Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8842 |
| ensemblid | ENSG00000007062.12 |
| hgncid | 9454 |
| symbol | PROM1 |
| name | prominin 1 |
| refseq_nuc | NM_006017.3 |
| refseq_prot | NP_006008.1 |
| ensembl_nuc | ENST00000447510.7 |
| ensembl_prot | ENSP00000415481.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 15968228 |
| end | 16084023 |
| strand | - |
| ver | v1.2 |
| region | chr4:15968228-16084023 |
| region5000 | chr4:15963228-16089023 |
| regionname0 | PROM1_chr4_15968228_16084023 |
| regionname5000 | PROM1_chr4_15963228_16089023 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 865 | 358 | 92 | 61 | 158 | 12 | 33 | 115 | PROM1_chr4_15963228_16089023 | PROM1 | MALVL others(860): Show |
chr4 | 15963228 | 16089023 |
| a0002 | 0/0 | 865 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | PROM1_chr4_15963228_16089023 | PROM1 | MALVL others(860): Show |
chr4 | 15963228 | 16089023 |
| a0003 | 0/0 | 865 | 3 | 0 | 1 | 2 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | MALVL others(860): Show |
chr4 | 15963228 | 16089023 |
| a0004 | 0/0 | 865 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | MALVL others(860): Show |
chr4 | 15963228 | 16089023 |
| a0005 | 0/0 | 865 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | MALVL others(860): Show |
chr4 | 15963228 | 16089023 |
| a0006 | 0/0 | 865 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | MALVL others(860): Show |
chr4 | 15963228 | 16089023 |
| a0007 | 0/0 | 865 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | MALVL others(860): Show |
chr4 | 15963228 | 16089023 |
| a0008 | 0/0 | 865 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | MALVL others(860): Show |
chr4 | 15963228 | 16089023 |
| a0009 | 0/0 | 865 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | MALVL others(860): Show |
chr4 | 15963228 | 16089023 |
| a0010 | 0/0 | 865 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | MALVL others(860): Show |
chr4 | 15963228 | 16089023 |
| a0011 | 0/0 | 865 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | MALVL others(860): Show |
chr4 | 15963228 | 16089023 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2595 | 272 | 58 | 48 | 125 | 11 | 28 | PROM1_chr4_15963228_16089023 | PROM1 | ATGGC others(2590): Show |
chr4 | 15963228 | 16089023 | ||
| a0001c0002 | 0/0 | 2595 | 53 | 5 | 12 | 32 | 1 | 3 | PROM1_chr4_15963228_16089023 | PROM1 | ATGGC others(2590): Show |
chr4 | 15963228 | 16089023 | ||
| a0001c0003 | 0/0 | 2595 | 12 | 12 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | ATGGC others(2590): Show |
chr4 | 15963228 | 16089023 | ||
| a0001c0004 | 0/0 | 2595 | 9 | 7 | 1 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | ATGGC others(2590): Show |
chr4 | 15963228 | 16089023 | ||
| a0001c0005 | 0/0 | 2595 | 8 | 8 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | ATGGC others(2590): Show |
chr4 | 15963228 | 16089023 | ||
| a0001c0011 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | ATGGC others(2590): Show |
chr4 | 15963228 | 16089023 | ||
| a0001c0016 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | ATGGC others(2590): Show |
chr4 | 15963228 | 16089023 | ||
| a0001c0018 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | ATGGC others(2590): Show |
chr4 | 15963228 | 16089023 | ||
| a0001c0019 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | ATGGC others(2590): Show |
chr4 | 15963228 | 16089023 | ||
| a0002c0006 | 0/0 | 2595 | 4 | 0 | 0 | 4 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | ATGGC others(2590): Show |
chr4 | 15963228 | 16089023 | ||
| a0003c0007 | 0/0 | 2595 | 3 | 0 | 1 | 2 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | ATGGC others(2590): Show |
chr4 | 15963228 | 16089023 | ||
| a0004c0008 | 0/0 | 2595 | 2 | 0 | 2 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | ATGGC others(2590): Show |
chr4 | 15963228 | 16089023 | ||
| a0005c0012 | 0/0 | 2595 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | ATGGC others(2590): Show |
chr4 | 15963228 | 16089023 | ||
| a0006c0010 | 0/0 | 2595 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | ATGGC others(2590): Show |
chr4 | 15963228 | 16089023 | ||
| a0007c0017 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | ATGGC others(2590): Show |
chr4 | 15963228 | 16089023 | ||
| a0008c0013 | 0/0 | 2595 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | ATGGC others(2590): Show |
chr4 | 15963228 | 16089023 | ||
| a0009c0014 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | ATGGC others(2590): Show |
chr4 | 15963228 | 16089023 | ||
| a0010c0015 | 0/0 | 2595 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | ATGGC others(2590): Show |
chr4 | 15963228 | 16089023 | ||
| a0011c0009 | 0/0 | 2595 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | ATGGC others(2590): Show |
chr4 | 15963228 | 16089023 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4021 | 102 | 20 | 8 | 54 | 4 | 16 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0001t0002 | 0/1 | 4021 | 75 | 17 | 13 | 35 | 3 | 6 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0001t0003 | 0/0 | 4021 | 64 | 2 | 19 | 34 | 4 | 5 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0001t0004 | 1/0 | 4021 | 19 | 13 | 4 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0001t0005 | 0/0 | 4020 | 4 | 4 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4015): Show |
chr4 | 15963228 | 16089023 |
| a0001c0001t0006 | 0/0 | 4021 | 2 | 2 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0001t0007 | 0/0 | 4021 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0001t0008 | 0/0 | 4021 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0001t0009 | 0/0 | 4021 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0001t0010 | 0/0 | 4021 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0001t0012 | 0/0 | 4021 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0001t0013 | 0/0 | 4021 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0002t0001 | 0/0 | 4021 | 20 | 0 | 8 | 10 | 0 | 2 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0002t0002 | 0/0 | 4021 | 20 | 1 | 1 | 17 | 1 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0002t0003 | 0/0 | 4021 | 8 | 0 | 2 | 5 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0002t0004 | 0/0 | 4021 | 5 | 4 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0003t0001 | 0/0 | 4021 | 3 | 3 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0003t0002 | 0/0 | 4021 | 6 | 6 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0003t0004 | 0/0 | 4021 | 2 | 2 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0003t0011 | 0/0 | 4020 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4015): Show |
chr4 | 15963228 | 16089023 |
| a0001c0004t0001 | 0/0 | 4021 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0004t0002 | 0/0 | 4021 | 5 | 4 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0004t0004 | 0/0 | 4021 | 3 | 2 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0005t0001 | 0/0 | 4021 | 4 | 4 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0005t0002 | 0/0 | 4021 | 2 | 2 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0005t0004 | 0/0 | 4021 | 2 | 2 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0011t0003 | 0/0 | 4021 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0016t0001 | 0/0 | 4021 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0018t0001 | 0/0 | 4021 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0001c0019t0005 | 0/0 | 4020 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4015): Show |
