Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 123036 |
| ensemblid | ENSG00000165929.13 |
| hgncid | 19859 |
| symbol | TC2N |
| name | tandem C2 domains, nuclear |
| refseq_nuc | NM_001128596.3 |
| refseq_prot | NP_001122068.2 |
| ensembl_nuc | ENST00000435962.7 |
| ensembl_prot | ENSP00000387882.2 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 91779746 |
| end | 91867536 |
| strand | - |
| ver | v1.2 |
| region | chr14:91779746-91867536 |
| region5000 | chr14:91774746-91872536 |
| regionname0 | TC2N_chr14_91779746_91867536 |
| regionname5000 | TC2N_chr14_91774746_91872536 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 490 | 332 | 87 | 58 | 136 | 14 | 36 | 98 | TC2N_chr14_91774746_91872536 | TC2N | MATEF others(485): Show |
chr14 | 91774746 | 91872536 |
| a0002 | 1/0 | 490 | 8 | 7 | 0 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | MATEF others(485): Show |
chr14 | 91774746 | 91872536 |
| a0003 | 0/0 | 490 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | MATEF others(485): Show |
chr14 | 91774746 | 91872536 |
| a0004 | 0/0 | 490 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | MATEF others(485): Show |
chr14 | 91774746 | 91872536 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1470 | 274 | 79 | 46 | 108 | 12 | 29 | TC2N_chr14_91774746_91872536 | TC2N | ATGGC others(1465): Show |
chr14 | 91774746 | 91872536 | ||
| a0001c0002 | 0/1 | 1470 | 56 | 7 | 12 | 27 | 2 | 7 | TC2N_chr14_91774746_91872536 | TC2N | ATGGC others(1465): Show |
chr14 | 91774746 | 91872536 | ||
| a0001c0006 | 0/0 | 1470 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | ATGGC others(1465): Show |
chr14 | 91774746 | 91872536 | ||
| a0001c0007 | 0/0 | 1470 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | ATGGC others(1465): Show |
chr14 | 91774746 | 91872536 | ||
| a0002c0003 | 1/0 | 1470 | 8 | 7 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | ATGGC others(1465): Show |
chr14 | 91774746 | 91872536 | ||
| a0003c0004 | 0/0 | 1470 | 3 | 3 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | ATGGC others(1465): Show |
chr14 | 91774746 | 91872536 | ||
| a0004c0005 | 0/0 | 1470 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | ATGGC others(1465): Show |
chr14 | 91774746 | 91872536 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5158 | 52 | 11 | 15 | 17 | 4 | 5 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0002 | 0/0 | 5158 | 102 | 11 | 25 | 56 | 3 | 7 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0003 | 0/0 | 5158 | 34 | 5 | 1 | 15 | 3 | 10 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0004 | 0/0 | 5158 | 14 | 0 | 0 | 10 | 0 | 4 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0005 | 0/0 | 5158 | 13 | 12 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0006 | 0/0 | 5158 | 11 | 11 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0008 | 0/0 | 5158 | 7 | 6 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0009 | 0/0 | 5158 | 7 | 6 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0010 | 0/0 | 5158 | 5 | 3 | 0 | 0 | 0 | 2 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0012 | 0/0 | 5158 | 3 | 0 | 0 | 3 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0013 | 0/0 | 5476 | 2 | 2 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5471): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0014 | 0/0 | 5158 | 2 | 0 | 0 | 0 | 2 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0015 | 0/0 | 5158 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0016 | 0/0 | 5489 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5484): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0017 | 0/0 | 5489 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5484): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0018 | 0/0 | 5490 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5485): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0019 | 0/0 | 5476 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5471): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0020 | 0/0 | 5158 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0021 | 0/0 | 5158 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0022 | 0/0 | 5158 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0024 | 0/0 | 5158 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0025 | 0/0 | 5477 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5472): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0026 | 0/0 | 5158 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0027 | 0/0 | 5158 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0029 | 0/0 | 5158 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0030 | 0/0 | 5158 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0031 | 0/0 | 5158 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0032 | 0/0 | 5158 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0033 | 0/0 | 5158 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0034 | 0/0 | 5158 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0035 | 0/0 | 5158 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0036 | 0/0 | 5158 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0037 | 0/0 | 5158 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0001t0038 | 0/0 | 5472 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5467): Show |
chr14 | 91774746 | 91872536 |
| a0001c0002t0001 | 0/0 | 5158 | 52 | 7 | 12 | 24 | 2 | 7 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0002t0011 | 0/0 | 5158 | 3 | 0 | 0 | 3 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0002t0023 | 0/1 | 5158 | 1 | 0 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0006t0002 | 0/0 | 5158 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0001c0007t0028 | 0/0 | 5158 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0002c0003t0007 | 1/0 | 5158 | 8 | 7 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0003c0004t0001 | 0/0 | 5158 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0003c0004t0002 | 0/0 | 5158 | 2 | 2 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| a0004c0005t0001 | 0/0 | 5158 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | AGTCA others(5153): Show |
chr14 | 91774746 | 91872536 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0005g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0005g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0005g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0005g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0008g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0008g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0008g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0008g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0008g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0009g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0009g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0010g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0010g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0010g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0010g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0010g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0012g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0012g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0012g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0013g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0013g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0014g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0014g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0015g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0016g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0017g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0018g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0019g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0020g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0021g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0022g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0024g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0025g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0026g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0027g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0029g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0030g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0031g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0032g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0033g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0034g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0035g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0036g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0037g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0038g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0011g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0011g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0023g0096 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0006t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0007t0028g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0002c0003t0007g0002 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0002c0003t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0002c0003t0007g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0002c0003t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0002c0003t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0003c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0003c0004t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0003c0004t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0004c0005t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0179 | EUR | GBR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0182 | EUR | GBR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0281 | EUR | GBR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00423 | hp1 | a0001 | c0001 | t0012 | g0318 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0186 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0277 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0131 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0116 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0102 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0138 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0297 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0149 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0298 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0139 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0151 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0294 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0142 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01109 | hp1 | a0001 | c0001 | t0009 | g0157 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01167 | hp2 | a0001 | c0001 | t0015 | g0069 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0130 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0291 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01175 | hp2 | a0001 | c0001 | t0035 | g0289 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01192 | hp2 | a0001 | c0001 | t0008 | g0084 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | CLM | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | CLM | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0091 | AMR | CLM | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | CLM | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0114 | AMR | CLM | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | CLM | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | IBS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0238 | EUR | IBS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0196 | EUR | IBS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01516 | hp2 | a0001 | c0001 | t0014 | g0304 | EUR | IBS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01517 | hp1 | a0001 | c0001 | t0014 | g0244 | EUR | IBS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0132 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0083 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01891 | hp2 | a0001 | c0001 | t0009 | g0155 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0106 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0288 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0181 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0115 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0260 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02040 | hp2 | a0001 | c0001 | t0032 | g0243 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0075 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02083 | hp2 | a0001 | c0001 | t0024 | g0127 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0259 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | CDX | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | CDX | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0087 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02258 | hp1 | a0002 | c0003 | t0007 | g0163 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0144 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0133 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0146 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02572 | hp1 | a0003 | c0004 | t0002 | g0279 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0101 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0321 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0148 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0153 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02630 | hp2 | a0001 | c0001 | t0025 | g0023 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0152 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0175 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0246 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0214 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02717 | hp2 | a0002 | c0003 | t0007 | g0002 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02723 | hp1 | a0001 | c0001 | t0031 | g0166 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0195 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0280 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02738 | hp1 | a0001 | c0001 | t0010 | g0170 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0017 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02809 | hp1 | a0001 | c0001 | t0026 | g0158 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02809 | hp2 | a0001 | c0001 | t0030 | g0147 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0004 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02818 | hp2 | a0001 | c0001 | t0027 | g0076 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02886 | hp1 | a0002 | c0003 | t0007 | g0164 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0247 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0065 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0071 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02922 | hp1 | a0003 | c0004 | t0001 | g0072 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0161 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0184 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02970 | hp1 | a0002 | c0003 | t0007 | g0162 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0004 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0086 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02976 | hp2 | a0002 | c0003 | t0007 | g0002 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03041 | hp1 | a0001 | c0001 | t0018 | g0085 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0081 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03098 | hp1 | a0001 | c0001 | t0010 | g0136 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0067 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0011 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0156 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03139 | hp1 | a0004 | c0005 | t0001 | g0049 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0154 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03195 | hp2 | a0001 | c0001 | t0008 | g0082 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0266 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03209 | hp2 | a0001 | c0001 | t0029 | g0197 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03225 | hp2 | a0001 | c0001 | t0017 | g0090 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0174 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03486 | hp1 | a0002 | c0003 | t0007 | g0094 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0095 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0143 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0315 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0064 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03516 | hp2 | a0003 | c0004 | t0002 | g0278 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03540 | hp1 | a0001 | c0001 | t0019 | g0089 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | STU | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03688 | hp2 | a0001 | c0001 | t0010 | g0135 | SAS | STU | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0183 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0299 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0129 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | BEB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0308 | SAS | BEB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0168 | SAS | BEB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0220 | SAS | BEB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0178 | SAS | BEB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0141 | SAS | BEB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0167 | SAS | STU | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0140 | SAS | STU | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0307 | SAS | STU | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG04204 | hp1 | a0001 | c0001 | t0021 | g0018 | SAS | STU | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0125 | SAS | STU | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0056 | AFR | YRI | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0173 | AFR | YRI | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18612 | hp1 | a0001 | c0006 | t0002 | g0253 | EAS | CHB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | CHB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18747 | hp1 | a0001 | c0001 | t0012 | g0317 | EAS | CHB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | CHB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0062 | AFR | YRI | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18906 | hp2 | a0001 | c0001 | t0013 | g0024 | AFR | YRI | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0309 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0313 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18960 | hp1 | a0001 | c0001 | t0012 | g0316 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18962 | hp1 | a0001 | c0001 | t0022 | g0054 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18964 | hp2 | a0001 | c0001 | t0033 | g0219 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18966 | hp2 | a0001 | c0002 | t0011 | g0008 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0311 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18970 | hp2 | a0001 | c0001 | t0036 | g0314 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0319 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18983 | hp1 | a0001 | c0002 | t0011 | g0008 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19001 | hp1 | a0001 | c0001 | t0037 | g0322 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0312 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0150 | AFR | LWK | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19043 | hp1 | a0002 | c0003 | t0007 | g0002 | AFR | LWK | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | LWK | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19054 | hp2 | a0001 | c0001 | t0020 | g0077 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19065 | hp2 | a0001 | c0002 | t0011 | g0112 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0310 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0320 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19240 | hp1 | a0001 | c0001 | t0034 | g0273 | AFR | YRI | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | YRI | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA20129 | hp1 | a0001 | c0001 | t0038 | g0323 | AFR | ASW | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA20129 | hp2 | a0001 | c0001 | t0010 | g0134 | AFR | ASW | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0117 | EUR | TSI | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0283 | EUR | TSI | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0118 | EUR | TSI | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | TSI | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0145 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0074 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0159 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02559 | hp1 | a0001 | c0001 | t0010 | g0137 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0160 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03471 | hp1 | a0001 | c0001 | t0016 | g0088 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0263 | AFR | USA | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | USA | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0255 | AFR | USA | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA20300 | hp2 | a0001 | c0001 | t0008 | g0080 | AFR | USA | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA21309 | hp1 | a0001 | c0001 | t0013 | g0022 | AFR | LWK | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA21309 | hp2 | a0001 | c0007 | t0028 | g0092 | AFR | LWK | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0023 | g0096 | REF | REF | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0007 | g0002 | REF | REF | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:91800327 | C | T | 1 | a0003 | 3 | HG02572.hp1 HG02922.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.515G>A | p.Ser172Asn | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/12 | 846/5158 | 515/1473 | 172/490 | chr14 | 91800327 | |||
| chr14:91802271 | T | A | 1 | a0001 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.452A>T | p.Lys151Met | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/12 | 783/5158 | 452/1473 | 151/490 | chr14 | 91802271 | |||
| chr14:91802271 | T | G | 3 | a0001 a0003 a0004 |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
missense_variant | MODERATE | c.452A>C | p.Lys151Thr | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/12 | 783/5158 | 452/1473 | 151/490 | chr14 | 91802271 | |||
| chr14:91812485 | A | G | 1 | a0004 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.128T>C | p.Val43Ala | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/12 | 459/5158 | 128/1473 | 43/490 | chr14 | 91812485 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:91783169 | G | A | 1 | a0001c0006 | 1 | NA18612.hp1 | synonymous_variant | LOW | c.1404C>T | p.Asn468Asn | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 1735/5158 | 1404/1473 | 468/490 | chr14 | 91783169 | |||
| chr14:91785243 | A | G | 1 | a0001c0002 | 55 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(52): Show |
synonymous_variant | LOW | c.1281T>C | p.Leu427Leu | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/12 | 1612/5158 | 1281/1473 | 427/490 | chr14 | 91785243 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:91779793 | C | T | 1 | a0001c0001t0022 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3307G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 3307 | chr14 | 91779793 | ||||||
| chr14:91779821 | C | A | 42 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(39): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
3_prime_UTR_variant | MODIFIER | c.*3279G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 3279 | chr14 | 91779821 | ||||||
| chr14:91780090 | T | A | 1 | a0001c0001t0037 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3010A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 3010 | chr14 | 91780090 | ||||||
| chr14:91780098 | G | A | 1 | a0001c0001t0029 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3002C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 3002 | chr14 | 91780098 | ||||||
| chr14:91780280 | A | T | 2 | a0001c0001t0005 a0001c0001t0030 |
14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2820T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2820 | chr14 | 91780280 | ||||||
| chr14:91780610 | A | G | 1 | a0001c0001t0021 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2490T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2490 | chr14 | 91780610 | ||||||
| chr14:91780905 | T | TAAAACAT others(311): Show |
1 | a0001c0001t0019 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2194_*2195insTTTT others(314): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2194 | chr14 | 91780905 | ||||||
| chr14:91780905 | T | TAAAACAT others(325): Show |
1 | a0001c0001t0018 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2194_*2195insTTTT others(328): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2194 | chr14 | 91780905 | ||||||
| chr14:91780905 | T | TAAAACAT others(324): Show |
1 | a0001c0001t0017 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2194_*2195insTTTT others(327): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2194 | chr14 | 91780905 | ||||||
| chr14:91780905 | T | TAAAACAT others(324): Show |
1 | a0001c0001t0016 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2194_*2195insTTTT others(327): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2194 | chr14 | 91780905 | ||||||
| chr14:91780905 | T | TAAAACAT others(307): Show |
1 | a0001c0001t0038 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2194_*2195insTTTT others(310): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2194 | chr14 | 91780905 | ||||||
| chr14:91780905 | T | TAAAACAT others(311): Show |
1 | a0001c0001t0013 | 2 | NA18906.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2194_*2195insTTTT others(314): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2194 | chr14 | 91780905 | ||||||
| chr14:91780905 | T | TAAAACAT others(312): Show |
1 | a0001c0001t0025 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2194_*2195insTTTT others(315): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2194 | chr14 | 91780905 | ||||||
| chr14:91780939 | C | T | 2 | a0001c0001t0009 a0001c0001t0026 |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2161G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2161 | chr14 | 91780939 | ||||||
| chr14:91780946 | T | G | 2 | a0001c0001t0010 a0001c0001t0034 |
6 | HG02559.hp1 HG02738.hp1 HG03098.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2154A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2154 | chr14 | 91780946 | ||||||
| chr14:91781004 | A | G | 1 | a0001c0001t0020 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2096T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2096 | chr14 | 91781004 | ||||||
| chr14:91781110 | T | C | 1 | a0001c0001t0024 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1990A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 1990 | chr14 | 91781110 | ||||||
| chr14:91781133 | A | C | 1 | a0001c0007t0028 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1967T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 1967 | chr14 | 91781133 | ||||||
| chr14:91781174 | A | T | 4 | a0001c0001t0016 a0001c0001t0017 a0001c0001t0018 others(1): Show |
4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1926T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 1926 | chr14 | 91781174 | ||||||
| chr14:91781338 | T | A | 1 | a0001c0002t0011 | 3 | NA18966.hp2 NA18983.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1762A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 1762 | chr14 | 91781338 | ||||||
| chr14:91781470 | G | T | 1 | a0001c0001t0031 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1630C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 1630 | chr14 | 91781470 | ||||||
| chr14:91781616 | A | G | 1 | a0001c0001t0015 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1484T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 1484 | chr14 | 91781616 | ||||||
