Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 196528 |
| ensemblid | ENSG00000189079.18 |
| hgncid | 18037 |
| symbol | ARID2 |
| name | AT-rich interaction domain 2 |
| refseq_nuc | NM_152641.4 |
| refseq_prot | NP_689854.2 |
| ensembl_nuc | ENST00000334344.11 |
| ensembl_prot | ENSP00000335044.6 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 45729706 |
| end | 45908037 |
| strand | + |
| ver | v1.2 |
| region | chr12:45729706-45908037 |
| region5000 | chr12:45724706-45913037 |
| regionname0 | ARID2_chr12_45729706_45908037 |
| regionname5000 | ARID2_chr12_45724706_45913037 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1835 | 285 | 67 | 63 | 103 | 12 | 38 | 74 | ARID2_chr12_45724706_45913037 | ARID2 | MANST others(1830): Show |
chr12 | 45724706 | 45913037 |
| a0002 | 0/0 | 1835 | 13 | 0 | 0 | 13 | 0 | 0 | 9 | ARID2_chr12_45724706_45913037 | ARID2 | MANST others(1830): Show |
chr12 | 45724706 | 45913037 |
| a0003 | 0/0 | 1835 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | MANST others(1830): Show |
chr12 | 45724706 | 45913037 |
| a0004 | 0/0 | 1835 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | ARID2_chr12_45724706_45913037 | ARID2 | MANST others(1830): Show |
chr12 | 45724706 | 45913037 |
| a0005 | 0/0 | 1835 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | MANST others(1830): Show |
chr12 | 45724706 | 45913037 |
| a0006 | 0/0 | 1835 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARID2_chr12_45724706_45913037 | ARID2 | MANST others(1830): Show |
chr12 | 45724706 | 45913037 |
| a0007 | 0/0 | 1835 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | MANST others(1830): Show |
chr12 | 45724706 | 45913037 |
| a0008 | 0/0 | 1835 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | MANST others(1830): Show |
chr12 | 45724706 | 45913037 |
| a0009 | 0/0 | 1835 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | MANST others(1830): Show |
chr12 | 45724706 | 45913037 |
| a0010 | 0/0 | 1835 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | MANST others(1830): Show |
chr12 | 45724706 | 45913037 |
| a0011 | 0/0 | 1835 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | MANST others(1830): Show |
chr12 | 45724706 | 45913037 |
| a0012 | 0/0 | 1835 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | MANST others(1830): Show |
chr12 | 45724706 | 45913037 |
| a0013 | 0/0 | 1835 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | MANST others(1830): Show |
chr12 | 45724706 | 45913037 |
| a0014 | 0/0 | 1835 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | MANST others(1830): Show |
chr12 | 45724706 | 45913037 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 5505 | 258 | 41 | 62 | 103 | 12 | 38 | ARID2_chr12_45724706_45913037 | ARID2 | ATGGC others(5500): Show |
chr12 | 45724706 | 45913037 | ||
| a0001c0002 | 0/0 | 5505 | 20 | 19 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | ATGGC others(5500): Show |
chr12 | 45724706 | 45913037 | ||
| a0001c0006 | 0/0 | 5505 | 3 | 3 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | ATGGC others(5500): Show |
chr12 | 45724706 | 45913037 | ||
| a0001c0009 | 0/0 | 5505 | 2 | 2 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | ATGGC others(5500): Show |
chr12 | 45724706 | 45913037 | ||
| a0001c0011 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | ATGGC others(5500): Show |
chr12 | 45724706 | 45913037 | ||
| a0001c0016 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | ATGGC others(5500): Show |
chr12 | 45724706 | 45913037 | ||
| a0002c0003 | 0/0 | 5505 | 12 | 0 | 0 | 12 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | ATGGC others(5500): Show |
chr12 | 45724706 | 45913037 | ||
| a0002c0020 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | ATGGC others(5500): Show |
chr12 | 45724706 | 45913037 | ||
| a0003c0004 | 0/0 | 5505 | 5 | 5 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | ATGGC others(5500): Show |
chr12 | 45724706 | 45913037 | ||
| a0004c0005 | 0/0 | 5505 | 3 | 0 | 0 | 3 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | ATGGC others(5500): Show |
chr12 | 45724706 | 45913037 | ||
| a0005c0008 | 0/0 | 5505 | 2 | 0 | 0 | 2 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | ATGGC others(5500): Show |
chr12 | 45724706 | 45913037 | ||
| a0006c0007 | 0/0 | 5505 | 2 | 0 | 0 | 2 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | ATGGC others(5500): Show |
chr12 | 45724706 | 45913037 | ||
| a0007c0019 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | ATGGC others(5500): Show |
chr12 | 45724706 | 45913037 | ||
| a0008c0013 | 0/0 | 5505 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | ATGGC others(5500): Show |
chr12 | 45724706 | 45913037 | ||
| a0009c0017 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | ATGGC others(5500): Show |
chr12 | 45724706 | 45913037 | ||
| a0010c0014 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | ATGGC others(5500): Show |
chr12 | 45724706 | 45913037 | ||
| a0011c0010 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | ATGGC others(5500): Show |
chr12 | 45724706 | 45913037 | ||
| a0012c0012 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | ATGGC others(5500): Show |
chr12 | 45724706 | 45913037 | ||
| a0013c0015 | 0/0 | 5505 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | ATGGC others(5500): Show |
chr12 | 45724706 | 45913037 | ||
| a0014c0018 | 0/0 | 5505 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | ATGGC others(5500): Show |
chr12 | 45724706 | 45913037 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 8598 | 227 | 26 | 58 | 100 | 12 | 29 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0001c0001t0003 | 0/0 | 8598 | 6 | 0 | 0 | 0 | 0 | 6 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0001c0001t0004 | 0/0 | 8599 | 5 | 5 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8594): Show |
chr12 | 45724706 | 45913037 |
| a0001c0001t0005 | 0/0 | 8598 | 4 | 4 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0001c0001t0007 | 0/0 | 8598 | 3 | 1 | 2 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0001c0001t0008 | 0/0 | 8598 | 3 | 3 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0001c0001t0009 | 0/0 | 8598 | 2 | 0 | 0 | 2 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0001c0001t0011 | 0/0 | 8598 | 2 | 0 | 1 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0001c0001t0012 | 0/0 | 8598 | 2 | 0 | 1 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0001c0001t0013 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0001c0001t0014 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0001c0001t0015 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0001c0001t0016 | 0/0 | 8598 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0001c0002t0002 | 0/0 | 8598 | 20 | 19 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0001c0006t0002 | 0/0 | 8598 | 3 | 3 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0001c0009t0010 | 0/0 | 8598 | 2 | 2 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0001c0011t0018 | 0/0 | 8586 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8581): Show |
chr12 | 45724706 | 45913037 |
| a0001c0016t0001 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0002c0003t0001 | 0/0 | 8598 | 12 | 0 | 0 | 12 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0002c0020t0001 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0003c0004t0006 | 0/0 | 8599 | 4 | 4 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8594): Show |
chr12 | 45724706 | 45913037 |
| a0003c0004t0017 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8594): Show |
chr12 | 45724706 | 45913037 |
| a0004c0005t0001 | 0/0 | 8598 | 3 | 0 | 0 | 3 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0005c0008t0001 | 0/0 | 8598 | 2 | 0 | 0 | 2 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0006c0007t0001 | 0/0 | 8598 | 2 | 0 | 0 | 2 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0007c0019t0001 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0008c0013t0001 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0009c0017t0001 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0010c0014t0007 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0011c0010t0002 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0012c0012t0001 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0013c0015t0001 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| a0014c0018t0001 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | GCCGG others(8593): Show |
chr12 | 45724706 | 45913037 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0029 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0200 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0007g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0007g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0007g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0008g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0008g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0009g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0009g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0011g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0011g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0012g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0012g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0013g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0014g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0015g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0016g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0006t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0006t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0006t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0009t0010g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0009t0010g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0011t0018g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0016t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0020t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0003c0004t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0003c0004t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0003c0004t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0003c0004t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0003c0004t0017g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0004c0005t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0004c0005t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0004c0005t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0005c0008t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0005c0008t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0006c0007t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0006c0007t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0007c0019t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0008c0013t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0009c0017t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0010c0014t0007g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0011c0010t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0012c0012t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0013c0015t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0014c0018t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0278 | EUR | GBR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | GBR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0276 | EUR | GBR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0069 | EUR | FIN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | FIN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00408 | hp2 | a0001 | c0001 | t0009 | g0179 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00597 | hp1 | a0007 | c0019 | t0001 | g0036 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00597 | hp2 | a0002 | c0003 | t0001 | g0307 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00673 | hp2 | a0002 | c0003 | t0001 | g0240 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00741 | hp1 | a0001 | c0001 | t0012 | g0251 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01167 | hp1 | a0001 | c0001 | t0007 | g0195 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01169 | hp2 | a0001 | c0001 | t0007 | g0267 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0256 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01358 | hp1 | a0001 | c0001 | t0011 | g0118 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01433 | hp1 | a0008 | c0013 | t0001 | g0238 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | IBS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01884 | hp1 | a0001 | c0011 | t0018 | g0271 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0311 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0286 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02135 | hp1 | a0005 | c0008 | t0001 | g0034 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02155 | hp1 | a0002 | c0003 | t0001 | g0246 | EAS | CDX | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CDX | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02165 | hp1 | a0002 | c0020 | t0001 | g0239 | EAS | CDX | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | CDX | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0219 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0285 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02280 | hp1 | a0009 | c0017 | t0001 | g0018 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0217 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02451 | hp1 | a0003 | c0004 | t0017 | g0205 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0211 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0133 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02622 | hp2 | a0001 | c0006 | t0002 | g0193 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0222 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0259 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0131 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02647 | hp2 | a0003 | c0004 | t0006 | g0107 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02698 | hp2 | a0001 | c0001 | t0011 | g0119 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02717 | hp1 | a0001 | c0009 | t0010 | g0208 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0314 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02809 | hp1 | a0001 | c0016 | t0001 | g0296 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0273 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02886 | hp1 | a0003 | c0004 | t0006 | g0105 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0213 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02895 | hp2 | a0001 | c0006 | t0002 | g0136 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0255 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0258 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02965 | hp1 | a0003 | c0004 | t0006 | g0106 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0210 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03098 | hp2 | a0003 | c0004 | t0006 | g0108 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03130 | hp1 | a0011 | c0010 | t0002 | g0206 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0288 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0221 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0215 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03209 | hp1 | a0001 | c0001 | t0015 | g0313 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0257 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0260 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0284 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0268 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0132 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03486 | hp1 | a0001 | c0001 | t0008 | g0128 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0261 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03516 | hp1 | a0001 | c0009 | t0010 | g0207 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0134 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0218 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03654 | hp2 | a0001 | c0001 | t0012 | g0252 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0282 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | BEB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03942 | hp1 | a0001 | c0001 | t0016 | g0116 | SAS | BEB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0283 | SAS | STU | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | BEB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | STU | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | STU | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0281 | SAS | STU | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18747 | hp1 | a0004 | c0005 | t0001 | g0111 | EAS | CHB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0253 | AFR | YRI | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0254 | AFR | YRI | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18940 | hp2 | a0012 | c0012 | t0001 | g0187 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18945 | hp1 | a0002 | c0003 | t0001 | g0236 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18956 | hp2 | a0004 | c0005 | t0001 | g0168 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18957 | hp2 | a0006 | c0007 | t0001 | g0020 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18962 | hp1 | a0002 | c0003 | t0001 | g0142 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18986 | hp2 | a0006 | c0007 | t0001 | g0051 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19001 | hp2 | a0005 | c0008 | t0001 | g0039 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19003 | hp2 | a0001 | c0001 | t0014 | g0175 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19011 | hp2 | a0002 | c0003 | t0001 | g0235 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19030 | hp1 | a0001 | c0006 | t0002 | g0194 | AFR | LWK | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | LWK | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19060 | hp2 | a0002 | c0003 | t0001 | g0243 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19062 | hp2 | a0002 | c0003 | t0001 | g0242 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19065 | hp1 | a0001 | c0001 | t0009 | g0109 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19070 | hp1 | a0002 | c0003 | t0001 | g0148 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19074 | hp2 | a0002 | c0003 | t0001 | g0237 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19077 | hp1 | a0004 | c0005 | t0001 | g0169 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19078 | hp1 | a0013 | c0015 | t0001 | g0295 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19088 | hp2 | a0002 | c0003 | t0001 | g0266 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19091 | hp1 | a0002 | c0003 | t0001 | g0310 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | TSI | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0130 | EUR | TSI | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0245 | EUR | TSI | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0280 | SAS | GIH | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | GIH | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0214 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0216 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02559 | hp1 | a0010 | c0014 | t0007 | g0269 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03471 | hp1 | a0001 | c0001 | t0013 | g0287 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0212 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0135 | AFR | USA | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | USA | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA20300 | hp1 | a0014 | c0018 | t0001 | g0262 | AFR | USA | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | USA | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0200 | REF | REF | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0029 | REF | REF | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:45836741 | A | G | 1 | a0007 | 1 | HG00597.hp1 | missense_variant&splice_region_variant | MODERATE | c.773A>G | p.Glu258Gly | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 8/21 | 904/8598 | 773/5508 | 258/1835 | chr12 | 45836741 | |||
| chr12:45839421 | C | T | 1 | a0014 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.1423C>T | p.His475Tyr | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/21 | 1554/8598 | 1423/5508 | 475/1835 | chr12 | 45839421 | |||
| chr12:45849582 | C | T | 1 | a0009 | 1 | HG02280.hp1 | missense_variant&splice_region_variant | MODERATE | c.1718C>T | p.Thr573Met | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 14/21 | 1849/8598 | 1718/5508 | 573/1835 | chr12 | 45849582 | |||
| chr12:45849623 | A | G | 1 | a0005 | 2 | HG02135.hp1 NA19001.hp2 |
missense_variant | MODERATE | c.1759A>G | p.Ser587Gly | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 14/21 | 1890/8598 | 1759/5508 | 587/1835 | chr12 | 45849623 | |||
| chr12:45850152 | G | A | 1 | a0006 | 2 | NA18957.hp2 NA18986.hp2 |
missense_variant | MODERATE | c.2029G>A | p.Val677Met | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 2160/8598 | 2029/5508 | 677/1835 | chr12 | 45850152 | |||
| chr12:45850551 | G | C | 1 | a0004 | 3 | NA18747.hp1 NA18956.hp2 NA19077.hp1 |
missense_variant | MODERATE | c.2428G>C | p.Ala810Pro | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 2559/8598 | 2428/5508 | 810/1835 | chr12 | 45850551 | |||
| chr12:45850887 | A | G | 1 | a0003 | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
missense_variant | MODERATE | c.2764A>G | p.Thr922Ala | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 2895/8598 | 2764/5508 | 922/1835 | chr12 | 45850887 | |||
| chr12:45850929 | G | T | 1 | a0013 | 1 | NA19078.hp1 | missense_variant | MODERATE | c.2806G>T | p.Gly936Cys | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 2937/8598 | 2806/5508 | 936/1835 | chr12 | 45850929 | |||
| chr12:45851868 | G | A | 1 | a0012 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.3745G>A | p.Glu1249Lys | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 3876/8598 | 3745/5508 | 1249/1835 | chr12 | 45851868 | |||
| chr12:45852423 | G | T | 1 | a0002 | 13 | HG00597.hp2 HG00673.hp2 HG02155.hp1 others(10): Show |
missense_variant | MODERATE | c.4300G>T | p.Ala1434Ser | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 4431/8598 | 4300/5508 | 1434/1835 | chr12 | 45852423 | |||
| chr12:45852465 | C | T | 1 | a0010 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.4342C>T | p.Leu1448Phe | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 4473/8598 | 4342/5508 | 1448/1835 | chr12 | 45852465 | |||
| chr12:45852615 | G | A | 1 | a0011 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.4492G>A | p.Ala1498Thr | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 4623/8598 | 4492/5508 | 1498/1835 | chr12 | 45852615 | |||
| chr12:45852847 | A | G | 1 | a0008 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.4724A>G | p.Gln1575Arg | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 4855/8598 | 4724/5508 | 1575/1835 | chr12 | 45852847 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:45730131 | C | T | 1 | a0002c0020 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.180C>T | p.Phe60Phe | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 2/21 | 311/8598 | 180/5508 | 60/1835 | chr12 | 45730131 | |||
| chr12:45811472 | A | C | 1 | a0001c0009 | 2 | HG02717.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.339A>C | p.Val113Val | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/21 | 470/8598 | 339/5508 | 113/1835 | chr12 | 45811472 | |||
| chr12:45850634 | A | T | 1 | a0001c0016 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.2511A>T | p.Ser837Ser | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 2642/8598 | 2511/5508 | 837/1835 | chr12 | 45850634 | |||
| chr12:45851294 | G | A | 3 | a0001c0002 a0001c0006 a0011c0010 |
24 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(21): Show |
synonymous_variant | LOW | c.3171G>A | p.Ser1057Ser | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 3302/8598 | 3171/5508 | 1057/1835 | chr12 | 45851294 | |||
| chr12:45851486 | G | A | 1 | a0001c0011 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.3363G>A | p.Leu1121Leu | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 3494/8598 | 3363/5508 | 1121/1835 | chr12 | 45851486 | |||
| chr12:45852311 | A | G | 1 | a0001c0006 | 3 | HG02622.hp2 HG02895.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.4188A>G | p.Gln1396Gln | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 4319/8598 | 4188/5508 | 1396/1835 | chr12 | 45852311 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:45729822 | T | A | 1 | a0001c0001t0013 | 1 | HG03471.hp1 | 5_prime_UTR_variant | MODIFIER | c.-15T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 1/21 | 15 | chr12 | 45729822 | ||||||
| chr12:45729823 | C | G | 1 | a0001c0001t0003 | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-14C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 1/21 | chr12 | 45729823 | |||||||
| chr12:45905383 | G | A | 1 | a0001c0001t0008 | 3 | HG02630.hp1 HG03195.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*305G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 305 | chr12 | 45905383 | ||||||
| chr12:45905466 | T | C | 1 | a0001c0001t0014 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*388T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 388 | chr12 | 45905466 | ||||||
| chr12:45905513 | G | A | 1 | a0001c0001t0009 | 2 | HG00408.hp2 NA19065.hp1 |
3_prime_UTR_variant | MODIFIER | c.*435G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 435 | chr12 | 45905513 | ||||||
| chr12:45905933 | CTTTTTTC others(5): Show |
C | 1 | a0001c0011t0018 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*874_*885delCTTTTT others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 874 | INFO_REALIGN_3_PRIME | chr12 | 45905933 | |||||
| chr12:45905940 | C | CT | 4 | a0001c0001t0001 a0001c0002t0002 a0010c0014t0007 others(1): Show |
23 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*873dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 874 | INFO_REALIGN_3_PRIME | chr12 | 45905940 | |||||
| chr12:45905952 | C | CT | 3 | a0001c0001t0004 a0003c0004t0006 a0003c0004t0017 |
10 | HG02451.hp1 HG02615.hp1 HG02647.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*885dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 886 | INFO_REALIGN_3_PRIME | chr12 | 45905952 | |||||
| chr12:45905952 | C | T | 2 | a0001c0001t0007 a0010c0014t0007 |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*874C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 874 | chr12 | 45905952 | ||||||
| chr12:45906057 | T | A | 1 | a0001c0009t0010 | 2 | HG02717.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*979T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 979 | chr12 | 45906057 | ||||||
| chr12:45906102 | G | A | 2 | a0003c0004t0006 a0003c0004t0017 |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1024G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 1024 | chr12 | 45906102 | ||||||
| chr12:45906317 | C | T | 1 | a0001c0001t0012 | 2 | HG00741.hp1 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1239C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 1239 | chr12 | 45906317 | ||||||
| chr12:45906324 | A | T | 2 | a0001c0001t0005 a0001c0001t0013 |
5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1246A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 1246 | chr12 | 45906324 | ||||||
| chr12:45906855 | T | G | 2 | a0003c0004t0006 a0003c0004t0017 |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1777T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 1777 | chr12 | 45906855 | ||||||
| chr12:45907096 | T | C | 1 | a0003c0004t0017 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2018T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 2018 | chr12 | 45907096 | ||||||
| chr12:45907285 | T | C | 1 | a0001c0001t0015 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2207T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 2207 | chr12 | 45907285 | ||||||
| chr12:45907298 | G | A | 4 | a0001c0001t0004 a0001c0002t0002 a0001c0006t0002 others(1): Show |
29 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2220G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 2220 | chr12 | 45907298 | ||||||
| chr12:45907420 | T | C | 1 | a0001c0001t0016 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2342T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 2342 | chr12 | 45907420 | ||||||
| chr12:45907877 | C | T | 1 | a0001c0001t0011 | 2 | HG01358.hp1 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2799C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 2799 | chr12 | 45907877 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:45730556 | A | T | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.186+419A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 2/20 | chr12 | 45730556 | |||||||
| chr12:45730612 | G | T | 1 | a0001c0001t0001g0315 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.186+475G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 2/20 | chr12 | 45730612 | |||||||
| chr12:45730630 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0110 a0001c0001t0001g0112 others(210): Show |
214 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.186+493A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 2/20 | chr12 | 45730630 | |||||||
| chr12:45730818 | G | GC | 29 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(26): Show |
29 | HG00438.hp1 HG00597.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.187-389dupC | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 45730818 | ||||||
| chr12:45730824 | C | A | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.187-393C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 2/20 | chr12 | 45730824 | |||||||
| chr12:45730873 | C | CT | 12 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0096 others(9): Show |
12 | HG00438.hp2 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.187-322dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 45730873 | ||||||
| chr12:45730873 | CT | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(107): Show |
111 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.187-322delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 45730873 | ||||||
| chr12:45731076 | T | A | 1 | a0003c0004t0017g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.187-141T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 2/20 | chr12 | 45731076 | |||||||
| chr12:45731077 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.187-140A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 2/20 | chr12 | 45731077 | |||||||
| chr12:45731346 | G | T | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+32G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45731346 | |||||||
| chr12:45731465 | G | A | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+151G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45731465 | |||||||
| chr12:45731809 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.284+495A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45731809 | |||||||
| chr12:45731859 | T | G | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+545T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45731859 | |||||||
| chr12:45732070 | C | A | 1 | a0011c0010t0002g0206 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.284+756C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45732070 | |||||||
| chr12:45732071 | G | C | 1 | a0001c0001t0001g0304 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.284+757G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45732071 | |||||||
| chr12:45732071 | G | GT | 11 | a0001c0001t0001g0092 a0001c0001t0001g0203 a0001c0001t0001g0204 others(8): Show |
11 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.284+768dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45732071 | ||||||
| chr12:45732239 | G | T | 10 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(7): Show |
10 | HG02647.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.284+925G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45732239 | |||||||
| chr12:45732383 | C | G | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+1069C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45732383 | |||||||
| chr12:45732734 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.284+1420A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45732734 | |||||||
| chr12:45732794 | A | C | 1 | a0001c0001t0001g0274 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.284+1480A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45732794 | |||||||
| chr12:45733320 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.284+2006G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45733320 | |||||||
| chr12:45733462 | C | T | 1 | a0001c0001t0015g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.284+2148C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45733462 | |||||||
| chr12:45733816 | G | A | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+2502G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45733816 | |||||||
| chr12:45733877 | C | T | 1 | a0001c0001t0005g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.284+2563C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45733877 | |||||||
| chr12:45733927 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.284+2613T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45733927 | |||||||
| chr12:45734016 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284+2702A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45734016 | |||||||
| chr12:45734131 | G | A | 1 | a0001c0001t0009g0109 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.284+2817G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45734131 | |||||||
| chr12:45734310 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.284+2996A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45734310 | |||||||
| chr12:45734340 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284+3026G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45734340 | |||||||
| chr12:45734350 | C | T | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.284+3036C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45734350 | |||||||
| chr12:45734384 | A | T | 3 | a0001c0001t0001g0272 a0001c0001t0001g0292 a0001c0011t0018g0271 |
3 | HG01884.hp1 HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.284+3070A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45734384 | |||||||
| chr12:45734593 | T | C | 1 | a0004c0005t0001g0111 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.284+3279T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45734593 | |||||||
| chr12:45735038 | A | G | 1 | a0001c0001t0015g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.284+3724A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45735038 | |||||||
| chr12:45735400 | T | C | 3 | a0001c0001t0001g0209 a0001c0009t0010g0207 a0001c0009t0010g0208 |
3 | HG02717.hp1 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.284+4086T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45735400 | |||||||
| chr12:45735417 | TCGTGTGT others(1): Show |
T | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+4104_284+4111d others(10): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45735417 | |||||||
| chr12:45735418 | C | CGT | 81 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0055 others(78): Show |
81 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.284+4145_284+4146d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45735418 | ||||||
| chr12:45735418 | C | CGTGT | 54 | a0001c0001t0001g0001 a0001c0001t0001g0044 a0001c0001t0001g0050 others(51): Show |
55 | HG00438.hp1 HG00639.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.284+4143_284+4146d others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45735418 | ||||||
| chr12:45735418 | C | CGTGTGT | 16 | a0001c0001t0001g0147 a0001c0001t0001g0153 a0001c0001t0001g0158 others(13): Show |
16 | HG00408.hp2 HG01358.hp1 HG02148.hp1 others(13): Show |
intron_variant | MODIFIER | c.284+4141_284+4146d others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45735418 | ||||||
| chr12:45735418 | C | CGTGTGTG others(1): Show |
9 | a0001c0001t0001g0145 a0001c0001t0001g0162 a0001c0001t0001g0265 others(6): Show |
9 | HG02615.hp1 HG02647.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.284+4139_284+4146d others(10): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45735418 | ||||||
| chr12:45735418 | CGT | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(47): Show |
50 | HG00140.hp2 HG00408.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.284+4145_284+4146d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45735418 | ||||||
| chr12:45735418 | CGTGT | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0068 a0006c0007t0001g0020 others(1): Show |
4 | NA18612.hp2 NA18957.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.284+4143_284+4146d others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45735418 | ||||||
| chr12:45735418 | CGTGTGT | C | 7 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0019 others(4): Show |
7 | HG00544.hp1 HG02132.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.284+4141_284+4146d others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45735418 | ||||||
| chr12:45735418 | CGTGTGTG others(1): Show |
C | 4 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+4139_284+4146d others(10): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45735418 | ||||||
| chr12:45735418 | CGTGTGTG others(3): Show |
C | 1 | a0002c0003t0001g0243 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.284+4137_284+4146d others(12): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45735418 | ||||||
| chr12:45735418 | CGTGTGTG others(17): Show |
C | 1 | a0001c0001t0001g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.284+4123_284+4146d others(26): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45735418 | ||||||
| chr12:45735487 | T | C | 1 | a0001c0001t0001g0005 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.284+4173T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45735487 | |||||||
| chr12:45735524 | G | T | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+4210G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45735524 | |||||||
| chr12:45735677 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.284+4363C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45735677 | |||||||
| chr12:45735771 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.284+4457C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45735771 | |||||||
| chr12:45736123 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.284+4809C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45736123 | |||||||
| chr12:45736172 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.284+4858A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45736172 | |||||||
| chr12:45736214 | A | G | 10 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(7): Show |
10 | HG02647.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.284+4900A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45736214 | |||||||
| chr12:45736351 | C | T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.284+5037C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45736351 | |||||||
| chr12:45736356 | G | GA | 6 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0003c0004t0006g0105 others(3): Show |
7 | HG02293.hp1 HG02647.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.284+5057dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45736356 | ||||||
| chr12:45736572 | A | G | 10 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(7): Show |
10 | HG02647.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.284+5258A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45736572 | |||||||
| chr12:45736602 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(1): Show |
4 | HG00408.hp1 HG00544.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+5288G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45736602 | |||||||
| chr12:45736843 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.284+5529G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45736843 | |||||||
| chr12:45737094 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0312 |
2 | NA18966.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.284+5780A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45737094 | |||||||
| chr12:45737251 | C | T | 14 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(11): Show |
14 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.284+5937C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45737251 | |||||||
| chr12:45737357 | C | T | 1 | a0002c0003t0001g0266 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.284+6043C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45737357 | |||||||
| chr12:45737633 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.284+6319A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45737633 | |||||||
| chr12:45737851 | A | C | 2 | a0001c0006t0002g0193 a0001c0006t0002g0194 |
2 | HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.284+6537A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45737851 | |||||||
| chr12:45737902 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.284+6588T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45737902 | |||||||
| chr12:45737904 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.284+6590T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45737904 | |||||||
| chr12:45738281 | T | C | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+6967T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45738281 | |||||||
| chr12:45738391 | T | A | 10 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(7): Show |
10 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.284+7077T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45738391 | |||||||
| chr12:45738725 | G | T | 4 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+7411G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45738725 | |||||||
| chr12:45738779 | C | CT | 28 | a0001c0001t0001g0004 a0001c0001t0001g0065 a0001c0001t0001g0066 others(25): Show |
28 | HG00280.hp1 HG01175.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.284+7499dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | ||||||
| chr12:45738779 | C | CTT | 20 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(17): Show |
20 | HG00621.hp1 HG00621.hp2 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.284+7498_284+7499d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | ||||||
| chr12:45738779 | C | CTTTT | 13 | a0001c0001t0001g0001 a0001c0001t0001g0083 a0001c0001t0001g0110 others(10): Show |
14 | HG01071.hp1 HG01109.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.284+7496_284+7499d others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | ||||||
| chr12:45738779 | C | CTTTTT | 45 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 others(42): Show |
45 | HG00609.hp2 HG01168.hp1 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.284+7495_284+7499d others(7): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | ||||||
| chr12:45738779 | C | CTTTTTT | 26 | a0001c0001t0001g0089 a0001c0001t0001g0176 a0001c0001t0001g0177 others(23): Show |
26 | HG00408.hp2 HG00673.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.284+7494_284+7499d others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | ||||||
| chr12:45738779 | C | CTTTTTTT others(1): Show |
6 | a0001c0001t0001g0192 a0001c0001t0001g0209 a0001c0001t0003g0281 others(3): Show |
6 | HG02738.hp2 HG03704.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.284+7492_284+7499d others(10): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | ||||||