chr4 | 15963228 | 16089023 |
| a0002c0006t0001 | 0/0 | 4021 | 2 | 0 | 0 | 2 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0002c0006t0002 | 0/0 | 4021 | 2 | 0 | 0 | 2 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0003c0007t0001 | 0/0 | 4021 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0003c0007t0002 | 0/0 | 4021 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0003c0007t0003 | 0/0 | 4021 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0004c0008t0002 | 0/0 | 4021 | 2 | 0 | 2 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0005c0012t0003 | 0/0 | 4021 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0006c0010t0002 | 0/0 | 4021 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0007c0017t0001 | 0/0 | 4021 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0008c0013t0003 | 0/0 | 4021 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0009c0014t0002 | 0/0 | 4021 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0010c0015t0003 | 0/0 | 4021 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| a0011c0009t0004 | 0/0 | 4021 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | AGATC others(4016): Show |
chr4 | 15963228 | 16089023 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0367 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0002g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0003g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0004g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0004g0142 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0004g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0005g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0005g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0007g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0008g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0009g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0010g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0012g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0001t0013g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0002g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0004g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0002t0004g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0003t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0003t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0003t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0003t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0003t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0003t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0003t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0003t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0003t0004g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0003t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0003t0011g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0004t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0004t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0004t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0004t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0004t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0004t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0004t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0004t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0004t0004g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0005t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0005t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0005t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0005t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0005t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0005t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0005t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0005t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0011t0003g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0016t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0018t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0001c0019t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0002c0006t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0002c0006t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0002c0006t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0002c0006t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0003c0007t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0003c0007t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0003c0007t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0004c0008t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0004c0008t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0005c0012t0003g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0006c0010t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0007c0017t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0008c0013t0003g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0009c0014t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0010c0015t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| a0011c0009t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0307 | EUR | FIN | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0333 | EUR | FIN | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | CHS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00423 | hp1 | a0001 | c0002 | t0002 | g0201 | EAS | CHS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0260 | EAS | CHS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | CHS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | CHS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | CHS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0305 | EAS | CHS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG00738 | hp2 | a0001 | c0002 | t0004 | g0268 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0128 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0166 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0318 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01081 | hp2 | a0001 | c0002 | t0003 | g0285 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01099 | hp1 | a0001 | c0004 | t0004 | g0321 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0129 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01106 | hp1 | a0005 | c0012 | t0003 | g0340 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0034 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0331 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0221 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0313 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0309 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0117 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0131 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0199 | AMR | PUR | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0125 | AMR | CLM | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | CLM | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0121 | AMR | CLM | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0228 | AMR | CLM | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0294 | AMR | CLM | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0229 | AMR | CLM | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | CLM | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01346 | hp1 | a0001 | c0001 | t0013 | g0366 | AMR | CLM | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0141 | AMR | CLM | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0273 | AMR | CLM | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0148 | AMR | CLM | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0247 | AMR | CLM | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0295 | AMR | CLM | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0124 | AMR | CLM | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0220 | EUR | IBS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0225 | EUR | IBS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | IBS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | IBS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | ACB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01884 | hp2 | a0001 | c0002 | t0004 | g0026 | AFR | ACB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01928 | hp2 | a0001 | c0002 | t0003 | g0226 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0281 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01943 | hp2 | a0004 | c0008 | t0002 | g0077 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01952 | hp2 | a0001 | c0001 | t0010 | g0126 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0245 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01981 | hp1 | a0006 | c0010 | t0002 | g0243 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0130 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01993 | hp1 | a0003 | c0007 | t0001 | g0174 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0246 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | KHV | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0334 | AFR | ACB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | ACB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0369 | EAS | KHV | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02056 | hp2 | a0001 | c0002 | t0003 | g0256 | EAS | KHV | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | KHV | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02074 | hp1 | a0003 | c0007 | t0002 | g0236 | EAS | KHV | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0181 | EAS | KHV | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0237 | EAS | KHV | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | KHV | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | KHV | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0300 | EAS | KHV | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0348 | AFR | ACB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02145 | hp2 | a0001 | c0004 | t0001 | g0046 | AFR | ACB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0132 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02148 | hp2 | a0004 | c0008 | t0002 | g0119 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | CDX | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CDX | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0371 | EAS | CDX | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02257 | hp2 | a0001 | c0003 | t0002 | g0017 | AFR | ACB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02258 | hp2 | a0001 | c0004 | t0004 | g0049 | AFR | ACB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0152 | AFR | ACB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02300 | hp1 | a0001 | c0001 | t0009 | g0076 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02300 | hp2 | a0001 | c0001 | t0004 | g0123 | AMR | PEL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0145 | AFR | ACB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02451 | hp2 | a0001 | c0003 | t0002 | g0008 | AFR | ACB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | KHV | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0045 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0266 | SAS | PJL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02630 | hp1 | a0001 | c0002 | t0004 | g0027 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02630 | hp2 | a0001 | c0003 | t0002 | g0009 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0053 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0277 | SAS | PJL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02717 | hp1 | a0001 | c0003 | t0011 | g0013 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0319 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0212 | SAS | PJL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0358 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02818 | hp2 | a0001 | c0019 | t0005 | g0018 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02886 | hp1 | a0001 | c0002 | t0004 | g0355 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0010 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02895 | hp1 | a0001 | c0005 | t0002 | g0338 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02922 | hp1 | a0001 | c0004 | t0002 | g0004 | AFR | ESN | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | ESN | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02965 | hp2 | a0001 | c0003 | t0004 | g0011 | AFR | ESN | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0297 | AFR | ESN | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02970 | hp2 | a0001 | c0004 | t0002 | g0349 | AFR | ESN | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0346 | AFR | ESN | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02976 | hp2 | a0001 | c0002 | t0004 | g0344 | AFR | ESN | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0337 | SAS | PJL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03017 | hp2 | a0001 | c0011 | t0003 | g0356 | SAS | PJL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0347 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0006 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | MSL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0031 | AFR | ESN | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03130 | hp2 | a0001 | c0003 | t0004 | g0007 | AFR | ESN | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03139 | hp1 | a0001 | c0001 | t0006 | g0032 | AFR | ESN | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03139 | hp2 | a0001 | c0004 | t0002 | g0135 | AFR | ESN | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03195 | hp1 | a0001 | c0018 | t0001 | g0215 | AFR | ESN | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0030 | AFR | ESN | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0080 | AFR | MSL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0351 | AFR | MSL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0342 | AFR | MSL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03486 | hp2 | a0001 | c0003 | t0002 | g0070 | AFR | MSL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0290 | SAS | PJL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0357 | SAS | PJL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0330 | SAS | PJL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03516 | hp1 | a0001 | c0005 | t0001 | g0219 | AFR | ESN | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0025 | AFR | ESN | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03540 | hp1 | a0001 | c0004 | t0004 | g0312 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | GWD | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03579 | hp2 | a0001 | c0003 | t0002 | g0012 | AFR | MSL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0082 | SAS | PJL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0227 | SAS | PJL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0291 | SAS | STU | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0329 | SAS | PJL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0339 | SAS | PJL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0320 | SAS | PJL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0203 | SAS | BEB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0364 | SAS | BEB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0292 | SAS | BEB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG04115 | hp1 | a0008 | c0013 | t0003 | g0335 | SAS | STU | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | STU | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG04199 | hp2 | a0001 | c0002 | t0003 | g0192 | SAS | STU | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0069 | SAS | STU | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | STU | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | STU | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | STU | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18522 | hp2 | a0001 | c0005 | t0004 | g0217 | AFR | YRI | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0370 | EAS | CHB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | CHB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | YRI | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0178 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18944 | hp1 | a0001 | c0001 | t0008 | g0234 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0365 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18952 | hp2 | a0001 | c0004 | t0002 | g0322 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18953 | hp1 | a0003 | c0007 | t0003 | g0314 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18959 | hp2 | a0002 | c0006 | t0002 | g0073 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0336 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0214 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0156 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18970 | hp1 | a0002 | c0006 | t0001 | g0206 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0055 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0332 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0158 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18982 | hp1 | a0001 | c0001 | t0012 | g0223 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18982 | hp2 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0368 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0359 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18993 | hp2 | a0009 | c0014 | t0002 | g0194 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18995 | hp2 | a0001 | c0002 | t0003 | g0202 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0341 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19001 | hp2 | a0001 | c0002 | t0003 | g0302 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19003 | hp2 | a0010 | c0015 | t0003 | g0093 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19009 | hp2 | a0001 | c0002 | t0003 | g0293 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19030 | hp1 | a0011 | c0009 | t0004 | g0317 | AFR | LWK | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19030 | hp2 | a0001 | c0005 | t0001 | g0216 | AFR | LWK | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19043 | hp1 | a0001 | c0005 | t0001 | g0218 | AFR | LWK | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19043 | hp2 | a0001 | c0005 | t0002 | g0022 | AFR | LWK | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19055 | hp2 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19060 | hp1 | a0001 | c0002 | t0003 | g0304 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19064 | hp1 | a0002 | c0006 | t0001 | g0208 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19078 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19088 | hp1 | a0002 | c0006 | t0002 | g0362 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19090 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0361 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0081 | AFR | YRI | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | YRI | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA20129 | hp1 | a0001 | c0005 | t0004 | g0075 | AFR | ASW | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA20129 | hp2 | a0001 | c0005 | t0001 | g0327 | AFR | ASW | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0259 | EUR | TSI | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0326 | EUR | TSI | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0296 | EUR | TSI | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0147 | EUR | TSI | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | GIH | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA20905 | hp2 | a0001 | c0016 | t0001 | g0143 | SAS | GIH | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02109 | hp1 | a0007 | c0017 | t0001 | g0019 | AFR | ACB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | ACB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0354 | AFR | ACB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0276 | AFR | ACB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02559 | hp1 | a0001 | c0003 | t0002 | g0020 | AFR | ACB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0298 | AFR | ACB | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0323 | AFR | MSL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG03471 | hp2 | a0001 | c0004 | t0002 | g0047 | AFR | MSL | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0343 | AFR | USA | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | USA | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0036 | AFR | USA | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | USA | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | LWK | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | LWK | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0367 | REF | REF | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0142 | REF | REF | PROM1_chr4_15963228_16089023 | PROM1 | chr4 | 15963228 | 16089023 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:15979426 | C | T | 1 | a0010 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.2551G>A | p.Val851Ile | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/28 | 2809/4021 | 2551/2598 | 851/865 | chr4 | 15979426 | |||
| chr4:15980426 | C | T | 1 | a0002 | 4 | NA18959.hp2 NA18970.hp1 NA19064.hp1 others(1): Show |
missense_variant | MODERATE | c.2485G>A | p.Asp829Asn | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 24/28 | 2743/4021 | 2485/2598 | 829/865 | chr4 | 15980426 | |||
| chr4:15980518 | A | G | 1 | a0009 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.2393T>C | p.Ile798Thr | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 24/28 | 2651/4021 | 2393/2598 | 798/865 | chr4 | 15980518 | |||
| chr4:15984327 | G | T | 1 | a0008 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.2309C>A | p.Pro770His | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/28 | 2567/4021 | 2309/2598 | 770/865 | chr4 | 15984327 | |||
| chr4:15994003 | T | C | 1 | a0007 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.1751A>G | p.His584Arg | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/28 | 2009/4021 | 1751/2598 | 584/865 | chr4 | 15994003 | |||