| chr14:91781715 | G | C | 3 | a0001c0001t0013 a0001c0001t0025 a0001c0001t0038 |
4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1385C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 1385 | chr14 | 91781715 | ||||||
| chr14:91781999 | A | T | 1 | a0001c0001t0037 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1101T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 1101 | chr14 | 91781999 | ||||||
| chr14:91782083 | G | T | 1 | a0001c0001t0033 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1017C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 1017 | chr14 | 91782083 | ||||||
| chr14:91782120 | C | T | 1 | a0001c0007t0028 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*980G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 980 | chr14 | 91782120 | ||||||
| chr14:91782268 | C | T | 1 | a0001c0001t0027 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*832G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 832 | chr14 | 91782268 | ||||||
| chr14:91782406 | A | G | 1 | a0001c0001t0008 | 7 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*694T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 694 | chr14 | 91782406 | ||||||
| chr14:91782475 | T | A | 1 | a0001c0001t0026 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*625A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 625 | chr14 | 91782475 | ||||||
| chr14:91782512 | A | C | 1 | a0001c0001t0030 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*588T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 588 | chr14 | 91782512 | ||||||
| chr14:91782541 | T | C | 8 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(5): Show |
43 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*559A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 559 | chr14 | 91782541 | ||||||
| chr14:91782608 | C | G | 1 | a0001c0001t0014 | 2 | HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*492G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 492 | chr14 | 91782608 | ||||||
| chr14:91782628 | A | G | 1 | a0001c0001t0032 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*472T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 472 | chr14 | 91782628 | ||||||
| chr14:91782695 | G | A | 2 | a0001c0001t0005 a0001c0001t0030 |
14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*405C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 405 | chr14 | 91782695 | ||||||
| chr14:91782757 | T | C | 4 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0031 others(1): Show |
39 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*343A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 343 | chr14 | 91782757 | ||||||
| chr14:91782782 | G | A | 41 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(38): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
3_prime_UTR_variant | MODIFIER | c.*318C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 318 | chr14 | 91782782 | ||||||
| chr14:91867267 | T | C | 8 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0032 others(5): Show |
111 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(108): Show |
5_prime_UTR_variant | MODIFIER | c.-62A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/12 | 53498 | chr14 | 91867267 | ||||||
| chr14:91867428 | G | A | 4 | a0001c0001t0004 a0001c0001t0012 a0001c0001t0036 others(1): Show |
19 | HG00423.hp1 HG02602.hp2 HG03491.hp1 others(16): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-223C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/12 | chr14 | 91867428 | |||||||
| chr14:91867492 | G | A | 1 | a0001c0001t0038 | 1 | NA20129.hp1 | 5_prime_UTR_variant | MODIFIER | c.-287C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/12 | 53723 | chr14 | 91867492 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:91783227 | G | C | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1363-17C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91783227 | |||||||
| chr14:91783260 | C | A | 1 | a0001c0001t0001g0033 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1363-50G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91783260 | |||||||
| chr14:91783510 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
11 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1363-300G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91783510 | |||||||
| chr14:91783623 | T | C | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1363-413A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91783623 | |||||||
| chr14:91784068 | T | C | 1 | a0001c0001t0004g0312 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1363-858A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91784068 | |||||||
| chr14:91784100 | G | A | 1 | a0001c0001t0018g0085 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1363-890C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91784100 | |||||||
| chr14:91784122 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1363-912G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91784122 | |||||||
| chr14:91784292 | T | C | 45 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(42): Show |
51 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1362+870A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91784292 | |||||||
| chr14:91784301 | T | C | 4 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0025g0023 others(1): Show |
4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1362+861A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91784301 | |||||||
| chr14:91784529 | T | C | 8 | a0001c0001t0006g0056 a0001c0001t0006g0062 a0001c0001t0006g0063 others(5): Show |
8 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1362+633A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91784529 | |||||||
| chr14:91784545 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1362+617C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91784545 | |||||||
| chr14:91784887 | A | C | 4 | a0001c0001t0016g0088 a0001c0001t0017g0090 a0001c0001t0018g0085 others(1): Show |
4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1362+275T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91784887 | |||||||
| chr14:91785019 | C | T | 317 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(314): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1362+143G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91785019 | |||||||
| chr14:91785034 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1362+128A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91785034 | |||||||
| chr14:91785120 | A | G | 2 | a0001c0001t0002g0218 a0001c0001t0033g0219 |
2 | NA18957.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1362+42T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91785120 | |||||||
| chr14:91785135 | T | C | 45 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(42): Show |
51 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1362+27A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91785135 | |||||||
| chr14:91785403 | A | T | 1 | a0001c0001t0018g0085 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1163-42T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91785403 | |||||||
| chr14:91785507 | C | T | 1 | a0001c0001t0031g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1163-146G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91785507 | |||||||
| chr14:91785574 | A | C | 2 | a0001c0001t0003g0061 a0001c0001t0003g0165 |
2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1163-213T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91785574 | |||||||
| chr14:91785603 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1163-242G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91785603 | |||||||
| chr14:91785685 | A | G | 317 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(314): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1163-324T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91785685 | |||||||
| chr14:91785820 | G | A | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1163-459C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91785820 | |||||||
| chr14:91785935 | C | T | 1 | a0001c0001t0002g0261 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1163-574G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91785935 | |||||||
| chr14:91786066 | G | C | 4 | a0001c0001t0003g0015 a0001c0001t0003g0059 a0001c0001t0003g0060 others(1): Show |
4 | NA18968.hp2 NA18998.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1163-705C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786066 | |||||||
| chr14:91786201 | A | G | 1 | a0001c0001t0013g0022 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1163-840T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786201 | |||||||
| chr14:91786300 | C | T | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1163-939G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786300 | |||||||
| chr14:91786363 | T | C | 1 | a0001c0001t0003g0017 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1163-1002A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786363 | |||||||
| chr14:91786495 | T | C | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1162+1018A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786495 | |||||||
| chr14:91786695 | T | C | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1162+818A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786695 | |||||||
| chr14:91786716 | T | A | 1 | a0001c0001t0001g0036 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1162+797A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786716 | |||||||
| chr14:91786718 | G | T | 1 | a0004c0005t0001g0049 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1162+795C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786718 | |||||||
| chr14:91786731 | T | C | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1162+782A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786731 | |||||||
| chr14:91786746 | T | C | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1162+767A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786746 | |||||||
| chr14:91786791 | A | G | 8 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(5): Show |
8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1162+722T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786791 | |||||||
| chr14:91786906 | G | A | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1162+607C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786906 | |||||||
| chr14:91786953 | T | A | 1 | a0001c0001t0005g0146 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1162+560A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786953 | |||||||
| chr14:91787011 | T | C | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1162+502A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91787011 | |||||||
| chr14:91787141 | A | T | 2 | a0001c0001t0002g0302 a0001c0001t0002g0305 |
2 | NA18962.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1162+372T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91787141 | |||||||
| chr14:91787212 | A | G | 1 | a0001c0001t0009g0160 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1162+301T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91787212 | |||||||
| chr14:91787262 | T | G | 2 | a0001c0001t0002g0221 a0001c0001t0002g0222 |
2 | NA18947.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1162+251A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91787262 | |||||||
| chr14:91787649 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0020g0077 |
2 | NA19000.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1048-22A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91787649 | |||||||
| chr14:91787728 | T | G | 4 | a0001c0001t0016g0088 a0001c0001t0017g0090 a0001c0001t0018g0085 others(1): Show |
4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1048-101A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91787728 | |||||||
| chr14:91787818 | T | A | 310 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(307): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.1048-191A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91787818 | |||||||
| chr14:91788359 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1048-732A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91788359 | |||||||
| chr14:91788428 | A | C | 17 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(14): Show |
19 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.1048-801T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91788428 | |||||||
| chr14:91788510 | A | G | 8 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(5): Show |
8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1048-883T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91788510 | |||||||
| chr14:91788659 | T | C | 318 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(315): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1048-1032A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91788659 | |||||||
| chr14:91788715 | A | C | 1 | a0001c0001t0032g0243 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1048-1088T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91788715 | |||||||
| chr14:91788961 | TA | T | 264 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1048-1335delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91788961 | |||||||
| chr14:91789022 | T | G | 37 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(34): Show |
43 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(40): Show |
intron_variant | MODIFIER | c.1048-1395A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789022 | |||||||
| chr14:91789136 | G | A | 1 | a0001c0001t0002g0230 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1048-1509C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789136 | |||||||
| chr14:91789197 | A | T | 13 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(10): Show |
15 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.1048-1570T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789197 | |||||||
| chr14:91789304 | G | T | 45 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(42): Show |
51 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1048-1677C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789304 | |||||||
| chr14:91789363 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0046 |
2 | HG04115.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1048-1736C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789363 | |||||||
| chr14:91789429 | TA | T | 10 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(7): Show |
10 | HG02630.hp2 HG02723.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.1048-1803delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789429 | |||||||
| chr14:91789440 | AAAG | A | 35 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(32): Show |
41 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1048-1816_1048-181 others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789440 | |||||||
| chr14:91789592 | CAGAG | C | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1048-1969_1048-196 others(8): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789592 | |||||||
| chr14:91789609 | T | A | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1048-1982A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789609 | |||||||
| chr14:91789623 | C | CA | 22 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(19): Show |
23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1048-1997dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789623 | |||||||
| chr14:91789630 | A | C | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1048-2003T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789630 | |||||||
| chr14:91789806 | T | G | 3 | a0003c0004t0001g0072 a0003c0004t0002g0278 a0003c0004t0002g0279 |
3 | HG02572.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1048-2179A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789806 | |||||||
| chr14:91789813 | C | A | 317 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(314): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1048-2186G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789813 | |||||||
| chr14:91789888 | C | A | 3 | a0003c0004t0001g0072 a0003c0004t0002g0278 a0003c0004t0002g0279 |
3 | HG02572.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1048-2261G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789888 | |||||||
| chr14:91790037 | C | G | 37 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(34): Show |
43 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(40): Show |
intron_variant | MODIFIER | c.1047+2330G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790037 | |||||||
| chr14:91790040 | A | C | 2 | a0001c0001t0001g0038 a0001c0001t0015g0069 |
2 | HG01109.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1047+2327T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790040 | |||||||
| chr14:91790080 | T | G | 1 | a0001c0001t0030g0147 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1047+2287A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790080 | |||||||
| chr14:91790391 | A | G | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1047+1976T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790391 | |||||||
| chr14:91790407 | C | T | 1 | a0001c0001t0002g0269 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1047+1960G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790407 | |||||||
| chr14:91790572 | T | C | 5 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1047+1795A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790572 | |||||||
| chr14:91790618 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1047+1749G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790618 | |||||||
| chr14:91790687 | T | C | 4 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0025g0023 others(1): Show |
4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1047+1680A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790687 | |||||||
| chr14:91790719 | T | C | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1047+1648A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790719 | |||||||
| chr14:91790842 | T | C | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1047+1525A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790842 | |||||||
| chr14:91790950 | A | G | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1047+1417T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790950 | |||||||
| chr14:91791064 | G | A | 6 | a0001c0001t0010g0134 a0001c0001t0010g0135 a0001c0001t0010g0136 others(3): Show |
6 | HG02559.hp1 HG02738.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1047+1303C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791064 | |||||||
| chr14:91791114 | G | C | 4 | a0001c0001t0016g0088 a0001c0001t0017g0090 a0001c0001t0018g0085 others(1): Show |
4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1047+1253C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791114 | |||||||
| chr14:91791176 | A | AGGAGG | 92 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(89): Show |
102 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1047+1186_1047+119 others(9): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791176 | |||||||
| chr14:91791176 | AGGAGG | A | 119 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(116): Show |
120 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.1047+1186_1047+119 others(9): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791176 | |||||||
| chr14:91791415 | C | T | 1 | a0001c0001t0003g0192 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1047+952G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791415 | |||||||
| chr14:91791485 | A | G | 7 | a0001c0001t0008g0080 a0001c0001t0008g0081 a0001c0001t0008g0082 others(4): Show |
7 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1047+882T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791485 | |||||||
| chr14:91791514 | T | A | 1 | a0001c0001t0009g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1047+853A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791514 | |||||||
| chr14:91791535 | T | TGA | 37 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(34): Show |
43 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(40): Show |
intron_variant | MODIFIER | c.1047+830_1047+831d others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791535 | |||||||
| chr14:91791562 | G | A | 1 | a0001c0001t0009g0133 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1047+805C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791562 | |||||||
| chr14:91791593 | A | G | 37 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(34): Show |
43 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(40): Show |
intron_variant | MODIFIER | c.1047+774T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791593 | |||||||
| chr14:91791639 | T | C | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1047+728A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791639 | |||||||
| chr14:91791757 | T | TA | 23 | a0001c0001t0005g0004 a0001c0001t0005g0011 a0001c0001t0005g0012 others(20): Show |
27 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1047+609dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791757 | |||||||
| chr14:91791757 | T | TAA | 13 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(10): Show |
15 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.1047+608_1047+609d others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791757 | |||||||
| chr14:91791758 | A | T | 3 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0025g0023 |
3 | HG02630.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1047+609T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791758 | |||||||
| chr14:91791836 | G | A | 2 | a0001c0001t0002g0232 a0001c0001t0036g0314 |
2 | NA18970.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1047+531C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791836 | |||||||
| chr14:91791913 | G | A | 8 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(5): Show |
8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1047+454C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791913 | |||||||
| chr14:91792011 | C | T | 10 | a0001c0001t0005g0004 a0001c0001t0005g0011 a0001c0001t0005g0012 others(7): Show |
14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1047+356G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91792011 | |||||||
| chr14:91792030 | A | G | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1047+337T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91792030 | |||||||
| chr14:91792118 | C | CA | 5 | a0001c0001t0001g0053 a0001c0001t0013g0022 a0001c0001t0013g0024 others(2): Show |
5 | HG02630.hp2 HG03471.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1047+248dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91792118 | |||||||
| chr14:91792121 | AG | A | 3 | a0001c0002t0001g0116 a0001c0002t0001g0117 a0001c0002t0001g0129 |
3 | HG00733.hp2 HG03710.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1047+245delC | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91792121 | |||||||
| chr14:91792122 | G | A | 314 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(311): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1047+245C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91792122 | |||||||
| chr14:91792155 | G | T | 4 | a0001c0001t0016g0088 a0001c0001t0017g0090 a0001c0001t0018g0085 others(1): Show |
4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1047+212C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91792155 | |||||||
| chr14:91792221 | T | TA | 317 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(314): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1047+145dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91792221 | |||||||
| chr14:91792353 | C | T | 10 | a0001c0001t0005g0004 a0001c0001t0005g0011 a0001c0001t0005g0012 others(7): Show |
14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1047+14G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91792353 | |||||||
| chr14:91792793 | C | T | 1 | a0001c0002t0001g0107 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.856-235G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91792793 | |||||||
| chr14:91793082 | A | G | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.856-524T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793082 | |||||||
| chr14:91793139 | T | C | 20 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0025 others(17): Show |
22 | HG00597.hp2 HG00673.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.856-581A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793139 | |||||||
| chr14:91793165 | A | G | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.856-607T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793165 | |||||||
| chr14:91793356 | A | G | 264 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.856-798T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793356 | |||||||
| chr14:91793441 | T | C | 3 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0025g0023 |
3 | HG02630.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.856-883A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793441 | |||||||
| chr14:91793463 | T | A | 4 | a0001c0001t0016g0088 a0001c0001t0017g0090 a0001c0001t0018g0085 others(1): Show |
4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-905A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793463 | |||||||
| chr14:91793559 | A | G | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.856-1001T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793559 | |||||||
| chr14:91793595 | C | T | 8 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(5): Show |
8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.856-1037G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793595 | |||||||
| chr14:91793846 | T | C | 8 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(5): Show |
8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.856-1288A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793846 | |||||||
| chr14:91793850 | C | T | 2 | a0001c0001t0002g0274 a0001c0001t0002g0292 |
2 | NA18968.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.856-1292G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793850 | |||||||
| chr14:91793930 | CT | C | 3 | a0001c0001t0003g0167 a0001c0001t0003g0174 a0001c0001t0003g0175 |
3 | HG02683.hp2 HG03239.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.856-1373delA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793930 | |||||||
| chr14:91794447 | G | A | 264 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.856-1889C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91794447 | |||||||
| chr14:91794509 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0042 |
2 | HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.856-1951C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91794509 | |||||||
| chr14:91794602 | TG | T | 47 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0002g0198 others(44): Show |
47 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.856-2045delC | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91794602 | |||||||
| chr14:91794656 | CA | C | 9 | a0001c0001t0002g0285 a0001c0001t0013g0022 a0001c0001t0013g0024 others(6): Show |
9 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.856-2099delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91794656 | |||||||
| chr14:91794748 | A | G | 1 | a0001c0001t0002g0299 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.856-2190T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91794748 | |||||||
| chr14:91794876 | T | C | 8 | a0001c0001t0006g0056 a0001c0001t0006g0062 a0001c0001t0006g0063 others(5): Show |
8 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.856-2318A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91794876 | |||||||
| chr14:91795098 | G | A | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.856-2540C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91795098 | |||||||
| chr14:91795153 | C | T | 2 | a0001c0001t0003g0061 a0001c0001t0003g0165 |
2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.856-2595G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91795153 | |||||||
| chr14:91795447 | G | A | 4 | a0001c0001t0016g0088 a0001c0001t0017g0090 a0001c0001t0018g0085 others(1): Show |
4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.855+2338C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91795447 | |||||||
| chr14:91795564 | T | C | 45 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(42): Show |
51 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(48): Show |