| chr12:45738779 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0303 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.284+7489_284+7499d others(13): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | ||||||
| chr12:45738779 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0003g0284 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.284+7486_284+7499d others(16): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | ||||||
| chr12:45738779 | CT | C | 21 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(18): Show |
21 | HG00140.hp2 HG00408.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.284+7499delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | ||||||
| chr12:45738779 | CTT | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0316 a0001c0001t0005g0286 others(4): Show |
7 | HG01257.hp1 HG01891.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.284+7498_284+7499d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | ||||||
| chr12:45738779 | CTTTTTTT others(2): Show |
C | 43 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(40): Show |
43 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.284+7491_284+7499d others(11): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | ||||||
| chr12:45738779 | CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0001g0225 a0001c0001t0007g0267 a0001c0001t0007g0268 |
3 | HG01074.hp1 HG01169.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.284+7490_284+7499d others(12): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | ||||||
| chr12:45738779 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0007g0195 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.284+7489_284+7499d others(13): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | ||||||
| chr12:45738779 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0010 a0001c0011t0018g0271 |
2 | HG01884.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.284+7488_284+7499d others(14): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | ||||||
| chr12:45738779 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0137 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.284+7484_284+7499d others(18): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | ||||||
| chr12:45738779 | CTTTTTTT others(10): Show |
C | 31 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0120 others(28): Show |
31 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.284+7483_284+7499d others(19): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | ||||||
| chr12:45738779 | CTTTTTTT others(11): Show |
C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0199 |
2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.284+7482_284+7499d others(20): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | ||||||
| chr12:45738952 | T | C | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.284+7638T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45738952 | |||||||
| chr12:45739019 | A | G | 1 | a0001c0001t0001g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.284+7705A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45739019 | |||||||
| chr12:45739143 | G | GT | 8 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0149 others(5): Show |
8 | HG01167.hp2 HG02602.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284+7836dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45739143 | ||||||
| chr12:45739322 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.284+8008A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45739322 | |||||||
| chr12:45739355 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.284+8041A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45739355 | |||||||
| chr12:45739383 | G | C | 1 | a0001c0001t0001g0028 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.284+8069G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45739383 | |||||||
| chr12:45739401 | T | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0084 a0001c0001t0001g0089 others(107): Show |
111 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.284+8087T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45739401 | |||||||
| chr12:45739438 | C | CT | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
202 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.284+8148dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45739438 | ||||||
| chr12:45739438 | C | CTT | 83 | a0001c0001t0001g0007 a0001c0001t0001g0063 a0001c0001t0001g0076 others(80): Show |
83 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.284+8147_284+8148d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45739438 | ||||||
| chr12:45739438 | C | CTTT | 10 | a0001c0001t0001g0245 a0001c0001t0001g0247 a0001c0001t0001g0278 others(7): Show |
10 | HG00099.hp1 HG01257.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.284+8146_284+8148d others(5): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45739438 | ||||||
| chr12:45739470 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284+8156C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45739470 | |||||||
| chr12:45739663 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+8349G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45739663 | |||||||
| chr12:45739737 | T | A | 1 | a0011c0010t0002g0206 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.284+8423T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45739737 | |||||||
| chr12:45740371 | T | C | 2 | a0001c0001t0001g0270 a0001c0001t0001g0291 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.284+9057T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45740371 | |||||||
| chr12:45740517 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0102 |
2 | HG00621.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.284+9203G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45740517 | |||||||
| chr12:45740595 | A | T | 5 | a0001c0001t0005g0273 a0001c0001t0005g0285 a0001c0001t0005g0286 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.284+9281A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45740595 | |||||||
| chr12:45740692 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0084 a0001c0001t0001g0089 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.284+9378T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45740692 | |||||||
| chr12:45740799 | G | C | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+9485G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45740799 | |||||||
| chr12:45740850 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0065 |
2 | HG02083.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.284+9536T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45740850 | |||||||
| chr12:45740909 | G | T | 1 | a0001c0001t0001g0062 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.284+9595G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45740909 | |||||||
| chr12:45741002 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0204 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.284+9688C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45741002 | |||||||
| chr12:45741029 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0084 a0001c0001t0001g0089 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.284+9715T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45741029 | |||||||
| chr12:45741184 | A | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
4 | NA18950.hp1 NA18980.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+9870A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45741184 | |||||||
| chr12:45741342 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.284+10028C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45741342 | |||||||
| chr12:45741384 | G | C | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+10070G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45741384 | |||||||
| chr12:45741591 | ATT | A | 47 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(44): Show |
47 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.284+10278_284+1027 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45741591 | |||||||
| chr12:45742360 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.284+11046G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45742360 | |||||||
| chr12:45742379 | G | A | 2 | a0001c0009t0010g0207 a0001c0009t0010g0208 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.284+11065G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45742379 | |||||||
| chr12:45742498 | A | G | 3 | a0001c0001t0001g0270 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.284+11184A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45742498 | |||||||
| chr12:45742570 | A | T | 1 | a0001c0001t0001g0190 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.284+11256A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45742570 | |||||||
| chr12:45742853 | C | T | 47 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(44): Show |
47 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.284+11539C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45742853 | |||||||
| chr12:45742999 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284+11685A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45742999 | |||||||
| chr12:45743026 | T | C | 2 | a0001c0009t0010g0207 a0001c0009t0010g0208 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.284+11712T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45743026 | |||||||
| chr12:45743045 | T | G | 1 | a0001c0001t0016g0116 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.284+11731T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45743045 | |||||||
| chr12:45743197 | T | TA | 9 | a0001c0001t0001g0220 a0001c0001t0001g0249 a0001c0001t0001g0263 others(6): Show |
9 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.284+11895dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45743197 | ||||||
| chr12:45743262 | G | A | 3 | a0001c0002t0002g0253 a0001c0002t0002g0258 a0001c0002t0002g0311 |
3 | HG01884.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.284+11948G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45743262 | |||||||
| chr12:45743450 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.284+12136C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45743450 | |||||||
| chr12:45743538 | T | C | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+12224T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45743538 | |||||||
| chr12:45744490 | T | G | 1 | a0001c0001t0001g0117 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.284+13176T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45744490 | |||||||
| chr12:45744561 | T | C | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+13247T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45744561 | |||||||
| chr12:45744622 | C | T | 1 | a0003c0004t0017g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.284+13308C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45744622 | |||||||
| chr12:45744811 | A | G | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+13497A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45744811 | |||||||
| chr12:45744853 | G | A | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+13539G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45744853 | |||||||
| chr12:45744941 | T | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0084 a0001c0001t0001g0089 others(103): Show |
107 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.284+13627T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45744941 | |||||||
| chr12:45744944 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.284+13630C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45744944 | |||||||
| chr12:45745482 | T | A | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.284+14168T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45745482 | |||||||
| chr12:45745582 | A | G | 3 | a0001c0001t0001g0201 a0001c0001t0001g0249 a0001c0001t0001g0263 |
3 | HG01109.hp2 HG02129.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.284+14268A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45745582 | |||||||
| chr12:45745612 | A | G | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+14298A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45745612 | |||||||
| chr12:45745672 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284+14358T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45745672 | |||||||
| chr12:45745715 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284+14401T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45745715 | |||||||
| chr12:45745763 | G | A | 5 | a0001c0002t0002g0254 a0001c0002t0002g0255 a0001c0002t0002g0259 others(2): Show |
5 | HG02630.hp2 HG02922.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.284+14449G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45745763 | |||||||
| chr12:45745807 | C | T | 1 | a0001c0001t0008g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.284+14493C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45745807 | |||||||
| chr12:45746100 | A | AT | 52 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0112 others(49): Show |
52 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.284+14801dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45746100 | ||||||
| chr12:45746100 | A | ATTTTTTT others(2): Show |
8 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(5): Show |
8 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.284+14793_284+1480 others(13): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45746100 | ||||||
| chr12:45746100 | A | ATTTTTTT others(3): Show |
2 | a0001c0001t0003g0283 a0001c0001t0003g0314 |
2 | HG02738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.284+14792_284+1480 others(14): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45746100 | ||||||
| chr12:45746214 | GATC | G | 29 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(26): Show |
29 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.284+14901_284+1490 others(7): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746214 | |||||||
| chr12:45746338 | T | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.284+15024T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746338 | |||||||
| chr12:45746377 | T | C | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+15063T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746377 | |||||||
| chr12:45746481 | A | G | 1 | a0013c0015t0001g0295 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.284+15167A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746481 | |||||||
| chr12:45746491 | G | GT | 40 | a0001c0001t0001g0292 a0001c0001t0003g0280 a0001c0001t0003g0281 others(37): Show |
40 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.284+15187dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45746491 | ||||||
| chr12:45746632 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.284+15318C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746632 | |||||||
| chr12:45746720 | A | G | 1 | a0001c0006t0002g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.284+15406A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746720 | |||||||
| chr12:45746738 | C | G | 45 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(42): Show |
45 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.284+15424C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746738 | |||||||
| chr12:45746789 | C | T | 9 | a0001c0001t0001g0226 a0001c0001t0001g0249 a0001c0001t0001g0263 others(6): Show |
9 | HG01109.hp2 HG01346.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.284+15475C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746789 | |||||||
| chr12:45746853 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.284+15539G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746853 | |||||||
| chr12:45746859 | C | T | 4 | a0001c0001t0001g0115 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG01099.hp2 HG01175.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.284+15545C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746859 | |||||||
| chr12:45746891 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0061 |
2 | HG04199.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.284+15577C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746891 | |||||||
| chr12:45746907 | C | A | 1 | a0001c0001t0005g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.284+15593C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746907 | |||||||
| chr12:45746930 | C | T | 1 | a0001c0001t0001g0005 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.284+15616C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746930 | |||||||
| chr12:45746969 | C | T | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+15655C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746969 | |||||||
| chr12:45746990 | C | T | 2 | a0001c0001t0003g0282 a0001c0001t0003g0314 |
2 | HG02738.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.284+15676C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746990 | |||||||
| chr12:45747003 | T | C | 3 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 |
3 | HG01167.hp1 HG01169.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.284+15689T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45747003 | |||||||
| chr12:45747011 | C | T | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+15697C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45747011 | |||||||
| chr12:45747209 | AT | A | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+15897delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45747209 | ||||||
| chr12:45747512 | A | G | 2 | a0001c0001t0001g0247 a0001c0001t0001g0278 |
2 | HG00099.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.284+16198A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45747512 | |||||||
| chr12:45747557 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.284+16243C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45747557 | |||||||
| chr12:45747589 | C | T | 44 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0021 others(41): Show |
44 | HG00099.hp2 HG00609.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.284+16275C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45747589 | |||||||
| chr12:45747759 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0312 |
2 | NA18966.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.284+16445A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45747759 | |||||||
| chr12:45747791 | A | G | 1 | a0001c0002t0002g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.284+16477A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45747791 | |||||||
| chr12:45747943 | C | G | 4 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+16629C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45747943 | |||||||
| chr12:45748116 | A | G | 1 | a0001c0001t0015g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.284+16802A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748116 | |||||||
| chr12:45748120 | T | G | 1 | a0001c0002t0002g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.284+16806T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748120 | |||||||
| chr12:45748344 | T | G | 45 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(42): Show |
45 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.284+17030T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748344 | |||||||
| chr12:45748352 | C | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0094 |
2 | NA18977.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.284+17038C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748352 | |||||||
| chr12:45748536 | A | AG | 47 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(44): Show |
47 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.284+17223dupG | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45748536 | ||||||
| chr12:45748572 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.284+17258A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748572 | |||||||
| chr12:45748607 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.284+17293C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748607 | |||||||
| chr12:45748681 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.284+17367C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748681 | |||||||
| chr12:45748715 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.284+17401T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748715 | |||||||
| chr12:45748844 | T | C | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+17530T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748844 | |||||||
| chr12:45748855 | G | C | 1 | a0001c0001t0001g0104 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.284+17541G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748855 | |||||||
| chr12:45748888 | A | C | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284+17574A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748888 | |||||||
| chr12:45748888 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.284+17574A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748888 | |||||||
| chr12:45749141 | T | C | 3 | a0001c0001t0001g0199 a0001c0001t0011g0118 a0001c0001t0011g0119 |
3 | HG01358.hp1 HG02698.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.284+17827T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45749141 | |||||||
| chr12:45749412 | TACAG | T | 3 | a0004c0005t0001g0111 a0004c0005t0001g0168 a0004c0005t0001g0169 |
3 | NA18747.hp1 NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.284+18104_284+1810 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45749412 | ||||||
| chr12:45749470 | T | C | 1 | a0001c0001t0001g0046 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.284+18156T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45749470 | |||||||
| chr12:45749541 | A | C | 1 | a0001c0001t0001g0091 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.284+18227A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45749541 | |||||||
| chr12:45749661 | A | G | 4 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+18347A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45749661 | |||||||
| chr12:45749778 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.284+18464C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45749778 | |||||||
| chr12:45750045 | T | C | 3 | a0004c0005t0001g0111 a0004c0005t0001g0168 a0004c0005t0001g0169 |
3 | NA18747.hp1 NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.284+18731T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45750045 | |||||||
| chr12:45750202 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.284+18888G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45750202 | |||||||
| chr12:45750480 | T | A | 1 | a0001c0001t0001g0010 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.284+19166T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45750480 | |||||||
| chr12:45750500 | C | T | 4 | a0001c0001t0001g0270 a0001c0001t0001g0290 a0001c0001t0001g0291 others(1): Show |
4 | HG02615.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.284+19186C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45750500 | |||||||
| chr12:45750534 | A | G | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+19220A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45750534 | |||||||
| chr12:45751044 | A | G | 2 | a0001c0001t0001g0002 a0001c0001t0001g0013 |
2 | HG00140.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.284+19730A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45751044 | |||||||
| chr12:45751072 | C | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0110 others(158): Show |
162 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.284+19758C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45751072 | |||||||
| chr12:45751429 | A | G | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(307): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.284+20115A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45751429 | |||||||
| chr12:45751629 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.284+20315C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45751629 | |||||||
| chr12:45751683 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.284+20369T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45751683 | |||||||
| chr12:45751820 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284+20506G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45751820 | |||||||
| chr12:45751938 | G | A | 3 | a0001c0001t0001g0227 a0001c0001t0001g0245 a0001c0001t0001g0306 |
3 | HG01168.hp2 HG02683.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.284+20624G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45751938 | |||||||
| chr12:45752153 | A | G | 3 | a0001c0001t0001g0249 a0001c0001t0001g0263 a0014c0018t0001g0262 |
3 | HG01109.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.284+20839A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45752153 | |||||||
| chr12:45752394 | A | G | 1 | a0001c0001t0015g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.284+21080A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45752394 | |||||||
| chr12:45752683 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0065 |
2 | HG02083.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.284+21369G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45752683 | |||||||
| chr12:45752776 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.284+21462G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45752776 | |||||||
| chr12:45753131 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0091 a0009c0017t0001g0018 |
3 | HG02280.hp1 HG03490.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.284+21817C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45753131 | |||||||
| chr12:45753268 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.284+21954C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45753268 | |||||||
| chr12:45753340 | G | A | 1 | a0001c0001t0005g0285 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.284+22026G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45753340 | |||||||
| chr12:45753594 | T | A | 1 | a0001c0001t0001g0220 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.284+22280T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45753594 | |||||||
| chr12:45753666 | G | A | 1 | a0014c0018t0001g0262 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.284+22352G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45753666 | |||||||
| chr12:45753963 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.284+22649C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45753963 | |||||||
| chr12:45754183 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.284+22869T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45754183 | |||||||
| chr12:45754241 | T | C | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.284+22927T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45754241 | |||||||
| chr12:45754333 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.284+23019A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45754333 | |||||||
| chr12:45754398 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.284+23084G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45754398 | |||||||
| chr12:45754408 | T | G | 1 | a0005c0008t0001g0034 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.284+23094T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45754408 | |||||||
| chr12:45754469 | A | G | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.284+23155A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45754469 | |||||||
| chr12:45754536 | T | C | 10 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(7): Show |
10 | HG02647.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.284+23222T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45754536 | |||||||
| chr12:45754637 | C | G | 2 | a0001c0009t0010g0207 a0001c0009t0010g0208 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.284+23323C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45754637 | |||||||
| chr12:45755175 | A | G | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+23861A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45755175 | |||||||
| chr12:45755233 | T | G | 1 | a0001c0002t0002g0254 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.284+23919T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45755233 | |||||||
| chr12:45755386 | G | T | 1 | a0001c0001t0001g0002 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.284+24072G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45755386 | |||||||
| chr12:45755485 | A | G | 3 | a0001c0001t0001g0270 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.284+24171A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45755485 | |||||||
| chr12:45755569 | T | C | 5 | a0001c0002t0002g0254 a0001c0002t0002g0255 a0001c0002t0002g0259 others(2): Show |
5 | HG02630.hp2 HG02922.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.284+24255T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45755569 | |||||||
| chr12:45755730 | T | G | 1 | a0001c0001t0001g0121 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.284+24416T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45755730 | |||||||
| chr12:45755760 | C | G | 29 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(26): Show |
29 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.284+24446C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45755760 | |||||||
| chr12:45755804 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.284+24490A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45755804 | |||||||
| chr12:45756235 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.284+24921C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45756235 | |||||||
| chr12:45756242 | C | A | 1 | a0001c0001t0001g0017 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.284+24928C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45756242 | |||||||
| chr12:45756375 | TG | T | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+25062delG | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45756375 | |||||||
| chr12:45756718 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.284+25404G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45756718 | |||||||
| chr12:45756803 | G | T | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+25489G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45756803 | |||||||
| chr12:45756813 | C | T | 1 | a0001c0006t0002g0193 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.284+25499C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45756813 | |||||||
| chr12:45757075 | T | G | 1 | a0001c0001t0014g0175 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.284+25761T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45757075 | |||||||
| chr12:45757342 | C | T | 39 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(36): Show |
39 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.284+26028C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45757342 | |||||||
| chr12:45757347 | T | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.284+26033T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45757347 | |||||||
| chr12:45757482 | A | G | 4 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+26168A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45757482 | |||||||
| chr12:45757552 | G | A | 4 | a0001c0001t0001g0147 a0001c0001t0001g0198 a0001c0001t0001g0297 others(1): Show |
4 | HG02602.hp2 HG04199.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.284+26238G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45757552 | |||||||
| chr12:45757564 | A | G | 1 | a0001c0001t0001g0007 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.284+26250A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45757564 | |||||||
| chr12:45757620 | A | G | 2 | a0001c0001t0001g0247 a0001c0001t0001g0278 |
2 | HG00099.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.284+26306A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45757620 | |||||||
| chr12:45757761 | C | G | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+26447C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45757761 | |||||||
| chr12:45757914 | C | T | 1 | a0001c0001t0004g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.284+26600C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45757914 | |||||||
| chr12:45758056 | C | T | 18 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0038 others(15): Show |
18 | HG00438.hp2 HG00621.hp1 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.284+26742C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45758056 | |||||||
| chr12:45758167 | TAGG | T | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+26854_284+2685 others(7): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45758167 | |||||||
| chr12:45758335 | A | G | 1 | a0014c0018t0001g0262 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.284+27021A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45758335 | |||||||
| chr12:45758513 | T | C | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+27199T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45758513 | |||||||
| chr12:45758548 | T | C | 1 | a0001c0001t0001g0202 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.284+27234T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45758548 | |||||||
| chr12:45758613 | C | T | 1 | a0003c0004t0006g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.284+27299C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45758613 | |||||||
| chr12:45758627 | A | G | 1 | a0001c0016t0001g0296 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.284+27313A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45758627 | |||||||
| chr12:45758960 | A | G | 44 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0001g0144 others(41): Show |
44 | HG00438.hp1 HG00738.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.284+27646A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45758960 | |||||||
| chr12:45758992 | A | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0102 others(1): Show |
4 | HG00597.hp1 HG00621.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+27678A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45758992 | |||||||
| chr12:45759132 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | NA19064.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.284+27818C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45759132 | |||||||
| chr12:45759150 | C | G | 2 | a0001c0001t0001g0082 a0001c0001t0001g0099 |
2 | HG00621.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.284+27836C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45759150 | |||||||
| chr12:45759845 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.284+28531C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45759845 | |||||||
| chr12:45759966 | A | G | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+28652A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45759966 | |||||||
| chr12:45760352 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.284+29038T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45760352 | |||||||
| chr12:45760392 | T | G | 2 | a0001c0001t0001g0249 a0001c0001t0001g0263 |
2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.284+29078T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45760392 | |||||||
| chr12:45760407 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.284+29093A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45760407 | |||||||
| chr12:45760487 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.284+29173G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45760487 | |||||||
| chr12:45760491 | G | A | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG00140.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.284+29177G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45760491 | |||||||
| chr12:45760493 | G | GT | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+29186dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45760493 | ||||||
| chr12:45760873 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.284+29559G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45760873 | |||||||
| chr12:45760896 | C | T | 1 | a0001c0001t0015g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.284+29582C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45760896 | |||||||
| chr12:45760925 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.284+29611G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45760925 | |||||||
| chr12:45761136 | AT | A | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+29823delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45761136 | |||||||
| chr12:45761199 | G | A | 1 | a0001c0002t0002g0311 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.284+29885G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45761199 | |||||||
| chr12:45761362 | T | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0047 a0001c0001t0001g0094 others(198): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.284+30048T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45761362 | |||||||
| chr12:45761724 | T | C | 10 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(7): Show |
10 | HG02647.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.284+30410T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45761724 | |||||||
| chr12:45761859 | C | A | 1 | a0001c0001t0001g0005 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.284+30545C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45761859 | |||||||
| chr12:45761887 | G | A | 2 | a0001c0009t0010g0207 a0001c0009t0010g0208 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.284+30573G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45761887 | |||||||
| chr12:45761994 | C | A | 2 | a0001c0009t0010g0207 a0001c0009t0010g0208 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.284+30680C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45761994 | |||||||
| chr12:45762011 | A | T | 1 | a0001c0001t0001g0203 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.284+30697A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45762011 | |||||||
| chr12:45762267 | A | C | 1 | a0001c0001t0001g0154 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.284+30953A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45762267 | |||||||
| chr12:45762476 | A | G | 5 | a0001c0001t0005g0273 a0001c0001t0005g0285 a0001c0001t0005g0286 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.284+31162A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45762476 | |||||||
| chr12:45762504 | T | C | 1 | a0013c0015t0001g0295 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.284+31190T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45762504 | |||||||
| chr12:45762852 | C | T | 1 | a0001c0001t0003g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.284+31538C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45762852 | |||||||
| chr12:45762875 | G | C | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+31561G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45762875 | |||||||
| chr12:45762918 | A | G | 29 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(26): Show |
29 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.284+31604A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45762918 | |||||||
| chr12:45763073 | A | G | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+31759A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763073 | |||||||
| chr12:45763109 | T | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.284+31795T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763109 | |||||||
| chr12:45763127 | A | G | 25 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(22): Show |
25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.284+31813A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763127 | |||||||
| chr12:45763353 | C | A | 1 | a0001c0001t0001g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.284+32039C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763353 | |||||||
| chr12:45763401 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.284+32087C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763401 | |||||||
| chr12:45763428 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.284+32114C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763428 | |||||||
| chr12:45763639 | C | CA | 6 | a0001c0001t0001g0005 a0001c0001t0001g0090 a0001c0001t0001g0098 others(3): Show |
6 | HG02135.hp1 HG02135.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+32338dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45763639 | ||||||
| chr12:45763652 | A | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0226 a0001c0001t0001g0305 |
3 | HG01346.hp1 HG02132.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.284+32338A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763652 | |||||||
| chr12:45763653 | T | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(141): Show |
145 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(142): Show |
intron_variant | MODIFIER | c.284+32339T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763653 | |||||||
| chr12:45763654 | T | A | 1 | a0001c0001t0001g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.284+32340T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763654 | |||||||
| chr12:45763660 | T | A | 6 | a0001c0001t0001g0071 a0001c0001t0001g0093 a0001c0001t0001g0096 others(3): Show |
6 | HG01346.hp1 HG02809.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+32346T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763660 | |||||||
| chr12:45763660 | TA | T | 10 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(7): Show |
10 | HG02647.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.284+32350delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45763660 | ||||||
| chr12:45763661 | A | T | 58 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0037 others(55): Show |
58 | HG00438.hp1 HG00673.hp2 HG01099.hp2 others(55): Show |
intron_variant | MODIFIER | c.284+32347A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763661 | |||||||
| chr12:45763699 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG00673.hp1 NA18944.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.284+32385C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763699 | |||||||
| chr12:45763729 | G | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
4 | NA18950.hp1 NA18980.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+32415G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763729 | |||||||
| chr12:45763784 | C | T | 1 | a0001c0001t0003g0280 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.284+32470C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763784 | |||||||
| chr12:45763840 | A | G | 3 | a0001c0001t0001g0270 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.284+32526A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763840 | |||||||
| chr12:45764125 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284+32811A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45764125 | |||||||
| chr12:45764612 | C | T | 39 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(36): Show |
39 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.284+33298C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45764612 | |||||||
| chr12:45764682 | C | T | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+33368C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45764682 | |||||||
| chr12:45764735 | A | G | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.284+33421A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45764735 | |||||||
| chr12:45765200 | GTTTTCTT others(4): Show |
G | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0075 |
3 | NA18947.hp1 NA18970.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.284+33897_284+3390 others(15): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45765200 | ||||||