| chr4:16006647 | C | T | 1 | a0005 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.1345G>A | p.Val449Met | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/28 | 1603/4021 | 1345/2598 | 449/865 | chr4 | 16006647 | |||
| chr4:16018457 | T | G | 1 | a0003 | 3 | HG01993.hp1 HG02074.hp1 NA18953.hp1 |
missense_variant | MODERATE | c.868A>C | p.Ser290Arg | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/28 | 1126/4021 | 868/2598 | 290/865 | chr4 | 16018457 | |||
| chr4:16025265 | C | T | 1 | a0006 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.557G>A | p.Arg186Gln | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 6/28 | 815/4021 | 557/2598 | 186/865 | chr4 | 16025265 | |||
| chr4:16033430 | T | C | 1 | a0011 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.383A>G | p.Tyr128Cys | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/28 | 641/4021 | 383/2598 | 128/865 | chr4 | 16033430 | |||
| chr4:16033478 | C | T | 1 | a0011 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.335G>A | p.Cys112Tyr | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/28 | 593/4021 | 335/2598 | 112/865 | chr4 | 16033478 | |||
| chr4:16075852 | A | C | 1 | a0004 | 2 | HG01943.hp2 HG02148.hp2 |
missense_variant | MODERATE | c.55T>G | p.Ser19Ala | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/28 | 313/4021 | 55/2598 | 19/865 | chr4 | 16075852 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:15980457 | G | A | 1 | a0007c0017 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.2454C>T | p.Tyr818Tyr | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 24/28 | 2712/4021 | 2454/2598 | 818/865 | chr4 | 15980457 | |||
| chr4:15986017 | T | C | 1 | a0001c0016 | 1 | NA20905.hp2 | synonymous_variant | LOW | c.2151A>G | p.Leu717Leu | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 21/28 | 2409/4021 | 2151/2598 | 717/865 | chr4 | 15986017 | |||
| chr4:15991228 | G | A | 1 | a0001c0011 | 1 | HG03017.hp2 | synonymous_variant | LOW | c.1977C>T | p.Asn659Asn | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/28 | 2235/4021 | 1977/2598 | 659/865 | chr4 | 15991228 | |||
| chr4:16006662 | G | A | 1 | a0001c0018 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.1330C>T | p.Leu444Leu | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/28 | 1588/4021 | 1330/2598 | 444/865 | chr4 | 16006662 | |||
| chr4:16018539 | C | T | 4 | a0001c0002 a0001c0011 a0002c0006 others(1): Show |
59 | HG00423.hp1 HG00438.hp2 HG00738.hp2 others(56): Show |
splice_region_variant&synonymous_variant | LOW | c.786G>A | p.Ala262Ala | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/28 | 1044/4021 | 786/2598 | 262/865 | chr4 | 16018539 | |||
| chr4:16024305 | T | C | 1 | a0001c0018 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.684A>G | p.Thr228Thr | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 7/28 | 942/4021 | 684/2598 | 228/865 | chr4 | 16024305 | |||
| chr4:16038994 | C | T | 2 | a0001c0004 a0001c0019 |
10 | HG01099.hp1 HG02145.hp2 HG02258.hp2 others(7): Show |
synonymous_variant | LOW | c.228G>A | p.Leu76Leu | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/28 | 486/4021 | 228/2598 | 76/865 | chr4 | 16038994 | |||
| chr4:16075778 | G | A | 4 | a0001c0003 a0001c0005 a0001c0018 others(1): Show |
22 | HG02257.hp2 HG02280.hp2 HG02451.hp2 others(19): Show |
synonymous_variant | LOW | c.129C>T | p.Thr43Thr | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/28 | 387/4021 | 129/2598 | 43/865 | chr4 | 16075778 | |||
| chr4:16075892 | G | A | 2 | a0001c0003 a0001c0019 |
13 | HG02257.hp2 HG02280.hp2 HG02451.hp2 others(10): Show |
synonymous_variant | LOW | c.15C>T | p.Leu5Leu | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/28 | 273/4021 | 15/2598 | 5/865 | chr4 | 16075892 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:15968315 | T | C | 25 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(22): Show |
224 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*1078A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 28/28 | 2752 | chr4 | 15968315 | ||||||
| chr4:15968527 | G | C | 1 | a0001c0003t0011 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*866C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 28/28 | 2540 | chr4 | 15968527 | ||||||
| chr4:15968578 | G | C | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(34): Show |
341 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(338): Show |
3_prime_UTR_variant | MODIFIER | c.*815C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 28/28 | 2489 | chr4 | 15968578 | ||||||
| chr4:15968709 | G | A | 1 | a0001c0001t0006 | 2 | HG03139.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*684C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 28/28 | 2358 | chr4 | 15968709 | ||||||
| chr4:15968726 | T | G | 11 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0010 others(8): Show |
81 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*667A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 28/28 | 2341 | chr4 | 15968726 | ||||||
| chr4:15969100 | G | A | 1 | a0001c0001t0012 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*293C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 28/28 | 1967 | chr4 | 15969100 | ||||||
| chr4:15969254 | G | A | 1 | a0001c0001t0013 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*139C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 28/28 | 1813 | chr4 | 15969254 | ||||||
| chr4:15969308 | TC | T | 3 | a0001c0001t0005 a0001c0003t0011 a0001c0019t0005 |
6 | HG02572.hp1 HG02717.hp1 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*84delG | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 28/28 | 1758 | chr4 | 15969308 | ||||||
| chr4:16075928 | A | G | 1 | a0001c0001t0010 | 1 | HG01952.hp2 | 5_prime_UTR_variant | MODIFIER | c.-22T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/28 | 22 | chr4 | 16075928 | ||||||
| chr4:16075931 | A | T | 1 | a0001c0001t0009 | 1 | HG02300.hp1 | 5_prime_UTR_variant | MODIFIER | c.-25T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/28 | 25 | chr4 | 16075931 | ||||||
| chr4:16076054 | C | T | 1 | a0001c0001t0008 | 1 | NA18944.hp1 | 5_prime_UTR_variant | MODIFIER | c.-148G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/28 | 148 | chr4 | 16076054 | ||||||
| chr4:16076074 | C | T | 1 | a0001c0001t0007 | 1 | HG01071.hp2 | 5_prime_UTR_variant | MODIFIER | c.-168G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/28 | 168 | chr4 | 16076074 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:15969459 | A | G | 105 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0050 others(102): Show |
107 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.*25-91T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15969459 | |||||||
| chr4:15969491 | G | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(120): Show |
124 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.*25-123C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15969491 | |||||||
| chr4:15969491 | G | C | 1 | a0001c0001t0001g0189 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.*25-123C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15969491 | |||||||
| chr4:15969648 | G | A | 1 | a0001c0001t0003g0225 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.*25-280C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15969648 | |||||||
| chr4:15969718 | G | T | 78 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0040 others(75): Show |