intron_variant | MODIFIER | c.855+2221A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91795564 | |||||||
| chr14:91795839 | C | G | 1 | a0001c0001t0002g0218 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.855+1946G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91795839 | |||||||
| chr14:91795846 | A | G | 242 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(239): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.855+1939T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91795846 | |||||||
| chr14:91795980 | T | C | 317 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(314): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.855+1805A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91795980 | |||||||
| chr14:91796066 | T | C | 4 | a0001c0001t0016g0088 a0001c0001t0017g0090 a0001c0001t0018g0085 others(1): Show |
4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.855+1719A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91796066 | |||||||
| chr14:91796358 | C | G | 1 | a0002c0003t0007g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.855+1427G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91796358 | |||||||
| chr14:91796614 | G | A | 35 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(32): Show |
41 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(38): Show |
intron_variant | MODIFIER | c.855+1171C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91796614 | |||||||
| chr14:91796659 | T | C | 7 | a0001c0001t0008g0080 a0001c0001t0008g0081 a0001c0001t0008g0082 others(4): Show |
7 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.855+1126A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91796659 | |||||||
| chr14:91796878 | C | T | 1 | a0001c0001t0003g0017 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.855+907G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91796878 | |||||||
| chr14:91796913 | A | G | 3 | a0001c0001t0002g0198 a0001c0001t0002g0229 a0001c0001t0002g0298 |
3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.855+872T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91796913 | |||||||
| chr14:91796971 | T | TTTTG | 317 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(314): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.855+810_855+813dup others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91796971 | |||||||
| chr14:91797103 | T | C | 1 | a0001c0001t0038g0323 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.855+682A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91797103 | |||||||
| chr14:91797324 | T | C | 13 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(10): Show |
15 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.855+461A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91797324 | |||||||
| chr14:91797327 | A | C | 194 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(191): Show |
202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.855+458T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91797327 | |||||||
| chr14:91797557 | C | A | 1 | a0004c0005t0001g0049 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.855+228G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91797557 | |||||||
| chr14:91797724 | A | C | 39 | a0001c0001t0001g0093 a0001c0001t0003g0013 a0001c0001t0003g0015 others(36): Show |
40 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.855+61T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91797724 | |||||||
| chr14:91797735 | AT | A | 39 | a0001c0001t0001g0093 a0001c0001t0003g0013 a0001c0001t0003g0015 others(36): Show |
40 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.855+49delA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91797735 | |||||||
| chr14:91797736 | TA | T | 238 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(235): Show |
249 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(246): Show |
intron_variant | MODIFIER | c.855+48delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91797736 | |||||||
| chr14:91797737 | A | C | 39 | a0001c0001t0001g0093 a0001c0001t0003g0013 a0001c0001t0003g0015 others(36): Show |
40 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.855+48T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91797737 | |||||||
| chr14:91797955 | C | T | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.739-54G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 7/11 | chr14 | 91797955 | |||||||
| chr14:91798037 | C | T | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.739-136G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 7/11 | chr14 | 91798037 | |||||||
| chr14:91798039 | C | T | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.739-138G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 7/11 | chr14 | 91798039 | |||||||
| chr14:91798087 | C | T | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.739-186G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 7/11 | chr14 | 91798087 | |||||||
| chr14:91798187 | A | C | 1 | a0001c0001t0004g0321 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.738+112T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 7/11 | chr14 | 91798187 | |||||||
| chr14:91798413 | G | C | 3 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0025g0023 |
3 | HG02630.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.638-14C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 6/11 | chr14 | 91798413 | |||||||
| chr14:91798681 | T | G | 1 | a0001c0001t0003g0188 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.638-282A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 6/11 | chr14 | 91798681 | |||||||
| chr14:91798816 | G | A | 264 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.637+173C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 6/11 | chr14 | 91798816 | |||||||
| chr14:91798922 | T | C | 5 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+67A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 6/11 | chr14 | 91798922 | |||||||
| chr14:91799182 | A | G | 1 | a0001c0001t0029g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.562-118T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91799182 | |||||||
| chr14:91799213 | G | GA | 17 | a0001c0001t0001g0097 a0001c0001t0002g0199 a0001c0001t0002g0264 others(14): Show |
17 | HG02145.hp1 HG02145.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.562-150dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91799213 | |||||||
| chr14:91799213 | GA | G | 42 | a0001c0001t0001g0093 a0001c0001t0003g0013 a0001c0001t0003g0015 others(39): Show |
43 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.562-150delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91799213 | |||||||
| chr14:91799322 | A | C | 13 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(10): Show |
15 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.562-258T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91799322 | |||||||
| chr14:91799668 | A | T | 2 | a0001c0001t0003g0061 a0001c0001t0003g0165 |
2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.562-604T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91799668 | |||||||
| chr14:91799761 | A | G | 1 | a0001c0001t0005g0144 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.561+520T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91799761 | |||||||
| chr14:91799863 | A | G | 10 | a0001c0001t0005g0004 a0001c0001t0005g0011 a0001c0001t0005g0012 others(7): Show |
14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.561+418T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91799863 | |||||||
| chr14:91799908 | A | C | 1 | a0001c0001t0031g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.561+373T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91799908 | |||||||
| chr14:91799917 | A | G | 3 | a0001c0001t0002g0198 a0001c0001t0002g0229 a0001c0001t0002g0298 |
3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.561+364T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91799917 | |||||||
| chr14:91800088 | T | G | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.561+193A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91800088 | |||||||
| chr14:91800143 | A | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(14): Show |
18 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.561+138T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91800143 | |||||||
| chr14:91800154 | T | C | 1 | a0001c0001t0002g0294 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.561+127A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91800154 | |||||||
| chr14:91800168 | C | A | 1 | a0001c0001t0034g0273 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.561+113G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91800168 | |||||||
| chr14:91800216 | C | T | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.561+65G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91800216 | |||||||
| chr14:91800443 | A | C | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-71T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91800443 | |||||||
| chr14:91800727 | A | G | 1 | a0001c0001t0002g0246 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.470-355T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91800727 | |||||||
| chr14:91800941 | GATAT | G | 3 | a0001c0001t0003g0167 a0001c0001t0003g0174 a0001c0001t0003g0175 |
3 | HG02683.hp2 HG03239.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.470-573_470-570del others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91800941 | |||||||
| chr14:91800943 | T | G | 1 | a0001c0001t0001g0048 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.470-571A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91800943 | |||||||
| chr14:91800953 | T | C | 1 | a0001c0001t0002g0221 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.470-581A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91800953 | |||||||
| chr14:91800955 | C | CACACACA others(27): Show |
59 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(56): Show |
60 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.470-617_470-584dup others(34): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91800955 | |||||||
| chr14:91800955 | C | CACACACA others(61): Show |
2 | a0001c0001t0002g0291 a0001c0001t0038g0323 |
2 | HG01175.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.470-651_470-584dup others(68): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91800955 | |||||||
| chr14:91800957 | C | CACACACA others(25): Show |
2 | a0001c0001t0013g0024 a0001c0001t0025g0023 |
2 | HG02630.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.470-617_470-586dup others(32): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91800957 | |||||||
| chr14:91801070 | ATG | A | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.470-700_470-699del others(2): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91801070 | |||||||
| chr14:91801080 | G | GTA | 9 | a0001c0001t0002g0255 a0001c0001t0002g0294 a0001c0001t0013g0022 others(6): Show |
9 | HG01081.hp2 HG01175.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.470-710_470-709dup others(2): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91801080 | |||||||
| chr14:91801080 | G | GTGTA | 4 | a0001c0001t0016g0088 a0001c0001t0017g0090 a0001c0001t0018g0085 others(1): Show |
4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-709_470-708ins others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91801080 | |||||||
| chr14:91801082 | A | G | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-710T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91801082 | |||||||
| chr14:91801690 | A | G | 264 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.469+564T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91801690 | |||||||
| chr14:91801735 | T | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(14): Show |
18 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.469+519A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91801735 | |||||||
| chr14:91801752 | C | T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(96): Show |
108 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.469+502G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91801752 | |||||||
| chr14:91801893 | G | T | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.469+361C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91801893 | |||||||
| chr14:91802132 | C | T | 7 | a0001c0001t0008g0080 a0001c0001t0008g0081 a0001c0001t0008g0082 others(4): Show |
7 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.469+122G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91802132 | |||||||
| chr14:91802161 | A | G | 8 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(5): Show |
8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.469+93T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91802161 | |||||||
| chr14:91802187 | C | T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(96): Show |
108 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.469+67G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91802187 | |||||||
| chr14:91802543 | T | C | 37 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(34): Show |
43 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(40): Show |
intron_variant | MODIFIER | c.302-122A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91802543 | |||||||
| chr14:91802565 | C | T | 1 | a0002c0003t0007g0164 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.302-144G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91802565 | |||||||
| chr14:91802708 | C | G | 1 | a0001c0001t0009g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.302-287G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91802708 | |||||||
| chr14:91802744 | T | TGG | 30 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(27): Show |
36 | HG02109.hp1 HG02451.hp2 HG02602.hp2 others(33): Show |
intron_variant | MODIFIER | c.302-325_302-324dup others(2): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91802744 | |||||||
| chr14:91802746 | G | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0047 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.302-325C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91802746 | |||||||
| chr14:91802776 | G | A | 1 | a0001c0001t0029g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.302-355C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91802776 | |||||||
| chr14:91802788 | T | C | 1 | a0001c0001t0035g0289 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.302-367A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91802788 | |||||||
| chr14:91802817 | G | A | 1 | a0001c0001t0030g0147 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.302-396C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91802817 | |||||||
| chr14:91802859 | C | T | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.302-438G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91802859 | |||||||
| chr14:91803084 | G | A | 53 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(50): Show |
59 | HG01081.hp1 HG01109.hp1 HG01891.hp2 others(56): Show |
intron_variant | MODIFIER | c.302-663C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803084 | |||||||
| chr14:91803097 | T | G | 1 | a0001c0002t0011g0112 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.302-676A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803097 | |||||||
| chr14:91803380 | T | C | 1 | a0001c0001t0003g0173 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.302-959A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803380 | |||||||
| chr14:91803380 | T | TAC | 61 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(58): Show |
64 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.302-961_302-960dup others(2): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803380 | |||||||
| chr14:91803380 | T | TACAC | 13 | a0001c0001t0001g0068 a0001c0001t0004g0319 a0001c0001t0005g0004 others(10): Show |
17 | HG01081.hp1 HG01975.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.302-963_302-960dup others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803380 | |||||||
| chr14:91803380 | T | TACACAC | 20 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(17): Show |
22 | HG02602.hp2 HG02647.hp1 HG02818.hp2 others(19): Show |
intron_variant | MODIFIER | c.302-965_302-960dup others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803380 | |||||||
| chr14:91803380 | T | TATAC | 8 | a0001c0001t0006g0074 a0001c0001t0006g0075 a0001c0001t0006g0159 others(5): Show |
8 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.302-960_302-959ins others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803380 | |||||||
| chr14:91803380 | TAC | T | 7 | a0001c0001t0002g0235 a0001c0001t0002g0302 a0001c0001t0002g0305 others(4): Show |
7 | HG00423.hp1 NA18747.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.302-961_302-960del others(2): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803380 | |||||||
| chr14:91803382 | C | T | 7 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0025g0023 others(4): Show |
7 | HG02572.hp1 HG02630.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.302-961G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803382 | |||||||
| chr14:91803403 | G | A | 1 | a0001c0001t0002g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.302-982C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803403 | |||||||
| chr14:91803412 | T | C | 2 | a0001c0001t0002g0248 a0001c0007t0028g0092 |
2 | HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.302-991A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803412 | |||||||
| chr14:91803412 | T | TAC | 3 | a0001c0002t0001g0138 a0001c0002t0001g0149 a0002c0003t0007g0094 |
3 | HG00738.hp1 HG01069.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.302-993_302-992dup others(2): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803412 | |||||||
| chr14:91803412 | TAC | T | 8 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(5): Show |
8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.302-993_302-992del others(2): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803412 | |||||||
| chr14:91803428 | C | CACACACA others(1): Show |
10 | a0001c0001t0005g0004 a0001c0001t0005g0011 a0001c0001t0005g0012 others(7): Show |
14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.302-1008_302-1007i others(10): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803428 | |||||||
| chr14:91803428 | C | CACACAT | 26 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(23): Show |
28 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(25): Show |
intron_variant | MODIFIER | c.302-1008_302-1007i others(8): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803428 | |||||||
| chr14:91803428 | C | CACAT | 4 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(1): Show |
4 | HG02145.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-1008_302-1007i others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803428 | |||||||
| chr14:91803428 | C | CAT | 254 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(251): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.302-1009_302-1008d others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803428 | |||||||
| chr14:91803428 | C | CATAT | 11 | a0001c0001t0001g0034 a0001c0001t0002g0228 a0001c0001t0009g0133 others(8): Show |
11 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.302-1011_302-1008d others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803428 | |||||||
| chr14:91803428 | C | T | 1 | a0001c0001t0002g0248 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.302-1007G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803428 | |||||||
| chr14:91803509 | G | A | 1 | a0001c0001t0001g0031 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.302-1088C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803509 | |||||||
| chr14:91803515 | T | C | 1 | a0001c0001t0003g0188 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.302-1094A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803515 | |||||||
| chr14:91803557 | A | T | 1 | a0001c0001t0004g0319 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.302-1136T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803557 | |||||||
| chr14:91803560 | C | T | 2 | a0001c0001t0003g0171 a0001c0001t0003g0184 |
2 | HG02647.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.302-1139G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803560 | |||||||
| chr14:91803577 | G | C | 317 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(314): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.302-1156C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803577 | |||||||
| chr14:91803609 | C | T | 1 | a0001c0002t0001g0116 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.302-1188G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803609 | |||||||
| chr14:91803767 | A | T | 1 | a0001c0001t0002g0224 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.302-1346T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803767 | |||||||
| chr14:91803836 | A | C | 1 | a0002c0003t0007g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.302-1415T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803836 | |||||||
| chr14:91803908 | C | A | 1 | a0001c0001t0002g0206 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.302-1487G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803908 | |||||||
| chr14:91803909 | C | G | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.302-1488G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803909 | |||||||
| chr14:91803963 | T | C | 3 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0025g0023 |
3 | HG02630.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.302-1542A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803963 | |||||||
| chr14:91803997 | G | A | 37 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(34): Show |
43 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(40): Show |
intron_variant | MODIFIER | c.302-1576C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803997 | |||||||
| chr14:91804102 | A | C | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.302-1681T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91804102 | |||||||
| chr14:91804142 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.302-1721G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91804142 | |||||||
| chr14:91804221 | C | T | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.302-1800G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91804221 | |||||||
| chr14:91804265 | T | C | 1 | a0002c0003t0007g0164 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.302-1844A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91804265 | |||||||
| chr14:91804270 | A | G | 5 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.302-1849T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91804270 | |||||||
| chr14:91804470 | T | C | 1 | a0001c0001t0022g0054 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.302-2049A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91804470 | |||||||
| chr14:91804633 | G | C | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.302-2212C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91804633 | |||||||
| chr14:91804744 | G | T | 1 | a0001c0002t0001g0124 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.302-2323C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91804744 | |||||||
| chr14:91804884 | G | A | 1 | a0001c0001t0004g0321 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.302-2463C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91804884 | |||||||
| chr14:91804943 | C | T | 4 | a0001c0001t0016g0088 a0001c0001t0017g0090 a0001c0001t0018g0085 others(1): Show |
4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.302-2522G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91804943 | |||||||
| chr14:91805260 | AG | A | 2 | a0001c0002t0001g0009 a0001c0002t0001g0119 |
3 | HG02895.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.302-2840delC | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91805260 | |||||||
| chr14:91805407 | G | A | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.302-2986C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91805407 | |||||||
| chr14:91805421 | C | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0015g0069 |
3 | HG01109.hp2 HG01167.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.302-3000G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91805421 | |||||||
| chr14:91805450 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 |
3 | HG01261.hp2 HG02004.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.302-3029G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91805450 | |||||||
| chr14:91805523 | T | A | 1 | a0001c0001t0002g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.302-3102A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91805523 | |||||||
| chr14:91805658 | C | T | 13 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(10): Show |
15 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.302-3237G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91805658 | |||||||
| chr14:91805749 | T | G | 10 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
11 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.302-3328A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91805749 | |||||||
| chr14:91805791 | G | A | 2 | a0001c0001t0003g0179 a0001c0001t0003g0196 |
2 | HG00099.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.302-3370C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91805791 | |||||||
| chr14:91805818 | T | C | 1 | a0001c0001t0002g0215 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.302-3397A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91805818 | |||||||
| chr14:91805933 | C | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0032 a0001c0001t0001g0042 |
3 | HG00673.hp2 HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.302-3512G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91805933 | |||||||
| chr14:91806111 | GC | G | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.302-3691delG | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91806111 | |||||||
| chr14:91806390 | T | G | 1 | a0001c0001t0004g0310 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.302-3969A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91806390 | |||||||
| chr14:91806497 | G | C | 4 | a0001c0001t0006g0074 a0001c0001t0006g0075 a0001c0001t0006g0159 others(1): Show |
4 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-4076C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91806497 | |||||||
| chr14:91806585 | C | T | 1 | a0001c0001t0004g0308 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.302-4164G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91806585 | |||||||
| chr14:91806671 | G | T | 1 | a0001c0001t0002g0230 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.302-4250C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91806671 | |||||||
| chr14:91806729 | G | A | 1 | a0001c0001t0002g0259 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.302-4308C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91806729 | |||||||
| chr14:91806829 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.302-4408T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91806829 | |||||||
| chr14:91806971 | C | T | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.302-4550G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91806971 | |||||||
| chr14:91807003 | A | T | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.302-4582T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91807003 | |||||||
| chr14:91807063 | C | T | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.302-4642G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91807063 | |||||||
| chr14:91807085 | G | C | 4 | a0001c0001t0016g0088 a0001c0001t0017g0090 a0001c0001t0018g0085 others(1): Show |
4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.302-4664C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91807085 | |||||||
| chr14:91807172 | C | T | 2 | a0001c0001t0003g0189 a0001c0001t0013g0022 |
2 | HG02155.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.302-4751G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91807172 | |||||||
| chr14:91807247 | C | T | 4 | a0001c0001t0003g0167 a0001c0001t0003g0173 a0001c0001t0003g0174 others(1): Show |
4 | HG02683.hp2 HG03239.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-4826G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91807247 | |||||||