| chr12:45765232 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284+33918A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45765232 | |||||||
| chr12:45765279 | C | T | 3 | a0001c0001t0008g0128 a0001c0001t0008g0221 a0001c0001t0008g0222 |
3 | HG02630.hp1 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.284+33965C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45765279 | |||||||
| chr12:45765348 | A | G | 29 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(26): Show |
29 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.284+34034A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45765348 | |||||||
| chr12:45765514 | G | GT | 17 | a0001c0001t0001g0028 a0001c0001t0001g0077 a0001c0001t0001g0121 others(14): Show |
17 | HG00621.hp2 HG00673.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.284+34215dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45765514 | ||||||
| chr12:45765811 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.284+34497A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45765811 | |||||||
| chr12:45765814 | G | A | 45 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(42): Show |
45 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.284+34500G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45765814 | |||||||
| chr12:45766093 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.284+34779A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766093 | |||||||
| chr12:45766123 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00408.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.284+34809G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766123 | |||||||
| chr12:45766164 | A | G | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+34850A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766164 | |||||||
| chr12:45766194 | G | C | 3 | a0001c0001t0001g0077 a0001c0001t0001g0102 a0007c0019t0001g0036 |
3 | HG00597.hp1 HG00621.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.284+34880G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766194 | |||||||
| chr12:45766376 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.284+35062C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766376 | |||||||
| chr12:45766377 | G | C | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+35063G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766377 | |||||||
| chr12:45766468 | A | G | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.284+35154A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766468 | |||||||
| chr12:45766659 | A | G | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+35345A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766659 | |||||||
| chr12:45766713 | A | C | 1 | a0001c0001t0001g0241 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.284+35399A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766713 | |||||||
| chr12:45766805 | C | T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.284+35491C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766805 | |||||||
| chr12:45766825 | A | C | 4 | a0001c0001t0001g0147 a0001c0001t0001g0198 a0001c0001t0001g0297 others(1): Show |
4 | HG02602.hp2 HG04199.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.284+35511A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766825 | |||||||
| chr12:45766848 | ATCCTAGC others(60): Show |
A | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+35535_284+3560 others(71): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766848 | |||||||
| chr12:45766915 | C | T | 9 | a0002c0003t0001g0235 a0002c0003t0001g0236 a0002c0003t0001g0237 others(6): Show |
9 | HG00597.hp2 HG02155.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.284+35601C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766915 | |||||||
| chr12:45766917 | A | T | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+35603A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766917 | |||||||
| chr12:45766918 | A | C | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+35604A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766918 | |||||||
| chr12:45766919 | G | C | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+35605G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766919 | |||||||
| chr12:45766921 | T | TTA | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+35607_284+3560 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766921 | |||||||
| chr12:45766923 | G | A | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+35609G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766923 | |||||||
| chr12:45766925 | G | T | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+35611G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766925 | |||||||
| chr12:45766926 | C | A | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+35612C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766926 | |||||||
| chr12:45767057 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.284+35743C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45767057 | |||||||
| chr12:45767084 | C | T | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+35770C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45767084 | |||||||
| chr12:45767162 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284+35848T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45767162 | |||||||
| chr12:45767477 | T | C | 6 | a0001c0001t0001g0114 a0001c0001t0001g0117 a0001c0001t0001g0125 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.284+36163T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45767477 | |||||||
| chr12:45767645 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(105): Show |
109 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.284+36331A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45767645 | |||||||
| chr12:45767689 | A | G | 10 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(7): Show |
10 | HG02647.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.284+36375A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45767689 | |||||||
| chr12:45767910 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.284+36596C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45767910 | |||||||
| chr12:45767995 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.284+36681T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45767995 | |||||||
| chr12:45768142 | A | G | 4 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+36828A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45768142 | |||||||
| chr12:45768468 | T | A | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+37154T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45768468 | |||||||
| chr12:45768506 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284+37192C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45768506 | |||||||
| chr12:45768596 | G | C | 9 | a0001c0001t0001g0226 a0001c0001t0001g0249 a0001c0001t0001g0263 others(6): Show |
9 | HG01109.hp2 HG01346.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.284+37282G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45768596 | |||||||
| chr12:45768810 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.284+37496A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45768810 | |||||||
| chr12:45768841 | CA | C | 5 | a0001c0001t0004g0131 a0001c0001t0004g0132 a0001c0001t0004g0133 others(2): Show |
5 | HG02615.hp1 HG02647.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.284+37529delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45768841 | ||||||
| chr12:45768843 | A | G | 3 | a0001c0001t0001g0294 a0001c0009t0010g0207 a0001c0009t0010g0208 |
3 | HG01975.hp1 HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.284+37529A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45768843 | |||||||
| chr12:45768873 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.284+37559C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45768873 | |||||||
| chr12:45768914 | C | T | 1 | a0001c0001t0001g0003 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.284+37600C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45768914 | |||||||
| chr12:45769021 | G | C | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+37707G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45769021 | |||||||
| chr12:45769065 | A | G | 9 | a0001c0001t0001g0226 a0001c0001t0001g0249 a0001c0001t0001g0263 others(6): Show |
9 | HG01109.hp2 HG01346.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.284+37751A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45769065 | |||||||
| chr12:45769195 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0065 |
2 | HG02083.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.284+37881A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45769195 | |||||||
| chr12:45769218 | A | T | 1 | a0001c0001t0001g0057 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.284+37904A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45769218 | |||||||
| chr12:45769285 | T | TTAAA | 10 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(7): Show |
10 | HG02647.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.284+37974_284+3797 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45769285 | ||||||
| chr12:45769574 | C | T | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+38260C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45769574 | |||||||
| chr12:45769902 | G | GA | 6 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0182 others(3): Show |
6 | NA18959.hp2 NA18973.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+38594dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45769902 | ||||||
| chr12:45769980 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.284+38666C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45769980 | |||||||
| chr12:45770063 | G | T | 1 | a0002c0003t0001g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.284+38749G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45770063 | |||||||
| chr12:45770174 | A | G | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.284+38860A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45770174 | |||||||
| chr12:45770178 | G | A | 4 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+38864G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45770178 | |||||||
| chr12:45770192 | G | A | 2 | a0001c0001t0001g0151 a0003c0004t0017g0205 |
2 | HG02451.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.284+38878G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45770192 | |||||||
| chr12:45770644 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.284+39330C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45770644 | |||||||
| chr12:45770711 | C | T | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+39397C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45770711 | |||||||
| chr12:45770759 | A | C | 1 | a0001c0001t0001g0016 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.284+39445A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45770759 | |||||||
| chr12:45770850 | A | G | 5 | a0001c0001t0005g0273 a0001c0001t0005g0285 a0001c0001t0005g0286 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.284+39536A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45770850 | |||||||
| chr12:45770882 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0094 |
2 | NA18977.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.284+39568A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45770882 | |||||||
| chr12:45771027 | C | T | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+39713C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45771027 | |||||||
| chr12:45771352 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.284+40038A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45771352 | |||||||
| chr12:45771356 | C | CA | 38 | a0001c0001t0001g0075 a0001c0001t0001g0228 a0001c0001t0001g0248 others(35): Show |
38 | HG00140.hp1 HG01175.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.285-40045dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45771356 | ||||||
| chr12:45771468 | C | T | 4 | a0001c0001t0001g0294 a0001c0001t0001g0304 a0001c0001t0001g0308 others(1): Show |
4 | HG01975.hp1 HG01981.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-39950C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45771468 | |||||||
| chr12:45771501 | C | CA | 6 | a0001c0001t0001g0067 a0001c0001t0001g0226 a0001c0001t0001g0305 others(3): Show |
6 | HG01346.hp1 HG02738.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.285-39902dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45771501 | ||||||
| chr12:45771501 | CA | C | 26 | a0001c0001t0001g0274 a0001c0001t0007g0195 a0001c0001t0007g0267 others(23): Show |
26 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.285-39902delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45771501 | ||||||
| chr12:45771639 | C | T | 1 | a0001c0001t0011g0119 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.285-39779C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45771639 | |||||||
| chr12:45771692 | C | CTA | 25 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0141 others(22): Show |
25 | HG00140.hp1 HG00673.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.285-39709_285-3970 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45771692 | ||||||
| chr12:45771692 | CTA | C | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-39709_285-3970 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45771692 | ||||||
| chr12:45771951 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.285-39467T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45771951 | |||||||
| chr12:45771991 | AAGG | A | 9 | a0001c0001t0001g0226 a0001c0001t0001g0249 a0001c0001t0001g0263 others(6): Show |
9 | HG01109.hp2 HG01346.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.285-39422_285-3942 others(7): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45771991 | ||||||
| chr12:45772012 | C | T | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-39406C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45772012 | |||||||
| chr12:45772073 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0074 a0001c0001t0001g0100 |
3 | HG02486.hp1 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.285-39345A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45772073 | |||||||
| chr12:45772150 | T | C | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-39268T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45772150 | |||||||
| chr12:45772209 | A | T | 1 | a0001c0001t0001g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285-39209A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45772209 | |||||||
| chr12:45772405 | C | T | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-39013C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45772405 | |||||||
| chr12:45772552 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.285-38866A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45772552 | |||||||
| chr12:45772621 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(214): Show |
218 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.285-38797T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45772621 | |||||||
| chr12:45772653 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.285-38765A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45772653 | |||||||
| chr12:45773516 | A | G | 1 | a0001c0001t0001g0005 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.285-37902A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45773516 | |||||||
| chr12:45773692 | A | C | 29 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(26): Show |
29 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.285-37726A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45773692 | |||||||
| chr12:45773906 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.285-37512G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45773906 | |||||||
| chr12:45774163 | T | A | 1 | a0001c0009t0010g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.285-37255T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45774163 | |||||||
| chr12:45774284 | AGTGTGAA others(5): Show |
A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0084 a0001c0001t0001g0089 others(104): Show |
108 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.285-37131_285-3712 others(16): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45774284 | ||||||
| chr12:45774509 | A | G | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(310): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.285-36909A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45774509 | |||||||
| chr12:45774511 | G | A | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.285-36907G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45774511 | |||||||
| chr12:45774612 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.285-36806G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45774612 | |||||||
| chr12:45774647 | C | T | 25 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(22): Show |
25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-36771C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45774647 | |||||||
| chr12:45774741 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.285-36677T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45774741 | |||||||
| chr12:45774890 | A | C | 4 | a0001c0001t0001g0270 a0001c0001t0001g0290 a0001c0001t0001g0291 others(1): Show |
4 | HG02615.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.285-36528A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45774890 | |||||||
| chr12:45774932 | T | C | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-36486T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45774932 | |||||||
| chr12:45774967 | C | T | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-36451C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45774967 | |||||||
| chr12:45775046 | C | A | 1 | a0001c0001t0015g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.285-36372C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45775046 | |||||||
| chr12:45775217 | C | T | 1 | a0002c0020t0001g0239 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.285-36201C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45775217 | |||||||
| chr12:45775248 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285-36170G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45775248 | |||||||
| chr12:45775311 | A | G | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-36107A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45775311 | |||||||
| chr12:45775459 | G | T | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-35959G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45775459 | |||||||
| chr12:45775847 | A | G | 1 | a0001c0001t0014g0175 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.285-35571A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45775847 | |||||||
| chr12:45775860 | A | G | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-35558A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45775860 | |||||||
| chr12:45776442 | G | A | 11 | a0001c0001t0001g0143 a0001c0001t0001g0151 a0001c0001t0001g0152 others(8): Show |
11 | HG00609.hp2 HG00673.hp1 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.285-34976G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45776442 | |||||||
| chr12:45776513 | A | G | 2 | a0001c0009t0010g0207 a0001c0009t0010g0208 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.285-34905A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45776513 | |||||||
| chr12:45776629 | T | A | 1 | a0001c0001t0001g0197 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.285-34789T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45776629 | |||||||
| chr12:45776724 | C | T | 3 | a0001c0001t0001g0249 a0001c0001t0001g0263 a0014c0018t0001g0262 |
3 | HG01109.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.285-34694C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45776724 | |||||||
| chr12:45776766 | A | T | 25 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(22): Show |
25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-34652A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45776766 | |||||||
| chr12:45776781 | C | CT | 22 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0026 others(19): Show |
22 | HG00741.hp1 HG01106.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.285-34616dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45776781 | ||||||
| chr12:45776781 | CT | C | 38 | a0001c0001t0001g0049 a0001c0001t0001g0153 a0001c0001t0003g0280 others(35): Show |
38 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.285-34616delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45776781 | ||||||
| chr12:45776840 | C | T | 1 | a0001c0001t0001g0022 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.285-34578C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45776840 | |||||||
| chr12:45776958 | G | T | 29 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(26): Show |
29 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.285-34460G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45776958 | |||||||
| chr12:45776970 | A | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(236): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.285-34448A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45776970 | |||||||
| chr12:45777199 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0084 a0001c0001t0001g0089 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.285-34219T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45777199 | |||||||
| chr12:45777292 | A | C | 25 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(22): Show |
25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-34126A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45777292 | |||||||
| chr12:45777527 | C | G | 1 | a0001c0001t0001g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285-33891C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45777527 | |||||||
| chr12:45777550 | T | G | 1 | a0001c0001t0001g0072 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.285-33868T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45777550 | |||||||
| chr12:45777705 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.285-33713G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45777705 | |||||||
| chr12:45777706 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.285-33712C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45777706 | |||||||
| chr12:45777932 | C | G | 10 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(7): Show |
10 | HG02647.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.285-33486C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45777932 | |||||||
| chr12:45778101 | G | C | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-33317G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778101 | |||||||
| chr12:45778121 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.285-33297C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778121 | |||||||
| chr12:45778123 | C | T | 5 | a0001c0001t0001g0056 a0001c0001t0001g0080 a0001c0001t0001g0083 others(2): Show |
5 | HG01071.hp1 HG01358.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.285-33295C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778123 | |||||||
| chr12:45778185 | G | A | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-33233G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778185 | |||||||
| chr12:45778251 | C | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0113 a0001c0001t0001g0114 others(121): Show |
125 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.285-33167C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778251 | |||||||
| chr12:45778255 | C | A | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.285-33163C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778255 | |||||||
| chr12:45778259 | C | G | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.285-33159C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778259 | |||||||
| chr12:45778294 | T | A | 4 | a0001c0001t0005g0273 a0001c0001t0005g0286 a0001c0001t0005g0288 others(1): Show |
4 | HG01891.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.285-33124T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778294 | |||||||
| chr12:45778298 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.285-33120A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778298 | |||||||
| chr12:45778307 | G | A | 1 | a0001c0001t0005g0286 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.285-33111G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778307 | |||||||
| chr12:45778380 | G | A | 10 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(7): Show |
10 | HG02647.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.285-33038G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778380 | |||||||
| chr12:45778421 | T | C | 1 | a0003c0004t0017g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.285-32997T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778421 | |||||||
| chr12:45778424 | A | G | 4 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-32994A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778424 | |||||||
| chr12:45778461 | GA | G | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-32956delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778461 | |||||||
| chr12:45778585 | A | G | 1 | a0001c0011t0018g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.285-32833A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778585 | |||||||
| chr12:45778759 | T | C | 1 | a0001c0016t0001g0296 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.285-32659T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778759 | |||||||
| chr12:45778828 | A | T | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-32590A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778828 | |||||||
| chr12:45779161 | C | A | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-32257C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45779161 | |||||||
| chr12:45779551 | A | G | 1 | a0001c0002t0002g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.285-31867A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45779551 | |||||||
| chr12:45779746 | T | A | 1 | a0001c0001t0001g0071 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.285-31672T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45779746 | |||||||
| chr12:45779756 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.285-31662A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45779756 | |||||||
| chr12:45780086 | A | G | 2 | a0004c0005t0001g0168 a0004c0005t0001g0169 |
2 | NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.285-31332A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45780086 | |||||||
| chr12:45780205 | C | A | 1 | a0001c0001t0001g0155 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.285-31213C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45780205 | |||||||
| chr12:45780207 | A | G | 2 | a0001c0001t0001g0270 a0001c0001t0001g0291 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.285-31211A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45780207 | |||||||
| chr12:45780229 | G | A | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-31189G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45780229 | |||||||
| chr12:45780384 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.285-31034T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45780384 | |||||||
| chr12:45780610 | A | AATT | 3 | a0001c0001t0001g0097 a0001c0001t0001g0272 a0001c0011t0018g0271 |
3 | HG01884.hp1 HG02257.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.285-30789_285-3078 others(7): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45780610 | ||||||
| chr12:45780728 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.285-30690C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45780728 | |||||||
| chr12:45780864 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0192 |
2 | NA18950.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.285-30554C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45780864 | |||||||
| chr12:45780973 | A | C | 1 | a0001c0002t0002g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.285-30445A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45780973 | |||||||
| chr12:45781114 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.285-30304C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45781114 | |||||||
| chr12:45781160 | T | G | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-30258T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45781160 | |||||||
| chr12:45781256 | A | G | 3 | a0001c0001t0001g0248 a0001c0001t0001g0265 a0010c0014t0007g0269 |
3 | HG02559.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.285-30162A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45781256 | |||||||
| chr12:45781322 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.285-30096A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45781322 | |||||||
| chr12:45781334 | C | T | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.285-30084C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45781334 | |||||||
| chr12:45781372 | T | TTGGCCAG others(1022): Show |
1 | a0001c0001t0008g0222 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1021): Show |
1 | a0001c0001t0008g0128 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1032): Show |
1 | a0001c0001t0001g0183 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1043): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1020): Show |
1 | a0001c0001t0003g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1019): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0009 |
2 | HG00544.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1030): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1017): Show |
1 | a0001c0001t0003g0314 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1028): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1021): Show |
1 | a0001c0001t0003g0280 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1017): Show |
1 | a0001c0001t0003g0281 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1028): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1015): Show |
1 | a0001c0001t0003g0284 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1013): Show |
1 | a0001c0001t0003g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1024): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1004): Show |
1 | a0001c0011t0018g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1015): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1003): Show |
1 | a0001c0001t0001g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1014): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(999): Show |
1 | a0001c0001t0001g0305 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1010): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1023): Show |
1 | a0001c0001t0001g0172 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1039): Show |
2 | a0001c0001t0001g0249 a0001c0001t0001g0263 |
2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1050): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1021): Show |
1 | a0014c0018t0001g0262 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1033): Show |
1 | a0001c0001t0001g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1044): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1032): Show |
1 | a0001c0001t0001g0122 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1043): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1027): Show |
1 | a0001c0001t0001g0290 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1038): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1022): Show |
1 | a0001c0001t0008g0221 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1020): Show |
1 | a0001c0001t0001g0085 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1020): Show |
1 | a0001c0001t0001g0223 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1021): Show |
1 | a0001c0001t0001g0198 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1025): Show |
1 | a0001c0001t0001g0224 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1036): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1026): Show |
1 | a0001c0001t0001g0098 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1037): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1015): Show |
1 | a0001c0001t0001g0008 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1016): Show |
2 | a0001c0001t0001g0075 a0005c0008t0001g0039 |
2 | NA19001.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1027): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1017): Show |
1 | a0001c0001t0001g0067 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1028): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1018): Show |
1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1029): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1021): Show |
1 | a0001c0001t0001g0125 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1015): Show |
1 | a0001c0009t0010g0207 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1016): Show |
3 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0149 |
3 | HG02129.hp1 HG02976.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1027): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1020): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0017 |
2 | HG01106.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1023): Show |
1 | a0001c0001t0001g0137 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1002): Show |
1 | a0001c0001t0001g0032 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1013): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1003): Show |
1 | a0001c0001t0001g0066 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1014): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(999): Show |
1 | a0001c0001t0001g0031 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1010): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1036): Show |
1 | a0001c0001t0001g0167 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1047): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1027): Show |
1 | a0001c0001t0014g0175 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1038): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1028): Show |
2 | a0001c0001t0001g0145 a0001c0001t0001g0150 |
2 | NA18953.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1039): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1025): Show |
1 | a0001c0001t0001g0157 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1036): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1026): Show |
1 | a0001c0001t0009g0179 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1037): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1026): Show |
1 | a0001c0001t0001g0299 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1037): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1021): Show |
1 | a0001c0001t0015g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1022): Show |
1 | a0001c0001t0001g0185 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1023): Show |
2 | a0001c0001t0001g0158 a0001c0001t0001g0300 |
2 | HG01109.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1024): Show |
1 | a0001c0001t0001g0170 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1035): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1023): Show |
2 | a0001c0001t0001g0037 a0001c0001t0001g0191 |
2 | HG01981.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1024): Show |
1 | a0001c0001t0001g0196 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1035): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1026): Show |
1 | a0013c0015t0001g0295 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1037): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1023): Show |
1 | a0004c0005t0001g0168 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(994): Show |
1 | a0001c0001t0001g0014 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1005): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1037): Show |
1 | a0001c0001t0001g0048 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1048): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1036): Show |
1 | a0001c0006t0002g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1047): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1033): Show |
1 | a0001c0006t0002g0193 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1044): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1028): Show |
1 | a0001c0001t0001g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1039): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1033): Show |
1 | a0001c0001t0001g0197 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1044): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1028): Show |
2 | a0001c0001t0001g0110 a0001c0001t0001g0115 |
2 | HG01346.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1039): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1020): Show |
1 | a0001c0001t0001g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1022): Show |
4 | a0001c0001t0001g0147 a0001c0001t0001g0270 a0001c0001t0001g0291 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1025): Show |
1 | a0001c0001t0001g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1036): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1030): Show |
1 | a0001c0001t0001g0060 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1041): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1015): Show |
1 | a0001c0001t0001g0007 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1016): Show |
2 | a0001c0001t0001g0073 a0001c0001t0001g0079 |
2 | HG02683.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1027): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1019): Show |
4 | a0001c0001t0001g0077 a0001c0001t0001g0086 a0001c0001t0001g0099 others(1): Show |
4 | HG00621.hp2 HG01433.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1030): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1020): Show |
4 | a0001c0001t0001g0040 a0001c0001t0001g0056 a0001c0001t0001g0058 others(1): Show |
4 | HG02083.hp1 HG02602.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1021): Show |
1 | a0001c0001t0001g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1022): Show |
1 | a0001c0001t0001g0279 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1025): Show |
1 | a0001c0001t0001g0126 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1036): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1015): Show |
2 | a0001c0001t0001g0090 a0001c0001t0001g0103 |
2 | HG02135.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1017): Show |
1 | a0001c0001t0001g0016 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1028): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1018): Show |
1 | a0001c0001t0001g0045 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1029): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1019): Show |
5 | a0001c0001t0001g0062 a0001c0001t0001g0097 a0001c0001t0001g0123 others(2): Show |
5 | HG01074.hp2 HG01106.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1030): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1020): Show |
2 | a0001c0001t0001g0022 a0001c0001t0001g0063 |
2 | HG04184.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1021): Show |
2 | a0001c0001t0001g0068 a0001c0001t0001g0199 |
2 | HG03704.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1024): Show |
1 | a0001c0001t0001g0293 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1035): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1009): Show |
1 | a0001c0001t0005g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1020): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1013): Show |
1 | a0001c0001t0001g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1024): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1015): Show |
6 | a0001c0001t0001g0059 a0001c0001t0001g0074 a0001c0001t0001g0080 others(3): Show |
6 | HG01168.hp1 HG01169.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1016): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0047 a0005c0008t0001g0034 |
3 | HG00099.hp2 HG02135.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1027): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1017): Show |
3 | a0001c0001t0001g0005 a0001c0001t0001g0070 a0001c0001t0001g0095 |
3 | HG00438.hp2 NA18956.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1028): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1018): Show |
6 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0065 others(3): Show |
7 | HG01993.hp2 HG02083.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1029): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1019): Show |
2 | a0001c0001t0001g0114 a0001c0001t0001g0117 |
2 | HG00639.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1030): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1020): Show |
1 | a0001c0001t0001g0127 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1021): Show |
3 | a0001c0001t0001g0129 a0001c0001t0001g0220 a0001c0001t0011g0119 |
3 | HG01515.hp2 HG02698.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1022): Show |
2 | a0001c0001t0001g0130 a0001c0001t0011g0118 |
2 | HG01358.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1008): Show |
1 | a0001c0001t0001g0083 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1019): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1012): Show |
1 | a0001c0001t0001g0027 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1023): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1013): Show |
3 | a0001c0001t0001g0061 a0006c0007t0001g0020 a0006c0007t0001g0051 |
3 | NA18941.hp2 NA18957.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1024): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1014): Show |
1 | a0001c0009t0010g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1025): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1015): Show |
3 | a0001c0001t0001g0041 a0001c0001t0001g0069 a0001c0002t0002g0253 |
3 | HG00280.hp1 NA18906.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1016): Show |
3 | a0001c0001t0001g0021 a0001c0001t0001g0044 a0001c0001t0001g0082 |
3 | HG00621.hp1 NA18747.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1027): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1017): Show |
4 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0019 others(1): Show |
4 | HG01257.hp1 HG01258.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1028): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1019): Show |
2 | a0001c0001t0001g0094 a0001c0016t0001g0296 |
2 | HG02809.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1030): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1021): Show |
1 | a0001c0001t0001g0104 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1015): Show |
2 | a0001c0001t0001g0146 a0001c0001t0001g0174 |
2 | HG01167.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1016): Show |
1 | a0001c0001t0001g0055 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1027): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1020): Show |
1 | a0001c0001t0016g0116 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1012): Show |
2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | NA18980.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1023): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1016): Show |
1 | a0001c0001t0001g0226 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1027): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1008): Show |
1 | a0001c0001t0001g0023 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1019): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1009): Show |
1 | a0001c0001t0005g0285 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1020): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1003): Show |