80 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.*25-350C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15969718 | |||||||
| chr4:15969738 | G | T | 1 | a0001c0001t0002g0292 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.*25-370C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15969738 | |||||||
| chr4:15969914 | G | A | 5 | a0001c0001t0005g0036 a0001c0001t0005g0045 a0001c0001t0005g0346 others(2): Show |
5 | HG02258.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.*25-546C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15969914 | |||||||
| chr4:15970015 | T | A | 27 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0033 others(24): Show |
27 | HG01243.hp1 HG02109.hp1 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.*25-647A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15970015 | |||||||
| chr4:15970162 | T | C | 79 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0038 others(76): Show |
81 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.*25-794A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15970162 | |||||||
| chr4:15970168 | CTT | C | 13 | a0001c0001t0001g0102 a0001c0001t0001g0183 a0001c0001t0001g0188 others(10): Show |
13 | HG00408.hp1 HG00438.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.*25-802_*25-801del others(2): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15970168 | |||||||
| chr4:15970173 | T | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0050 a0001c0001t0001g0106 others(5): Show |
8 | HG02280.hp2 HG03579.hp1 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.*25-805A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15970173 | |||||||
| chr4:15970175 | T | C | 13 | a0001c0001t0001g0102 a0001c0001t0001g0183 a0001c0001t0001g0188 others(10): Show |
13 | HG00408.hp1 HG00438.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.*25-807A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15970175 | |||||||
| chr4:15970221 | A | G | 81 | a0001c0001t0001g0190 a0001c0001t0002g0052 a0001c0001t0003g0002 others(78): Show |
83 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.*24+822T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15970221 | |||||||
| chr4:15970339 | G | A | 13 | a0001c0001t0001g0102 a0001c0001t0001g0183 a0001c0001t0001g0188 others(10): Show |
13 | HG00408.hp1 HG00438.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.*24+704C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15970339 | |||||||
| chr4:15970347 | T | A | 15 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0050 others(12): Show |
15 | HG01243.hp1 HG02109.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.*24+696A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15970347 | |||||||
| chr4:15970388 | G | T | 77 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0038 others(74): Show |
79 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.*24+655C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15970388 | |||||||
| chr4:15970419 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.*24+624G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15970419 | |||||||
| chr4:15970455 | G | A | 102 | a0001c0001t0001g0213 a0001c0001t0002g0005 a0001c0001t0002g0016 others(99): Show |
102 | HG00423.hp1 HG00597.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.*24+588C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15970455 | |||||||
| chr4:15970516 | T | A | 2 | a0001c0001t0003g0316 a0001c0001t0003g0341 |
2 | NA18993.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.*24+527A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15970516 | |||||||
| chr4:15970555 | T | C | 42 | a0001c0001t0002g0048 a0001c0001t0002g0066 a0001c0001t0002g0089 others(39): Show |
42 | HG00423.hp1 HG00597.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.*24+488A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15970555 | |||||||
| chr4:15970678 | G | A | 333 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(330): Show |
336 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(333): Show |
intron_variant | MODIFIER | c.*24+365C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15970678 | |||||||
| chr4:15970811 | TA | T | 335 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(332): Show |
338 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(335): Show |
intron_variant | MODIFIER | c.*24+231delT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15970811 | |||||||
| chr4:15970820 | A | T | 2 | a0001c0001t0003g0222 a0001c0005t0001g0218 |
2 | NA18939.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.*24+223T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15970820 | |||||||
| chr4:15970884 | T | A | 3 | a0001c0001t0001g0094 a0001c0001t0001g0171 a0001c0001t0009g0076 |
3 | HG02300.hp1 HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.*24+159A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15970884 | |||||||
| chr4:15970926 | G | A | 333 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(330): Show |
336 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(333): Show |
intron_variant | MODIFIER | c.*24+117C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 27/27 | chr4 | 15970926 | |||||||
| chr4:15971184 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2583-102G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15971184 | |||||||
| chr4:15971282 | T | C | 54 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0213 others(51): Show |
54 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.2583-200A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15971282 | |||||||
| chr4:15971373 | C | T | 1 | a0001c0001t0003g0163 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2583-291G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15971373 | |||||||
| chr4:15971481 | G | A | 1 | a0001c0001t0005g0036 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2583-399C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15971481 | |||||||
| chr4:15971537 | G | T | 2 | a0001c0001t0002g0083 a0001c0003t0002g0009 |
2 | HG02630.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2583-455C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15971537 | |||||||
| chr4:15971574 | G | T | 13 | a0001c0001t0001g0102 a0001c0001t0001g0183 a0001c0001t0001g0188 others(10): Show |
13 | HG00408.hp1 HG00438.hp1 HG01993.hp1 others(10): Show |
intron_variant | MODIFIER | c.2583-492C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15971574 | |||||||
| chr4:15972097 | G | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0345 |
2 | HG02129.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.2583-1015C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15972097 | |||||||
| chr4:15972105 | G | C | 14 | a0001c0001t0001g0102 a0001c0001t0001g0183 a0001c0001t0001g0188 others(11): Show |
14 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(11): Show |
intron_variant | MODIFIER | c.2583-1023C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15972105 | |||||||
| chr4:15972163 | C | G | 45 | a0001c0001t0003g0002 a0001c0001t0003g0038 a0001c0001t0003g0057 others(42): Show |
46 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.2583-1081G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15972163 | |||||||
| chr4:15972258 | G | A | 1 | a0001c0003t0002g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2583-1176C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15972258 | |||||||