| chr14:91807340 | T | C | 7 | a0001c0001t0002g0241 a0001c0001t0002g0256 a0001c0001t0002g0262 others(4): Show |
7 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.302-4919A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91807340 | |||||||
| chr14:91807634 | T | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(14): Show |
18 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.301+4678A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91807634 | |||||||
| chr14:91807926 | G | A | 1 | a0001c0001t0002g0215 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.301+4386C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91807926 | |||||||
| chr14:91807932 | T | C | 2 | a0001c0001t0002g0241 a0001c0002t0001g0095 |
2 | HG00544.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.301+4380A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91807932 | |||||||
| chr14:91808160 | C | T | 1 | a0001c0001t0020g0077 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.301+4152G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91808160 | |||||||
| chr14:91808291 | A | G | 1 | a0001c0001t0001g0027 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.301+4021T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91808291 | |||||||
| chr14:91808351 | G | A | 2 | a0001c0001t0002g0302 a0001c0001t0002g0305 |
2 | NA18962.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.301+3961C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91808351 | |||||||
| chr14:91808837 | T | C | 4 | a0001c0001t0002g0265 a0001c0001t0002g0267 a0001c0001t0002g0268 others(1): Show |
4 | HG00423.hp2 NA18960.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+3475A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91808837 | |||||||
| chr14:91808978 | T | A | 1 | a0002c0003t0007g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.301+3334A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91808978 | |||||||
| chr14:91809377 | C | A | 44 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(41): Show |
47 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.301+2935G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91809377 | |||||||
| chr14:91809602 | T | G | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.301+2710A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91809602 | |||||||
| chr14:91809775 | A | G | 1 | a0001c0001t0002g0282 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.301+2537T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91809775 | |||||||
| chr14:91809881 | A | T | 1 | a0001c0001t0005g0144 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.301+2431T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91809881 | |||||||
| chr14:91810040 | A | G | 2 | a0001c0001t0003g0186 a0001c0001t0003g0187 |
2 | HG00558.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.301+2272T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810040 | |||||||
| chr14:91810041 | T | C | 1 | a0001c0002t0011g0112 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.301+2271A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810041 | |||||||
| chr14:91810138 | C | T | 1 | a0001c0001t0029g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.301+2174G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810138 | |||||||
| chr14:91810316 | TG | T | 13 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(10): Show |
15 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.301+1995delC | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810316 | |||||||
| chr14:91810333 | C | G | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.301+1979G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810333 | |||||||
| chr14:91810477 | A | G | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.301+1835T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810477 | |||||||
| chr14:91810496 | T | C | 1 | a0001c0001t0029g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.301+1816A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810496 | |||||||
| chr14:91810558 | T | C | 11 | a0001c0001t0002g0203 a0001c0001t0002g0213 a0001c0001t0002g0218 others(8): Show |
11 | HG00673.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.301+1754A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810558 | |||||||
| chr14:91810573 | A | G | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.301+1739T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810573 | |||||||
| chr14:91810581 | C | T | 1 | a0001c0001t0002g0252 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.301+1731G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810581 | |||||||
| chr14:91810681 | A | C | 1 | a0001c0001t0009g0156 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.301+1631T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810681 | |||||||
| chr14:91810734 | C | A | 1 | a0001c0001t0009g0160 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.301+1578G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810734 | |||||||
| chr14:91810841 | C | G | 4 | a0001c0001t0016g0088 a0001c0001t0017g0090 a0001c0001t0018g0085 others(1): Show |
4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+1471G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810841 | |||||||
| chr14:91810868 | G | GA | 8 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(5): Show |
8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.301+1443dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810868 | |||||||
| chr14:91810909 | G | A | 10 | a0001c0001t0005g0004 a0001c0001t0005g0011 a0001c0001t0005g0012 others(7): Show |
14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.301+1403C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810909 | |||||||
| chr14:91810991 | T | A | 1 | a0001c0001t0002g0277 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.301+1321A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810991 | |||||||
| chr14:91811041 | C | T | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.301+1271G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811041 | |||||||
| chr14:91811150 | C | T | 3 | a0001c0001t0005g0004 a0001c0001t0005g0148 a0001c0001t0005g0152 |
5 | HG02615.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+1162G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811150 | |||||||
| chr14:91811151 | G | A | 8 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(5): Show |
8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.301+1161C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811151 | |||||||
| chr14:91811248 | A | AT | 37 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(34): Show |
43 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(40): Show |
intron_variant | MODIFIER | c.301+1063dupA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811248 | |||||||
| chr14:91811360 | G | GT | 17 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(14): Show |
18 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.301+951dupA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811360 | |||||||
| chr14:91811504 | TTCTC | T | 8 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(5): Show |
8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.301+804_301+807del others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811504 | |||||||
| chr14:91811587 | T | C | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.301+725A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811587 | |||||||
| chr14:91811639 | T | C | 8 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(5): Show |
8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.301+673A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811639 | |||||||
| chr14:91811754 | G | C | 1 | a0001c0001t0024g0127 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.301+558C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811754 | |||||||
| chr14:91811873 | T | A | 1 | a0001c0001t0029g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.301+439A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811873 | |||||||
| chr14:91811974 | T | C | 10 | a0001c0001t0005g0004 a0001c0001t0005g0011 a0001c0001t0005g0012 others(7): Show |
14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.301+338A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811974 | |||||||
| chr14:91812014 | T | A | 2 | a0001c0001t0002g0218 a0001c0001t0033g0219 |
2 | NA18957.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.301+298A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91812014 | |||||||
| chr14:91812296 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0046 |
2 | HG04115.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.301+16G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91812296 | |||||||
| chr14:91812298 | A | G | 1 | a0001c0001t0038g0323 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.301+14T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91812298 | |||||||
| chr14:91812686 | C | G | 4 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0025g0023 others(1): Show |
4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-141G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 2/11 | chr14 | 91812686 | |||||||
| chr14:91812838 | T | C | 264 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.68-293A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 2/11 | chr14 | 91812838 | |||||||
| chr14:91813386 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.67+317A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 2/11 | chr14 | 91813386 | |||||||
| chr14:91813412 | C | T | 1 | a0001c0001t0002g0249 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67+291G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 2/11 | chr14 | 91813412 | |||||||
| chr14:91813437 | C | G | 1 | a0001c0001t0010g0134 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.67+266G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 2/11 | chr14 | 91813437 | |||||||
| chr14:91813639 | T | G | 50 | a0001c0001t0024g0127 a0001c0002t0001g0001 a0001c0002t0001g0009 others(47): Show |
56 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.67+64A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 2/11 | chr14 | 91813639 | |||||||
| chr14:91813693 | T | C | 110 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0036 others(107): Show |
111 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.67+10A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 2/11 | chr14 | 91813693 | |||||||
| chr14:91813893 | A | T | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-68T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91813893 | |||||||
| chr14:91813993 | T | C | 1 | a0001c0001t0002g0296 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-56-168A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91813993 | |||||||
| chr14:91814056 | GA | G | 6 | a0001c0001t0010g0134 a0001c0001t0010g0135 a0001c0001t0010g0136 others(3): Show |
6 | HG02559.hp1 HG02738.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56-232delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91814056 | |||||||
| chr14:91814310 | T | C | 1 | a0002c0003t0007g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-56-485A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91814310 | |||||||
| chr14:91814331 | G | A | 46 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(43): Show |
47 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.-56-506C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91814331 | |||||||
| chr14:91814357 | CA | C | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.-56-533delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91814357 | |||||||
| chr14:91814391 | T | C | 35 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(32): Show |
41 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(38): Show |
intron_variant | MODIFIER | c.-56-566A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91814391 | |||||||
| chr14:91814944 | TATACAAT others(6): Show |
T | 3 | a0001c0001t0002g0198 a0001c0001t0002g0229 a0001c0001t0002g0298 |
3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-56-1132_-56-1120d others(15): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91814944 | |||||||
| chr14:91815042 | T | C | 7 | a0001c0001t0008g0080 a0001c0001t0008g0081 a0001c0001t0008g0082 others(4): Show |
7 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-1217A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815042 | |||||||
| chr14:91815161 | C | T | 1 | a0001c0001t0002g0208 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-56-1336G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815161 | |||||||
| chr14:91815200 | G | A | 8 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(5): Show |
8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-56-1375C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815200 | |||||||
| chr14:91815248 | C | A | 2 | a0001c0001t0002g0221 a0001c0001t0002g0222 |
2 | NA18947.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-56-1423G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815248 | |||||||
| chr14:91815347 | A | ATGAAT | 8 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(5): Show |
8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-56-1523_-56-1522i others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815347 | |||||||
| chr14:91815348 | C | A | 8 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(5): Show |
8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-56-1523G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815348 | |||||||
| chr14:91815349 | T | A | 8 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(5): Show |
8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-56-1524A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815349 | |||||||
| chr14:91815429 | C | A | 1 | a0001c0001t0002g0199 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-56-1604G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815429 | |||||||
| chr14:91815434 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-56-1609G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815434 | |||||||
| chr14:91815447 | G | A | 264 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-56-1622C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815447 | |||||||
| chr14:91815765 | T | C | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.-56-1940A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815765 | |||||||
| chr14:91815772 | T | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-56-1947A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815772 | |||||||
| chr14:91815932 | T | C | 264 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(261): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-56-2107A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815932 | |||||||
| chr14:91816011 | A | G | 1 | a0001c0001t0031g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-56-2186T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91816011 | |||||||
| chr14:91816039 | A | T | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-2214T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91816039 | |||||||
| chr14:91816189 | T | C | 7 | a0001c0001t0008g0080 a0001c0001t0008g0081 a0001c0001t0008g0082 others(4): Show |
7 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-2364A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91816189 | |||||||
| chr14:91816378 | G | A | 13 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(10): Show |
15 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.-56-2553C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91816378 | |||||||
| chr14:91816482 | T | C | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-2657A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91816482 | |||||||
| chr14:91816526 | G | T | 1 | a0002c0003t0007g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-56-2701C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91816526 | |||||||
| chr14:91816649 | T | C | 1 | a0001c0001t0002g0274 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-56-2824A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91816649 | |||||||
| chr14:91816779 | T | A | 1 | a0001c0001t0031g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-56-2954A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91816779 | |||||||
| chr14:91816959 | C | A | 1 | a0001c0001t0002g0281 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-56-3134G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91816959 | |||||||
| chr14:91817008 | C | T | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-3183G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91817008 | |||||||
| chr14:91817338 | T | C | 1 | a0001c0001t0002g0231 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-56-3513A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91817338 | |||||||
| chr14:91817818 | G | A | 13 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(10): Show |
15 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.-56-3993C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91817818 | |||||||
| chr14:91817828 | T | G | 39 | a0001c0001t0001g0093 a0001c0001t0003g0013 a0001c0001t0003g0015 others(36): Show |
40 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.-56-4003A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91817828 | |||||||
| chr14:91818089 | T | C | 148 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(145): Show |
150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.-56-4264A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818089 | |||||||
| chr14:91818168 | C | T | 1 | a0001c0001t0002g0203 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-56-4343G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818168 | |||||||
| chr14:91818169 | G | A | 10 | a0001c0001t0005g0004 a0001c0001t0005g0011 a0001c0001t0005g0012 others(7): Show |
14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-56-4344C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818169 | |||||||
| chr14:91818179 | A | G | 3 | a0001c0001t0004g0311 a0001c0001t0004g0312 a0001c0001t0037g0322 |
3 | NA18969.hp2 NA19001.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-56-4354T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818179 | |||||||
| chr14:91818441 | A | G | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-4616T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818441 | |||||||
| chr14:91818476 | T | A | 41 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(38): Show |
47 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(44): Show |
intron_variant | MODIFIER | c.-56-4651A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818476 | |||||||
| chr14:91818799 | C | T | 17 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(14): Show |
18 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-56-4974G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818799 | |||||||
| chr14:91818825 | C | G | 17 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(14): Show |
18 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-56-5000G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818825 | |||||||
| chr14:91818865 | A | G | 1 | a0001c0001t0003g0195 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-56-5040T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818865 | |||||||
| chr14:91818897 | A | T | 1 | a0001c0001t0003g0174 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-56-5072T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818897 | |||||||
| chr14:91818947 | G | C | 2 | a0001c0001t0001g0093 a0001c0002t0001g0121 |
2 | NA19030.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-56-5122C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818947 | |||||||
| chr14:91818982 | T | G | 1 | a0001c0001t0001g0046 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-56-5157A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818982 | |||||||
| chr14:91818995 | A | T | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-5170T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818995 | |||||||
| chr14:91819028 | C | G | 41 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(38): Show |
47 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(44): Show |
intron_variant | MODIFIER | c.-56-5203G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91819028 | |||||||
| chr14:91819040 | C | A | 4 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0025g0023 others(1): Show |
4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-5215G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91819040 | |||||||
| chr14:91819528 | C | T | 3 | a0001c0002t0001g0103 a0001c0002t0001g0105 a0001c0002t0001g0107 |
3 | NA19079.hp1 NA19080.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-56-5703G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91819528 | |||||||
| chr14:91819756 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
11 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-56-5931G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91819756 | |||||||
| chr14:91819765 | C | T | 1 | a0001c0001t0038g0323 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-56-5940G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91819765 | |||||||
| chr14:91819766 | G | A | 1 | a0002c0003t0007g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-56-5941C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91819766 | |||||||
| chr14:91819884 | T | C | 1 | a0001c0001t0009g0154 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-56-6059A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91819884 | |||||||
| chr14:91819918 | A | C | 38 | a0001c0001t0003g0013 a0001c0001t0003g0015 a0001c0001t0003g0017 others(35): Show |
39 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.-56-6093T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91819918 | |||||||
| chr14:91819943 | T | A | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-6118A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91819943 | |||||||
| chr14:91820131 | A | T | 1 | a0001c0001t0001g0045 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-56-6306T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820131 | |||||||
| chr14:91820196 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-56-6371G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820196 | |||||||
| chr14:91820283 | A | G | 1 | a0001c0001t0031g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-56-6458T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820283 | |||||||
| chr14:91820297 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-56-6472G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820297 | |||||||
| chr14:91820380 | A | T | 4 | a0001c0001t0001g0172 a0001c0001t0002g0263 a0001c0001t0002g0264 others(1): Show |
4 | HG02145.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-6555T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820380 | |||||||
| chr14:91820387 | CAATA | C | 8 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(5): Show |
8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-56-6566_-56-6563d others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820387 | |||||||
| chr14:91820513 | G | C | 154 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(151): Show |
161 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-56-6688C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820513 | |||||||
| chr14:91820545 | G | A | 1 | a0001c0001t0002g0242 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-56-6720C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820545 | |||||||
| chr14:91820688 | A | G | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-6863T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820688 | |||||||
| chr14:91820703 | T | TA | 147 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(144): Show |
154 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.-56-6879dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820703 | |||||||
| chr14:91820729 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-56-6904G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820729 | |||||||
| chr14:91820931 | A | G | 10 | a0001c0001t0005g0004 a0001c0001t0005g0011 a0001c0001t0005g0012 others(7): Show |
14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-56-7106T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820931 | |||||||
| chr14:91821173 | A | C | 1 | a0001c0001t0002g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-56-7348T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91821173 | |||||||
| chr14:91821399 | G | C | 99 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(96): Show |
108 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.-56-7574C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91821399 | |||||||
| chr14:91821471 | C | G | 2 | a0001c0001t0003g0186 a0001c0001t0003g0187 |
2 | HG00558.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-56-7646G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91821471 | |||||||
| chr14:91821662 | A | G | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-7837T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91821662 | |||||||
| chr14:91821672 | C | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0045 a0001c0001t0001g0057 others(1): Show |
5 | HG00099.hp2 HG02683.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-7847G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91821672 | |||||||
| chr14:91821917 | G | C | 10 | a0001c0001t0005g0004 a0001c0001t0005g0011 a0001c0001t0005g0012 others(7): Show |
14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-56-8092C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91821917 | |||||||
| chr14:91822232 | A | T | 1 | a0001c0002t0001g0125 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-56-8407T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91822232 | |||||||
| chr14:91822235 | T | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(34): Show |
40 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-56-8410A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91822235 | |||||||
| chr14:91822466 | G | GTTC | 317 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(314): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-56-8644_-56-8642d others(5): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91822466 | |||||||
| chr14:91822668 | G | C | 1 | a0001c0001t0010g0136 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-56-8843C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91822668 | |||||||
| chr14:91822694 | G | C | 1 | a0001c0001t0002g0260 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-56-8869C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91822694 | |||||||
| chr14:91822714 | C | CT | 153 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(150): Show |
160 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.-56-8890dupA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91822714 | |||||||
| chr14:91822802 | T | C | 318 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(315): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-56-8977A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91822802 | |||||||
| chr14:91822874 | A | G | 1 | a0001c0001t0002g0237 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-56-9049T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91822874 | |||||||
| chr14:91822916 | C | T | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-9091G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91822916 | |||||||
| chr14:91822957 | C | T | 94 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(91): Show |
103 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.-56-9132G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91822957 | |||||||
| chr14:91823023 | T | C | 1 | a0002c0003t0007g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-56-9198A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823023 | |||||||
| chr14:91823212 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-56-9387G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823212 | |||||||
| chr14:91823394 | C | CTGG | 5 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-9570_-56-9569i others(5): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823394 | |||||||
| chr14:91823395 | C | G | 5 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-9570G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823395 | |||||||
| chr14:91823396 | T | A | 5 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-9571A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823396 | |||||||
| chr14:91823530 | A | G | 117 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(114): Show |