1 | a0001c0001t0001g0042 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1014): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1000): Show |
1 | a0001c0001t0001g0033 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1011): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(997): Show |
1 | a0001c0001t0001g0028 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1008): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1038): Show |
1 | a0001c0001t0001g0176 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1049): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1030): Show |
1 | a0012c0012t0001g0187 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1041): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1032): Show |
1 | a0001c0001t0001g0151 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1043): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1026): Show |
1 | a0001c0001t0001g0143 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1037): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1023): Show |
1 | a0001c0001t0001g0159 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1024): Show |
1 | a0001c0001t0001g0160 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1035): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1026): Show |
1 | a0001c0001t0001g0161 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1037): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1022): Show |
1 | a0001c0001t0001g0189 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1023): Show |
1 | a0001c0001t0001g0302 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1024): Show |
2 | a0001c0001t0001g0298 a0001c0001t0009g0109 |
2 | HG03927.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1035): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1025): Show |
1 | a0001c0001t0001g0177 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1036): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1029): Show |
1 | a0001c0001t0001g0303 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1040): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1023): Show |
3 | a0001c0001t0001g0171 a0001c0001t0001g0181 a0001c0001t0001g0204 |
3 | HG00673.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1024): Show |
1 | a0001c0001t0001g0154 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1035): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1025): Show |
2 | a0001c0001t0001g0203 a0001c0001t0001g0312 |
2 | HG00609.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1036): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1033): Show |
1 | a0001c0001t0001g0188 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1044): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1012): Show |
2 | a0001c0001t0001g0144 a0001c0001t0001g0184 |
2 | NA18950.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1023): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1014): Show |
1 | a0001c0001t0001g0186 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1025): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1021): Show |
1 | a0001c0001t0001g0162 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1022): Show |
6 | a0001c0001t0001g0089 a0001c0001t0001g0153 a0001c0001t0001g0163 others(3): Show |
6 | HG01975.hp2 NA18612.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1023): Show |
5 | a0001c0001t0001g0156 a0001c0001t0001g0165 a0001c0001t0001g0166 others(2): Show |
5 | HG01934.hp2 HG02273.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1024): Show |
3 | a0001c0001t0001g0182 a0001c0001t0001g0201 a0001c0001t0001g0315 |
3 | HG02129.hp2 NA18959.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1035): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1022): Show |
4 | a0001c0001t0001g0038 a0001c0001t0001g0084 a0001c0001t0001g0152 others(1): Show |
4 | NA18944.hp1 NA18977.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1023): Show |
1 | a0001c0001t0001g0190 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1024): Show |
1 | a0001c0001t0001g0155 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1035): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1021): Show |
2 | a0001c0001t0001g0202 a0004c0005t0001g0169 |
2 | NA19077.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1029): Show |
1 | a0001c0001t0001g0049 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1040): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1014): Show |
1 | a0001c0001t0001g0093 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1025): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1015): Show |
1 | a0001c0001t0001g0003 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1018): Show |
1 | a0001c0001t0001g0053 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1029): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1013): Show |
1 | a0001c0001t0001g0071 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1024): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1014): Show |
1 | a0001c0001t0001g0046 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1025): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1010): Show |
2 | a0001c0001t0001g0054 a0001c0001t0001g0072 |
2 | HG02165.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1021): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1012): Show |
1 | a0001c0001t0001g0096 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1023): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1011): Show |
1 | a0001c0001t0001g0057 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1022): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1044): Show |
1 | a0001c0002t0002g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1055): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1036): Show |
1 | a0001c0002t0002g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1047): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1032): Show |
1 | a0011c0010t0002g0206 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1043): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1039): Show |
1 | a0001c0006t0002g0136 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1050): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1036): Show |
3 | a0001c0001t0004g0131 a0001c0002t0002g0210 a0001c0002t0002g0259 |
3 | HG02630.hp2 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1047): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1034): Show |
1 | a0001c0002t0002g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1045): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1035): Show |
1 | a0001c0002t0002g0216 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1046): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1036): Show |
1 | a0001c0002t0002g0211 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1047): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1031): Show |
1 | a0001c0002t0002g0217 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1042): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1033): Show |
2 | a0001c0002t0002g0212 a0001c0002t0002g0214 |
2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1044): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1035): Show |
1 | a0001c0002t0002g0218 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1046): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1025): Show |
1 | a0001c0002t0002g0260 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1036): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1030): Show |
1 | a0001c0001t0004g0132 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1041): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1032): Show |
1 | a0001c0002t0002g0213 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1043): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1028): Show |
1 | a0001c0001t0004g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1039): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1030): Show |
1 | a0003c0004t0017g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1041): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1022): Show |
1 | a0001c0002t0002g0256 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1026): Show |
2 | a0001c0001t0004g0133 a0001c0001t0004g0134 |
2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1037): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1019): Show |
1 | a0001c0001t0001g0102 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1030): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1017): Show |
1 | a0007c0019t0001g0036 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1028): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1019): Show |
1 | a0001c0002t0002g0261 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1030): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1020): Show |
1 | a0001c0001t0001g0121 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1005): Show |
1 | a0001c0001t0005g0286 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1016): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1006): Show |
1 | a0001c0001t0013g0287 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1017): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1014): Show |
1 | a0001c0002t0002g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1025): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1016): Show |
1 | a0001c0002t0002g0311 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1027): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1001): Show |
1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1012): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1003): Show |
1 | a0001c0001t0005g0288 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1014): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1005): Show |
1 | a0001c0002t0002g0219 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1016): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1009): Show |
1 | a0010c0014t0007g0269 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1020): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1008): Show |
1 | a0001c0001t0007g0267 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1019): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1009): Show |
2 | a0001c0001t0007g0195 a0001c0001t0007g0268 |
2 | HG01167.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1020): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1019): Show |
1 | a0001c0001t0001g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1030): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1023): Show |
1 | a0001c0001t0001g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(996): Show |
2 | a0003c0004t0006g0105 a0003c0004t0006g0108 |
2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1007): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(994): Show |
1 | a0003c0004t0006g0106 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1005): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(995): Show |
1 | a0003c0004t0006g0107 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1006): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1028): Show |
1 | a0001c0001t0001g0228 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1039): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1002): Show |
1 | a0001c0001t0001g0229 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1013): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1003): Show |
1 | a0001c0001t0001g0308 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1014): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1006): Show |
1 | a0001c0001t0001g0244 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1017): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1036): Show |
1 | a0002c0003t0001g0266 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1047): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1039): Show |
1 | a0008c0013t0001g0238 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1050): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1035): Show |
1 | a0002c0003t0001g0240 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1046): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1031): Show |
1 | a0001c0001t0001g0141 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1042): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1033): Show |
1 | a0001c0001t0001g0230 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1044): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1029): Show |
2 | a0001c0001t0001g0275 a0002c0003t0001g0142 |
2 | HG01934.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1040): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1031): Show |
1 | a0001c0001t0001g0241 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1042): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1033): Show |
2 | a0001c0001t0001g0139 a0001c0001t0001g0250 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1044): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1029): Show |
2 | a0001c0001t0001g0112 a0001c0001t0012g0252 |
2 | HG02293.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1040): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1033): Show |
1 | a0001c0001t0001g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1044): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1026): Show |
1 | a0001c0001t0001g0231 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1037): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1024): Show |
1 | a0001c0001t0001g0232 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1035): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1020): Show |
1 | a0001c0001t0001g0138 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1023): Show |
2 | a0001c0001t0001g0225 a0001c0001t0001g0233 |
2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1031): Show |
1 | a0001c0001t0001g0274 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1042): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1013): Show |
1 | a0001c0001t0001g0277 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1024): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1013): Show |
1 | a0001c0001t0001g0276 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1024): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1018): Show |
1 | a0001c0001t0001g0306 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1029): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1019): Show |
1 | a0002c0003t0001g0242 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1030): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1020): Show |
1 | a0001c0001t0001g0140 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1015): Show |
1 | a0002c0020t0001g0239 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1022): Show |
1 | a0001c0001t0001g0234 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1014): Show |
1 | a0002c0003t0001g0235 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1025): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1016): Show |
2 | a0001c0001t0001g0245 a0002c0003t0001g0243 |
2 | NA19060.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1027): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1011): Show |
1 | a0001c0001t0012g0251 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1022): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1013): Show |
2 | a0002c0003t0001g0236 a0002c0003t0001g0310 |
2 | NA18945.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1024): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1014): Show |
2 | a0002c0003t0001g0237 a0002c0003t0001g0307 |
2 | HG00597.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1025): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1015): Show |
1 | a0001c0001t0001g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1014): Show |
1 | a0002c0003t0001g0246 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1025): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1010): Show |
1 | a0001c0001t0001g0247 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1021): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1006): Show |
1 | a0001c0001t0001g0317 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1017): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1007): Show |
1 | a0001c0001t0001g0316 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1018): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1012): Show |
1 | a0001c0001t0001g0278 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1023): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1001): Show |
2 | a0001c0001t0001g0294 a0001c0001t0001g0304 |
2 | HG01975.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1012): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781372 | T | TTGGCCAG others(1002): Show |
1 | a0001c0001t0001g0309 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1013): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | ||||||
| chr12:45781508 | G | A | 5 | a0001c0001t0001g0112 a0001c0001t0001g0139 a0001c0001t0001g0229 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.285-29910G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45781508 | |||||||
| chr12:45781686 | A | G | 45 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(42): Show |
45 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.285-29732A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45781686 | |||||||
| chr12:45781776 | T | C | 1 | a0001c0001t0009g0179 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.285-29642T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45781776 | |||||||
| chr12:45781820 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.285-29598T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45781820 | |||||||
| chr12:45781959 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0312 |
2 | NA18966.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.285-29459A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45781959 | |||||||
| chr12:45782093 | A | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(95): Show |
99 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.285-29325A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45782093 | |||||||
| chr12:45782120 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285-29298A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45782120 | |||||||
| chr12:45782137 | T | TA | 3 | a0001c0001t0001g0022 a0001c0001t0001g0063 a0001c0001t0001g0097 |
3 | HG04184.hp2 NA19077.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.285-29278dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45782137 | ||||||
| chr12:45782168 | A | G | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.285-29250A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45782168 | |||||||
| chr12:45782486 | G | A | 9 | a0002c0003t0001g0235 a0002c0003t0001g0236 a0002c0003t0001g0237 others(6): Show |
9 | HG00597.hp2 HG02155.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.285-28932G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45782486 | |||||||
| chr12:45782487 | G | T | 1 | a0001c0001t0001g0141 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.285-28931G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45782487 | |||||||
| chr12:45782578 | G | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
4 | NA18950.hp1 NA18980.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-28840G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45782578 | |||||||
| chr12:45782610 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.285-28808C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45782610 | |||||||
| chr12:45782809 | C | T | 1 | a0001c0002t0002g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.285-28609C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45782809 | |||||||
| chr12:45783044 | A | T | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | HG00140.hp1 HG01934.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.285-28374A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45783044 | |||||||
| chr12:45783111 | A | G | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG01168.hp1 HG01169.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.285-28307A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45783111 | |||||||
| chr12:45783166 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285-28252T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45783166 | |||||||
| chr12:45783654 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.285-27764G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45783654 | |||||||
| chr12:45783704 | A | C | 3 | a0001c0002t0002g0253 a0001c0002t0002g0258 a0001c0002t0002g0311 |
3 | HG01884.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.285-27714A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45783704 | |||||||
| chr12:45783751 | A | T | 29 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(26): Show |
29 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.285-27667A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45783751 | |||||||
| chr12:45783886 | TAAGTTA | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(158): Show |
162 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.285-27529_285-2752 others(10): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45783886 | ||||||
| chr12:45783913 | A | G | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-27505A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45783913 | |||||||
| chr12:45783939 | A | G | 1 | a0001c0001t0001g0003 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.285-27479A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45783939 | |||||||
| chr12:45784190 | G | T | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-27228G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45784190 | |||||||
| chr12:45784375 | T | A | 23 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0155 others(20): Show |
23 | HG01109.hp1 HG01934.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.285-27043T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45784375 | |||||||
| chr12:45784613 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.285-26805G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45784613 | |||||||
| chr12:45785202 | C | T | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0075 others(1): Show |
4 | NA18940.hp1 NA18947.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.285-26216C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785202 | |||||||
| chr12:45785391 | C | T | 2 | a0001c0001t0001g0197 a0001c0001t0001g0279 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.285-26027C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785391 | |||||||
| chr12:45785392 | G | A | 3 | a0001c0006t0002g0136 a0001c0006t0002g0193 a0001c0006t0002g0194 |
3 | HG02622.hp2 HG02895.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.285-26026G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785392 | |||||||
| chr12:45785499 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.285-25919G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785499 | |||||||
| chr12:45785617 | A | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0090 a0001c0001t0001g0099 |
3 | HG00621.hp1 HG02135.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.285-25801A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785617 | |||||||
| chr12:45785714 | C | A | 1 | a0001c0001t0001g0075 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.285-25704C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785714 | |||||||
| chr12:45785764 | A | C | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-25654A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785764 | |||||||
| chr12:45785862 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.285-25556G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785862 | |||||||
| chr12:45785913 | G | A | 1 | a0001c0016t0001g0296 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.285-25505G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785913 | |||||||
| chr12:45785954 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.285-25464A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785954 | |||||||
| chr12:45785998 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0066 |
2 | HG01192.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.285-25420T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785998 | |||||||
| chr12:45786095 | A | C | 8 | a0001c0001t0001g0225 a0001c0001t0001g0231 a0001c0001t0001g0233 others(5): Show |
8 | HG00642.hp1 HG01074.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.285-25323A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45786095 | |||||||
| chr12:45786113 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.285-25305A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45786113 | |||||||
| chr12:45786137 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.285-25281A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45786137 | |||||||
| chr12:45786238 | TTAAAG | T | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-25177_285-2517 others(9): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45786238 | ||||||
| chr12:45786280 | A | T | 1 | a0001c0001t0001g0155 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.285-25138A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45786280 | |||||||
| chr12:45786370 | C | G | 1 | a0010c0014t0007g0269 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.285-25048C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45786370 | |||||||
| chr12:45786401 | A | G | 1 | a0001c0002t0002g0215 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.285-25017A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45786401 | |||||||
| chr12:45786525 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.285-24893G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45786525 | |||||||
| chr12:45786644 | T | C | 1 | a0001c0001t0001g0041 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.285-24774T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45786644 | |||||||
| chr12:45786902 | G | A | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-24516G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45786902 | |||||||
| chr12:45786959 | A | G | 1 | a0001c0001t0001g0004 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.285-24459A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45786959 | |||||||
| chr12:45787209 | A | G | 1 | a0003c0004t0006g0105 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.285-24209A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45787209 | |||||||
| chr12:45787218 | C | CTTTT | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-24187_285-2418 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45787218 | ||||||
| chr12:45787282 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.285-24136A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45787282 | |||||||
| chr12:45787573 | C | G | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.285-23845C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45787573 | |||||||
| chr12:45787713 | A | T | 3 | a0001c0001t0001g0249 a0001c0001t0001g0263 a0014c0018t0001g0262 |
3 | HG01109.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.285-23705A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45787713 | |||||||
| chr12:45788026 | G | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(22): Show |
25 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-23392G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45788026 | |||||||
| chr12:45788029 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.285-23389T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45788029 | |||||||
| chr12:45788209 | A | G | 1 | a0001c0001t0005g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.285-23209A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45788209 | |||||||
| chr12:45788484 | A | C | 1 | a0001c0001t0001g0041 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.285-22934A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45788484 | |||||||
| chr12:45788609 | G | A | 25 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(22): Show |
25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-22809G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45788609 | |||||||
| chr12:45788632 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.285-22786T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45788632 | |||||||
| chr12:45788665 | A | T | 1 | a0001c0001t0001g0181 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.285-22753A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45788665 | |||||||
| chr12:45788907 | A | C | 40 | a0001c0001t0001g0292 a0001c0001t0003g0280 a0001c0001t0003g0281 others(37): Show |
40 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.285-22511A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45788907 | |||||||
| chr12:45789047 | A | G | 1 | a0001c0001t0001g0022 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.285-22371A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45789047 | |||||||
| chr12:45789049 | CA | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(161): Show |
165 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.285-22368delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45789049 | |||||||
| chr12:45789068 | A | G | 47 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(44): Show |
47 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.285-22350A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45789068 | |||||||
| chr12:45789742 | G | A | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-21676G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45789742 | |||||||
| chr12:45790004 | T | A | 1 | a0002c0003t0001g0307 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.285-21414T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45790004 | |||||||
| chr12:45790005 | C | G | 1 | a0002c0003t0001g0307 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.285-21413C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45790005 | |||||||
| chr12:45790006 | A | C | 1 | a0002c0003t0001g0307 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.285-21412A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45790006 | |||||||
| chr12:45790341 | TTGTA | T | 9 | a0002c0003t0001g0235 a0002c0003t0001g0236 a0002c0003t0001g0237 others(6): Show |
9 | HG00597.hp2 HG02155.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.285-21074_285-2107 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45790341 | ||||||
| chr12:45790351 | T | C | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-21067T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45790351 | |||||||
| chr12:45790376 | A | G | 1 | a0001c0001t0003g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.285-21042A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45790376 | |||||||
| chr12:45790487 | C | T | 3 | a0001c0001t0001g0249 a0001c0001t0001g0263 a0014c0018t0001g0262 |
3 | HG01109.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.285-20931C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45790487 | |||||||
| chr12:45790488 | A | C | 5 | a0001c0001t0005g0273 a0001c0001t0005g0285 a0001c0001t0005g0286 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.285-20930A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45790488 | |||||||
| chr12:45790690 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0003g0280 |
2 | NA20752.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.285-20728C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45790690 | |||||||
| chr12:45790840 | A | C | 1 | a0001c0001t0001g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285-20578A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45790840 | |||||||
| chr12:45790940 | G | A | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-20478G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45790940 | |||||||
| chr12:45791066 | T | G | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.285-20352T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45791066 | |||||||
| chr12:45791204 | C | CTG | 8 | a0001c0001t0001g0076 a0001c0001t0001g0127 a0001c0001t0001g0154 others(5): Show |
8 | HG00738.hp2 HG01099.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.285-20185_285-2018 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45791204 | ||||||
| chr12:45791204 | C | CTGTG | 3 | a0001c0001t0001g0023 a0001c0001t0001g0292 a0001c0011t0018g0271 |
3 | HG01884.hp1 HG02300.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.285-20187_285-2018 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45791204 | ||||||
| chr12:45791204 | CTG | C | 92 | a0001c0001t0001g0058 a0001c0001t0001g0110 a0001c0001t0001g0112 others(89): Show |
92 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.285-20185_285-2018 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45791204 | ||||||
| chr12:45791204 | CTGTG | C | 19 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(16): Show |
19 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.285-20187_285-2018 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45791204 | ||||||
| chr12:45791373 | A | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.285-20045A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45791373 | |||||||
| chr12:45791384 | C | T | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-20034C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45791384 | |||||||
| chr12:45791483 | C | A | 6 | a0001c0001t0001g0138 a0001c0001t0001g0140 a0001c0001t0001g0228 others(3): Show |
6 | HG00639.hp2 HG01081.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-19935C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45791483 | |||||||
| chr12:45791646 | T | C | 29 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(26): Show |
29 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.285-19772T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45791646 | |||||||
| chr12:45791662 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0094 |
2 | NA18977.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.285-19756C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45791662 | |||||||
| chr12:45791782 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.285-19636A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45791782 | |||||||
| chr12:45792010 | C | T | 3 | a0001c0001t0001g0226 a0001c0001t0001g0305 a0001c0001t0003g0283 |
3 | HG01346.hp1 HG02809.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.285-19408C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45792010 | |||||||
| chr12:45792493 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.285-18925G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45792493 | |||||||
| chr12:45792520 | C | T | 1 | a0001c0001t0005g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.285-18898C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45792520 | |||||||
| chr12:45792528 | C | T | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-18890C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45792528 | |||||||
| chr12:45792610 | GAGAT | G | 3 | a0001c0001t0001g0270 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.285-18805_285-1880 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45792610 | ||||||
| chr12:45792942 | T | G | 1 | a0001c0001t0001g0015 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.285-18476T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45792942 | |||||||
| chr12:45793037 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.285-18381G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793037 | |||||||
| chr12:45793121 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.285-18297G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793121 | |||||||
| chr12:45793157 | G | A | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.285-18261G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793157 | |||||||
| chr12:45793159 | G | C | 4 | a0001c0001t0001g0153 a0001c0001t0001g0172 a0001c0001t0001g0196 others(1): Show |
4 | NA18966.hp2 NA19001.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.285-18259G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793159 | |||||||
| chr12:45793205 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00408.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.285-18213C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793205 | |||||||
| chr12:45793216 | C | G | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.285-18202C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793216 | |||||||
| chr12:45793227 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285-18191G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793227 | |||||||
| chr12:45793346 | C | CT | 215 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.285-18065dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45793346 | ||||||
| chr12:45793543 | C | CTG | 5 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0174 others(2): Show |
5 | HG01167.hp2 HG01346.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.285-17855_285-1785 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45793543 | ||||||
| chr12:45793543 | C | CTGTG | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-17857_285-1785 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45793543 | ||||||
| chr12:45793543 | CTGTG | C | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-17857_285-1785 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45793543 | ||||||
| chr12:45793565 | A | G | 3 | a0001c0002t0002g0253 a0001c0002t0002g0258 a0001c0002t0002g0311 |
3 | HG01884.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.285-17853A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793565 | |||||||
| chr12:45793602 | A | C | 1 | a0001c0006t0002g0193 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.285-17816A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793602 | |||||||
| chr12:45793730 | C | CAT | 5 | a0002c0003t0001g0237 a0003c0004t0006g0105 a0003c0004t0006g0106 others(2): Show |
5 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.285-17676_285-1767 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45793730 | ||||||
| chr12:45793826 | A | T | 6 | a0001c0001t0001g0114 a0001c0001t0001g0117 a0001c0001t0001g0125 others(3): Show |
6 | HG00280.hp2 HG00639.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.285-17592A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793826 | |||||||
| chr12:45793837 | T | G | 1 | a0001c0001t0001g0153 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.285-17581T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793837 | |||||||
| chr12:45793960 | G | T | 6 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0182 others(3): Show |
6 | NA18959.hp2 NA18973.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-17458G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793960 | |||||||
| chr12:45793971 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285-17447T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793971 | |||||||
| chr12:45794143 | C | A | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.285-17275C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45794143 | |||||||
| chr12:45794282 | T | C | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-17136T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45794282 | |||||||
| chr12:45794328 | G | A | 1 | a0001c0001t0005g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.285-17090G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45794328 | |||||||
| chr12:45794343 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.285-17075G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45794343 | |||||||
| chr12:45794362 | T | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0044 |
3 | NA18979.hp1 NA19064.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.285-17056T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45794362 | |||||||
| chr12:45794709 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.285-16709C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45794709 | |||||||
| chr12:45794734 | T | G | 3 | a0001c0001t0001g0270 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.285-16684T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45794734 | |||||||
| chr12:45794772 | G | A | 1 | a0001c0001t0015g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.285-16646G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45794772 | |||||||
| chr12:45794927 | C | G | 1 | a0001c0001t0001g0279 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.285-16491C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45794927 | |||||||
| chr12:45795084 | T | C | 2 | a0001c0001t0001g0197 a0001c0001t0001g0279 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.285-16334T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45795084 | |||||||
| chr12:45795411 | C | T | 3 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 |
3 | HG01167.hp1 HG01169.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.285-16007C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45795411 | |||||||
| chr12:45795445 | T | A | 1 | a0001c0001t0005g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.285-15973T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45795445 | |||||||
| chr12:45795452 | G | A | 1 | a0001c0001t0005g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.285-15966G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45795452 | |||||||
| chr12:45795471 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.285-15947G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45795471 | |||||||
| chr12:45795501 | G | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(22): Show |
25 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-15917G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45795501 | |||||||
| chr12:45795519 | G | A | 1 | a0001c0001t0007g0268 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.285-15899G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45795519 | |||||||
| chr12:45795542 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.285-15876C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45795542 | |||||||
| chr12:45795577 | C | A | 1 | a0001c0001t0001g0199 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.285-15841C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45795577 | |||||||
| chr12:45795702 | C | CTG | 111 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(108): Show |
112 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.285-15715_285-1571 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45795702 | ||||||
| chr12:45795918 | A | T | 1 | a0001c0002t0002g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.285-15500A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45795918 | |||||||
| chr12:45796081 | AC | A | 5 | a0001c0002t0002g0254 a0001c0002t0002g0255 a0001c0002t0002g0259 others(2): Show |
5 | HG02630.hp2 HG02922.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.285-15335delC | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45796081 | ||||||
| chr12:45796217 | C | A | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.285-15201C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45796217 | |||||||
| chr12:45796231 | G | A | 1 | a0001c0001t0016g0116 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.285-15187G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45796231 | |||||||
| chr12:45796444 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.285-14974A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45796444 | |||||||
| chr12:45796502 | G | GTTTATTT others(13): Show |
4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-14907_285-1488 others(24): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45796502 | ||||||
| chr12:45796593 | A | G | 23 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(20): Show |
23 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.285-14825A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45796593 | |||||||