| chr4:15972269 | C | T | 17 | a0001c0001t0001g0023 a0001c0001t0001g0095 a0001c0001t0001g0098 others(14): Show |
17 | HG00735.hp2 HG02258.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.2583-1187G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15972269 | |||||||
| chr4:15972351 | A | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(219): Show |
225 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.2583-1269T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15972351 | |||||||
| chr4:15972392 | T | A | 3 | a0001c0001t0002g0120 a0001c0003t0002g0020 a0001c0004t0002g0349 |
3 | HG02559.hp1 HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.2583-1310A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15972392 | |||||||
| chr4:15972442 | C | A | 9 | a0001c0001t0001g0033 a0001c0001t0001g0054 a0001c0001t0001g0084 others(6): Show |
9 | HG02145.hp2 HG02257.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.2583-1360G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15972442 | |||||||
| chr4:15972497 | T | C | 1 | a0001c0002t0001g0359 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2583-1415A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15972497 | |||||||
| chr4:15972599 | C | A | 342 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(339): Show |
345 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(342): Show |
intron_variant | MODIFIER | c.2583-1517G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15972599 | |||||||
| chr4:15972651 | G | A | 1 | a0001c0001t0004g0141 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2583-1569C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15972651 | |||||||
| chr4:15972833 | T | C | 2 | a0001c0001t0006g0030 a0001c0001t0006g0032 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2583-1751A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15972833 | |||||||
| chr4:15972902 | C | T | 11 | a0001c0001t0001g0023 a0001c0001t0001g0095 a0001c0001t0001g0190 others(8): Show |
11 | HG00735.hp2 HG02572.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.2583-1820G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15972902 | |||||||
| chr4:15972910 | A | C | 4 | a0001c0001t0003g0065 a0001c0001t0003g0222 a0001c0001t0003g0286 others(1): Show |
4 | NA18939.hp1 NA18953.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.2583-1828T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15972910 | |||||||
| chr4:15972985 | T | C | 1 | a0001c0001t0005g0346 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2583-1903A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15972985 | |||||||
| chr4:15972986 | G | A | 14 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0054 others(11): Show |
14 | HG02145.hp2 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.2583-1904C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15972986 | |||||||
| chr4:15972993 | G | A | 1 | a0001c0001t0002g0282 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2583-1911C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15972993 | |||||||
| chr4:15973152 | A | C | 1 | a0001c0001t0004g0323 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2583-2070T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15973152 | |||||||
| chr4:15973313 | G | C | 1 | a0001c0001t0002g0103 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2583-2231C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15973313 | |||||||
| chr4:15973362 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2583-2280C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15973362 | |||||||
| chr4:15973540 | G | T | 3 | a0001c0001t0004g0069 a0001c0001t0004g0123 a0001c0001t0004g0141 |
3 | HG01346.hp2 HG02300.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2583-2458C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15973540 | |||||||
| chr4:15973620 | G | C | 57 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0050 others(54): Show |
57 | HG00438.hp1 HG00738.hp2 HG01099.hp1 others(54): Show |
intron_variant | MODIFIER | c.2583-2538C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15973620 | |||||||
| chr4:15973735 | T | C | 13 | a0001c0001t0001g0024 a0001c0001t0001g0051 a0001c0001t0001g0071 others(10): Show |
13 | HG02257.hp2 HG02451.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.2583-2653A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15973735 | |||||||
| chr4:15973739 | A | G | 1 | a0001c0001t0003g0132 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2583-2657T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15973739 | |||||||
| chr4:15973860 | T | C | 1 | a0001c0001t0002g0354 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2583-2778A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15973860 | |||||||
| chr4:15973900 | T | C | 1 | a0001c0001t0005g0346 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2583-2818A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15973900 | |||||||
| chr4:15973916 | G | A | 1 | a0001c0003t0002g0020 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2583-2834C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15973916 | |||||||
| chr4:15973918 | A | C | 290 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0023 others(287): Show |
292 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(289): Show |
intron_variant | MODIFIER | c.2583-2836T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15973918 | |||||||
| chr4:15973949 | G | A | 25 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0085 others(22): Show |
25 | HG01099.hp1 HG01109.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.2583-2867C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15973949 | |||||||
| chr4:15974025 | T | C | 4 | a0001c0001t0001g0230 a0001c0002t0001g0131 a0001c0002t0001g0221 others(1): Show |
4 | HG01167.hp2 HG01192.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.2583-2943A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974025 | |||||||
| chr4:15974109 | T | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0054 others(5): Show |
8 | HG01243.hp1 HG02630.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2583-3027A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974109 | |||||||
| chr4:15974118 | T | C | 1 | a0001c0018t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2583-3036A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974118 | |||||||
| chr4:15974118 | T | TTC | 17 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0054 others(14): Show |
17 | HG01099.hp1 HG01243.hp1 HG01346.hp2 others(14): Show |
intron_variant | MODIFIER | c.2583-3038_2583-303 others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974118 | |||||||
| chr4:15974118 | T | TTCTC | 56 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0113 others(53): Show |
56 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.2583-3040_2583-303 others(8): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974118 | |||||||
| chr4:15974118 | T | TTCTCTC | 140 | a0001c0001t0001g0021 a0001c0001t0001g0056 a0001c0001t0001g0095 others(137): Show |
141 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.2583-3042_2583-303 others(10): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974118 | |||||||
| chr4:15974118 | T | TTCTCTCT others(1): Show |
3 | a0001c0001t0003g0117 a0001c0002t0003g0226 a0001c0002t0003g0285 |
3 | HG01081.hp2 HG01192.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.2583-3044_2583-303 others(12): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974118 | |||||||