118 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.-56-9705T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823530 | |||||||
| chr14:91823535 | A | AAG | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-9711_-56-9710i others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823535 | |||||||
| chr14:91823535 | A | G | 2 | a0001c0001t0008g0082 a0001c0002t0001g0113 |
2 | HG03195.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.-56-9710T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823535 | |||||||
| chr14:91823536 | G | A | 10 | a0001c0001t0008g0082 a0001c0001t0009g0133 a0001c0001t0009g0153 others(7): Show |
10 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-9711C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823536 | |||||||
| chr14:91823536 | G | GA | 307 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(304): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-56-9712dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823536 | |||||||
| chr14:91823579 | A | G | 8 | a0001c0001t0006g0056 a0001c0001t0006g0062 a0001c0001t0006g0063 others(5): Show |
8 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-9754T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823579 | |||||||
| chr14:91823768 | A | G | 1 | a0001c0001t0002g0227 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-56-9943T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823768 | |||||||
| chr14:91823840 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-56-10015A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823840 | |||||||
| chr14:91823890 | A | AAAC | 13 | a0001c0001t0001g0026 a0001c0001t0002g0210 a0001c0001t0002g0211 others(10): Show |
13 | HG02015.hp1 HG02523.hp1 NA18947.hp1 others(10): Show |
intron_variant | MODIFIER | c.-56-10068_-56-1006 others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823890 | |||||||
| chr14:91823890 | A | C | 2 | a0001c0001t0013g0024 a0001c0001t0025g0023 |
2 | HG02630.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-56-10065T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823890 | |||||||
| chr14:91824337 | A | G | 154 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(151): Show |
161 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-56-10512T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91824337 | |||||||
| chr14:91824400 | A | G | 99 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(96): Show |
108 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.-56-10575T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91824400 | |||||||
| chr14:91824511 | A | T | 3 | a0001c0001t0003g0167 a0001c0001t0003g0174 a0001c0001t0003g0175 |
3 | HG02683.hp2 HG03239.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-56-10686T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91824511 | |||||||
| chr14:91824536 | C | T | 4 | a0001c0001t0002g0198 a0001c0001t0002g0229 a0001c0001t0002g0230 others(1): Show |
4 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-10711G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91824536 | |||||||
| chr14:91824639 | G | T | 9 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(6): Show |
9 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.-56-10814C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91824639 | |||||||
| chr14:91824682 | G | A | 1 | a0001c0001t0002g0240 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-56-10857C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91824682 | |||||||
| chr14:91824840 | G | C | 1 | a0001c0001t0002g0255 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-56-11015C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91824840 | |||||||
| chr14:91824950 | G | C | 1 | a0001c0001t0001g0042 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-56-11125C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91824950 | |||||||
| chr14:91825026 | CT | C | 231 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(228): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.-56-11202delA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825026 | |||||||
| chr14:91825026 | CTT | C | 10 | a0001c0001t0001g0041 a0001c0001t0002g0235 a0001c0001t0002g0296 others(7): Show |
10 | HG01981.hp2 HG02647.hp1 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-11203_-56-1120 others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825026 | |||||||
| chr14:91825026 | CTTT | C | 40 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(37): Show |
46 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(43): Show |
intron_variant | MODIFIER | c.-56-11204_-56-1120 others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825026 | |||||||
| chr14:91825026 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0002g0246 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-56-11217_-56-1120 others(20): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825026 | |||||||
| chr14:91825027 | T | C | 1 | a0002c0003t0007g0002 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-56-11202A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825027 | |||||||
| chr14:91825035 | T | C | 2 | a0001c0001t0013g0024 a0001c0001t0025g0023 |
2 | HG02630.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-56-11210A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825035 | |||||||
| chr14:91825036 | T | C | 1 | a0001c0001t0010g0136 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-56-11211A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825036 | |||||||
| chr14:91825267 | C | T | 1 | a0001c0001t0002g0200 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-56-11442G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825267 | |||||||
| chr14:91825283 | C | T | 1 | a0001c0001t0015g0069 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-56-11458G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825283 | |||||||
| chr14:91825284 | G | A | 1 | a0001c0001t0026g0158 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-56-11459C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825284 | |||||||
| chr14:91825338 | G | A | 10 | a0001c0001t0005g0004 a0001c0001t0005g0011 a0001c0001t0005g0012 others(7): Show |
14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-56-11513C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825338 | |||||||
| chr14:91825544 | T | C | 1 | a0001c0001t0038g0323 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-56-11719A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825544 | |||||||
| chr14:91825646 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-56-11821A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825646 | |||||||
| chr14:91825667 | C | T | 1 | a0001c0001t0010g0170 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-56-11842G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825667 | |||||||
| chr14:91825700 | T | C | 8 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(5): Show |
8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-56-11875A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825700 | |||||||
| chr14:91825764 | A | T | 318 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(315): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-56-11939T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825764 | |||||||
| chr14:91825862 | T | C | 10 | a0001c0001t0005g0004 a0001c0001t0005g0011 a0001c0001t0005g0012 others(7): Show |
14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-56-12037A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825862 | |||||||
| chr14:91825893 | G | A | 22 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(19): Show |
23 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-56-12068C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825893 | |||||||
| chr14:91826144 | C | A | 1 | a0001c0001t0002g0285 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-56-12319G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826144 | |||||||
| chr14:91826198 | T | C | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-12373A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826198 | |||||||
| chr14:91826212 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-56-12387G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826212 | |||||||
| chr14:91826213 | G | T | 4 | a0001c0001t0002g0207 a0001c0001t0002g0251 a0001c0001t0002g0261 others(1): Show |
4 | NA18995.hp2 NA19077.hp2 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-12388C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826213 | |||||||
| chr14:91826231 | G | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0025 others(16): Show |
21 | HG00597.hp2 HG00673.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.-56-12406C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826231 | |||||||
| chr14:91826313 | T | C | 317 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(314): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-56-12488A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826313 | |||||||
| chr14:91826315 | G | T | 13 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(10): Show |
15 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.-56-12490C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826315 | |||||||
| chr14:91826318 | T | TG | 4 | a0001c0001t0002g0198 a0001c0001t0002g0229 a0001c0001t0002g0230 others(1): Show |
4 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-12494dupC | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826318 | |||||||
| chr14:91826319 | G | GA | 291 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(288): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.-56-12495dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826319 | |||||||
| chr14:91826319 | G | GAA | 21 | a0001c0001t0001g0032 a0001c0001t0002g0205 a0001c0001t0002g0216 others(18): Show |
21 | HG00673.hp2 HG01175.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.-56-12496_-56-1249 others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826319 | |||||||
| chr14:91826425 | T | G | 117 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(114): Show |
118 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.-56-12600A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826425 | |||||||
| chr14:91826861 | C | T | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-13036G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826861 | |||||||
| chr14:91826877 | T | C | 1 | a0001c0001t0038g0323 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-56-13052A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826877 | |||||||
| chr14:91827111 | T | C | 1 | a0001c0001t0002g0216 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-56-13286A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91827111 | |||||||
| chr14:91827174 | A | G | 154 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(151): Show |
161 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-56-13349T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91827174 | |||||||
| chr14:91827210 | C | T | 1 | a0001c0001t0002g0282 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-56-13385G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91827210 | |||||||
| chr14:91827787 | C | A | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-13962G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91827787 | |||||||
| chr14:91827795 | T | G | 1 | a0001c0001t0002g0225 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-56-13970A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91827795 | |||||||
| chr14:91827930 | T | G | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-14105A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91827930 | |||||||
| chr14:91828165 | T | C | 1 | a0001c0001t0009g0156 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-56-14340A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91828165 | |||||||
| chr14:91828250 | A | G | 1 | a0001c0001t0038g0323 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-56-14425T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91828250 | |||||||
| chr14:91828347 | A | G | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.-56-14522T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91828347 | |||||||
| chr14:91828357 | T | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(34): Show |
40 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-56-14532A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91828357 | |||||||
| chr14:91828363 | T | C | 117 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(114): Show |
118 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.-56-14538A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91828363 | |||||||
| chr14:91828459 | TTA | T | 3 | a0001c0001t0002g0263 a0001c0001t0002g0264 a0001c0001t0002g0266 |
3 | HG02145.hp2 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-56-14636_-56-1463 others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91828459 | |||||||
| chr14:91828500 | C | A | 1 | a0004c0005t0001g0049 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-56-14675G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91828500 | |||||||
| chr14:91828508 | C | T | 155 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.-56-14683G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91828508 | |||||||
| chr14:91828797 | T | C | 4 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0025g0023 others(1): Show |
4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-14972A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91828797 | |||||||
| chr14:91829051 | T | TA | 6 | a0001c0001t0002g0233 a0001c0001t0002g0256 a0001c0001t0006g0063 others(3): Show |
6 | HG02040.hp1 HG02040.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56-15227dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91829051 | |||||||
| chr14:91829051 | TA | T | 47 | a0001c0001t0001g0016 a0001c0001t0001g0078 a0001c0001t0002g0275 others(44): Show |
48 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.-56-15227delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91829051 | |||||||
| chr14:91829056 | A | T | 10 | a0001c0001t0005g0004 a0001c0001t0005g0011 a0001c0001t0005g0012 others(7): Show |
14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-56-15231T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91829056 | |||||||
| chr14:91829091 | T | C | 4 | a0001c0001t0016g0088 a0001c0001t0017g0090 a0001c0001t0018g0085 others(1): Show |
4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-15266A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91829091 | |||||||
| chr14:91829280 | T | G | 13 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(10): Show |
15 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.-56-15455A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91829280 | |||||||
| chr14:91829530 | T | C | 1 | a0001c0001t0025g0023 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-56-15705A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91829530 | |||||||
| chr14:91829727 | T | C | 117 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(114): Show |
118 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.-56-15902A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91829727 | |||||||
| chr14:91829789 | C | T | 2 | a0001c0001t0003g0061 a0001c0001t0003g0165 |
2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-56-15964G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91829789 | |||||||
| chr14:91830167 | T | C | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-16342A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91830167 | |||||||
| chr14:91830344 | C | T | 1 | a0001c0002t0001g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-56-16519G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91830344 | |||||||
| chr14:91830569 | C | T | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-16744G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91830569 | |||||||
| chr14:91830655 | C | CA | 136 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(133): Show |
139 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.-56-16831dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91830655 | |||||||
| chr14:91830664 | A | C | 1 | a0001c0001t0001g0032 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-56-16839T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91830664 | |||||||
| chr14:91830681 | A | G | 109 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(106): Show |
110 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.-56-16856T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91830681 | |||||||
| chr14:91830738 | A | AT | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-16914_-56-1691 others(5): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91830738 | |||||||
| chr14:91830908 | G | C | 2 | a0001c0001t0005g0012 a0001c0001t0005g0146 |
3 | HG02451.hp2 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-56-17083C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91830908 | |||||||
| chr14:91830965 | T | C | 1 | a0001c0001t0002g0206 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-56-17140A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91830965 | |||||||
| chr14:91831022 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-56-17197A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831022 | |||||||
| chr14:91831088 | G | C | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-17263C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831088 | |||||||
| chr14:91831135 | G | C | 3 | a0003c0004t0001g0072 a0003c0004t0002g0278 a0003c0004t0002g0279 |
3 | HG02572.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-56-17310C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831135 | |||||||
| chr14:91831137 | TAA | T | 3 | a0003c0004t0001g0072 a0003c0004t0002g0278 a0003c0004t0002g0279 |
3 | HG02572.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-56-17314_-56-1731 others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831137 | |||||||
| chr14:91831142 | C | G | 3 | a0003c0004t0001g0072 a0003c0004t0002g0278 a0003c0004t0002g0279 |
3 | HG02572.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-56-17317G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831142 | |||||||
| chr14:91831143 | C | A | 3 | a0003c0004t0001g0072 a0003c0004t0002g0278 a0003c0004t0002g0279 |
3 | HG02572.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-56-17318G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831143 | |||||||
| chr14:91831145 | A | T | 3 | a0003c0004t0001g0072 a0003c0004t0002g0278 a0003c0004t0002g0279 |
3 | HG02572.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-56-17320T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831145 | |||||||
| chr14:91831147 | C | G | 3 | a0003c0004t0001g0072 a0003c0004t0002g0278 a0003c0004t0002g0279 |
3 | HG02572.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-56-17322G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831147 | |||||||
| chr14:91831227 | C | T | 154 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.-56-17402G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831227 | |||||||
| chr14:91831575 | T | C | 8 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(5): Show |
8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-56-17750A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831575 | |||||||
| chr14:91831602 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-56-17777T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831602 | |||||||
| chr14:91831885 | G | C | 4 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0025g0023 others(1): Show |
4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-18060C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831885 | |||||||
| chr14:91831902 | G | A | 1 | a0001c0001t0003g0066 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-56-18077C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831902 | |||||||
| chr14:91831924 | C | G | 9 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(6): Show |
9 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.-56-18099G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831924 | |||||||
| chr14:91832173 | G | A | 5 | a0001c0001t0002g0209 a0001c0001t0002g0220 a0001c0001t0002g0227 others(2): Show |
5 | HG00642.hp2 HG00738.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-18348C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832173 | |||||||
| chr14:91832203 | A | G | 7 | a0001c0001t0009g0133 a0001c0001t0009g0154 a0001c0001t0009g0155 others(4): Show |
7 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-18378T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832203 | |||||||
| chr14:91832390 | C | CA | 30 | a0001c0001t0002g0269 a0001c0001t0004g0005 a0001c0001t0004g0307 others(27): Show |
36 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.-56-18566dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832390 | |||||||
| chr14:91832390 | C | CAA | 266 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(263): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.-56-18567_-56-1856 others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832390 | |||||||
| chr14:91832390 | C | CAAA | 21 | a0001c0001t0001g0006 a0001c0001t0001g0057 a0001c0001t0002g0199 others(18): Show |
22 | HG00099.hp2 HG01109.hp1 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.-56-18568_-56-1856 others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832390 | |||||||
| chr14:91832547 | C | T | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-18722G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832547 | |||||||
| chr14:91832566 | A | G | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.-56-18741T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832566 | |||||||
| chr14:91832592 | G | A | 317 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(314): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-56-18767C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832592 | |||||||
| chr14:91832737 | A | G | 1 | a0001c0002t0001g0122 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-56-18912T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832737 | |||||||
| chr14:91832755 | T | C | 4 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0025g0023 others(1): Show |
4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-18930A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832755 | |||||||
| chr14:91832853 | A | G | 1 | a0001c0001t0003g0184 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-56-19028T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832853 | |||||||
| chr14:91832893 | G | A | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.-56-19068C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832893 | |||||||
| chr14:91833166 | C | T | 4 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0025g0023 others(1): Show |
4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-19341G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91833166 | |||||||
| chr14:91833524 | A | T | 7 | a0001c0001t0009g0133 a0001c0001t0009g0154 a0001c0001t0009g0155 others(4): Show |
7 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-19699T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91833524 | |||||||
| chr14:91833629 | C | T | 1 | a0001c0001t0004g0307 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-56-19804G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91833629 | |||||||
| chr14:91833754 | A | T | 8 | a0001c0001t0006g0056 a0001c0001t0006g0062 a0001c0001t0006g0063 others(5): Show |
8 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-19929T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91833754 | |||||||
| chr14:91833825 | C | T | 4 | a0001c0001t0016g0088 a0001c0001t0017g0090 a0001c0001t0018g0085 others(1): Show |
4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-20000G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91833825 | |||||||
| chr14:91833867 | C | A | 1 | a0001c0001t0001g0031 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-56-20042G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91833867 | |||||||
| chr14:91833918 | G | C | 1 | a0001c0001t0010g0136 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-56-20093C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91833918 | |||||||
| chr14:91833920 | G | T | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-20095C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91833920 | |||||||
| chr14:91834080 | T | G | 1 | a0001c0001t0002g0306 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-56-20255A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91834080 | |||||||
| chr14:91834276 | T | G | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-20451A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91834276 | |||||||
| chr14:91834368 | G | A | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-20543C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91834368 | |||||||
| chr14:91834444 | C | T | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-20619G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91834444 | |||||||
| chr14:91834494 | A | C | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-20669T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91834494 | |||||||
| chr14:91834703 | C | T | 2 | a0001c0001t0002g0208 a0001c0001t0002g0217 |
2 | NA19060.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-56-20878G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91834703 | |||||||
| chr14:91834848 | T | G | 4 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0025g0023 others(1): Show |
4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-21023A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91834848 | |||||||
| chr14:91834850 | G | T | 36 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(33): Show |
42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.-56-21025C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91834850 | |||||||
| chr14:91835205 | G | T | 1 | a0001c0001t0004g0310 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-56-21380C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91835205 | |||||||
| chr14:91835307 | A | C | 2 | a0001c0001t0002g0242 a0001c0001t0032g0243 |
2 | HG02040.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-56-21482T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91835307 | |||||||
| chr14:91835802 | C | A | 1 | a0001c0001t0002g0234 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-56-21977G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91835802 | |||||||
| chr14:91835813 | A | G | 8 | a0001c0001t0006g0056 a0001c0001t0006g0062 a0001c0001t0006g0063 others(5): Show |
8 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-21988T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91835813 | |||||||
| chr14:91835815 | G | C | 1 | a0001c0001t0001g0055 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-56-21990C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91835815 | |||||||
| chr14:91835918 | C | T | 4 | a0001c0001t0003g0015 a0001c0001t0003g0059 a0001c0001t0003g0060 others(1): Show |
4 | NA18968.hp2 NA18998.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-22093G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91835918 | |||||||
| chr14:91836217 | A | G | 301 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(298): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.-56-22392T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836217 | |||||||
| chr14:91836350 | C | T | 1 | a0001c0001t0002g0292 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-56-22525G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836350 | |||||||
| chr14:91836376 | G | A | 4 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0025g0023 others(1): Show |
4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-22551C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836376 | |||||||
| chr14:91836405 | C | T | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-22580G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836405 | |||||||
| chr14:91836484 | C | G | 1 | a0001c0001t0029g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-56-22659G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836484 | |||||||
| chr14:91836550 | G | A | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-22725C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836550 | |||||||
| chr14:91836574 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-56-22749C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836574 | |||||||