| chr12:45796786 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.285-14632A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45796786 | |||||||
| chr12:45797080 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0063 a0001c0001t0001g0097 |
3 | HG04184.hp2 NA19077.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.285-14338C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45797080 | |||||||
| chr12:45797295 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0233 |
2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.285-14123C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45797295 | |||||||
| chr12:45797309 | A | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
4 | NA18950.hp1 NA18980.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-14109A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45797309 | |||||||
| chr12:45797526 | T | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(201): Show |
205 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.285-13892T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45797526 | |||||||
| chr12:45797564 | A | C | 1 | a0001c0001t0001g0154 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.285-13854A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45797564 | |||||||
| chr12:45797591 | A | G | 2 | a0001c0001t0001g0249 a0001c0001t0001g0263 |
2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.285-13827A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45797591 | |||||||
| chr12:45797865 | T | A | 2 | a0001c0001t0003g0282 a0001c0001t0003g0314 |
2 | HG02738.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.285-13553T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45797865 | |||||||
| chr12:45798208 | GT | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(97): Show |
101 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.285-13200delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45798208 | ||||||
| chr12:45798383 | T | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0061 |
2 | NA18941.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.285-13035T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45798383 | |||||||
| chr12:45798443 | A | G | 1 | a0001c0016t0001g0296 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.285-12975A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45798443 | |||||||
| chr12:45798574 | A | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(209): Show |
213 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.285-12844A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45798574 | |||||||
| chr12:45798732 | AC | A | 25 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(22): Show |
25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-12685delC | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45798732 | |||||||
| chr12:45798799 | A | G | 2 | a0001c0009t0010g0207 a0001c0009t0010g0208 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.285-12619A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45798799 | |||||||
| chr12:45798869 | T | C | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-12549T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45798869 | |||||||
| chr12:45798904 | C | T | 2 | a0001c0009t0010g0207 a0001c0009t0010g0208 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.285-12514C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45798904 | |||||||
| chr12:45799444 | G | A | 39 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(36): Show |
39 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.285-11974G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45799444 | |||||||
| chr12:45799596 | C | G | 39 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(36): Show |
39 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.285-11822C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45799596 | |||||||
| chr12:45799788 | G | A | 1 | a0001c0002t0002g0216 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.285-11630G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45799788 | |||||||
| chr12:45800070 | G | A | 1 | a0001c0001t0001g0043 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.285-11348G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45800070 | |||||||
| chr12:45800128 | G | A | 2 | a0001c0001t0001g0249 a0001c0001t0001g0263 |
2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.285-11290G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45800128 | |||||||
| chr12:45800162 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.285-11256G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45800162 | |||||||
| chr12:45800521 | C | CAT | 213 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(210): Show |
214 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.285-10897_285-1089 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45800521 | |||||||
| chr12:45800650 | A | AAAG | 217 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(214): Show |
218 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.285-10767_285-1076 others(7): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45800650 | ||||||
| chr12:45800799 | A | C | 1 | a0001c0001t0001g0130 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.285-10619A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45800799 | |||||||
| chr12:45800978 | GAA | G | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-10438_285-1043 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45800978 | ||||||
| chr12:45801051 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0250 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.285-10367G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801051 | |||||||
| chr12:45801073 | G | C | 1 | a0001c0001t0001g0055 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.285-10345G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801073 | |||||||
| chr12:45801185 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.285-10233G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801185 | |||||||
| chr12:45801306 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.285-10112C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801306 | |||||||
| chr12:45801319 | G | GA | 28 | a0001c0001t0001g0008 a0001c0001t0001g0063 a0001c0001t0001g0244 others(25): Show |
28 | HG00544.hp2 HG01175.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.285-10086dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45801319 | ||||||
| chr12:45801332 | A | AAG | 45 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(42): Show |
45 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.285-10086_285-1008 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801332 | |||||||
| chr12:45801333 | G | T | 45 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(42): Show |
45 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.285-10085G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801333 | |||||||
| chr12:45801334 | T | G | 2 | a0001c0009t0010g0207 a0001c0009t0010g0208 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.285-10084T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801334 | |||||||
| chr12:45801370 | G | A | 7 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0070 others(4): Show |
7 | HG00438.hp2 HG00621.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.285-10048G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801370 | |||||||
| chr12:45801378 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.285-10040A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801378 | |||||||
| chr12:45801505 | C | G | 25 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(22): Show |
25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-9913C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801505 | |||||||
| chr12:45801968 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0057 |
2 | HG02165.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.285-9450G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801968 | |||||||
| chr12:45801971 | T | C | 2 | a0001c0001t0001g0137 a0001c0001t0016g0116 |
2 | HG03831.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.285-9447T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801971 | |||||||
| chr12:45802066 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(214): Show |
218 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.285-9352A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45802066 | |||||||
| chr12:45802473 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.285-8945G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45802473 | |||||||
| chr12:45802978 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.285-8440C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45802978 | |||||||
| chr12:45803084 | A | C | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-8334A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45803084 | |||||||
| chr12:45803189 | T | C | 3 | a0001c0001t0001g0153 a0001c0001t0001g0196 a0001c0001t0001g0312 |
3 | NA18966.hp2 NA19001.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.285-8229T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45803189 | |||||||
| chr12:45803243 | A | G | 3 | a0001c0001t0001g0249 a0001c0001t0001g0263 a0014c0018t0001g0262 |
3 | HG01109.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.285-8175A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45803243 | |||||||
| chr12:45803479 | A | C | 1 | a0001c0001t0001g0164 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.285-7939A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45803479 | |||||||
| chr12:45803535 | A | G | 1 | a0001c0002t0002g0219 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.285-7883A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45803535 | |||||||
| chr12:45803540 | G | A | 3 | a0001c0001t0001g0270 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.285-7878G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45803540 | |||||||
| chr12:45803612 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0185 |
2 | HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.285-7806C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45803612 | |||||||
| chr12:45803693 | G | T | 1 | a0001c0001t0001g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.285-7725G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45803693 | |||||||
| chr12:45803704 | G | T | 1 | a0001c0001t0001g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.285-7714G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45803704 | |||||||
| chr12:45803973 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.285-7445A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45803973 | |||||||
| chr12:45804042 | A | G | 6 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0044 others(3): Show |
6 | HG02135.hp1 NA18612.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-7376A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45804042 | |||||||
| chr12:45804251 | A | G | 4 | a0001c0001t0001g0110 a0001c0001t0001g0209 a0001c0009t0010g0207 others(1): Show |
4 | HG02717.hp1 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-7167A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45804251 | |||||||
| chr12:45804481 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.285-6937T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45804481 | |||||||
| chr12:45804728 | A | C | 5 | a0001c0001t0005g0273 a0001c0001t0005g0285 a0001c0001t0005g0286 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.285-6690A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45804728 | |||||||
| chr12:45804812 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.285-6606T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45804812 | |||||||
| chr12:45804867 | T | G | 1 | a0001c0001t0001g0234 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.285-6551T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45804867 | |||||||
| chr12:45805429 | G | T | 1 | a0001c0001t0001g0094 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.285-5989G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45805429 | |||||||
| chr12:45805600 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.285-5818G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45805600 | |||||||
| chr12:45805806 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(214): Show |
218 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.285-5612T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45805806 | |||||||
| chr12:45805822 | C | T | 44 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.285-5596C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45805822 | |||||||
| chr12:45806015 | T | C | 2 | a0001c0001t0012g0251 a0001c0001t0012g0252 |
2 | HG00741.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.285-5403T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45806015 | |||||||
| chr12:45806203 | A | AT | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-5203dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45806203 | ||||||
| chr12:45806226 | A | G | 39 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(36): Show |
39 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.285-5192A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45806226 | |||||||
| chr12:45806245 | T | C | 3 | a0001c0001t0001g0171 a0001c0001t0001g0189 a0001c0001t0001g0204 |
3 | HG00738.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.285-5173T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45806245 | |||||||
| chr12:45806613 | G | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(22): Show |
25 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-4805G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45806613 | |||||||
| chr12:45806792 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.285-4626G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45806792 | |||||||
| chr12:45807407 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(111): Show |
115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.285-4011A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45807407 | |||||||
| chr12:45807596 | A | G | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-3822A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45807596 | |||||||
| chr12:45807693 | AAC | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
4 | NA18950.hp1 NA18980.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-3723_285-3722d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45807693 | ||||||
| chr12:45807987 | C | T | 1 | a0001c0011t0018g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.285-3431C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45807987 | |||||||
| chr12:45808038 | A | G | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.285-3380A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808038 | |||||||
| chr12:45808117 | T | G | 66 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0084 others(63): Show |
66 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.285-3301T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808117 | |||||||
| chr12:45808119 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.285-3299C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808119 | |||||||
| chr12:45808167 | A | G | 39 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(36): Show |
39 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.285-3251A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808167 | |||||||
| chr12:45808316 | A | G | 45 | a0001c0001t0001g0054 a0001c0001t0001g0112 a0001c0001t0001g0138 others(42): Show |
45 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.285-3102A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808316 | |||||||
| chr12:45808358 | A | T | 25 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(22): Show |
25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-3060A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808358 | |||||||
| chr12:45808413 | A | G | 27 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(24): Show |
27 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.285-3005A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808413 | |||||||
| chr12:45808567 | A | G | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-2851A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808567 | |||||||
| chr12:45808688 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.285-2730C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808688 | |||||||
| chr12:45808690 | A | G | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG00140.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.285-2728A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808690 | |||||||
| chr12:45808732 | C | CGTGT | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-2683_285-2682i others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45808732 | ||||||
| chr12:45808736 | C | T | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-2682C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808736 | |||||||
| chr12:45808736 | CGT | C | 54 | a0001c0001t0001g0046 a0001c0001t0001g0050 a0001c0001t0001g0054 others(51): Show |
54 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.285-2659_285-2658d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45808736 | ||||||
| chr12:45808736 | CGTGT | C | 8 | a0001c0001t0001g0249 a0001c0001t0001g0263 a0001c0001t0001g0270 others(5): Show |
8 | HG01109.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.285-2661_285-2658d others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45808736 | ||||||
| chr12:45808753 | GTGTGTGT others(1): Show |
G | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-2657_285-2650d others(10): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45808753 | ||||||
| chr12:45808801 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.285-2617G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808801 | |||||||
| chr12:45808835 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.285-2583G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808835 | |||||||
| chr12:45808898 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.285-2520G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808898 | |||||||
| chr12:45808932 | T | G | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-2486T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808932 | |||||||
| chr12:45809235 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.285-2183A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45809235 | |||||||
| chr12:45809285 | C | G | 25 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(22): Show |
25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-2133C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45809285 | |||||||
| chr12:45809305 | A | G | 1 | a0008c0013t0001g0238 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.285-2113A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45809305 | |||||||
| chr12:45809494 | CCTT | C | 25 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(22): Show |
25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-1920_285-1918d others(5): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45809494 | ||||||
| chr12:45809875 | A | G | 1 | a0001c0001t0001g0004 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.285-1543A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45809875 | |||||||
| chr12:45810131 | T | G | 11 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(8): Show |
11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.285-1287T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45810131 | |||||||
| chr12:45810207 | G | T | 1 | a0001c0001t0001g0019 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.285-1211G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45810207 | |||||||
| chr12:45810686 | C | G | 1 | a0001c0001t0015g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.285-732C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45810686 | |||||||
| chr12:45810693 | G | T | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.285-725G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45810693 | |||||||
| chr12:45810694 | C | T | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.285-724C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45810694 | |||||||
| chr12:45810937 | C | T | 7 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(4): Show |
7 | HG02559.hp1 HG02738.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.285-481C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45810937 | |||||||
| chr12:45810983 | G | A | 1 | a0001c0002t0002g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.285-435G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45810983 | |||||||
| chr12:45811025 | C | T | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-393C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45811025 | |||||||
| chr12:45811131 | C | T | 4 | a0001c0001t0001g0294 a0001c0001t0001g0304 a0001c0001t0001g0308 others(1): Show |
4 | HG01975.hp1 HG01981.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-287C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45811131 | |||||||
| chr12:45811147 | T | G | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.285-271T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45811147 | |||||||
| chr12:45811247 | C | T | 1 | a0001c0011t0018g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.285-171C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45811247 | |||||||
| chr12:45811349 | T | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.285-69T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45811349 | |||||||
| chr12:45811908 | C | T | 3 | a0001c0006t0002g0136 a0001c0006t0002g0193 a0001c0006t0002g0194 |
3 | HG02622.hp2 HG02895.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.418+357C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45811908 | |||||||
| chr12:45812058 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.418+507A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45812058 | |||||||
| chr12:45812145 | A | T | 2 | a0001c0009t0010g0207 a0001c0009t0010g0208 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.418+594A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45812145 | |||||||
| chr12:45812310 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.418+759G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45812310 | |||||||
| chr12:45812346 | C | T | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.418+795C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45812346 | |||||||
| chr12:45812354 | G | A | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.418+803G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45812354 | |||||||
| chr12:45812509 | TCTG | T | 3 | a0001c0001t0001g0077 a0001c0001t0001g0102 a0007c0019t0001g0036 |
3 | HG00597.hp1 HG00621.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.418+959_418+961del others(3): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45812509 | |||||||
| chr12:45812513 | A | G | 3 | a0001c0001t0001g0077 a0001c0001t0001g0102 a0007c0019t0001g0036 |
3 | HG00597.hp1 HG00621.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.418+962A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45812513 | |||||||
| chr12:45812766 | C | T | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+1215C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45812766 | |||||||
| chr12:45813039 | G | C | 11 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(8): Show |
11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.418+1488G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45813039 | |||||||
| chr12:45813218 | CTG | C | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+1668_418+1669d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45813218 | |||||||
| chr12:45813458 | T | TA | 61 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(58): Show |
61 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.418+1923dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 45813458 | ||||||
| chr12:45813458 | T | TAA | 24 | a0001c0001t0001g0272 a0001c0002t0002g0210 a0001c0002t0002g0212 others(21): Show |
24 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.418+1922_418+1923d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 45813458 | ||||||
| chr12:45813458 | TA | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(104): Show |
108 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.418+1923delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 45813458 | ||||||
| chr12:45813548 | G | A | 2 | a0001c0001t0007g0195 a0001c0001t0007g0267 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.418+1997G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45813548 | |||||||
| chr12:45813573 | C | T | 2 | a0001c0002t0002g0256 a0001c0002t0002g0261 |
2 | HG01175.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.418+2022C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45813573 | |||||||
| chr12:45814073 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.418+2522G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814073 | |||||||
| chr12:45814151 | C | G | 2 | a0001c0001t0001g0151 a0001c0001t0001g0176 |
2 | NA18962.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.418+2600C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814151 | |||||||
| chr12:45814263 | C | G | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.418+2712C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814263 | |||||||
| chr12:45814371 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.418+2820C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814371 | |||||||
| chr12:45814539 | A | G | 2 | a0001c0001t0001g0249 a0001c0001t0001g0263 |
2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.418+2988A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814539 | |||||||
| chr12:45814581 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.418+3030C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814581 | |||||||
| chr12:45814588 | T | C | 3 | a0001c0001t0001g0270 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.418+3037T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814588 | |||||||
| chr12:45814599 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.418+3048G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814599 | |||||||
| chr12:45814636 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.419-3034A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814636 | |||||||
| chr12:45814655 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(104): Show |
108 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.419-3015A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814655 | |||||||
| chr12:45814890 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.419-2780G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814890 | |||||||
| chr12:45815286 | A | C | 1 | a0001c0001t0001g0167 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.419-2384A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45815286 | |||||||
| chr12:45815475 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.419-2195G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45815475 | |||||||
| chr12:45815599 | T | TTG | 36 | a0001c0001t0001g0032 a0001c0001t0001g0066 a0001c0001t0001g0071 others(33): Show |
36 | HG01109.hp2 HG01175.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.419-2049_419-2048d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 45815599 | ||||||
| chr12:45815599 | TTG | T | 3 | a0001c0001t0001g0122 a0001c0001t0004g0131 a0001c0006t0002g0194 |
3 | HG00642.hp2 HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.419-2049_419-2048d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 45815599 | ||||||
| chr12:45815654 | G | A | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.419-2016G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45815654 | |||||||
| chr12:45815698 | G | A | 8 | a0001c0001t0001g0141 a0001c0001t0001g0146 a0001c0001t0001g0147 others(5): Show |
8 | HG01167.hp2 HG02602.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-1972G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45815698 | |||||||
| chr12:45815737 | C | T | 2 | a0001c0001t0012g0251 a0001c0001t0012g0252 |
2 | HG00741.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.419-1933C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45815737 | |||||||
| chr12:45815849 | C | G | 1 | a0001c0001t0001g0046 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.419-1821C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45815849 | |||||||
| chr12:45816341 | A | G | 1 | a0001c0006t0002g0193 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.419-1329A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45816341 | |||||||
| chr12:45816383 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.419-1287T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45816383 | |||||||
| chr12:45816674 | C | T | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.419-996C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45816674 | |||||||
| chr12:45816805 | A | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | NA19064.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.419-865A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45816805 | |||||||
| chr12:45816960 | C | T | 1 | a0013c0015t0001g0295 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.419-710C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45816960 | |||||||
| chr12:45817128 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.419-542G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45817128 | |||||||
| chr12:45817294 | C | T | 1 | a0001c0002t0002g0217 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.419-376C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45817294 | |||||||
| chr12:45817431 | T | A | 46 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(43): Show |
46 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.419-239T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45817431 | |||||||
| chr12:45817506 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.419-164G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45817506 | |||||||
| chr12:45817526 | T | TTATATTT others(32): Show |
4 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.419-137_419-99dupT others(38): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 45817526 | ||||||
| chr12:45817613 | T | C | 43 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(40): Show |
43 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.419-57T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45817613 | |||||||
| chr12:45817967 | T | C | 1 | a0001c0001t0001g0306 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.637+79T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45817967 | |||||||
| chr12:45818157 | T | C | 1 | a0011c0010t0002g0206 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.637+269T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45818157 | |||||||
| chr12:45818390 | C | A | 22 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0117 others(19): Show |
22 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.637+502C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45818390 | |||||||
| chr12:45818392 | A | G | 2 | a0001c0001t0001g0249 a0001c0001t0001g0263 |
2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.637+504A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45818392 | |||||||
| chr12:45818761 | T | G | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.637+873T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45818761 | |||||||
| chr12:45818908 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.637+1020A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45818908 | |||||||
| chr12:45819093 | A | G | 5 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0004c0005t0001g0111 others(2): Show |
5 | NA18747.hp1 NA18956.hp2 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+1205A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45819093 | |||||||
| chr12:45819130 | T | A | 5 | a0001c0002t0002g0254 a0001c0002t0002g0255 a0001c0002t0002g0259 others(2): Show |
5 | HG02630.hp2 HG02922.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+1242T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45819130 | |||||||
| chr12:45819251 | C | G | 28 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(25): Show |
28 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+1363C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45819251 | |||||||
| chr12:45819510 | T | C | 11 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(8): Show |
11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.637+1622T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45819510 | |||||||
| chr12:45819656 | A | G | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-1764A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45819656 | |||||||
| chr12:45819684 | C | A | 1 | a0001c0002t0002g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.638-1736C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45819684 | |||||||
| chr12:45819808 | G | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(200): Show |
204 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.638-1612G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45819808 | |||||||
| chr12:45819930 | G | C | 2 | a0001c0001t0005g0285 a0001c0001t0005g0286 |
2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.638-1490G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45819930 | |||||||
| chr12:45819967 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.638-1453C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45819967 | |||||||
| chr12:45820035 | T | A | 1 | a0001c0001t0001g0013 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.638-1385T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45820035 | |||||||
| chr12:45820084 | A | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(23): Show |
26 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.638-1336A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45820084 | |||||||
| chr12:45820208 | A | G | 4 | a0001c0001t0001g0053 a0001c0001t0001g0071 a0001c0001t0001g0093 others(1): Show |
4 | NA18966.hp1 NA18969.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-1212A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45820208 | |||||||
| chr12:45820321 | T | C | 1 | a0001c0006t0002g0136 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.638-1099T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45820321 | |||||||
| chr12:45820526 | C | T | 1 | a0001c0011t0018g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.638-894C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45820526 | |||||||
| chr12:45820616 | T | C | 2 | a0001c0001t0001g0227 a0001c0001t0001g0245 |
2 | HG02683.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.638-804T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45820616 | |||||||
| chr12:45820717 | T | C | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-703T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45820717 | |||||||
| chr12:45820775 | T | C | 1 | a0001c0001t0012g0251 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.638-645T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45820775 | |||||||
| chr12:45821018 | T | C | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.638-402T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45821018 | |||||||
| chr12:45821364 | A | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.638-56A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45821364 | |||||||
| chr12:45821380 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(161): Show |
165 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.638-40G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45821380 | |||||||
| chr12:45821585 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.705+98A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45821585 | |||||||
| chr12:45821611 | T | C | 1 | a0005c0008t0001g0034 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.705+124T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45821611 | |||||||
| chr12:45821673 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0075 |
3 | NA18947.hp1 NA18970.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.705+186C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45821673 | |||||||
| chr12:45822112 | T | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+625T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45822112 | |||||||
| chr12:45822135 | A | G | 1 | a0001c0001t0001g0027 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.705+648A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45822135 | |||||||
| chr12:45822377 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.705+890T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45822377 | |||||||
| chr12:45822623 | T | G | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.705+1136T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45822623 | |||||||
| chr12:45822876 | C | T | 45 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(42): Show |
45 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.705+1389C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45822876 | |||||||
| chr12:45823180 | A | G | 1 | a0002c0003t0001g0142 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.705+1693A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45823180 | |||||||
| chr12:45823256 | T | C | 1 | a0001c0016t0001g0296 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.705+1769T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45823256 | |||||||
| chr12:45823580 | CAAAT | C | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.705+2097_705+2100d others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45823580 | ||||||
| chr12:45823688 | G | GA | 24 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(21): Show |
24 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.705+2207dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45823688 | ||||||
| chr12:45823722 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.705+2235C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45823722 | |||||||
| chr12:45823889 | A | G | 5 | a0001c0001t0001g0231 a0001c0001t0001g0294 a0001c0001t0001g0304 others(2): Show |
5 | HG01975.hp1 HG01981.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.705+2402A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45823889 | |||||||
| chr12:45824012 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.705+2525G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45824012 | |||||||
| chr12:45824096 | T | C | 11 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(8): Show |
11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.705+2609T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45824096 | |||||||
| chr12:45824125 | A | G | 3 | a0001c0001t0001g0143 a0001c0001t0001g0177 a0012c0012t0001g0187 |
3 | NA18940.hp2 NA18947.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.705+2638A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45824125 | |||||||
| chr12:45824331 | GGAAAAAC others(15): Show |
G | 1 | a0001c0001t0001g0050 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.705+2857_705+2878d others(24): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45824331 | ||||||
| chr12:45824427 | A | G | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.705+2940A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45824427 | |||||||
| chr12:45824491 | A | G | 2 | a0001c0001t0001g0032 a0001c0001t0001g0066 |
2 | HG01192.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.705+3004A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45824491 | |||||||
| chr12:45824540 | A | C | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.705+3053A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45824540 | |||||||
| chr12:45824689 | T | G | 2 | a0001c0001t0008g0128 a0001c0001t0008g0222 |
2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.705+3202T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45824689 | |||||||
| chr12:45824713 | C | T | 24 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(21): Show |
24 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.705+3226C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45824713 | |||||||
| chr12:45824758 | A | G | 1 | a0001c0009t0010g0208 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.705+3271A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45824758 | |||||||
| chr12:45824840 | G | A | 24 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(21): Show |
24 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.705+3353G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45824840 | |||||||
| chr12:45824866 | C | CAT | 12 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(9): Show |
13 | HG00438.hp1 HG02056.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.705+3394_705+3395d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45824866 | ||||||
| chr12:45824866 | CAT | C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0154 a0001c0001t0001g0292 others(1): Show |
4 | HG02132.hp2 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+3394_705+3395d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45824866 | ||||||
| chr12:45825022 | G | T | 1 | a0001c0011t0018g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.705+3535G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45825022 | |||||||
| chr12:45825161 | A | G | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.705+3674A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45825161 | |||||||
| chr12:45825735 | A | G | 45 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(42): Show |
45 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.705+4248A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45825735 | |||||||
| chr12:45825837 | A | G | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.705+4350A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45825837 | |||||||
| chr12:45825871 | A | G | 1 | a0003c0004t0006g0107 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.705+4384A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45825871 | |||||||
| chr12:45825911 | A | G | 1 | a0001c0001t0001g0005 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.705+4424A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45825911 | |||||||
| chr12:45825930 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.705+4443G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45825930 | |||||||
| chr12:45825992 | C | T | 1 | a0010c0014t0007g0269 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.705+4505C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45825992 | |||||||
| chr12:45826327 | G | A | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.705+4840G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45826327 | |||||||
| chr12:45826361 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.705+4874G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45826361 | |||||||
| chr12:45826425 | T | C | 4 | a0001c0001t0001g0294 a0001c0001t0001g0304 a0001c0001t0001g0308 others(1): Show |
4 | HG01975.hp1 HG01981.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+4938T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45826425 | |||||||
| chr12:45826458 | T | C | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.705+4971T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45826458 | |||||||
| chr12:45826569 | C | CA | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.705+5083dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45826569 | ||||||
| chr12:45826617 | A | T | 1 | a0001c0001t0001g0298 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.705+5130A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45826617 | |||||||
| chr12:45826671 | G | A | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.705+5184G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45826671 | |||||||
| chr12:45826684 | G | A | 2 | a0002c0003t0001g0237 a0002c0003t0001g0243 |
2 | NA19060.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.705+5197G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45826684 | |||||||
| chr12:45826727 | A | G | 1 | a0001c0001t0012g0251 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.705+5240A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45826727 | |||||||
| chr12:45827091 | C | A | 5 | a0001c0001t0001g0112 a0001c0001t0001g0139 a0001c0001t0001g0229 others(2): Show |
5 | HG01069.hp1 HG01071.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.705+5604C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45827091 | |||||||
| chr12:45827110 | T | G | 1 | a0001c0002t0002g0211 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.705+5623T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45827110 | |||||||
| chr12:45827149 | A | T | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.705+5662A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45827149 | |||||||
| chr12:45827811 | T | C | 1 | a0001c0001t0001g0008 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.705+6324T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45827811 | |||||||
| chr12:45828113 | G | A | 11 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(8): Show |
11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.705+6626G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828113 | |||||||
| chr12:45828143 | A | C | 1 | a0001c0001t0001g0094 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.705+6656A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828143 | |||||||
| chr12:45828143 | A | G | 1 | a0001c0002t0002g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.705+6656A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828143 | |||||||
| chr12:45828339 | G | T | 4 | a0001c0001t0005g0273 a0001c0001t0005g0286 a0001c0001t0005g0288 others(1): Show |
4 | HG01891.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.705+6852G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828339 | |||||||
| chr12:45828540 | T | C | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.705+7053T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828540 | |||||||
| chr12:45828564 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.705+7077G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828564 | |||||||
| chr12:45828595 | C | T | 1 | a0002c0003t0001g0307 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.705+7108C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828595 | |||||||
| chr12:45828662 | G | C | 1 | a0003c0004t0017g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.705+7175G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828662 | |||||||
| chr12:45828686 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.705+7199G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828686 | |||||||
| chr12:45828746 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0095 |
2 | HG00438.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.705+7259A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828746 | |||||||
| chr12:45828945 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.705+7458A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828945 | |||||||
| chr12:45829365 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(111): Show |
115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.706-7224T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45829365 | |||||||
| chr12:45829600 | T | A | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-6989T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45829600 | |||||||
| chr12:45829638 | T | A | 4 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.706-6951T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45829638 | |||||||
| chr12:45829792 | T | TTTC | 75 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(72): Show |
75 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.706-6788_706-6786d others(5): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45829792 | ||||||
| chr12:45829802 | T | TTC | 136 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0084 others(133): Show |
137 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.706-6786_706-6785i others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45829802 | ||||||
| chr12:45829803 | T | TC | 5 | a0001c0001t0001g0038 a0001c0001t0001g0121 a0001c0001t0001g0160 others(2): Show |
5 | HG01069.hp2 HG01256.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.706-6786_706-6785i others(3): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45829803 | |||||||
| chr12:45829898 | G | C | 28 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(25): Show |
28 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.706-6691G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45829898 | |||||||
| chr12:45829991 | G | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.706-6598G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45829991 | |||||||
| chr12:45830136 | G | A | 11 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(8): Show |
11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.706-6453G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45830136 | |||||||
| chr12:45830195 | T | G | 1 | a0001c0001t0001g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.706-6394T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45830195 | |||||||
| chr12:45830280 | A | G | 26 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(23): Show |
26 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.706-6309A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45830280 | |||||||
| chr12:45830356 | T | G | 3 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | HG00140.hp1 HG01934.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.706-6233T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45830356 | |||||||
| chr12:45830358 | C | T | 6 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0182 others(3): Show |
6 | NA18959.hp2 NA18973.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-6231C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45830358 | |||||||
| chr12:45830368 | G | A | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-6221G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45830368 | |||||||
| chr12:45830831 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0095 |
2 | HG00438.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.706-5758A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45830831 | |||||||
| chr12:45830912 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.706-5677G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45830912 | |||||||
| chr12:45830913 | C | A | 1 | a0001c0001t0001g0062 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.706-5676C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45830913 | |||||||
| chr12:45830988 | G | A | 2 | a0001c0001t0001g0249 a0001c0001t0001g0263 |
2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.706-5601G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45830988 | |||||||
| chr12:45831031 | C | T | 23 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(20): Show |
23 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.706-5558C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45831031 | |||||||
| chr12:45831236 | C | T | 4 | a0001c0001t0001g0270 a0001c0001t0001g0290 a0001c0001t0001g0291 others(1): Show |
4 | HG02615.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.706-5353C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45831236 | |||||||
| chr12:45831250 | C | A | 1 | a0001c0001t0015g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.706-5339C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45831250 | |||||||
| chr12:45831364 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0082 |
2 | HG00621.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.706-5225C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45831364 | |||||||
| chr12:45831369 | GTTAT | G | 6 | a0001c0001t0001g0123 a0001c0001t0001g0143 a0001c0001t0001g0151 others(3): Show |
6 | HG01074.hp2 NA18940.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.706-5212_706-5209d others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45831369 | ||||||
| chr12:45831536 | T | C | 1 | a0001c0001t0001g0027 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.706-5053T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45831536 | |||||||
| chr12:45831627 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.706-4962A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45831627 | |||||||
| chr12:45831724 | A | G | 5 | a0001c0001t0005g0273 a0001c0001t0005g0285 a0001c0001t0005g0286 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.706-4865A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45831724 | |||||||
| chr12:45831811 | C | G | 11 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(8): Show |
11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.706-4778C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45831811 | |||||||
| chr12:45832414 | G | A | 11 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(8): Show |
11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.706-4175G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45832414 | |||||||
| chr12:45832702 | C | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(107): Show |
111 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.706-3887C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45832702 | |||||||
| chr12:45832760 | C | G | 1 | a0001c0001t0001g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.706-3829C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45832760 | |||||||
| chr12:45832957 | A | G | 11 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(8): Show |
11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.706-3632A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45832957 | |||||||
| chr12:45833867 | A | G | 24 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(21): Show |
24 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.706-2722A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45833867 | |||||||
| chr12:45833883 | T | C | 1 | a0003c0004t0017g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.706-2706T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45833883 | |||||||
| chr12:45834199 | A | G | 3 | a0001c0001t0001g0068 a0005c0008t0001g0034 a0005c0008t0001g0039 |
3 | HG02135.hp1 NA18612.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.706-2390A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45834199 | |||||||
| chr12:45834260 | C | CT | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-2317dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45834260 | ||||||
| chr12:45834272 | T | C | 1 | a0001c0011t0018g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.706-2317T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45834272 | |||||||
| chr12:45834458 | T | C | 1 | a0001c0001t0001g0315 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.706-2131T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45834458 | |||||||
| chr12:45834464 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.706-2125G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45834464 | |||||||
| chr12:45834487 | A | G | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-2102A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45834487 | |||||||
| chr12:45834697 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(110): Show |
114 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.706-1892G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45834697 | |||||||
| chr12:45834843 | C | G | 1 | a0001c0001t0001g0229 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.706-1746C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45834843 | |||||||
| chr12:45835083 | T | A | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.706-1506T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45835083 | |||||||
| chr12:45835289 | G | C | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.706-1300G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45835289 | |||||||
| chr12:45835346 | A | G | 1 | a0001c0002t0002g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.706-1243A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45835346 | |||||||
| chr12:45835499 | C | CA | 26 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(23): Show |
26 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.706-1080dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45835499 | ||||||
| chr12:45835628 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0052 |
2 | NA18747.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.706-961G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45835628 | |||||||
| chr12:45835684 | A | G | 11 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(8): Show |
11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.706-905A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45835684 | |||||||
| chr12:45835900 | C | CA | 7 | a0001c0001t0001g0038 a0001c0001t0003g0280 a0001c0001t0003g0281 others(4): Show |
7 | HG02486.hp2 HG02738.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.706-678dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45835900 | ||||||
| chr12:45835906 | A | C | 1 | a0001c0001t0015g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.706-683A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45835906 | |||||||
| chr12:45835912 | C | A | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-677C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45835912 | |||||||
| chr12:45835912 | C | CAAA | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.706-674_706-672dup others(3): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45835912 | ||||||
| chr12:45835918 | C | A | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-671C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45835918 | |||||||
| chr12:45835925 | G | C | 11 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(8): Show |
11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.706-664G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45835925 | |||||||
| chr12:45835949 | TTA | T | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-639_706-638del others(2): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45835949 | |||||||
| chr12:45836248 | C | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(94): Show |
98 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.706-341C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45836248 | |||||||
| chr12:45836556 | A | C | 1 | a0001c0011t0018g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.706-33A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45836556 | |||||||
| chr12:45836727 | A | C | 5 | a0001c0001t0004g0131 a0001c0001t0004g0132 a0001c0001t0004g0133 others(2): Show |
5 | HG02615.hp1 HG02647.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.773-14A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 7/20 | chr12 | 45836727 | |||||||
| chr12:45837141 | A | C | 1 | a0001c0001t0001g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1023+150A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 8/20 | chr12 | 45837141 | |||||||
| chr12:45838102 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1330+395T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45838102 | |||||||
| chr12:45838170 | C | T | 22 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0117 others(19): Show |
22 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.1330+463C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45838170 | |||||||
| chr12:45838322 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1330+615A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45838322 | |||||||
| chr12:45838389 | T | C | 2 | a0001c0009t0010g0207 a0001c0009t0010g0208 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1330+682T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45838389 | |||||||
| chr12:45838868 | G | GT | 41 | a0001c0001t0001g0067 a0001c0001t0001g0076 a0001c0001t0001g0086 others(38): Show |
41 | HG00544.hp2 HG01167.hp1 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.1331-446dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr12 | 45838868 | ||||||
| chr12:45838868 | G | GTT | 7 | a0001c0001t0003g0314 a0001c0002t0002g0211 a0003c0004t0006g0105 others(4): Show |
7 | HG02451.hp1 HG02451.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1331-447_1331-446d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr12 | 45838868 | ||||||
| chr12:45838868 | G | T | 2 | a0001c0001t0008g0128 a0001c0001t0008g0222 |
2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1331-461G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45838868 | |||||||
| chr12:45838873 | T | G | 2 | a0001c0009t0010g0207 a0001c0009t0010g0208 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1331-456T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45838873 | |||||||
| chr12:45838965 | A | G | 1 | a0014c0018t0001g0262 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1331-364A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45838965 | |||||||
| chr12:45839020 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1331-309G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45839020 | |||||||
| chr12:45839110 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1331-219C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45839110 | |||||||
| chr12:45839217 | T | G | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1331-112T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45839217 | |||||||
| chr12:45839259 | T | C | 4 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1331-70T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45839259 | |||||||
| chr12:45839753 | T | C | 1 | a0001c0001t0001g0045 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1498+257T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45839753 | |||||||
| chr12:45839814 | G | A | 1 | a0001c0001t0014g0175 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1498+318G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45839814 | |||||||
| chr12:45839847 | A | G | 1 | a0001c0011t0018g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1498+351A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45839847 | |||||||
| chr12:45839946 | G | C | 1 | a0001c0001t0001g0096 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1498+450G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45839946 | |||||||
| chr12:45840196 | C | A | 1 | a0002c0003t0001g0246 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1498+700C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45840196 | |||||||
| chr12:45840228 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1498+732A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45840228 | |||||||
| chr12:45840262 | A | G | 5 | a0001c0001t0005g0273 a0001c0001t0005g0285 a0001c0001t0005g0286 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498+766A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45840262 | |||||||
| chr12:45840684 | A | G | 4 | a0001c0001t0005g0285 a0001c0001t0008g0128 a0001c0001t0008g0221 others(1): Show |
4 | HG02258.hp1 HG02630.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1498+1188A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45840684 | |||||||
| chr12:45840738 | T | C | 1 | a0014c0018t0001g0262 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1498+1242T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45840738 | |||||||
| chr12:45840788 | C | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0164 |
3 | HG02056.hp2 NA18612.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1498+1292C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45840788 | |||||||
| chr12:45841019 | C | T | 2 | a0001c0001t0001g0245 a0001c0001t0001g0306 |
2 | HG01168.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1498+1523C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45841019 | |||||||
| chr12:45841087 | G | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1498+1591G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45841087 | |||||||
| chr12:45841211 | A | G | 5 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(2): Show |
5 | HG03239.hp2 HG03704.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498+1715A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45841211 | |||||||
| chr12:45841211 | A | T | 1 | a0001c0001t0003g0314 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1498+1715A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45841211 | |||||||
| chr12:45841404 | G | C | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1498+1908G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45841404 | |||||||
| chr12:45841884 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1498+2388C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45841884 | |||||||
| chr12:45842085 | C | T | 2 | a0001c0001t0001g0272 a0001c0011t0018g0271 |
2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1498+2589C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45842085 | |||||||
| chr12:45842109 | A | T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1498+2613A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45842109 | |||||||
| chr12:45842234 | C | CA | 23 | a0001c0001t0001g0022 a0001c0001t0001g0063 a0001c0001t0001g0097 others(20): Show |
23 | HG01175.hp1 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1498+2753dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 45842234 | ||||||
| chr12:45842234 | CA | C | 13 | a0001c0001t0001g0248 a0001c0001t0001g0265 a0001c0001t0001g0270 others(10): Show |
13 | HG02615.hp2 HG02738.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.1498+2753delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 45842234 | ||||||
| chr12:45842250 | T | A | 1 | a0001c0002t0002g0255 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1498+2754T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45842250 | |||||||
| chr12:45842295 | GTGTATAT others(17): Show |
G | 3 | a0001c0001t0001g0125 a0001c0001t0001g0171 a0001c0001t0001g0204 |
3 | HG01192.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1498+2833_1498+285 others(28): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 45842295 | ||||||
| chr12:45842481 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1498+2985G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45842481 | |||||||
| chr12:45842574 | T | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0185 |
2 | HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1498+3078T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45842574 | |||||||
| chr12:45842683 | G | A | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498+3187G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45842683 | |||||||
| chr12:45842847 | A | G | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498+3351A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45842847 | |||||||
| chr12:45843137 | G | C | 4 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1498+3641G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843137 | |||||||
| chr12:45843279 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1499-3577C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843279 | |||||||
| chr12:45843286 | T | TTTAGCTA others(507): Show |
5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1499-3570_1499-356 others(518): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843286 | |||||||
| chr12:45843329 | A | C | 7 | a0001c0001t0001g0004 a0001c0001t0001g0114 a0001c0001t0001g0117 others(4): Show |
7 | HG00280.hp2 HG00639.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.1499-3527A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843329 | |||||||
| chr12:45843375 | C | CT | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1499-3466dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 45843375 | ||||||
| chr12:45843378 | T | C | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1499-3478T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843378 | |||||||
| chr12:45843401 | C | T | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1499-3455C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843401 | |||||||
| chr12:45843471 | A | G | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1499-3385A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843471 | |||||||
| chr12:45843750 | T | G | 5 | a0001c0001t0005g0273 a0001c0001t0005g0285 a0001c0001t0005g0286 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1499-3106T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843750 | |||||||
| chr12:45843754 | T | C | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | NA19064.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1499-3102T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843754 | |||||||
| chr12:45843841 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1499-3015C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843841 | |||||||
| chr12:45843850 | C | G | 4 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1499-3006C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843850 | |||||||
| chr12:45843938 | C | T | 7 | a0001c0001t0001g0226 a0001c0001t0001g0270 a0001c0001t0001g0290 others(4): Show |
7 | HG01346.hp1 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1499-2918C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843938 | |||||||
| chr12:45843982 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1499-2874C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843982 | |||||||
| chr12:45844141 | G | A | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1499-2715G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45844141 | |||||||
| chr12:45844141 | G | C | 1 | a0001c0001t0001g0041 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1499-2715G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45844141 | |||||||
| chr12:45844258 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1499-2598A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45844258 | |||||||
| chr12:45844378 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1499-2478G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45844378 | |||||||
| chr12:45844576 | G | C | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1499-2280G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45844576 | |||||||
| chr12:45844728 | C | G | 2 | a0001c0001t0001g0249 a0001c0001t0001g0263 |
2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1499-2128C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45844728 | |||||||
| chr12:45844781 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1499-2075C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45844781 | |||||||
| chr12:45844857 | C | T | 44 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.1499-1999C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45844857 | |||||||
| chr12:45844891 | C | T | 2 | a0001c0001t0001g0270 a0001c0001t0001g0291 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1499-1965C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45844891 | |||||||
| chr12:45845161 | C | T | 2 | a0001c0009t0010g0207 a0001c0009t0010g0208 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1499-1695C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45845161 | |||||||
| chr12:45845229 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1499-1627G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45845229 | |||||||
| chr12:45845317 | T | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0185 |
2 | HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1499-1539T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45845317 | |||||||
| chr12:45845346 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0074 a0001c0001t0001g0100 |
3 | HG02486.hp1 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1499-1510T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45845346 | |||||||
| chr12:45845369 | T | G | 3 | a0001c0001t0001g0270 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1499-1487T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45845369 | |||||||
| chr12:45845635 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1499-1221G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45845635 | |||||||
| chr12:45845742 | A | G | 2 | a0001c0001t0007g0195 a0001c0001t0007g0267 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1499-1114A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45845742 | |||||||
| chr12:45845826 | G | T | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1499-1030G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45845826 | |||||||
| chr12:45845934 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1499-922T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45845934 | |||||||
| chr12:45846378 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1499-478G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45846378 | |||||||
| chr12:45846397 | C | T | 2 | a0001c0002t0002g0256 a0001c0002t0002g0261 |
2 | HG01175.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1499-459C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45846397 | |||||||
| chr12:45846480 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1499-376T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45846480 | |||||||
| chr12:45846505 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1499-351C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45846505 | |||||||
| chr12:45846615 | T | C | 3 | a0001c0001t0001g0249 a0001c0001t0001g0263 a0014c0018t0001g0262 |
3 | HG01109.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1499-241T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45846615 | |||||||
| chr12:45846679 | A | G | 1 | a0002c0003t0001g0148 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1499-177A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45846679 | |||||||
| chr12:45846744 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1499-112C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45846744 | |||||||
| chr12:45846775 | G | T | 1 | a0001c0001t0001g0043 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1499-81G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45846775 | |||||||
| chr12:45847039 | T | C | 3 | a0004c0005t0001g0111 a0004c0005t0001g0168 a0004c0005t0001g0169 |
3 | NA18747.hp1 NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1580+102T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45847039 | |||||||
| chr12:45847380 | T | A | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(310): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1580+443T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45847380 | |||||||
| chr12:45847397 | T | G | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1580+460T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45847397 | |||||||
| chr12:45847436 | A | T | 1 | a0001c0001t0001g0279 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1580+499A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45847436 | |||||||
| chr12:45847483 | C | G | 1 | a0013c0015t0001g0295 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1580+546C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45847483 | |||||||
| chr12:45847636 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1580+699C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45847636 | |||||||
| chr12:45847687 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0204 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1580+750C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45847687 | |||||||
| chr12:45847703 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1580+766G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45847703 | |||||||
| chr12:45847911 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1581-925A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45847911 | |||||||
| chr12:45848114 | T | A | 3 | a0001c0001t0001g0008 a0001c0009t0010g0207 a0001c0009t0010g0208 |
3 | HG02056.hp1 HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1581-722T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45848114 | |||||||
| chr12:45848400 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1581-436C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45848400 | |||||||
| chr12:45848412 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1581-424G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45848412 | |||||||
| chr12:45848632 | T | C | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1581-204T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45848632 | |||||||
| chr12:45848658 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1581-178C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45848658 | |||||||
| chr12:45848701 | C | T | 2 | a0001c0002t0002g0256 a0001c0002t0002g0261 |
2 | HG01175.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1581-135C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45848701 | |||||||
| chr12:45849099 | G | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1715+129G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 13/20 | chr12 | 45849099 | |||||||
| chr12:45849106 | T | C | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1715+136T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 13/20 | chr12 | 45849106 | |||||||
| chr12:45849336 | T | G | 3 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 |
3 | HG01167.hp1 HG01169.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1716-244T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 13/20 | chr12 | 45849336 | |||||||
| chr12:45849411 | G | A | 2 | a0001c0001t0001g0023 a0001c0001t0001g0048 |
2 | HG00609.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1716-169G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 13/20 | chr12 | 45849411 | |||||||
| chr12:45853204 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4773+308G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45853204 | |||||||
| chr12:45853286 | G | A | 1 | a0001c0001t0015g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4773+390G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45853286 | |||||||
| chr12:45853515 | A | G | 7 | a0001c0001t0001g0248 a0001c0001t0001g0265 a0003c0004t0006g0105 others(4): Show |
7 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.4773+619A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45853515 | |||||||
| chr12:45853807 | A | G | 1 | a0001c0011t0018g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4773+911A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45853807 | |||||||
| chr12:45853870 | G | A | 40 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(37): Show |
40 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(37): Show |
intron_variant | MODIFIER | c.4773+974G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45853870 | |||||||
| chr12:45853888 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4773+992C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45853888 | |||||||
| chr12:45853961 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0095 |
2 | HG00438.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.4773+1065C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45853961 | |||||||
| chr12:45854004 | C | T | 2 | a0001c0001t0001g0270 a0001c0001t0001g0291 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4773+1108C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45854004 | |||||||
| chr12:45854005 | G | A | 6 | a0002c0003t0001g0246 a0003c0004t0006g0105 a0003c0004t0006g0106 others(3): Show |
6 | HG02155.hp1 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.4773+1109G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45854005 | |||||||
| chr12:45854021 | G | A | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+1125G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45854021 | |||||||
| chr12:45854125 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0009 |
2 | HG00544.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.4773+1229C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45854125 | |||||||
| chr12:45854145 | C | T | 1 | a0001c0001t0011g0119 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4773+1249C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45854145 | |||||||
| chr12:45854308 | G | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0174 |
3 | HG01167.hp2 HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4773+1412G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45854308 | |||||||
| chr12:45854383 | G | A | 2 | a0004c0005t0001g0168 a0004c0005t0001g0169 |
2 | NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.4773+1487G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45854383 | |||||||
| chr12:45855017 | T | C | 45 | a0001c0001t0001g0003 a0001c0001t0003g0280 a0001c0001t0003g0281 others(42): Show |
45 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(42): Show |
intron_variant | MODIFIER | c.4773+2121T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855017 | |||||||
| chr12:45855036 | T | G | 3 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 |
3 | HG01167.hp1 HG01169.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4773+2140T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855036 | |||||||
| chr12:45855104 | G | A | 22 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0117 others(19): Show |
22 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.4773+2208G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855104 | |||||||
| chr12:45855271 | C | G | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+2375C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855271 | |||||||
| chr12:45855376 | A | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0245 |
2 | HG02683.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.4773+2480A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855376 | |||||||
| chr12:45855563 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4773+2667A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855563 | |||||||
| chr12:45855644 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(214): Show |
218 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.4773+2748T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855644 | |||||||
| chr12:45855670 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4773+2774A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855670 | |||||||
| chr12:45855731 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4773+2835G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855731 | |||||||
| chr12:45855859 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.4773+2963C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855859 | |||||||
| chr12:45855889 | T | C | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+2993T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855889 | |||||||
| chr12:45855904 | T | G | 1 | a0001c0001t0001g0185 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4773+3008T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855904 | |||||||
| chr12:45855909 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4773+3013G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855909 | |||||||
| chr12:45855947 | T | C | 1 | a0003c0004t0017g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4773+3051T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855947 | |||||||
| chr12:45856004 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4773+3108T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45856004 | |||||||
| chr12:45856067 | C | CT | 46 | a0001c0001t0001g0015 a0001c0001t0001g0024 a0001c0001t0001g0025 others(43): Show |
46 | HG01106.hp2 HG01109.hp2 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.4773+3196dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr12 | 45856067 | ||||||
| chr12:45856067 | C | CTT | 36 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(33): Show |
36 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.4773+3195_4773+319 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr12 | 45856067 | ||||||
| chr12:45856067 | CT | C | 13 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0081 others(10): Show |
13 | HG01167.hp1 HG01256.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.4773+3196delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr12 | 45856067 | ||||||
| chr12:45856067 | CTTTTTTT others(4): Show |
C | 1 | a0001c0016t0001g0296 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4773+3186_4773+319 others(15): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr12 | 45856067 | ||||||
| chr12:45856067 | CTTTTTTT others(5): Show |
C | 7 | a0001c0001t0001g0023 a0001c0001t0001g0048 a0003c0004t0006g0105 others(4): Show |
7 | HG00609.hp1 HG02300.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.4773+3185_4773+319 others(16): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr12 | 45856067 | ||||||
| chr12:45856067 | CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0005g0273 a0001c0001t0005g0286 a0001c0001t0005g0288 others(1): Show |
4 | HG01891.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4773+3184_4773+319 others(17): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr12 | 45856067 | ||||||
| chr12:45856075 | T | C | 5 | a0001c0001t0003g0281 a0001c0001t0003g0282 a0001c0001t0003g0283 others(2): Show |
5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+3179T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45856075 | |||||||
| chr12:45856076 | T | C | 1 | a0001c0001t0003g0280 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4773+3180T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45856076 | |||||||
| chr12:45857018 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4774-3783A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45857018 | |||||||
| chr12:45857049 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4774-3752T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45857049 | |||||||
| chr12:45857228 | A | C | 1 | a0001c0001t0001g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4774-3573A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45857228 | |||||||
| chr12:45857406 | A | T | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4774-3395A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45857406 | |||||||
| chr12:45857435 | A | G | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-3366A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45857435 | |||||||
| chr12:45857486 | T | C | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4774-3315T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45857486 | |||||||
| chr12:45857791 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4774-3010G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45857791 | |||||||
| chr12:45858049 | C | T | 29 | a0001c0001t0004g0131 a0001c0001t0004g0132 a0001c0001t0004g0133 others(26): Show |
29 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4774-2752C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45858049 | |||||||
| chr12:45858454 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4774-2347G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45858454 | |||||||
| chr12:45858946 | A | C | 8 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0052 others(5): Show |
8 | HG02129.hp1 NA18747.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.4774-1855A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45858946 | |||||||
| chr12:45859188 | A | C | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4774-1613A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45859188 | |||||||
| chr12:45859253 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4774-1548A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45859253 | |||||||
| chr12:45859283 | G | A | 1 | a0001c0001t0005g0286 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4774-1518G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45859283 | |||||||