| chr14:91836577 | A | AGGCGAGG others(13): Show |
5 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-22753_-56-2275 others(24): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836577 | |||||||
| chr14:91836577 | A | AGGCGAGG others(13): Show |
123 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0036 others(120): Show |
125 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.-56-22772_-56-2275 others(24): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836577 | |||||||
| chr14:91836577 | A | AGGCGAGG others(33): Show |
49 | a0001c0001t0001g0016 a0001c0001t0001g0047 a0001c0001t0002g0210 others(46): Show |
50 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.-56-22792_-56-2275 others(44): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836577 | |||||||
| chr14:91836577 | A | AGGCGAGG others(53): Show |
47 | a0001c0001t0001g0020 a0001c0001t0003g0017 a0001c0001t0003g0186 others(44): Show |
52 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.-56-22753_-56-2275 others(64): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836577 | |||||||
| chr14:91836577 | A | AGGCGAGG others(73): Show |
34 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0021 others(31): Show |
37 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.-56-22753_-56-2275 others(84): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836577 | |||||||
| chr14:91836577 | A | AGGCGAGG others(93): Show |
11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0048 others(8): Show |
11 | HG01074.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-56-22753_-56-2275 others(104): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836577 | |||||||
| chr14:91836577 | A | AGGCGAGG others(113): Show |
2 | a0001c0001t0010g0137 a0004c0005t0001g0049 |
2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-56-22753_-56-2275 others(124): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836577 | |||||||
| chr14:91836577 | AGGCGAGG others(13): Show |
A | 8 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(5): Show |
8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-56-22772_-56-2275 others(24): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836577 | |||||||
| chr14:91836607 | A | AGGCGGGG others(13): Show |
1 | a0001c0001t0029g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-56-22802_-56-2278 others(24): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836607 | |||||||
| chr14:91836628 | G | A | 162 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(159): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-56-22803C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836628 | |||||||
| chr14:91836635 | C | A | 9 | a0001c0001t0002g0212 a0001c0001t0002g0257 a0001c0001t0002g0258 others(6): Show |
9 | HG00609.hp2 HG01258.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.-56-22810G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836635 | |||||||
| chr14:91836820 | G | A | 1 | a0001c0001t0029g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-56-22995C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836820 | |||||||
| chr14:91837132 | G | C | 1 | a0001c0001t0012g0317 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-56-23307C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91837132 | |||||||
| chr14:91837219 | A | G | 2 | a0001c0001t0002g0302 a0001c0001t0002g0305 |
2 | NA18962.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-56-23394T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91837219 | |||||||
| chr14:91837246 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(2): Show |
6 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-23421C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91837246 | |||||||
| chr14:91837270 | T | C | 317 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(314): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-56-23445A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91837270 | |||||||
| chr14:91837298 | C | T | 8 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0016g0088 others(5): Show |
8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-56-23473G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91837298 | |||||||
| chr14:91837368 | A | C | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-23543T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91837368 | |||||||
| chr14:91837525 | A | T | 1 | a0001c0002t0001g0095 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-56-23700T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91837525 | |||||||
| chr14:91837533 | A | G | 155 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(152): Show |
162 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.-56-23708T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91837533 | |||||||
| chr14:91837534 | G | T | 1 | a0001c0002t0001g0009 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-56-23709C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91837534 | |||||||
| chr14:91837788 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(2): Show |
6 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-23963T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91837788 | |||||||
| chr14:91838065 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-56-24240T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838065 | |||||||
| chr14:91838072 | CA | C | 4 | a0001c0001t0016g0088 a0001c0001t0017g0090 a0001c0001t0018g0085 others(1): Show |
4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-24248delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838072 | |||||||
| chr14:91838074 | A | T | 4 | a0001c0001t0016g0088 a0001c0001t0017g0090 a0001c0001t0018g0085 others(1): Show |
4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-24249T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838074 | |||||||
| chr14:91838146 | C | CT | 45 | a0001c0001t0001g0038 a0001c0001t0002g0249 a0001c0001t0002g0267 others(42): Show |
51 | HG01081.hp1 HG01109.hp2 HG02055.hp2 others(48): Show |
intron_variant | MODIFIER | c.-56-24322dupA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838146 | |||||||
| chr14:91838146 | C | CTT | 10 | a0001c0001t0004g0319 a0001c0001t0005g0152 a0001c0001t0009g0133 others(7): Show |
10 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-24323_-56-2432 others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838146 | |||||||
| chr14:91838146 | CT | C | 7 | a0001c0001t0001g0093 a0001c0001t0003g0061 a0001c0001t0003g0165 others(4): Show |
7 | HG02622.hp1 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-24322delA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838146 | |||||||
| chr14:91838358 | C | G | 1 | a0002c0003t0007g0162 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-56-24533G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838358 | |||||||
| chr14:91838376 | C | A | 2 | a0001c0001t0004g0005 a0001c0001t0004g0309 |
4 | NA18945.hp1 NA19057.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-24551G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838376 | |||||||
| chr14:91838528 | C | A | 5 | a0001c0002t0001g0010 a0001c0002t0001g0140 a0001c0002t0001g0141 others(2): Show |
6 | HG01106.hp1 HG03490.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-24703G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838528 | |||||||
| chr14:91838728 | C | A | 1 | a0001c0001t0002g0202 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-56-24903G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838728 | |||||||
| chr14:91838973 | A | G | 162 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(159): Show |
169 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.-56-25148T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838973 | |||||||
| chr14:91839112 | C | A | 29 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(26): Show |
35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-56-25287G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91839112 | |||||||
| chr14:91839241 | G | A | 1 | a0001c0002t0001g0095 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-56-25416C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91839241 | |||||||
| chr14:91839370 | C | T | 29 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(26): Show |
35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-56-25545G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91839370 | |||||||
| chr14:91839461 | C | G | 1 | a0001c0001t0001g0093 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-56-25636G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91839461 | |||||||
| chr14:91839704 | C | T | 1 | a0001c0001t0006g0075 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-56-25879G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91839704 | |||||||
| chr14:91840457 | A | G | 1 | a0001c0001t0002g0240 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-56-26632T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91840457 | |||||||
| chr14:91840561 | T | A | 59 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(56): Show |
60 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.-57+26701A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91840561 | |||||||
| chr14:91840613 | G | A | 8 | a0001c0001t0009g0133 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57+26649C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91840613 | |||||||
| chr14:91841033 | G | A | 308 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(305): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-57+26229C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91841033 | |||||||
| chr14:91841226 | G | T | 1 | a0001c0001t0002g0220 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-57+26036C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91841226 | |||||||
| chr14:91841432 | A | C | 14 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(11): Show |
16 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(13): Show |
intron_variant | MODIFIER | c.-57+25830T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91841432 | |||||||
| chr14:91841701 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0042 a0001c0001t0013g0024 others(1): Show |
4 | HG02071.hp1 HG02523.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+25561G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91841701 | |||||||
| chr14:91841763 | G | A | 1 | a0001c0001t0002g0302 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-57+25499C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91841763 | |||||||
| chr14:91841908 | A | G | 1 | a0001c0001t0031g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-57+25354T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91841908 | |||||||
| chr14:91841909 | T | G | 4 | a0001c0001t0016g0088 a0001c0001t0017g0090 a0001c0001t0018g0085 others(1): Show |
4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+25353A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91841909 | |||||||
| chr14:91841916 | T | C | 1 | a0001c0001t0002g0285 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-57+25346A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91841916 | |||||||
| chr14:91841976 | C | CT | 198 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(195): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.-57+25285dupA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91841976 | |||||||
| chr14:91841976 | C | CTT | 80 | a0001c0001t0001g0007 a0001c0001t0001g0041 a0001c0001t0001g0046 others(77): Show |
87 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.-57+25284_-57+2528 others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91841976 | |||||||
| chr14:91842022 | G | A | 1 | a0001c0001t0004g0307 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-57+25240C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842022 | |||||||
| chr14:91842193 | C | A | 30 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(27): Show |
36 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.-57+25069G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842193 | |||||||
| chr14:91842237 | G | A | 1 | a0002c0003t0007g0164 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-57+25025C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842237 | |||||||
| chr14:91842348 | T | A | 2 | a0001c0001t0003g0195 a0001c0001t0003g0196 |
2 | HG01516.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-57+24914A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842348 | |||||||
| chr14:91842441 | G | T | 1 | a0001c0001t0002g0246 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-57+24821C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842441 | |||||||
| chr14:91842482 | T | C | 2 | a0001c0001t0001g0040 a0001c0001t0001g0046 |
2 | HG04115.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-57+24780A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842482 | |||||||
| chr14:91842729 | C | T | 4 | a0001c0001t0006g0074 a0001c0001t0006g0075 a0001c0001t0006g0159 others(1): Show |
4 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+24533G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842729 | |||||||
| chr14:91842742 | A | T | 45 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(42): Show |
51 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(48): Show |
intron_variant | MODIFIER | c.-57+24520T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842742 | |||||||
| chr14:91842885 | A | G | 154 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(151): Show |
161 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-57+24377T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842885 | |||||||
| chr14:91842896 | C | T | 1 | a0001c0001t0002g0282 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-57+24366G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842896 | |||||||
| chr14:91842911 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-57+24351G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842911 | |||||||
| chr14:91842914 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-57+24348G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842914 | |||||||
| chr14:91842935 | A | C | 1 | a0001c0001t0002g0294 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-57+24327T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842935 | |||||||
| chr14:91842981 | A | G | 162 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(159): Show |
169 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.-57+24281T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842981 | |||||||
| chr14:91843223 | AT | A | 50 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0002g0198 others(47): Show |
50 | HG00639.hp1 HG00642.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.-57+24038delA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843223 | |||||||
| chr14:91843259 | G | C | 1 | a0001c0001t0002g0294 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-57+24003C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843259 | |||||||
| chr14:91843394 | A | G | 1 | a0001c0001t0002g0202 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-57+23868T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843394 | |||||||
| chr14:91843440 | C | G | 1 | a0001c0001t0001g0050 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-57+23822G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843440 | |||||||
| chr14:91843500 | A | G | 318 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(315): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-57+23762T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843500 | |||||||
| chr14:91843617 | C | G | 8 | a0001c0001t0006g0056 a0001c0001t0006g0062 a0001c0001t0006g0063 others(5): Show |
8 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57+23645G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843617 | |||||||
| chr14:91843649 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | NA19002.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.-57+23613G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843649 | |||||||
| chr14:91843687 | G | A | 1 | a0001c0001t0038g0323 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-57+23575C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843687 | |||||||
| chr14:91843720 | T | C | 1 | a0001c0001t0002g0290 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-57+23542A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843720 | |||||||
| chr14:91843762 | C | T | 1 | a0001c0001t0008g0086 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-57+23500G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843762 | |||||||
| chr14:91843882 | AT | A | 44 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(41): Show |
50 | HG01081.hp1 HG01109.hp1 HG01891.hp2 others(47): Show |
intron_variant | MODIFIER | c.-57+23379delA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843882 | |||||||
| chr14:91843910 | C | T | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-57+23352G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843910 | |||||||
| chr14:91843946 | T | C | 17 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(14): Show |
18 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-57+23316A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843946 | |||||||
| chr14:91844053 | G | GA | 136 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0002g0014 others(133): Show |
143 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.-57+23208dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844053 | |||||||
| chr14:91844130 | G | C | 29 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(26): Show |
35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57+23132C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844130 | |||||||
| chr14:91844140 | T | C | 4 | a0001c0001t0003g0066 a0001c0001t0012g0316 a0001c0001t0012g0317 others(1): Show |
4 | HG00423.hp1 NA18747.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+23122A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844140 | |||||||
| chr14:91844186 | G | T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0020 others(23): Show |
28 | HG00597.hp2 HG00673.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.-57+23076C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844186 | |||||||
| chr14:91844206 | G | A | 1 | a0001c0001t0006g0067 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-57+23056C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844206 | |||||||
| chr14:91844355 | G | T | 137 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0002g0014 others(134): Show |
144 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.-57+22907C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844355 | |||||||
| chr14:91844521 | T | C | 7 | a0001c0001t0009g0153 a0001c0001t0009g0154 a0001c0001t0009g0155 others(4): Show |
7 | HG01109.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+22741A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844521 | |||||||
| chr14:91844534 | C | T | 1 | a0001c0001t0002g0204 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-57+22728G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844534 | |||||||
| chr14:91844535 | G | A | 1 | a0001c0001t0006g0064 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-57+22727C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844535 | |||||||
| chr14:91844693 | G | A | 8 | a0001c0002t0001g0009 a0001c0002t0001g0101 a0001c0002t0001g0102 others(5): Show |
9 | HG00733.hp2 HG00735.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+22569C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844693 | |||||||
| chr14:91844740 | G | A | 157 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(154): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.-57+22522C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844740 | |||||||
| chr14:91844760 | C | CA | 55 | a0001c0001t0001g0021 a0001c0001t0001g0041 a0001c0001t0001g0042 others(52): Show |
58 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.-57+22501dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844760 | |||||||
| chr14:91844760 | C | CAA | 17 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0003g0167 others(14): Show |
17 | HG00642.hp1 HG01109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-57+22500_-57+2250 others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844760 | |||||||
| chr14:91844760 | CA | C | 11 | a0001c0001t0003g0013 a0001c0001t0008g0081 a0001c0001t0008g0082 others(8): Show |
12 | HG01192.hp2 HG01884.hp2 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57+22501delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844760 | |||||||
| chr14:91844760 | CAAAAAAA others(3): Show |
C | 7 | a0001c0001t0002g0213 a0001c0001t0002g0226 a0001c0001t0002g0227 others(4): Show |
7 | HG00642.hp2 HG02109.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+22492_-57+2250 others(14): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844760 | |||||||
| chr14:91844760 | CAAAAAAA others(4): Show |
C | 130 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0002g0014 others(127): Show |
137 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.-57+22491_-57+2250 others(15): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844760 | |||||||
| chr14:91845066 | G | A | 29 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(26): Show |
35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57+22196C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845066 | |||||||
| chr14:91845085 | G | A | 1 | a0001c0001t0009g0154 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-57+22177C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845085 | |||||||
| chr14:91845121 | G | A | 1 | a0001c0001t0002g0294 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-57+22141C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845121 | |||||||
| chr14:91845232 | A | AAAAT | 98 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0002g0014 others(95): Show |
98 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.-57+22026_-57+2202 others(8): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845232 | |||||||
| chr14:91845232 | A | AAAATAAA others(1): Show |
21 | a0001c0001t0002g0014 a0001c0001t0002g0208 a0001c0001t0002g0209 others(18): Show |
21 | HG00609.hp2 HG00738.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-57+22022_-57+2202 others(12): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845232 | |||||||
| chr14:91845232 | AAAAT | A | 46 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0001c0001t0001g0180 others(43): Show |
46 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.-57+22026_-57+2202 others(8): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845232 | |||||||
| chr14:91845232 | AAAATAAA others(1): Show |
A | 108 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(105): Show |
118 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(115): Show |
intron_variant | MODIFIER | c.-57+22022_-57+2202 others(12): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845232 | |||||||
| chr14:91845232 | AAAATAAA others(5): Show |
A | 29 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(26): Show |
35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57+22018_-57+2202 others(16): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845232 | |||||||
| chr14:91845232 | AAAATAAA others(13): Show |
A | 6 | a0001c0001t0010g0134 a0001c0001t0010g0135 a0001c0001t0010g0136 others(3): Show |
6 | HG02559.hp1 HG03098.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+22010_-57+2202 others(24): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845232 | |||||||
| chr14:91845269 | A | G | 10 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
11 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+21993T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845269 | |||||||
| chr14:91845274 | T | A | 1 | a0001c0001t0002g0282 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-57+21988A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845274 | |||||||
| chr14:91845442 | T | G | 1 | a0001c0001t0029g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57+21820A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845442 | |||||||
| chr14:91845454 | T | C | 4 | a0001c0001t0002g0280 a0001c0001t0002g0281 a0001c0001t0002g0283 others(1): Show |
4 | HG00140.hp2 HG01175.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+21808A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845454 | |||||||
| chr14:91845561 | G | T | 48 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0002g0198 others(45): Show |
48 | HG00639.hp1 HG00642.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.-57+21701C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845561 | |||||||
| chr14:91846015 | T | C | 107 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0002g0014 others(104): Show |
108 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-57+21247A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91846015 | |||||||
| chr14:91846025 | A | G | 140 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0002g0014 others(137): Show |
147 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.-57+21237T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91846025 | |||||||
| chr14:91846128 | GC | G | 3 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0025g0023 |
3 | HG02630.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-57+21133delG | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91846128 | |||||||
| chr14:91846130 | T | A | 3 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0025g0023 |
3 | HG02630.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-57+21132A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91846130 | |||||||
| chr14:91846551 | G | A | 3 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0025g0023 |
3 | HG02630.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-57+20711C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91846551 | |||||||
| chr14:91846984 | G | A | 29 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(26): Show |
35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57+20278C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91846984 | |||||||
| chr14:91846986 | G | A | 1 | a0001c0001t0036g0314 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-57+20276C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91846986 | |||||||
| chr14:91847006 | C | T | 1 | a0001c0001t0010g0134 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-57+20256G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847006 | |||||||
| chr14:91847033 | G | A | 14 | a0001c0001t0008g0080 a0001c0001t0008g0081 a0001c0001t0008g0082 others(11): Show |
14 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57+20229C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847033 | |||||||
| chr14:91847166 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-57+20096C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847166 | |||||||
| chr14:91847207 | G | A | 10 | a0001c0001t0005g0004 a0001c0001t0005g0011 a0001c0001t0005g0012 others(7): Show |
14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57+20055C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847207 | |||||||
| chr14:91847259 | G | GA | 8 | a0001c0001t0009g0153 a0001c0001t0009g0154 a0001c0001t0009g0155 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57+20002dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847259 | |||||||
| chr14:91847259 | G | GAA | 11 | a0001c0001t0006g0056 a0001c0001t0006g0062 a0001c0001t0006g0063 others(8): Show |
11 | HG02630.hp2 HG02818.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+20001_-57+2000 others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847259 | |||||||
| chr14:91847259 | G | GAAA | 41 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(38): Show |
47 | HG01081.hp1 HG01192.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.-57+20000_-57+2000 others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847259 | |||||||
| chr14:91847347 | C | T | 1 | a0001c0001t0002g0202 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-57+19915G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847347 | |||||||
| chr14:91847362 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-57+19900G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847362 | |||||||
| chr14:91847363 | T | A | 29 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(26): Show |
35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57+19899A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847363 | |||||||