| chr12:45859540 | C | G | 1 | a0001c0002t0002g0216 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4774-1261C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45859540 | |||||||
| chr12:45859608 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4774-1193A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45859608 | |||||||
| chr12:45859675 | T | G | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4774-1126T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45859675 | |||||||
| chr12:45859879 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4774-922G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45859879 | |||||||
| chr12:45860175 | T | C | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4774-626T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45860175 | |||||||
| chr12:45860310 | A | T | 1 | a0001c0001t0001g0033 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4774-491A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45860310 | |||||||
| chr12:45860612 | T | C | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.4774-189T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45860612 | |||||||
| chr12:45860660 | G | A | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4774-141G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45860660 | |||||||
| chr12:45860665 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.4774-136C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45860665 | |||||||
| chr12:45860716 | CAT | C | 45 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(42): Show |
45 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.4774-83_4774-82del others(2): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr12 | 45860716 | ||||||
| chr12:45860722 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.4774-79C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45860722 | |||||||
| chr12:45861176 | C | T | 2 | a0001c0001t0001g0249 a0001c0001t0001g0263 |
2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.4922+227C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45861176 | |||||||
| chr12:45861212 | A | G | 28 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(25): Show |
28 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.4922+263A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45861212 | |||||||
| chr12:45861253 | G | T | 1 | a0001c0001t0001g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4922+304G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45861253 | |||||||
| chr12:45861264 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | NA18974.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.4922+315C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45861264 | |||||||
| chr12:45861296 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.4922+347A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45861296 | |||||||
| chr12:45861329 | A | T | 1 | a0001c0001t0001g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4922+380A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45861329 | |||||||
| chr12:45861554 | T | C | 2 | a0002c0003t0001g0237 a0002c0003t0001g0243 |
2 | NA19060.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.4922+605T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45861554 | |||||||
| chr12:45861580 | C | CT | 8 | a0001c0001t0001g0248 a0001c0001t0001g0265 a0001c0001t0003g0280 others(5): Show |
8 | HG02738.hp2 HG03098.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.4922+652dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45861580 | ||||||
| chr12:45861580 | CT | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0028 others(197): Show |
201 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.4922+652delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45861580 | ||||||
| chr12:45861750 | A | G | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.4922+801A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45861750 | |||||||
| chr12:45861890 | A | G | 7 | a0001c0001t0001g0163 a0001c0001t0001g0166 a0001c0001t0001g0170 others(4): Show |
7 | HG01109.hp1 HG01934.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.4922+941A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45861890 | |||||||
| chr12:45862067 | T | C | 1 | a0001c0001t0008g0221 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4922+1118T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45862067 | |||||||
| chr12:45862161 | T | A | 3 | a0001c0001t0008g0128 a0001c0001t0008g0221 a0001c0001t0008g0222 |
3 | HG02630.hp1 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4922+1212T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45862161 | |||||||
| chr12:45862166 | G | T | 1 | a0004c0005t0001g0111 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.4922+1217G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45862166 | |||||||
| chr12:45862167 | GT | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0067 a0001c0001t0001g0069 |
3 | HG00280.hp1 HG01993.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.4922+1223delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45862167 | ||||||
| chr12:45862170 | T | C | 2 | a0001c0001t0001g0151 a0001c0001t0001g0176 |
2 | NA18962.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.4922+1221T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45862170 | |||||||
| chr12:45862646 | C | G | 1 | a0001c0001t0011g0118 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4922+1697C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45862646 | |||||||
| chr12:45862892 | A | AT | 164 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0037 others(161): Show |
165 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.4922+1953dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45862892 | ||||||
| chr12:45862955 | A | T | 1 | a0001c0001t0001g0038 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.4922+2006A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45862955 | |||||||
| chr12:45863082 | G | A | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4922+2133G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45863082 | |||||||
| chr12:45863313 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4922+2364A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45863313 | |||||||
| chr12:45863391 | G | A | 1 | a0001c0001t0003g0284 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4922+2442G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45863391 | |||||||
| chr12:45863592 | A | T | 1 | a0001c0001t0001g0164 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4922+2643A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45863592 | |||||||
| chr12:45863669 | ATTGTAAA others(5): Show |
A | 1 | a0001c0001t0001g0220 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.4922+2726_4922+273 others(16): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45863669 | ||||||
| chr12:45863703 | C | T | 28 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(25): Show |
28 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.4922+2754C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45863703 | |||||||
| chr12:45863818 | CT | C | 5 | a0001c0002t0002g0253 a0001c0002t0002g0254 a0001c0002t0002g0259 others(2): Show |
5 | HG02630.hp2 HG03130.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+2878delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45863818 | ||||||
| chr12:45863855 | TTG | T | 23 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(20): Show |
23 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.4922+2908_4922+290 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45863855 | ||||||
| chr12:45863856 | TG | T | 5 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+2908delG | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45863856 | |||||||
| chr12:45863857 | G | T | 11 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(8): Show |
11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.4922+2908G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45863857 | |||||||
| chr12:45863857 | GT | G | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.4922+2918delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45863857 | ||||||
| chr12:45863901 | A | G | 4 | a0001c0001t0001g0153 a0001c0001t0001g0172 a0001c0001t0001g0196 others(1): Show |
4 | NA18966.hp2 NA19001.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.4922+2952A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45863901 | |||||||
| chr12:45863929 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4922+2980C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45863929 | |||||||
| chr12:45864031 | T | A | 24 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(21): Show |
24 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.4922+3082T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45864031 | |||||||
| chr12:45864118 | A | G | 1 | a0005c0008t0001g0039 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.4922+3169A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45864118 | |||||||
| chr12:45864289 | A | G | 2 | a0001c0009t0010g0207 a0001c0009t0010g0208 |
2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4922+3340A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45864289 | |||||||
| chr12:45864522 | G | GA | 6 | a0001c0001t0003g0283 a0003c0004t0006g0105 a0003c0004t0006g0106 others(3): Show |
6 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4922+3585dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45864522 | ||||||
| chr12:45864534 | A | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(105): Show |
109 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.4922+3585A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45864534 | |||||||
| chr12:45864591 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.4922+3642A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45864591 | |||||||
| chr12:45864713 | T | C | 1 | a0005c0008t0001g0034 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4922+3764T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45864713 | |||||||
| chr12:45864799 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4922+3850A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45864799 | |||||||
| chr12:45864835 | T | C | 1 | a0001c0001t0009g0109 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.4922+3886T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45864835 | |||||||
| chr12:45865405 | C | A | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+4456C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45865405 | |||||||
| chr12:45865633 | A | G | 1 | a0002c0003t0001g0142 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4922+4684A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45865633 | |||||||
| chr12:45865914 | A | T | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+4965A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45865914 | |||||||
| chr12:45866065 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0185 |
2 | HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.4922+5116A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45866065 | |||||||
| chr12:45866250 | G | A | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+5301G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45866250 | |||||||
| chr12:45866293 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0001g0241 |
2 | HG00738.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.4922+5344C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45866293 | |||||||
| chr12:45866554 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4922+5605T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45866554 | |||||||
| chr12:45866736 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.4922+5787A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45866736 | |||||||
| chr12:45866827 | A | G | 11 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(8): Show |
11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.4922+5878A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45866827 | |||||||
| chr12:45866836 | T | C | 4 | a0001c0001t0005g0273 a0001c0001t0005g0286 a0001c0001t0005g0288 others(1): Show |
4 | HG01891.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4922+5887T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45866836 | |||||||
| chr12:45866881 | A | T | 1 | a0001c0001t0001g0264 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4922+5932A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45866881 | |||||||
| chr12:45866926 | A | G | 4 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4922+5977A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45866926 | |||||||
| chr12:45866928 | T | TTTG | 75 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(72): Show |
75 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.4922+6015_4922+601 others(7): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45866928 | ||||||
| chr12:45866928 | T | TTTGTTG | 13 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0072 others(10): Show |
13 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.4922+6012_4922+601 others(10): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45866928 | ||||||
| chr12:45866928 | TTTG | T | 13 | a0001c0001t0001g0055 a0001c0001t0001g0094 a0001c0001t0001g0226 others(10): Show |
13 | HG01346.hp1 HG02273.hp2 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.4922+6015_4922+601 others(7): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45866928 | ||||||
| chr12:45866928 | TTTGTTGT others(2): Show |
T | 4 | a0001c0001t0005g0273 a0001c0001t0005g0286 a0001c0001t0005g0288 others(1): Show |
4 | HG01891.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4922+6009_4922+601 others(13): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45866928 | ||||||
| chr12:45866928 | TTTGTTGT others(5): Show |
T | 29 | a0001c0001t0004g0131 a0001c0001t0004g0132 a0001c0001t0004g0133 others(26): Show |
29 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4922+6006_4922+601 others(16): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45866928 | ||||||
| chr12:45867002 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4922+6053G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45867002 | |||||||
| chr12:45867025 | A | T | 1 | a0001c0001t0001g0030 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.4922+6076A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45867025 | |||||||
| chr12:45867031 | A | G | 4 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4922+6082A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45867031 | |||||||
| chr12:45867229 | A | G | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+6280A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45867229 | |||||||
| chr12:45867365 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4922+6416C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45867365 | |||||||
| chr12:45867518 | T | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(214): Show |
218 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.4922+6569T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45867518 | |||||||
| chr12:45867538 | C | T | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+6589C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45867538 | |||||||
| chr12:45867599 | C | T | 28 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(25): Show |
28 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.4922+6650C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45867599 | |||||||
| chr12:45867870 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4922+6921C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45867870 | |||||||
| chr12:45867890 | C | T | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4922+6941C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45867890 | |||||||
| chr12:45868369 | A | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0094 |
2 | NA18977.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.4922+7420A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45868369 | |||||||
| chr12:45868434 | C | CT | 3 | a0001c0001t0001g0022 a0001c0001t0001g0063 a0001c0001t0001g0097 |
3 | HG04184.hp2 NA19077.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.4922+7486dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45868434 | ||||||
| chr12:45868642 | T | C | 1 | a0014c0018t0001g0262 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4922+7693T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45868642 | |||||||
| chr12:45868749 | T | C | 9 | a0001c0001t0001g0226 a0001c0001t0001g0249 a0001c0001t0001g0263 others(6): Show |
9 | HG01109.hp2 HG01346.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.4922+7800T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45868749 | |||||||
| chr12:45868793 | C | G | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4922+7844C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45868793 | |||||||
| chr12:45868883 | C | T | 1 | a0013c0015t0001g0295 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4922+7934C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45868883 | |||||||
| chr12:45869026 | GT | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(197): Show |
201 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.4922+8088delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45869026 | ||||||
| chr12:45869076 | T | G | 44 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(41): Show |
44 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.4922+8127T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45869076 | |||||||
| chr12:45869128 | G | T | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+8179G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45869128 | |||||||
| chr12:45869450 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4922+8501G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45869450 | |||||||
| chr12:45869672 | C | G | 1 | a0001c0001t0001g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4922+8723C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45869672 | |||||||
| chr12:45869756 | G | C | 1 | a0001c0001t0001g0102 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4922+8807G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45869756 | |||||||
| chr12:45869883 | A | AAAAAC | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+8949_4922+895 others(9): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45869883 | ||||||
| chr12:45869900 | AAAAC | A | 5 | a0001c0001t0003g0281 a0001c0001t0003g0282 a0001c0001t0003g0283 others(2): Show |
5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+8962_4922+896 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45869900 | ||||||
| chr12:45870071 | C | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0093 a0001c0001t0001g0096 |
3 | NA18966.hp1 NA18969.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.4922+9122C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45870071 | |||||||
| chr12:45870134 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4922+9185C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45870134 | |||||||
| chr12:45870150 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4922+9201T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45870150 | |||||||
| chr12:45870152 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4922+9203A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45870152 | |||||||
| chr12:45870168 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4922+9219T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45870168 | |||||||
| chr12:45870364 | C | G | 1 | a0001c0001t0001g0071 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.4922+9415C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45870364 | |||||||
| chr12:45870870 | C | T | 1 | a0001c0011t0018g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4922+9921C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45870870 | |||||||
| chr12:45870987 | T | C | 2 | a0001c0001t0001g0270 a0001c0001t0001g0291 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4922+10038T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45870987 | |||||||
| chr12:45870997 | A | G | 2 | a0001c0001t0001g0209 a0002c0020t0001g0239 |
2 | HG02165.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4922+10048A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45870997 | |||||||
| chr12:45871105 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4922+10156A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45871105 | |||||||
| chr12:45871717 | A | T | 3 | a0001c0001t0004g0131 a0001c0001t0004g0132 a0001c0001t0004g0134 |
3 | HG02647.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4922+10768A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45871717 | |||||||
| chr12:45871847 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.4922+10898G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45871847 | |||||||
| chr12:45871865 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.4922+10916C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45871865 | |||||||
| chr12:45871941 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4922+10992G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45871941 | |||||||
| chr12:45872133 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(154): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.4922+11184C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872133 | |||||||
| chr12:45872136 | T | A | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4922+11187T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872136 | |||||||
| chr12:45872180 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(154): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.4922+11231C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872180 | |||||||
| chr12:45872228 | T | C | 5 | a0001c0001t0005g0273 a0001c0001t0005g0285 a0001c0001t0005g0286 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.4922+11279T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872228 | |||||||
| chr12:45872245 | T | C | 1 | a0001c0001t0001g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4922+11296T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872245 | |||||||
| chr12:45872338 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0147 |
2 | NA18969.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.4922+11389C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872338 | |||||||
| chr12:45872480 | A | T | 29 | a0001c0001t0004g0131 a0001c0001t0004g0132 a0001c0001t0004g0133 others(26): Show |
29 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4922+11531A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872480 | |||||||
| chr12:45872569 | A | G | 2 | a0001c0001t0001g0226 a0001c0001t0001g0305 |
2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.4922+11620A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872569 | |||||||
| chr12:45872614 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4922+11665C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872614 | |||||||
| chr12:45872648 | C | G | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4922+11699C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872648 | |||||||
| chr12:45872980 | A | G | 1 | a0002c0003t0001g0307 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4922+12031A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872980 | |||||||
| chr12:45873081 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4922+12132A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45873081 | |||||||
| chr12:45873100 | T | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
2 | HG00408.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.4922+12151T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45873100 | |||||||
| chr12:45873302 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4922+12353C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45873302 | |||||||
| chr12:45873302 | C | T | 16 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0117 others(13): Show |
16 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.4922+12353C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45873302 | |||||||
| chr12:45873477 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(1): Show |
4 | HG00140.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.4922+12528G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45873477 | |||||||
| chr12:45873507 | T | C | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG01168.hp1 HG01169.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.4922+12558T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45873507 | |||||||
| chr12:45873936 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4922+12987C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45873936 | |||||||
| chr12:45873966 | G | A | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+13017G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45873966 | |||||||
| chr12:45874348 | T | A | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4922+13399T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45874348 | |||||||
| chr12:45874436 | C | G | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4922+13487C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45874436 | |||||||
| chr12:45874455 | G | A | 8 | a0001c0001t0001g0225 a0001c0001t0001g0231 a0001c0001t0001g0233 others(5): Show |
8 | HG00642.hp1 HG01074.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.4922+13506G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45874455 | |||||||
| chr12:45874468 | C | T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4922+13519C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45874468 | |||||||
| chr12:45874517 | T | C | 2 | a0001c0001t0001g0249 a0001c0001t0001g0263 |
2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.4922+13568T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45874517 | |||||||
| chr12:45874913 | T | C | 11 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(8): Show |
11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.4922+13964T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45874913 | |||||||
| chr12:45874967 | A | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(214): Show |
218 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.4922+14018A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45874967 | |||||||
| chr12:45874983 | G | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(211): Show |
215 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.4922+14034G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45874983 | |||||||
| chr12:45875150 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4922+14201G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45875150 | |||||||
| chr12:45875301 | A | T | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4922+14352A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45875301 | |||||||
| chr12:45875435 | A | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0052 |
2 | NA18747.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.4922+14486A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45875435 | |||||||
| chr12:45875780 | G | A | 1 | a0001c0001t0011g0119 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4922+14831G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45875780 | |||||||
| chr12:45876302 | G | A | 5 | a0001c0001t0005g0273 a0001c0001t0005g0285 a0001c0001t0005g0286 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.4922+15353G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876302 | |||||||
| chr12:45876333 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0063 a0001c0001t0001g0097 |
3 | HG04184.hp2 NA19077.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.4922+15384G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876333 | |||||||
| chr12:45876353 | C | T | 1 | a0001c0002t0002g0218 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4922+15404C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876353 | |||||||
| chr12:45876382 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4923-15398T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876382 | |||||||
| chr12:45876569 | GA | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(108): Show |
112 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.4923-15198delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45876569 | ||||||
| chr12:45876627 | A | T | 1 | a0001c0002t0002g0258 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4923-15153A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876627 | |||||||
| chr12:45876628 | A | G | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-15152A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876628 | |||||||
| chr12:45876707 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.4923-15073G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876707 | |||||||
| chr12:45876793 | TA | T | 8 | a0001c0001t0001g0087 a0001c0001t0001g0272 a0001c0001t0003g0280 others(5): Show |
8 | HG01168.hp1 HG02257.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.4923-14973delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45876793 | ||||||
| chr12:45876846 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4923-14934T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876846 | |||||||
| chr12:45876885 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4923-14895C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876885 | |||||||
| chr12:45876917 | A | G | 1 | a0001c0001t0005g0286 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4923-14863A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876917 | |||||||
| chr12:45876960 | T | C | 11 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(8): Show |
11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.4923-14820T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876960 | |||||||
| chr12:45877091 | C | CA | 35 | a0001c0001t0001g0100 a0001c0001t0001g0157 a0001c0001t0001g0176 others(32): Show |
35 | HG01175.hp1 HG01175.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.4923-14670dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45877091 | ||||||
| chr12:45877091 | CA | C | 13 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0087 others(10): Show |
13 | HG01168.hp1 HG02451.hp1 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.4923-14670delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45877091 | ||||||
| chr12:45877219 | G | C | 1 | a0001c0001t0001g0130 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4923-14561G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45877219 | |||||||
| chr12:45877321 | C | G | 1 | a0001c0001t0001g0158 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.4923-14459C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45877321 | |||||||
| chr12:45877341 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.4923-14439G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45877341 | |||||||
| chr12:45877343 | A | G | 33 | a0001c0001t0004g0131 a0001c0001t0004g0132 a0001c0001t0004g0133 others(30): Show |
33 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.4923-14437A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45877343 | |||||||
| chr12:45877385 | T | C | 8 | a0001c0001t0001g0141 a0001c0001t0001g0146 a0001c0001t0001g0147 others(5): Show |
8 | HG01167.hp2 HG02602.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.4923-14395T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45877385 | |||||||
| chr12:45877573 | G | A | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4923-14207G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45877573 | |||||||
| chr12:45877953 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4923-13827G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45877953 | |||||||
| chr12:45877991 | G | T | 1 | a0001c0001t0001g0015 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4923-13789G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45877991 | |||||||
| chr12:45878292 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4923-13488C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45878292 | |||||||
| chr12:45878776 | G | T | 5 | a0001c0001t0004g0131 a0001c0001t0004g0132 a0001c0001t0004g0133 others(2): Show |
5 | HG02615.hp1 HG02647.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.4923-13004G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45878776 | |||||||
| chr12:45878800 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4923-12980C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45878800 | |||||||
| chr12:45879063 | C | G | 44 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.4923-12717C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45879063 | |||||||
| chr12:45879295 | T | C | 4 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(1): Show |
4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4923-12485T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45879295 | |||||||
| chr12:45879354 | C | T | 1 | a0003c0004t0006g0107 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4923-12426C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45879354 | |||||||
| chr12:45879419 | A | T | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-12361A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45879419 | |||||||
| chr12:45879572 | A | G | 1 | a0001c0001t0001g0015 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4923-12208A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45879572 | |||||||
| chr12:45879955 | G | A | 1 | a0001c0001t0005g0288 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4923-11825G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45879955 | |||||||
| chr12:45879986 | AGT | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | HG02074.hp2 HG02523.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.4923-11791_4923-11 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45879986 | ||||||
| chr12:45880002 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.4923-11778G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45880002 | |||||||
| chr12:45880099 | T | G | 45 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(42): Show |
45 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.4923-11681T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45880099 | |||||||
| chr12:45880172 | G | A | 1 | a0001c0016t0001g0296 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4923-11608G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45880172 | |||||||
| chr12:45880411 | T | G | 1 | a0001c0016t0001g0296 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4923-11369T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45880411 | |||||||
| chr12:45880427 | C | T | 2 | a0001c0001t0001g0249 a0001c0001t0001g0263 |
2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.4923-11353C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45880427 | |||||||
| chr12:45880534 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4923-11246T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45880534 | |||||||
| chr12:45880554 | C | G | 1 | a0001c0001t0015g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4923-11226C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45880554 | |||||||
| chr12:45880608 | A | T | 1 | a0001c0011t0018g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4923-11172A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45880608 | |||||||
| chr12:45880638 | A | T | 1 | a0001c0001t0001g0062 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4923-11142A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45880638 | |||||||
| chr12:45880654 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4923-11126C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45880654 | |||||||
| chr12:45881075 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.4923-10705G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45881075 | |||||||
| chr12:45881513 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4923-10267A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45881513 | |||||||
| chr12:45881564 | A | G | 2 | a0006c0007t0001g0020 a0006c0007t0001g0051 |
2 | NA18957.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.4923-10216A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45881564 | |||||||
| chr12:45881654 | GTCT | G | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-10120_4923-10 others(9): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45881654 | ||||||
| chr12:45881968 | G | A | 4 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4923-9812G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45881968 | |||||||
| chr12:45882154 | A | G | 114 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(111): Show |
115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.4923-9626A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45882154 | |||||||
| chr12:45882315 | C | T | 2 | a0001c0001t0003g0282 a0001c0001t0003g0314 |
2 | HG02738.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.4923-9465C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45882315 | |||||||
| chr12:45882906 | G | T | 3 | a0004c0005t0001g0111 a0004c0005t0001g0168 a0004c0005t0001g0169 |
3 | NA18747.hp1 NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.4923-8874G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45882906 | |||||||
| chr12:45883003 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4923-8777C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45883003 | |||||||
| chr12:45883212 | T | A | 4 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0067 others(1): Show |
4 | HG00280.hp1 HG01993.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.4923-8568T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45883212 | |||||||
| chr12:45883875 | C | A | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4923-7905C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45883875 | |||||||
| chr12:45883943 | T | C | 29 | a0001c0001t0004g0131 a0001c0001t0004g0132 a0001c0001t0004g0133 others(26): Show |
29 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4923-7837T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45883943 | |||||||
| chr12:45884028 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4923-7752T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45884028 | |||||||
| chr12:45884224 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4923-7556C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45884224 | |||||||
| chr12:45884394 | T | TCAAA | 12 | a0001c0001t0001g0067 a0001c0001t0003g0280 a0001c0001t0003g0281 others(9): Show |
12 | HG02451.hp1 HG02647.hp2 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.4923-7365_4923-736 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45884394 | ||||||
| chr12:45884401 | A | G | 1 | a0002c0003t0001g0242 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.4923-7379A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45884401 | |||||||
| chr12:45884594 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4923-7186T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45884594 | |||||||
| chr12:45884603 | C | T | 1 | a0001c0001t0001g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4923-7177C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45884603 | |||||||
| chr12:45884879 | C | T | 4 | a0001c0001t0001g0270 a0001c0001t0001g0290 a0001c0001t0001g0291 others(1): Show |
4 | HG02615.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.4923-6901C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45884879 | |||||||
| chr12:45884886 | A | T | 10 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(7): Show |
10 | HG00438.hp2 HG00621.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.4923-6894A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45884886 | |||||||
| chr12:45884976 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.4923-6804C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45884976 | |||||||
| chr12:45885116 | G | T | 1 | a0001c0001t0001g0019 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4923-6664G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885116 | |||||||
| chr12:45885285 | C | T | 44 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.4923-6495C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885285 | |||||||
| chr12:45885319 | A | G | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-6461A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885319 | |||||||
| chr12:45885371 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.4923-6409G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885371 | |||||||
| chr12:45885530 | T | C | 1 | a0001c0001t0001g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4923-6250T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885530 | |||||||
| chr12:45885554 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.4923-6226T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885554 | |||||||
| chr12:45885596 | T | C | 4 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4923-6184T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885596 | |||||||
| chr12:45885600 | G | A | 24 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(21): Show |
24 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.4923-6180G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885600 | |||||||
| chr12:45885641 | A | G | 3 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0174 |
3 | HG01167.hp2 HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4923-6139A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885641 | |||||||
| chr12:45885775 | G | A | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4923-6005G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885775 | |||||||
| chr12:45885883 | A | C | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-5897A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885883 | |||||||
| chr12:45885983 | C | A | 1 | a0001c0001t0001g0005 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.4923-5797C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885983 | |||||||
| chr12:45886104 | A | G | 4 | a0001c0001t0001g0270 a0001c0001t0001g0290 a0001c0001t0001g0291 others(1): Show |
4 | HG02615.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.4923-5676A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45886104 | |||||||
| chr12:45886132 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.4923-5648A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45886132 | |||||||
| chr12:45886146 | GTGGGATA others(30): Show |
G | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-5628_4923-559 others(41): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45886146 | ||||||
| chr12:45886228 | A | G | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-5552A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45886228 | |||||||
| chr12:45886385 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(87): Show |
91 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.4923-5395C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45886385 | |||||||
| chr12:45886456 | T | G | 4 | a0001c0001t0001g0115 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
4 | HG01099.hp2 HG01175.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.4923-5324T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45886456 | |||||||
| chr12:45886731 | G | A | 66 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0084 others(63): Show |
66 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.4923-5049G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45886731 | |||||||
| chr12:45886766 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.4923-5014G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45886766 | |||||||
| chr12:45886832 | A | C | 3 | a0001c0001t0001g0249 a0001c0001t0001g0263 a0014c0018t0001g0262 |
3 | HG01109.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4923-4948A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45886832 | |||||||
| chr12:45886995 | A | C | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4923-4785A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45886995 | |||||||
| chr12:45887251 | T | A | 1 | a0001c0001t0001g0226 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.4923-4529T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45887251 | |||||||
| chr12:45887254 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.4923-4526A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45887254 | |||||||
| chr12:45887445 | A | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(106): Show |
110 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.4923-4335A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45887445 | |||||||
| chr12:45887452 | T | C | 1 | a0001c0011t0018g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4923-4328T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45887452 | |||||||
| chr12:45887494 | AAG | A | 5 | a0001c0001t0001g0270 a0001c0001t0001g0272 a0001c0001t0001g0290 others(2): Show |
5 | HG02257.hp2 HG02615.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-4283_4923-428 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45887494 | ||||||
| chr12:45887548 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4923-4232C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45887548 | |||||||
| chr12:45887813 | C | T | 44 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.4923-3967C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45887813 | |||||||
| chr12:45888119 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4923-3661T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45888119 | |||||||
| chr12:45888194 | C | CA | 39 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0017 others(36): Show |
39 | HG00408.hp1 HG00597.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.4923-3571dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45888194 | ||||||
| chr12:45888223 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(209): Show |
213 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.4923-3557G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45888223 | |||||||
| chr12:45888260 | A | G | 1 | a0001c0001t0001g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4923-3520A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45888260 | |||||||
| chr12:45888475 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.4923-3305C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45888475 | |||||||
| chr12:45888509 | T | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | NA18950.hp1 NA18980.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.4923-3271T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45888509 | |||||||
| chr12:45888825 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4923-2955T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45888825 | |||||||
| chr12:45889058 | C | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0149 a0001c0001t0001g0174 |
3 | HG01167.hp2 HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4923-2722C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45889058 | |||||||
| chr12:45889182 | AAATAAT | A | 4 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4923-2588_4923-258 others(10): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45889182 | ||||||
| chr12:45889247 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4923-2533A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45889247 | |||||||
| chr12:45889348 | A | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4923-2432A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45889348 | |||||||
| chr12:45889430 | T | A | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-2350T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45889430 | |||||||
| chr12:45889653 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4923-2127C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45889653 | |||||||
| chr12:45889711 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.4923-2069G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45889711 | |||||||
| chr12:45889806 | C | T | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4923-1974C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45889806 | |||||||
| chr12:45890214 | A | G | 28 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(25): Show |
28 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.4923-1566A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45890214 | |||||||
| chr12:45890660 | A | G | 1 | a0002c0003t0001g0237 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.4923-1120A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45890660 | |||||||
| chr12:45890927 | G | C | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG01168.hp1 HG01169.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.4923-853G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45890927 | |||||||
| chr12:45890937 | C | T | 1 | a0001c0001t0001g0302 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4923-843C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45890937 | |||||||
| chr12:45891001 | C | A | 1 | a0001c0001t0001g0035 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4923-779C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45891001 | |||||||
| chr12:45891041 | T | C | 3 | a0001c0001t0001g0077 a0001c0001t0001g0102 a0007c0019t0001g0036 |
3 | HG00597.hp1 HG00621.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.4923-739T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45891041 | |||||||
| chr12:45891058 | G | A | 5 | a0001c0002t0002g0253 a0001c0002t0002g0255 a0001c0002t0002g0259 others(2): Show |
5 | HG02630.hp2 HG02922.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-722G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45891058 | |||||||
| chr12:45891163 | C | CA | 6 | a0001c0001t0001g0017 a0001c0001t0001g0137 a0001c0001t0001g0272 others(3): Show |
6 | HG02074.hp1 HG02257.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.4923-600dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45891163 | ||||||
| chr12:45891163 | CA | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(102): Show |
105 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.4923-600delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45891163 | ||||||
| chr12:45891441 | T | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0067 |
2 | HG02738.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.4923-339T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45891441 | |||||||
| chr12:45891538 | G | A | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-242G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45891538 | |||||||
| chr12:45891553 | G | C | 1 | a0001c0001t0001g0122 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.4923-227G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45891553 | |||||||
| chr12:45891966 | A | G | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.5062-45A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 17/20 | chr12 | 45891966 | |||||||
| chr12:45892181 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5147+85T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | chr12 | 45892181 | |||||||
| chr12:45892479 | C | CAT | 209 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(206): Show |
210 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.5147+397_5147+398d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr12 | 45892479 | ||||||
| chr12:45892479 | C | CATAT | 4 | a0001c0001t0001g0130 a0001c0001t0001g0270 a0001c0001t0001g0290 others(1): Show |
4 | HG02615.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.5147+395_5147+398d others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr12 | 45892479 | ||||||
| chr12:45892567 | T | G | 1 | a0001c0001t0001g0197 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5147+471T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | chr12 | 45892567 | |||||||
| chr12:45892719 | A | G | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.5147+623A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | chr12 | 45892719 | |||||||
| chr12:45892723 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0278 |
2 | HG00099.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.5147+627C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | chr12 | 45892723 | |||||||
| chr12:45892829 | G | A | 1 | a0001c0011t0018g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5148-591G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | chr12 | 45892829 | |||||||
| chr12:45892900 | A | G | 5 | a0001c0001t0005g0273 a0001c0001t0005g0285 a0001c0001t0005g0286 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.5148-520A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | chr12 | 45892900 | |||||||
| chr12:45893116 | C | T | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.5148-304C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | chr12 | 45893116 | |||||||
| chr12:45893184 | T | C | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.5148-236T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | chr12 | 45893184 | |||||||
| chr12:45893313 | G | A | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.5148-107G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | chr12 | 45893313 | |||||||
| chr12:45893375 | G | A | 1 | a0001c0001t0001g0245 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.5148-45G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | chr12 | 45893375 | |||||||
| chr12:45893732 | T | C | 1 | a0001c0001t0001g0265 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5363+11T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45893732 | |||||||
| chr12:45893828 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.5363+107A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45893828 | |||||||
| chr12:45894153 | A | G | 4 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.5363+432A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45894153 | |||||||
| chr12:45894397 | G | GGCCC | 8 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0165 others(5): Show |
8 | HG02129.hp2 NA18959.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.5363+677_5363+680d others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45894397 | ||||||
| chr12:45894554 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.5363+833G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45894554 | |||||||
| chr12:45894650 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0063 a0001c0001t0001g0097 |
3 | HG04184.hp2 NA19077.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.5363+929T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45894650 | |||||||
| chr12:45894699 | G | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(212): Show |
216 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.5363+978G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45894699 | |||||||
| chr12:45894833 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5363+1112C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45894833 | |||||||
| chr12:45894840 | A | ACCTCTTT others(281): Show |
1 | a0001c0001t0013g0287 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5363+1129_5363+113 others(292): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45894840 | ||||||
| chr12:45894876 | A | T | 4 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(1): Show |
4 | NA18950.hp1 NA18980.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.5363+1155A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45894876 | |||||||
| chr12:45894955 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.5363+1234T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45894955 | |||||||
| chr12:45895321 | T | C | 11 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(8): Show |
11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.5363+1600T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45895321 | |||||||
| chr12:45895387 | A | G | 5 | a0001c0001t0004g0131 a0001c0001t0004g0132 a0001c0001t0004g0133 others(2): Show |
5 | HG02615.hp1 HG02647.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.5363+1666A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45895387 | |||||||
| chr12:45895541 | C | G | 29 | a0001c0001t0004g0131 a0001c0001t0004g0132 a0001c0001t0004g0133 others(26): Show |
29 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.5363+1820C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45895541 | |||||||
| chr12:45895604 | G | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | HG02523.hp1 NA18952.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.5363+1883G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45895604 | |||||||
| chr12:45895695 | G | A | 10 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(7): Show |
10 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.5363+1974G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45895695 | |||||||
| chr12:45896099 | T | A | 2 | a0001c0001t0001g0063 a0001c0001t0001g0097 |
2 | HG04184.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.5363+2378T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896099 | |||||||
| chr12:45896165 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(105): Show |
109 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.5363+2444G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896165 | |||||||
| chr12:45896191 | A | G | 4 | a0001c0001t0001g0294 a0001c0001t0001g0304 a0001c0001t0001g0308 others(1): Show |
4 | HG01975.hp1 HG01981.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.5363+2470A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896191 | |||||||
| chr12:45896282 | G | C | 2 | a0001c0002t0002g0254 a0001c0002t0002g0311 |
2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.5363+2561G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896282 | |||||||
| chr12:45896403 | A | G | 4 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.5363+2682A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896403 | |||||||
| chr12:45896449 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5363+2728C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896449 | |||||||
| chr12:45896459 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5363+2738G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896459 | |||||||
| chr12:45896627 | C | CT | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.5363+2909dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45896627 | ||||||
| chr12:45896674 | G | A | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0164 |
3 | HG02056.hp2 NA18612.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.5363+2953G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896674 | |||||||
| chr12:45896682 | G | A | 1 | a0001c0001t0001g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5363+2961G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896682 | |||||||
| chr12:45896827 | G | A | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.5363+3106G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896827 | |||||||
| chr12:45896976 | A | C | 1 | a0001c0001t0001g0072 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.5363+3255A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896976 | |||||||
| chr12:45897107 | G | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0085 |
2 | HG01071.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.5363+3386G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45897107 | |||||||
| chr12:45897354 | C | T | 1 | a0001c0006t0002g0194 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5363+3633C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45897354 | |||||||
| chr12:45897360 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.5363+3639C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45897360 | |||||||
| chr12:45897382 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.5363+3661A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45897382 | |||||||
| chr12:45897867 | C | T | 1 | a0001c0001t0004g0133 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.5363+4146C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45897867 | |||||||
| chr12:45898462 | G | A | 28 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(25): Show |
28 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.5363+4741G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45898462 | |||||||
| chr12:45898644 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0070 |
2 | HG02083.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.5363+4923G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45898644 | |||||||
| chr12:45898829 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5363+5108G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45898829 | |||||||
| chr12:45898911 | C | A | 1 | a0001c0002t0002g0257 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5363+5190C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45898911 | |||||||
| chr12:45898981 | T | A | 1 | a0001c0001t0001g0302 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5363+5260T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45898981 | |||||||
| chr12:45898994 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.5363+5273C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45898994 | |||||||
| chr12:45899068 | T | C | 4 | a0002c0003t0001g0235 a0002c0003t0001g0236 a0002c0003t0001g0307 others(1): Show |
4 | HG00597.hp2 NA18945.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.5363+5347T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899068 | |||||||
| chr12:45899212 | C | T | 45 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(42): Show |
45 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.5363+5491C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899212 | |||||||
| chr12:45899249 | C | T | 4 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0085 others(1): Show |
4 | HG01071.hp1 HG01358.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.5363+5528C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899249 | |||||||
| chr12:45899270 | C | CA | 52 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0013 others(49): Show |
52 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.5363+5576dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899270 | ||||||
| chr12:45899270 | CA | C | 7 | a0001c0001t0001g0088 a0001c0001t0001g0114 a0001c0001t0001g0125 others(4): Show |
7 | HG00544.hp2 HG01169.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.5363+5576delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899270 | ||||||
| chr12:45899270 | CAAAAAAA others(4): Show |
C | 44 | a0001c0001t0001g0112 a0001c0001t0001g0138 a0001c0001t0001g0139 others(41): Show |
44 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.5363+5566_5363+557 others(15): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899270 | ||||||
| chr12:45899270 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0298 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.5363+5562_5363+557 others(19): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899270 | ||||||
| chr12:45899367 | G | C | 4 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.5364-5567G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899367 | |||||||
| chr12:45899401 | A | G | 1 | a0001c0001t0005g0286 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5364-5533A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899401 | |||||||
| chr12:45899421 | A | G | 1 | a0001c0001t0005g0286 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5364-5513A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899421 | |||||||
| chr12:45899432 | A | G | 1 | a0001c0001t0001g0060 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.5364-5502A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899432 | |||||||
| chr12:45899462 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.5364-5472T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899462 | |||||||
| chr12:45899474 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0204 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.5364-5460C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899474 | |||||||
| chr12:45899478 | C | T | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.5364-5456C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899478 | |||||||
| chr12:45899516 | G | C | 1 | a0001c0001t0003g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5364-5418G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899516 | |||||||
| chr12:45899592 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.5364-5342C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899592 | |||||||
| chr12:45899597 | T | C | 52 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0053 others(49): Show |
52 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.5364-5337T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899597 | |||||||
| chr12:45899621 | G | GTATATAT others(11): Show |
3 | a0001c0001t0001g0249 a0001c0001t0001g0263 a0014c0018t0001g0262 |
3 | HG01109.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.5364-5305_5364-528 others(22): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899621 | ||||||
| chr12:45899633 | T | TTA | 3 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 |
3 | HG02647.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.5364-5287_5364-528 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899633 | ||||||
| chr12:45899649 | TTGGTTAT others(21): Show |
T | 1 | a0001c0011t0018g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5364-5269_5364-524 others(32): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899649 | ||||||
| chr12:45899653 | T | TTA | 3 | a0001c0001t0001g0110 a0001c0001t0001g0248 a0001c0001t0001g0265 |
3 | HG02965.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5364-5267_5364-526 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899653 | ||||||
| chr12:45899655 | ATATATAT others(33): Show |
A | 7 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0190 others(4): Show |
7 | HG02886.hp1 HG02965.hp1 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.5364-5255_5364-521 others(44): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899655 | ||||||
| chr12:45899657 | ATATATAT others(17): Show |
A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0113 a0001c0001t0001g0114 others(44): Show |
48 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.5364-5255_5364-523 others(28): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899657 | ||||||
| chr12:45899657 | ATATATAT others(47): Show |
A | 1 | a0003c0004t0006g0107 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5364-5255_5364-520 others(58): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899657 | ||||||
| chr12:45899661 | ATATATAT others(3): Show |
A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0010 others(131): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.5364-5255_5364-524 others(14): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899661 | ||||||
| chr12:45899671 | T | TTATA | 9 | a0001c0001t0001g0064 a0001c0001t0001g0149 a0001c0001t0001g0174 others(6): Show |
9 | HG00738.hp1 HG01891.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.5364-5259_5364-525 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | ||||||
| chr12:45899671 | T | TTATATA | 27 | a0001c0001t0001g0082 a0001c0001t0001g0112 a0001c0001t0001g0138 others(24): Show |
27 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.5364-5261_5364-525 others(10): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | ||||||
| chr12:45899671 | T | TTATATAT others(13): Show |
1 | a0001c0001t0004g0135 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5364-5256_5364-525 others(24): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | ||||||
| chr12:45899671 | T | TTATATAT others(95): Show |
1 | a0001c0001t0012g0251 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5364-5256_5364-525 others(106): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | ||||||
| chr12:45899671 | T | TTATATAT others(29): Show |
1 | a0001c0001t0001g0248 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5364-5256_5364-525 others(40): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | ||||||
| chr12:45899671 | T | TTATATAT others(59): Show |
1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5364-5256_5364-525 others(70): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | ||||||
| chr12:45899671 | T | TTATATAT others(89): Show |
1 | a0001c0001t0001g0277 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5364-5256_5364-525 others(100): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | ||||||
| chr12:45899671 | T | TTATATAT others(91): Show |
17 | a0001c0001t0001g0099 a0001c0001t0001g0230 a0001c0001t0001g0231 others(14): Show |
17 | HG01071.hp2 HG01081.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.5364-5256_5364-525 others(102): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | ||||||
| chr12:45899671 | T | TTATATAT others(93): Show |
2 | a0001c0001t0001g0225 a0001c0001t0001g0233 |
2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.5364-5256_5364-525 others(104): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | ||||||
| chr12:45899671 | T | TTATATAT others(13): Show |
5 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0061 others(2): Show |
5 | HG01978.hp2 HG01981.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.5364-5256_5364-525 others(24): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | ||||||
| chr12:45899671 | T | TTATATAT others(27): Show |
2 | a0001c0001t0001g0050 a0001c0002t0002g0257 |
2 | HG02129.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.5364-5256_5364-525 others(38): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | ||||||
| chr12:45899671 | T | TTATATAT others(119): Show |
2 | a0001c0001t0001g0077 a0001c0001t0001g0102 |
2 | HG00621.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.5364-5256_5364-525 others(130): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | ||||||
| chr12:45899671 | TTATATAT others(7): Show |
T | 1 | a0001c0001t0001g0017 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.5364-5241_5364-522 others(18): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | ||||||
| chr12:45899673 | ATATATGG others(1): Show |
A | 14 | a0001c0001t0007g0195 a0001c0001t0007g0267 a0001c0001t0007g0268 others(11): Show |
14 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.5364-5255_5364-524 others(12): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899673 | ||||||
| chr12:45899673 | ATATATGG others(31): Show |
A | 6 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0001t0003g0280 others(3): Show |
6 | HG03516.hp2 HG03704.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.5364-5255_5364-521 others(42): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899673 | ||||||
| chr12:45899673 | ATATATGG others(45): Show |
A | 1 | a0001c0001t0004g0134 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5364-5255_5364-520 others(56): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899673 | ||||||
| chr12:45899694 | G | GTT | 23 | a0001c0001t0001g0077 a0001c0001t0001g0099 a0001c0001t0001g0102 others(20): Show |
23 | HG00621.hp2 HG00642.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.5364-5239_5364-523 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899694 | ||||||
| chr12:45899694 | G | GTTATATA others(85): Show |
1 | a0001c0001t0001g0276 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5364-5198_5364-519 others(96): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899694 | ||||||
| chr12:45899694 | G | GTTATATA others(87): Show |
20 | a0001c0001t0001g0082 a0001c0001t0001g0138 a0001c0001t0001g0139 others(17): Show |
20 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.5364-5198_5364-519 others(98): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899694 | ||||||
| chr12:45899694 | G | GTTATATA others(85): Show |
1 | a0001c0001t0001g0275 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.5364-5198_5364-519 others(96): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899694 | ||||||
| chr12:45899694 | G | GTTATATA others(87): Show |
1 | a0001c0001t0001g0112 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.5364-5198_5364-519 others(98): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899694 | ||||||
| chr12:45899695 | TTA | T | 15 | a0001c0001t0001g0064 a0001c0001t0007g0195 a0001c0001t0007g0267 others(12): Show |
15 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.5364-5227_5364-522 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899695 | ||||||
| chr12:45899697 | A | ATATATAT others(7): Show |
7 | a0001c0001t0001g0149 a0001c0001t0001g0174 a0001c0001t0005g0273 others(4): Show |
7 | HG01891.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.5364-5207_5364-519 others(18): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899697 | ||||||
| chr12:45899697 | A | ATATATAT others(101): Show |
1 | a0001c0001t0001g0278 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.5364-5198_5364-519 others(112): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899697 | ||||||
| chr12:45899697 | A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5364-5228_5364-522 others(16): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899697 | ||||||
| chr12:45899697 | A | ATATATAT others(35): Show |
1 | a0003c0004t0017g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5364-5228_5364-522 others(46): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899697 | ||||||
| chr12:45899697 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.5364-5237A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899697 | |||||||
| chr12:45899697 | ATATATAT others(7): Show |
A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0066 a0001c0001t0001g0152 others(2): Show |
5 | HG00673.hp1 HG01192.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.5364-5207_5364-519 others(18): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899697 | ||||||
| chr12:45899699 | ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0068 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.5364-5225_5364-521 others(16): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899699 | ||||||
| chr12:45899711 | T | TTA | 4 | a0001c0001t0001g0064 a0001c0001t0001g0249 a0001c0001t0001g0263 others(1): Show |
4 | HG01109.hp2 HG02258.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.5364-5213_5364-521 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899711 | ||||||
| chr12:45899711 | T | TTATATAT others(41): Show |
1 | a0001c0001t0001g0244 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.5364-5198_5364-519 others(52): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899711 | ||||||
| chr12:45899711 | T | TTTTA | 10 | a0001c0002t0002g0210 a0001c0002t0002g0211 a0001c0002t0002g0212 others(7): Show |
10 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.5364-5222_5364-522 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899711 | ||||||
| chr12:45899727 | ATATATAT others(7): Show |
A | 1 | a0001c0001t0001g0064 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.5364-5197_5364-518 others(18): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899727 | ||||||
| chr12:45899740 | T | TATATATA others(83): Show |
1 | a0001c0001t0001g0274 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.5364-5194_5364-519 others(94): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899740 | |||||||
| chr12:45899741 | T | A | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5364-5193T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899741 | |||||||
| chr12:45899743 | A | T | 1 | a0001c0001t0001g0274 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.5364-5191A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899743 | |||||||
| chr12:45899785 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5364-5149C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899785 | |||||||
| chr12:45899786 | CT | C | 36 | a0001c0001t0001g0001 a0001c0001t0001g0110 a0001c0001t0001g0114 others(33): Show |
37 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.5364-5147delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899786 | |||||||
| chr12:45899787 | T | C | 7 | a0001c0001t0001g0113 a0001c0001t0001g0129 a0001c0001t0001g0185 others(4): Show |
7 | HG00280.hp2 HG01358.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5364-5147T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899787 | |||||||
| chr12:45900083 | CAG | C | 5 | a0003c0004t0006g0105 a0003c0004t0006g0106 a0003c0004t0006g0107 others(2): Show |
5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.5364-4848_5364-484 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45900083 | ||||||
| chr12:45900091 | C | T | 1 | a0001c0016t0001g0296 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.5364-4843C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45900091 | |||||||
| chr12:45900092 | G | A | 3 | a0001c0001t0001g0152 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG00673.hp1 NA18944.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.5364-4842G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45900092 | |||||||
| chr12:45900144 | T | G | 1 | a0001c0001t0001g0006 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5364-4790T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45900144 | |||||||
| chr12:45900160 | A | T | 2 | a0001c0001t0001g0248 a0001c0001t0001g0265 |
2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5364-4774A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45900160 | |||||||
| chr12:45900230 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5364-4704T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45900230 | |||||||
| chr12:45900423 | C | T | 1 | a0001c0001t0001g0019 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.5364-4511C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45900423 | |||||||
| chr12:45900540 | A | G | 1 | a0001c0002t0002g0217 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5364-4394A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45900540 | |||||||
| chr12:45900909 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5364-4025C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45900909 | |||||||
| chr12:45900911 | C | T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5364-4023C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45900911 | |||||||
| chr12:45901089 | TTTTTC | T | 6 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(3): Show |
6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.5364-3838_5364-383 others(9): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901089 | ||||||
| chr12:45901125 | G | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(154): Show |
158 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.5364-3809G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45901125 | |||||||
| chr12:45901150 | CTTAATTT others(7): Show |
C | 2 | a0001c0001t0003g0284 a0001c0001t0003g0314 |
2 | HG02738.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.5364-3781_5364-376 others(18): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901150 | ||||||
| chr12:45901150 | CTTAATTT others(8): Show |
C | 4 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0003g0282 others(1): Show |
4 | HG03704.hp1 HG04115.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.5364-3781_5364-376 others(19): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901150 | ||||||
| chr12:45901154 | A | AT | 18 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0078 others(15): Show |
18 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.5364-3746dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901154 | ||||||
| chr12:45901154 | A | ATT | 6 | a0001c0001t0001g0075 a0001c0001t0001g0228 a0001c0001t0001g0263 others(3): Show |
6 | HG01109.hp2 HG01433.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.5364-3747_5364-374 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901154 | ||||||
| chr12:45901154 | AT | A | 63 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(60): Show |
63 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.5364-3746delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901154 | ||||||
| chr12:45901154 | ATT | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(54): Show |
57 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.5364-3747_5364-374 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901154 | ||||||
| chr12:45901154 | ATTT | A | 25 | a0001c0001t0001g0006 a0001c0001t0001g0024 a0001c0001t0001g0025 others(22): Show |
25 | HG01167.hp2 HG01168.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.5364-3748_5364-374 others(7): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901154 | ||||||
| chr12:45901154 | ATTTT | A | 7 | a0001c0001t0001g0027 a0001c0001t0001g0209 a0001c0001t0001g0297 others(4): Show |
7 | HG02451.hp1 HG02602.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.5364-3749_5364-374 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901154 | ||||||
| chr12:45901154 | ATTTTTTT others(8): Show |
A | 3 | a0001c0001t0001g0170 a0001c0001t0001g0181 a0001c0001t0001g0191 |
3 | HG00673.hp1 HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.5364-3760_5364-374 others(19): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901154 | ||||||
| chr12:45901154 | ATTTTTTT others(9): Show |
A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0037 a0001c0001t0001g0038 others(85): Show |
89 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.5364-3761_5364-374 others(20): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901154 | ||||||
| chr12:45901316 | G | T | 1 | a0001c0002t0002g0219 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5364-3618G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45901316 | |||||||
| chr12:45901695 | C | G | 1 | a0001c0001t0003g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.5364-3239C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45901695 | |||||||
| chr12:45901748 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.5364-3186A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45901748 | |||||||
| chr12:45902100 | A | G | 4 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0164 others(1): Show |
4 | HG00438.hp1 HG02056.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.5364-2834A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45902100 | |||||||
| chr12:45902109 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5364-2825A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45902109 | |||||||
| chr12:45902240 | A | G | 1 | a0001c0001t0012g0252 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.5364-2694A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45902240 | |||||||
| chr12:45902295 | A | G | 66 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0084 others(63): Show |
66 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.5364-2639A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45902295 | |||||||
| chr12:45902422 | A | C | 1 | a0014c0018t0001g0262 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5364-2512A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45902422 | |||||||
| chr12:45902446 | A | G | 1 | a0010c0014t0007g0269 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5364-2488A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45902446 | |||||||
| chr12:45902527 | T | G | 13 | a0002c0003t0001g0142 a0002c0003t0001g0148 a0002c0003t0001g0235 others(10): Show |
13 | HG00597.hp2 HG00673.hp2 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.5364-2407T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45902527 | |||||||
| chr12:45902535 | AT | A | 9 | a0001c0001t0001g0110 a0001c0001t0001g0123 a0001c0001t0001g0144 others(6): Show |
9 | HG01074.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.5364-2385delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45902535 | ||||||
| chr12:45902779 | G | A | 2 | a0001c0001t0001g0270 a0001c0001t0001g0291 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5364-2155G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45902779 | |||||||
| chr12:45902807 | C | T | 1 | a0001c0011t0018g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5364-2127C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45902807 | |||||||
| chr12:45902861 | A | G | 1 | a0001c0001t0015g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5364-2073A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45902861 | |||||||
| chr12:45903269 | G | A | 5 | a0001c0001t0005g0273 a0001c0001t0005g0285 a0001c0001t0005g0286 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.5364-1665G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45903269 | |||||||
| chr12:45903812 | T | C | 5 | a0001c0001t0005g0273 a0001c0001t0005g0285 a0001c0001t0005g0286 others(2): Show |
5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.5364-1122T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45903812 | |||||||
| chr12:45904155 | A | C | 1 | a0001c0001t0001g0004 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.5364-779A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45904155 | |||||||
| chr12:45904233 | G | A | 3 | a0001c0001t0001g0171 a0001c0001t0001g0189 a0001c0001t0001g0204 |
3 | HG00738.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.5364-701G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45904233 | |||||||
| chr12:45904495 | G | A | 1 | a0001c0001t0003g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5364-439G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45904495 | |||||||
| chr12:45904507 | A | G | 1 | a0011c0010t0002g0206 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5364-427A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45904507 | |||||||
| chr12:45904560 | A | G | 2 | a0001c0001t0001g0316 a0001c0001t0001g0317 |
2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.5364-374A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45904560 | |||||||
| chr12:45904563 | C | T | 25 | a0001c0001t0001g0316 a0001c0001t0001g0317 a0001c0002t0002g0210 others(22): Show |
25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.5364-371C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45904563 | |||||||
| chr12:45904652 | T | C | 219 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0037 others(216): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.5364-282T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45904652 | |||||||
| chr12:45904654 | A | G | 219 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0037 others(216): Show |
220 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.5364-280A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45904654 | |||||||
| chr12:45904689 | C | CA | 39 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0017 others(36): Show |
39 | HG00544.hp1 HG00639.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.5364-220dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45904689 | ||||||
| chr12:45904689 | C | CAA | 7 | a0001c0001t0001g0091 a0001c0001t0001g0123 a0001c0001t0001g0263 others(4): Show |
7 | HG01074.hp2 HG01109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.5364-221_5364-220d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45904689 | ||||||
| chr12:45904689 | CA | C | 36 | a0001c0001t0001g0002 a0001c0001t0001g0033 a0001c0001t0001g0145 others(33): Show |
36 | HG01175.hp1 HG01256.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.5364-220delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45904689 | ||||||
| chr12:45904726 | G | C | 5 | a0001c0001t0001g0249 a0001c0001t0001g0263 a0001c0001t0001g0270 others(2): Show |
5 | HG01109.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.5364-208G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45904726 | |||||||
| chr12:45904911 | A | G | 2 | a0001c0001t0001g0270 a0001c0001t0001g0291 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5364-23A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45904911 |