| chr14:91847557 | C | T | 1 | a0001c0002t0001g0101 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-57+19705G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847557 | |||||||
| chr14:91847792 | T | C | 1 | a0001c0001t0002g0215 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-57+19470A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847792 | |||||||
| chr14:91847828 | G | A | 14 | a0001c0001t0002g0198 a0001c0001t0002g0203 a0001c0001t0002g0213 others(11): Show |
14 | HG00673.hp1 HG00735.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57+19434C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847828 | |||||||
| chr14:91847873 | A | G | 1 | a0001c0001t0003g0192 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-57+19389T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847873 | |||||||
| chr14:91848031 | G | A | 29 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(26): Show |
35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57+19231C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848031 | |||||||
| chr14:91848051 | T | C | 39 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(36): Show |
42 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.-57+19211A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848051 | |||||||
| chr14:91848098 | A | T | 1 | a0001c0001t0006g0062 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-57+19164T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848098 | |||||||
| chr14:91848174 | A | G | 3 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 |
3 | HG02145.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-57+19088T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848174 | |||||||
| chr14:91848313 | G | A | 28 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(25): Show |
34 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-57+18949C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848313 | |||||||
| chr14:91848356 | G | C | 3 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 |
3 | HG02145.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-57+18906C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848356 | |||||||
| chr14:91848432 | C | A | 257 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(254): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-57+18830G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848432 | |||||||
| chr14:91848548 | C | T | 1 | a0001c0001t0002g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-57+18714G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848548 | |||||||
| chr14:91848574 | C | T | 1 | a0001c0001t0029g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57+18688G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848574 | |||||||
| chr14:91848599 | T | G | 1 | a0001c0001t0004g0315 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-57+18663A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848599 | |||||||
| chr14:91848605 | G | T | 1 | a0001c0001t0002g0299 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-57+18657C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848605 | |||||||
| chr14:91848897 | T | C | 28 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(25): Show |
34 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-57+18365A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848897 | |||||||
| chr14:91849158 | A | C | 1 | a0001c0001t0033g0219 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-57+18104T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91849158 | |||||||
| chr14:91849230 | G | A | 1 | a0001c0001t0002g0235 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-57+18032C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91849230 | |||||||
| chr14:91849288 | T | C | 7 | a0001c0001t0009g0153 a0001c0001t0009g0154 a0001c0001t0009g0155 others(4): Show |
7 | HG01109.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+17974A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91849288 | |||||||
| chr14:91849399 | T | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0047 |
2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-57+17863A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91849399 | |||||||
| chr14:91849595 | T | A | 1 | a0001c0001t0029g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57+17667A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91849595 | |||||||
| chr14:91849684 | G | A | 4 | a0001c0001t0031g0166 a0003c0004t0001g0072 a0003c0004t0002g0278 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+17578C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91849684 | |||||||
| chr14:91849786 | C | G | 315 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(312): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-57+17476G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91849786 | |||||||
| chr14:91849830 | C | T | 30 | a0001c0001t0002g0204 a0001c0001t0004g0005 a0001c0001t0004g0307 others(27): Show |
36 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.-57+17432G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91849830 | |||||||
| chr14:91849941 | C | T | 29 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(26): Show |
35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57+17321G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91849941 | |||||||
| chr14:91849971 | C | A | 29 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(26): Show |
35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57+17291G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91849971 | |||||||
| chr14:91850004 | A | G | 29 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(26): Show |
35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57+17258T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850004 | |||||||
| chr14:91850049 | C | CA | 9 | a0001c0001t0002g0272 a0001c0001t0009g0153 a0001c0001t0009g0154 others(6): Show |
9 | HG01109.hp1 HG01891.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+17212dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850049 | |||||||
| chr14:91850049 | CA | C | 249 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(246): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.-57+17212delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850049 | |||||||
| chr14:91850049 | CAAA | C | 28 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(25): Show |
34 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-57+17210_-57+1721 others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850049 | |||||||
| chr14:91850049 | CAAAAA | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(2): Show |
6 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+17208_-57+1721 others(9): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850049 | |||||||
| chr14:91850180 | C | T | 40 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0001c0001t0001g0180 others(37): Show |
41 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.-57+17082G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850180 | |||||||
| chr14:91850182 | T | TA | 265 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(262): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-57+17079dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850182 | |||||||
| chr14:91850324 | A | G | 1 | a0001c0001t0002g0297 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-57+16938T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850324 | |||||||
| chr14:91850348 | T | C | 11 | a0001c0001t0006g0056 a0001c0001t0006g0062 a0001c0001t0006g0063 others(8): Show |
11 | HG02630.hp2 HG02818.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+16914A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850348 | |||||||
| chr14:91850411 | G | A | 179 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-57+16851C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850411 | |||||||
| chr14:91850490 | A | C | 1 | a0001c0001t0001g0026 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-57+16772T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850490 | |||||||
| chr14:91850496 | A | G | 2 | a0001c0002t0001g0138 a0001c0002t0001g0149 |
2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.-57+16766T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850496 | |||||||
| chr14:91850603 | G | A | 1 | a0001c0001t0034g0273 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-57+16659C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850603 | |||||||
| chr14:91850659 | A | G | 286 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(283): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-57+16603T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850659 | |||||||
| chr14:91850736 | G | T | 1 | a0001c0001t0002g0301 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-57+16526C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850736 | |||||||
| chr14:91850794 | G | A | 2 | a0001c0001t0002g0211 a0001c0001t0002g0236 |
2 | HG02523.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-57+16468C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850794 | |||||||
| chr14:91850835 | A | G | 286 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(283): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-57+16427T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850835 | |||||||
| chr14:91850836 | G | C | 286 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(283): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-57+16426C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850836 | |||||||
| chr14:91850966 | G | T | 179 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-57+16296C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850966 | |||||||
| chr14:91851012 | A | G | 286 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(283): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-57+16250T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851012 | |||||||
| chr14:91851197 | G | A | 1 | a0001c0002t0001g0095 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-57+16065C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851197 | |||||||
| chr14:91851213 | G | A | 179 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-57+16049C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851213 | |||||||
| chr14:91851312 | G | A | 6 | a0001c0001t0002g0237 a0001c0001t0002g0238 a0001c0001t0002g0239 others(3): Show |
6 | HG00639.hp1 HG00733.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+15950C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851312 | |||||||
| chr14:91851435 | G | T | 316 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(313): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.-57+15827C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851435 | |||||||
| chr14:91851438 | G | T | 2 | a0001c0001t0002g0263 a0001c0001t0002g0264 |
2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-57+15824C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851438 | |||||||
| chr14:91851511 | T | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(43): Show |
49 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.-57+15751A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851511 | |||||||
| chr14:91851522 | C | T | 7 | a0001c0001t0009g0153 a0001c0001t0009g0154 a0001c0001t0009g0155 others(4): Show |
7 | HG01109.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+15740G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851522 | |||||||
| chr14:91851807 | A | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-57+15455T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851807 | |||||||
| chr14:91851828 | C | T | 178 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.-57+15434G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851828 | |||||||
| chr14:91851990 | G | A | 179 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-57+15272C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851990 | |||||||
| chr14:91852111 | T | C | 286 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(283): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.-57+15151A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852111 | |||||||
| chr14:91852154 | G | A | 179 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-57+15108C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852154 | |||||||
| chr14:91852191 | G | A | 2 | a0001c0001t0003g0171 a0001c0001t0003g0184 |
2 | HG02647.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-57+15071C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852191 | |||||||
| chr14:91852198 | C | T | 1 | a0001c0007t0028g0092 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-57+15064G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852198 | |||||||
| chr14:91852287 | C | T | 2 | a0001c0001t0003g0061 a0001c0001t0003g0165 |
2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-57+14975G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852287 | |||||||
| chr14:91852315 | C | T | 49 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0002g0198 others(46): Show |
49 | HG00639.hp1 HG00642.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.-57+14947G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852315 | |||||||
| chr14:91852345 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-57+14917G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852345 | |||||||
| chr14:91852472 | A | G | 150 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.-57+14790T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852472 | |||||||
| chr14:91852485 | C | T | 179 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-57+14777G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852485 | |||||||
| chr14:91852591 | G | A | 208 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(205): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-57+14671C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852591 | |||||||
| chr14:91852699 | T | C | 1 | a0001c0001t0010g0137 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-57+14563A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852699 | |||||||
| chr14:91852779 | T | G | 1 | a0001c0001t0002g0198 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-57+14483A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852779 | |||||||
| chr14:91852815 | G | A | 179 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-57+14447C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852815 | |||||||
| chr14:91852935 | G | A | 11 | a0001c0001t0008g0080 a0001c0001t0008g0081 a0001c0001t0008g0082 others(8): Show |
11 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+14327C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852935 | |||||||
| chr14:91852948 | G | A | 179 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-57+14314C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852948 | |||||||
| chr14:91853028 | G | A | 179 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-57+14234C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853028 | |||||||
| chr14:91853136 | GCTACT | G | 11 | a0001c0001t0008g0080 a0001c0001t0008g0081 a0001c0001t0008g0082 others(8): Show |
11 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+14121_-57+1412 others(9): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853136 | |||||||
| chr14:91853375 | T | C | 179 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-57+13887A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853375 | |||||||
| chr14:91853380 | A | G | 179 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-57+13882T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853380 | |||||||
| chr14:91853381 | C | T | 3 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0025g0023 |
3 | HG02630.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-57+13881G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853381 | |||||||
| chr14:91853397 | G | T | 1 | a0002c0003t0007g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-57+13865C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853397 | |||||||
| chr14:91853435 | G | A | 179 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-57+13827C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853435 | |||||||
| chr14:91853539 | A | G | 1 | a0001c0001t0009g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-57+13723T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853539 | |||||||
| chr14:91853558 | A | G | 1 | a0001c0001t0002g0245 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-57+13704T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853558 | |||||||
| chr14:91853629 | ATTT | A | 163 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(160): Show |
173 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.-57+13630_-57+1363 others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853629 | |||||||
| chr14:91853629 | ATTTT | A | 5 | a0001c0001t0003g0013 a0001c0001t0003g0015 a0001c0001t0003g0182 others(2): Show |
6 | HG00140.hp1 HG03490.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+13629_-57+1363 others(8): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853629 | |||||||
| chr14:91853642 | TTTA | T | 11 | a0001c0001t0006g0056 a0001c0001t0006g0062 a0001c0001t0006g0063 others(8): Show |
11 | HG02630.hp2 HG02818.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+13617_-57+1361 others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853642 | |||||||
| chr14:91853649 | TACAC | T | 16 | a0001c0001t0002g0240 a0001c0001t0002g0263 a0001c0001t0002g0264 others(13): Show |
16 | HG00423.hp2 HG02145.hp2 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.-57+13609_-57+1361 others(8): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853649 | |||||||
| chr14:91853649 | TACACAC | T | 117 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0002g0014 others(114): Show |
124 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.-57+13607_-57+1361 others(10): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853649 | |||||||
| chr14:91853649 | TACACACA others(5): Show |
T | 179 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-57+13601_-57+1361 others(16): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853649 | |||||||
| chr14:91853665 | C | A | 7 | a0001c0001t0009g0153 a0001c0001t0009g0154 a0001c0001t0009g0155 others(4): Show |
7 | HG01109.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+13597G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853665 | |||||||
| chr14:91853675 | C | A | 179 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(176): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-57+13587G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853675 | |||||||
| chr14:91853951 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-57+13311G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853951 | |||||||
| chr14:91854010 | C | T | 1 | a0001c0001t0002g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-57+13252G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854010 | |||||||
| chr14:91854061 | G | A | 154 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(151): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.-57+13201C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854061 | |||||||
| chr14:91854178 | G | A | 11 | a0001c0001t0006g0056 a0001c0001t0006g0062 a0001c0001t0006g0063 others(8): Show |
11 | HG02630.hp2 HG02818.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+13084C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854178 | |||||||
| chr14:91854413 | A | G | 1 | a0001c0001t0004g0310 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-57+12849T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854413 | |||||||
| chr14:91854420 | G | GGAGGGGG others(26): Show |
7 | a0001c0001t0009g0153 a0001c0001t0009g0154 a0001c0001t0009g0155 others(4): Show |
7 | HG01109.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+12809_-57+1284 others(37): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854420 | |||||||
| chr14:91854508 | TGGA | T | 10 | a0001c0001t0005g0004 a0001c0001t0005g0011 a0001c0001t0005g0012 others(7): Show |
14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57+12751_-57+1275 others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854508 | |||||||
| chr14:91854508 | TGGAGGA | T | 174 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(171): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.-57+12748_-57+1275 others(10): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854508 | |||||||
| chr14:91854649 | G | A | 3 | a0001c0001t0013g0022 a0001c0001t0013g0024 a0001c0001t0025g0023 |
3 | HG02630.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-57+12613C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854649 | |||||||
| chr14:91854674 | A | G | 2 | a0001c0001t0003g0186 a0001c0001t0003g0187 |
2 | HG00558.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-57+12588T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854674 | |||||||
| chr14:91854817 | C | G | 1 | a0001c0001t0002g0296 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-57+12445G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854817 | |||||||
| chr14:91854866 | A | G | 109 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0002g0014 others(106): Show |
110 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.-57+12396T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854866 | |||||||
| chr14:91855009 | C | T | 1 | a0001c0001t0009g0154 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-57+12253G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91855009 | |||||||
| chr14:91855176 | C | T | 10 | a0001c0001t0005g0004 a0001c0001t0005g0011 a0001c0001t0005g0012 others(7): Show |
14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57+12086G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91855176 | |||||||
| chr14:91855241 | C | G | 316 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(313): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.-57+12021G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91855241 | |||||||
| chr14:91855414 | C | G | 1 | a0001c0001t0003g0167 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-57+11848G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91855414 | |||||||
| chr14:91855782 | C | T | 1 | a0001c0001t0004g0307 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-57+11480G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91855782 | |||||||
| chr14:91855787 | G | T | 11 | a0001c0001t0008g0080 a0001c0001t0008g0081 a0001c0001t0008g0082 others(8): Show |
11 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+11475C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91855787 | |||||||
| chr14:91855811 | G | A | 4 | a0001c0001t0006g0074 a0001c0001t0006g0075 a0001c0001t0006g0159 others(1): Show |
4 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+11451C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91855811 | |||||||
| chr14:91856072 | T | C | 110 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0002g0014 others(107): Show |
111 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.-57+11190A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91856072 | |||||||
| chr14:91856214 | C | T | 1 | a0001c0002t0001g0185 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-57+11048G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91856214 | |||||||
| chr14:91856215 | G | A | 7 | a0001c0001t0003g0017 a0001c0001t0009g0133 a0001c0001t0010g0134 others(4): Show |
7 | HG02280.hp1 HG02559.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+11047C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91856215 | |||||||
| chr14:91856270 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(2): Show |
6 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+10992G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91856270 | |||||||
| chr14:91856442 | G | A | 1 | a0001c0001t0029g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57+10820C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91856442 | |||||||
| chr14:91856486 | CA | C | 141 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(138): Show |
154 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.-57+10775delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91856486 | |||||||
| chr14:91856486 | CAA | C | 44 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(41): Show |
47 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.-57+10774_-57+1077 others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91856486 | |||||||
| chr14:91856672 | C | T | 9 | a0001c0001t0006g0159 a0001c0001t0006g0161 a0001c0001t0009g0153 others(6): Show |
9 | HG01109.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+10590G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91856672 | |||||||
| chr14:91856699 | C | A | 15 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(12): Show |
20 | HG01081.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-57+10563G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91856699 | |||||||
| chr14:91857095 | G | C | 16 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(13): Show |
21 | HG01081.hp1 HG01891.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.-57+10167C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857095 | |||||||
| chr14:91857096 | C | T | 9 | a0001c0001t0006g0159 a0001c0001t0006g0161 a0001c0001t0009g0153 others(6): Show |
9 | HG01109.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+10166G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857096 | |||||||
| chr14:91857109 | T | A | 1 | a0002c0003t0007g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-57+10153A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857109 | |||||||
| chr14:91857298 | A | G | 1 | a0001c0001t0002g0217 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-57+9964T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857298 | |||||||
| chr14:91857422 | G | A | 1 | a0002c0003t0007g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-57+9840C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857422 | |||||||
| chr14:91857520 | A | T | 1 | a0001c0002t0001g0111 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-57+9742T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857520 | |||||||
| chr14:91857566 | G | A | 37 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(34): Show |
40 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-57+9696C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857566 | |||||||
| chr14:91857609 | G | A | 1 | a0002c0003t0007g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-57+9653C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857609 | |||||||
| chr14:91857742 | C | T | 2 | a0001c0001t0014g0244 a0001c0001t0014g0304 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-57+9520G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857742 | |||||||
| chr14:91857893 | G | T | 1 | a0001c0002t0001g0131 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-57+9369C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857893 | |||||||
| chr14:91857965 | CTTTG | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(34): Show |
40 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-57+9293_-57+9296d others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857965 | |||||||
| chr14:91858008 | C | G | 8 | a0001c0001t0003g0061 a0001c0001t0006g0056 a0001c0001t0006g0062 others(5): Show |
8 | HG02723.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57+9254G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858008 | |||||||
| chr14:91858114 | C | T | 202 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0093 others(199): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.-57+9148G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858114 | |||||||
| chr14:91858140 | T | TTTC | 3 | a0001c0001t0003g0015 a0001c0001t0003g0184 a0001c0002t0001g0099 |
3 | HG02965.hp2 NA19054.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-57+9119_-57+9121d others(5): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858140 | |||||||
| chr14:91858152 | C | CT | 21 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0021 others(18): Show |
22 | HG01891.hp1 HG01928.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.-57+9109dupA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858152 | |||||||
| chr14:91858152 | C | CTT | 18 | a0001c0001t0006g0159 a0001c0001t0008g0080 a0001c0001t0008g0081 others(15): Show |
18 | HG01109.hp1 HG01192.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-57+9108_-57+9109d others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858152 | |||||||
| chr14:91858152 | C | CTTCT | 88 | a0001c0001t0001g0070 a0001c0001t0001g0093 a0001c0001t0001g0172 others(85): Show |
89 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.-57+9109_-57+9110i others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858152 | |||||||
| chr14:91858152 | C | CTTCTT | 54 | a0001c0001t0001g0073 a0001c0001t0002g0014 a0001c0001t0002g0202 others(51): Show |
55 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.-57+9109_-57+9110i others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858152 | |||||||
| chr14:91858152 | C | T | 2 | a0001c0001t0002g0280 a0001c0001t0002g0281 |
2 | HG00140.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-57+9110G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858152 | |||||||
| chr14:91858155 | T | C | 2 | a0001c0001t0002g0241 a0001c0002t0001g0095 |
2 | HG00544.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-57+9107A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858155 | |||||||
| chr14:91858271 | C | T | 40 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(37): Show |
43 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.-57+8991G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858271 | |||||||
| chr14:91858535 | T | C | 33 | a0001c0001t0003g0066 a0001c0001t0004g0005 a0001c0001t0004g0307 others(30): Show |
35 | HG00423.hp1 HG01192.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.-57+8727A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858535 | |||||||
| chr14:91858747 | C | T | 8 | a0001c0001t0003g0061 a0001c0001t0006g0056 a0001c0001t0006g0062 others(5): Show |
8 | HG02723.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57+8515G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858747 | |||||||
| chr14:91858850 | C | T | 49 | a0001c0001t0001g0097 a0001c0001t0024g0127 a0001c0002t0001g0001 others(46): Show |
55 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-57+8412G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858850 | |||||||
| chr14:91858898 | G | T | 307 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(304): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-57+8364C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858898 | |||||||
| chr14:91859053 | T | C | 22 | a0001c0001t0003g0066 a0001c0001t0004g0005 a0001c0001t0004g0307 others(19): Show |
24 | HG00423.hp1 HG02055.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-57+8209A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859053 | |||||||
| chr14:91859078 | C | T | 9 | a0001c0001t0006g0159 a0001c0001t0006g0161 a0001c0001t0009g0153 others(6): Show |
9 | HG01109.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+8184G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859078 | |||||||
| chr14:91859084 | G | A | 11 | a0001c0001t0008g0080 a0001c0001t0008g0081 a0001c0001t0008g0082 others(8): Show |
11 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+8178C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859084 | |||||||
| chr14:91859305 | A | T | 5 | a0001c0001t0001g0172 a0001c0001t0003g0167 a0001c0001t0003g0173 others(2): Show |
5 | HG02683.hp2 HG03239.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+7957T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859305 | |||||||
| chr14:91859351 | C | T | 30 | a0001c0001t0003g0066 a0001c0001t0004g0005 a0001c0001t0004g0307 others(27): Show |
32 | HG00423.hp1 HG01109.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.-57+7911G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859351 | |||||||
| chr14:91859410 | C | T | 20 | a0001c0001t0003g0066 a0001c0001t0004g0005 a0001c0001t0004g0307 others(17): Show |
22 | HG00423.hp1 HG02055.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-57+7852G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859410 | |||||||
| chr14:91859412 | T | C | 7 | a0001c0001t0008g0080 a0001c0001t0008g0081 a0001c0001t0008g0082 others(4): Show |
7 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+7850A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859412 | |||||||
| chr14:91859670 | C | T | 1 | a0001c0002t0001g0130 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-57+7592G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859670 | |||||||
| chr14:91859754 | T | C | 7 | a0001c0001t0002g0214 a0001c0001t0002g0242 a0001c0001t0002g0280 others(4): Show |
7 | HG00140.hp2 HG01175.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+7508A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859754 | |||||||
| chr14:91859926 | A | G | 147 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0093 others(144): Show |
149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.-57+7336T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859926 | |||||||
| chr14:91859968 | A | C | 3 | a0001c0001t0005g0004 a0001c0001t0005g0148 a0001c0001t0005g0152 |
5 | HG02615.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+7294T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859968 | |||||||
| chr14:91859970 | G | T | 1 | a0001c0001t0002g0215 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-57+7292C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859970 | |||||||
| chr14:91860071 | G | T | 41 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(38): Show |
44 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.-57+7191C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91860071 | |||||||
| chr14:91860074 | C | G | 2 | a0001c0001t0006g0074 a0001c0001t0006g0075 |
2 | HG02055.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-57+7188G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91860074 | |||||||
| chr14:91860287 | G | T | 318 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(315): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-57+6975C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91860287 | |||||||
| chr14:91860331 | C | CA | 24 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(21): Show |
27 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-57+6930dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91860331 | |||||||
| chr14:91860331 | CA | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(90): Show |
96 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.-57+6930delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91860331 | |||||||
| chr14:91860735 | C | T | 9 | a0001c0001t0006g0159 a0001c0001t0006g0161 a0001c0001t0009g0153 others(6): Show |
9 | HG01109.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+6527G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91860735 | |||||||
| chr14:91860765 | T | C | 9 | a0001c0001t0003g0061 a0001c0001t0006g0056 a0001c0001t0006g0062 others(6): Show |
9 | HG02723.hp2 HG02895.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+6497A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91860765 | |||||||
| chr14:91860891 | C | G | 71 | a0001c0001t0001g0007 a0001c0001t0001g0050 a0001c0001t0001g0051 others(68): Show |
82 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(79): Show |
intron_variant | MODIFIER | c.-57+6371G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91860891 | |||||||
| chr14:91861105 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-57+6157A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861105 | |||||||
| chr14:91861136 | T | C | 1 | a0001c0001t0003g0192 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-57+6126A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861136 | |||||||
| chr14:91861138 | C | T | 18 | a0001c0001t0003g0066 a0001c0001t0004g0005 a0001c0001t0004g0307 others(15): Show |
20 | HG00423.hp1 HG02602.hp2 HG03491.hp1 others(17): Show |
intron_variant | MODIFIER | c.-57+6124G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861138 | |||||||
| chr14:91861440 | C | T | 1 | a0001c0001t0029g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57+5822G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861440 | |||||||
| chr14:91861515 | G | C | 1 | a0001c0001t0003g0193 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-57+5747C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861515 | |||||||
| chr14:91861533 | C | T | 1 | a0001c0002t0001g0110 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-57+5729G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861533 | |||||||
| chr14:91861558 | G | A | 31 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0001c0001t0001g0180 others(28): Show |
32 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.-57+5704C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861558 | |||||||
| chr14:91861705 | C | T | 2 | a0001c0001t0038g0323 a0002c0003t0007g0094 |
2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-57+5557G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861705 | |||||||
| chr14:91861721 | G | A | 1 | a0001c0001t0002g0200 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-57+5541C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861721 | |||||||
| chr14:91861734 | C | T | 1 | a0001c0001t0029g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57+5528G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861734 | |||||||
| chr14:91861765 | A | G | 32 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0001c0001t0001g0180 others(29): Show |
33 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.-57+5497T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861765 | |||||||
| chr14:91861814 | A | G | 1 | a0001c0001t0002g0213 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-57+5448T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861814 | |||||||
| chr14:91861823 | G | A | 1 | a0001c0001t0003g0165 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-57+5439C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861823 | |||||||
| chr14:91861827 | G | A | 1 | a0001c0001t0029g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57+5435C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861827 | |||||||
| chr14:91861845 | T | C | 1 | a0001c0001t0038g0323 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-57+5417A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861845 | |||||||
| chr14:91861913 | A | AAT | 252 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0016 others(249): Show |
268 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(265): Show |
intron_variant | MODIFIER | c.-57+5347_-57+5348d others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861913 | |||||||
| chr14:91861958 | GTA | G | 10 | a0001c0001t0001g0097 a0001c0002t0001g0098 a0001c0002t0001g0099 others(7): Show |
10 | HG01928.hp2 NA18989.hp1 NA19001.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57+5302_-57+5303d others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861958 | |||||||
| chr14:91862142 | G | A | 136 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
150 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(147): Show |
intron_variant | MODIFIER | c.-57+5120C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862142 | |||||||
| chr14:91862255 | G | A | 4 | a0001c0001t0016g0088 a0001c0001t0017g0090 a0001c0001t0018g0085 others(1): Show |
4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+5007C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862255 | |||||||
| chr14:91862339 | C | CA | 12 | a0001c0001t0001g0079 a0001c0001t0002g0284 a0001c0001t0002g0285 others(9): Show |
12 | HG00597.hp1 HG02055.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.-57+4922dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862339 | |||||||
| chr14:91862339 | C | CAAAAAAA others(2): Show |
9 | a0001c0001t0008g0080 a0001c0001t0008g0082 a0001c0001t0008g0083 others(6): Show |
9 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+4914_-57+4922d others(11): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862339 | |||||||
| chr14:91862339 | CAAAAAA | C | 11 | a0001c0001t0005g0004 a0001c0001t0005g0011 a0001c0001t0005g0012 others(8): Show |
15 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57+4917_-57+4922d others(8): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862339 | |||||||
| chr14:91862339 | CAAAAAAA | C | 117 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
127 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.-57+4916_-57+4922d others(9): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862339 | |||||||
| chr14:91862418 | G | C | 1 | a0001c0001t0001g0055 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-57+4844C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862418 | |||||||
| chr14:91862485 | T | A | 11 | a0001c0001t0003g0169 a0001c0001t0003g0186 a0001c0001t0003g0187 others(8): Show |
11 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+4777A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862485 | |||||||
| chr14:91862509 | G | A | 18 | a0001c0001t0003g0066 a0001c0001t0004g0005 a0001c0001t0004g0307 others(15): Show |
20 | HG00423.hp1 HG02602.hp2 HG03491.hp1 others(17): Show |
intron_variant | MODIFIER | c.-57+4753C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862509 | |||||||
| chr14:91862605 | G | A | 3 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 |
3 | HG02145.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-57+4657C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862605 | |||||||
| chr14:91862669 | G | A | 1 | a0001c0001t0006g0159 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-57+4593C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862669 | |||||||
| chr14:91862760 | G | A | 12 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(9): Show |
12 | HG01109.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57+4502C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862760 | |||||||
| chr14:91862856 | A | C | 1 | a0001c0001t0003g0171 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-57+4406T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862856 | |||||||
| chr14:91862858 | A | G | 1 | a0001c0001t0006g0056 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-57+4404T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862858 | |||||||
| chr14:91862971 | T | C | 12 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(9): Show |
12 | HG01109.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57+4291A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862971 | |||||||
| chr14:91863113 | C | G | 2 | a0001c0002t0001g0091 a0001c0007t0028g0092 |
2 | HG01261.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-57+4149G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863113 | |||||||
| chr14:91863273 | G | A | 1 | a0001c0001t0038g0323 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-57+3989C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863273 | |||||||
| chr14:91863323 | G | A | 3 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 |
3 | HG02145.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-57+3939C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863323 | |||||||
| chr14:91863404 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-57+3858T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863404 | |||||||
| chr14:91863519 | G | A | 9 | a0001c0001t0006g0159 a0001c0001t0006g0161 a0001c0001t0009g0153 others(6): Show |
9 | HG01109.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+3743C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863519 | |||||||
| chr14:91863711 | C | A | 64 | a0001c0001t0001g0097 a0001c0001t0005g0004 a0001c0001t0005g0011 others(61): Show |
74 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.-57+3551G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863711 | |||||||
| chr14:91863772 | C | T | 67 | a0001c0001t0001g0097 a0001c0001t0002g0199 a0001c0001t0002g0200 others(64): Show |
77 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(74): Show |
intron_variant | MODIFIER | c.-57+3490G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863772 | |||||||
| chr14:91863829 | C | CA | 72 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0097 others(69): Show |
78 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.-57+3432dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863829 | |||||||
| chr14:91863829 | CA | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(53): Show |
60 | HG00099.hp2 HG00673.hp2 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.-57+3432delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863829 | |||||||
| chr14:91863884 | C | A | 76 | a0001c0001t0001g0097 a0001c0001t0002g0199 a0001c0001t0002g0200 others(73): Show |
86 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.-57+3378G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863884 | |||||||
| chr14:91863889 | A | G | 32 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0001c0001t0001g0180 others(29): Show |
33 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.-57+3373T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863889 | |||||||
| chr14:91864069 | C | T | 76 | a0001c0001t0001g0097 a0001c0001t0002g0199 a0001c0001t0002g0200 others(73): Show |
86 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.-57+3193G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864069 | |||||||
| chr14:91864182 | C | G | 1 | a0001c0001t0005g0144 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-57+3080G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864182 | |||||||
| chr14:91864446 | T | C | 64 | a0001c0001t0001g0097 a0001c0001t0005g0004 a0001c0001t0005g0011 others(61): Show |
74 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.-57+2816A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864446 | |||||||
| chr14:91864475 | G | A | 151 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(148): Show |
165 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.-57+2787C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864475 | |||||||
| chr14:91864509 | A | G | 1 | a0001c0001t0018g0085 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-57+2753T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864509 | |||||||
| chr14:91864522 | G | T | 17 | a0001c0001t0004g0005 a0001c0001t0004g0307 a0001c0001t0004g0308 others(14): Show |
19 | HG00423.hp1 HG02602.hp2 HG03491.hp1 others(16): Show |
intron_variant | MODIFIER | c.-57+2740C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864522 | |||||||
| chr14:91864596 | A | C | 1 | a0002c0003t0007g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-57+2666T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864596 | |||||||
| chr14:91864709 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-57+2553T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864709 | |||||||
| chr14:91864739 | CT | C | 9 | a0001c0001t0006g0159 a0001c0001t0006g0161 a0001c0001t0009g0153 others(6): Show |
9 | HG01109.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+2522delA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864739 | |||||||
| chr14:91864777 | CT | C | 262 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(259): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-57+2484delA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864777 | |||||||
| chr14:91864777 | CTT | C | 18 | a0001c0001t0002g0293 a0001c0001t0002g0294 a0001c0001t0003g0195 others(15): Show |
22 | HG01069.hp1 HG01081.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.-57+2483_-57+2484d others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864777 | |||||||
| chr14:91864777 | CTTT | C | 11 | a0001c0001t0008g0080 a0001c0001t0008g0081 a0001c0001t0008g0082 others(8): Show |
11 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+2482_-57+2484d others(5): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864777 | |||||||
| chr14:91864805 | A | T | 1 | a0001c0001t0002g0207 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-57+2457T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864805 | |||||||
| chr14:91864814 | C | A | 1 | a0001c0002t0001g0129 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-57+2448G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864814 | |||||||
| chr14:91864821 | G | T | 1 | a0001c0001t0001g0093 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-57+2441C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864821 | |||||||
| chr14:91864868 | G | T | 2 | a0001c0002t0001g0130 a0001c0002t0001g0131 |
2 | HG00642.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-57+2394C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864868 | |||||||
| chr14:91864969 | C | T | 4 | a0001c0001t0008g0081 a0001c0001t0008g0082 a0001c0001t0008g0083 others(1): Show |
4 | HG01192.hp2 HG01884.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+2293G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864969 | |||||||
| chr14:91865031 | C | T | 2 | a0001c0002t0001g0091 a0001c0007t0028g0092 |
2 | HG01261.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-57+2231G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865031 | |||||||
| chr14:91865075 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-57+2187C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865075 | |||||||
| chr14:91865144 | A | G | 2 | a0001c0002t0001g0091 a0001c0007t0028g0092 |
2 | HG01261.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-57+2118T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865144 | |||||||
| chr14:91865217 | T | C | 1 | a0001c0001t0002g0295 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-57+2045A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865217 | |||||||
| chr14:91865221 | GATTT | G | 73 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(70): Show |
77 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.-57+2037_-57+2040d others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865221 | |||||||
| chr14:91865303 | TC | T | 36 | a0001c0001t0001g0097 a0001c0001t0024g0127 a0001c0002t0001g0001 others(33): Show |
41 | HG00544.hp1 HG00733.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.-57+1958delG | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865303 | |||||||
| chr14:91865367 | TG | T | 8 | a0001c0001t0006g0159 a0001c0001t0009g0153 a0001c0001t0009g0154 others(5): Show |
8 | HG01109.hp1 HG01891.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57+1894delC | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865367 | |||||||
| chr14:91865369 | G | GT | 7 | a0001c0001t0002g0198 a0001c0001t0002g0199 a0001c0001t0002g0203 others(4): Show |
7 | HG00438.hp2 HG00735.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+1892dupA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865369 | |||||||
| chr14:91865369 | GT | G | 67 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(64): Show |
71 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.-57+1892delA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865369 | |||||||
| chr14:91865369 | GTT | G | 16 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0001t0002g0305 others(13): Show |
16 | HG01167.hp2 HG01192.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57+1891_-57+1892d others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865369 | |||||||
| chr14:91865377 | T | G | 1 | a0002c0003t0007g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-57+1885A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865377 | |||||||
| chr14:91865390 | T | A | 3 | a0001c0001t0029g0197 a0001c0002t0001g0091 a0001c0007t0028g0092 |
3 | HG01261.hp1 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-57+1872A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865390 | |||||||
| chr14:91865390 | TA | T | 61 | a0001c0001t0001g0097 a0001c0001t0002g0202 a0001c0001t0004g0310 others(58): Show |
70 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.-57+1871delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865390 | |||||||
| chr14:91865391 | A | T | 22 | a0001c0001t0002g0267 a0001c0001t0002g0268 a0001c0001t0003g0184 others(19): Show |
24 | HG00423.hp1 HG02602.hp2 HG02965.hp2 others(21): Show |
intron_variant | MODIFIER | c.-57+1871T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865391 | |||||||
| chr14:91865392 | A | T | 1 | a0001c0002t0001g0095 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-57+1870T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865392 | |||||||
| chr14:91865566 | C | T | 12 | a0001c0001t0008g0080 a0001c0001t0008g0081 a0001c0001t0008g0082 others(9): Show |
12 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-57+1696G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865566 | |||||||
| chr14:91865572 | T | G | 1 | a0001c0001t0031g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-57+1690A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865572 | |||||||
| chr14:91865670 | A | G | 1 | a0001c0001t0038g0323 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-57+1592T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865670 | |||||||
| chr14:91865671 | C | T | 151 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(148): Show |
165 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.-57+1591G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865671 | |||||||
| chr14:91865740 | T | G | 32 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0001c0001t0001g0180 others(29): Show |
33 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.-57+1522A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865740 | |||||||
| chr14:91866129 | A | G | 9 | a0001c0001t0006g0159 a0001c0001t0006g0161 a0001c0001t0009g0153 others(6): Show |
9 | HG01109.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+1133T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866129 | |||||||
| chr14:91866204 | C | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(72): Show |
79 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.-57+1058G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866204 | |||||||
| chr14:91866311 | C | T | 1 | a0001c0001t0002g0202 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-57+951G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866311 | |||||||
| chr14:91866378 | T | C | 78 | a0001c0001t0001g0093 a0001c0001t0001g0097 a0001c0001t0005g0004 others(75): Show |
88 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(85): Show |
intron_variant | MODIFIER | c.-57+884A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866378 | |||||||
| chr14:91866459 | A | G | 3 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 |
3 | HG02145.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-57+803T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866459 | |||||||
| chr14:91866472 | T | C | 64 | a0001c0001t0001g0097 a0001c0001t0005g0004 a0001c0001t0005g0011 others(61): Show |
74 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.-57+790A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866472 | |||||||
| chr14:91866506 | G | A | 285 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(282): Show |
302 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(299): Show |
intron_variant | MODIFIER | c.-57+756C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866506 | |||||||
| chr14:91866524 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(71): Show |
78 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.-57+738G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866524 | |||||||
| chr14:91866605 | G | C | 4 | a0001c0001t0001g0093 a0001c0002t0001g0091 a0001c0007t0028g0092 others(1): Show |
4 | HG01261.hp1 HG03486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+657C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866605 | |||||||
| chr14:91866657 | G | A | 64 | a0001c0001t0001g0097 a0001c0001t0005g0004 a0001c0001t0005g0011 others(61): Show |
74 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(71): Show |
intron_variant | MODIFIER | c.-57+605C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866657 | |||||||
| chr14:91866691 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-57+571G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866691 | |||||||
| chr14:91866852 | A | G | 1 | a0001c0001t0004g0307 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-57+410T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866852 | |||||||
| chr14:91867067 | T | C | 1 | a0001c0001t0002g0306 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-57+195A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91867067 | |||||||
| chr14:91867087 | C | CCTCT | 276 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(273): Show |
293 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(290): Show |
intron_variant | MODIFIER | c.-57+174_-57+175ins others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91867087 | |||||||
| chr14:91867184 | T | C | 1 | a0001c0001t0029g0197 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57+78A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91867184 |