| chr4:15974118 | T | TTCTCTCT others(3): Show |
3 | a0001c0001t0001g0033 a0001c0001t0001g0085 a0001c0001t0001g0337 |
3 | HG02895.hp2 HG02897.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2583-3046_2583-303 others(14): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974118 | |||||||
| chr4:15974118 | T | TTCTCTCT others(5): Show |
1 | a0001c0001t0002g0140 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2583-3048_2583-303 others(16): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974118 | |||||||
| chr4:15974118 | TTCTC | T | 76 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0042 others(73): Show |
77 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.2583-3040_2583-303 others(8): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974118 | |||||||
| chr4:15974216 | A | G | 296 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(293): Show |
298 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(295): Show |
intron_variant | MODIFIER | c.2583-3134T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974216 | |||||||
| chr4:15974254 | A | G | 1 | a0001c0003t0011g0013 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2583-3172T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974254 | |||||||
| chr4:15974332 | A | G | 1 | a0001c0001t0002g0196 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2583-3250T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974332 | |||||||
| chr4:15974532 | G | A | 1 | a0001c0001t0002g0354 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2583-3450C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974532 | |||||||
| chr4:15974708 | T | A | 1 | a0001c0001t0003g0231 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2583-3626A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974708 | |||||||
| chr4:15974753 | G | A | 1 | a0001c0001t0001g0284 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2583-3671C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974753 | |||||||
| chr4:15974759 | C | T | 1 | a0001c0003t0002g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2583-3677G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974759 | |||||||
| chr4:15974761 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0005g0080 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2583-3679C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974761 | |||||||
| chr4:15974763 | A | C | 1 | a0001c0001t0002g0354 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2583-3681T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974763 | |||||||
| chr4:15974858 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2583-3776G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974858 | |||||||
| chr4:15974877 | A | G | 2 | a0001c0001t0001g0263 a0001c0001t0001g0311 |
2 | HG00544.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.2583-3795T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974877 | |||||||
| chr4:15974976 | G | A | 38 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0039 others(35): Show |
39 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.2583-3894C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974976 | |||||||
| chr4:15974982 | T | C | 295 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(292): Show |
297 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(294): Show |
intron_variant | MODIFIER | c.2583-3900A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974982 | |||||||
| chr4:15974988 | T | C | 1 | a0001c0003t0002g0070 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2583-3906A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15974988 | |||||||
| chr4:15975137 | G | A | 295 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(292): Show |
297 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(294): Show |
intron_variant | MODIFIER | c.2583-4055C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15975137 | |||||||
| chr4:15975184 | C | A | 1 | a0001c0003t0011g0013 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2583-4102G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15975184 | |||||||
| chr4:15975205 | C | T | 1 | a0001c0002t0002g0276 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2583-4123G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15975205 | |||||||
| chr4:15975242 | C | T | 9 | a0001c0001t0001g0042 a0001c0001t0001g0165 a0001c0001t0001g0198 others(6): Show |
9 | HG01074.hp2 HG01109.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2582+4153G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15975242 | |||||||
| chr4:15975282 | C | A | 1 | a0001c0001t0001g0339 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2582+4113G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15975282 | |||||||
| chr4:15975283 | A | G | 4 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0002g0083 others(1): Show |
4 | HG01243.hp1 HG02630.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2582+4112T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15975283 | |||||||
| chr4:15975322 | C | A | 1 | a0001c0001t0002g0220 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2582+4073G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15975322 | |||||||
| chr4:15975346 | A | G | 1 | a0001c0004t0002g0349 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2582+4049T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15975346 | |||||||
| chr4:15975575 | T | C | 5 | a0001c0001t0001g0230 a0001c0002t0001g0131 a0001c0002t0001g0221 others(2): Show |
5 | HG01167.hp2 HG01192.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.2582+3820A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15975575 | |||||||
| chr4:15975646 | C | A | 1 | a0001c0001t0001g0084 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2582+3749G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15975646 | |||||||
| chr4:15975900 | T | C | 257 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0024 others(254): Show |
258 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.2582+3495A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15975900 | |||||||
| chr4:15975949 | T | C | 368 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(365): Show |
371 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(368): Show |
intron_variant | MODIFIER | c.2582+3446A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15975949 | |||||||
| chr4:15976108 | C | T | 73 | a0001c0001t0001g0035 a0001c0001t0001g0042 a0001c0001t0001g0061 others(70): Show |
74 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.2582+3287G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15976108 | |||||||
| chr4:15976185 | G | A | 1 | a0001c0003t0011g0013 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2582+3210C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15976185 | |||||||
| chr4:15976200 | A | C | 75 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0054 others(72): Show |
76 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.2582+3195T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15976200 | |||||||
| chr4:15976205 | C | G | 75 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0054 others(72): Show |
76 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.2582+3190G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15976205 | |||||||
| chr4:15976254 | C | T | 4 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0002g0120 others(1): Show |
4 | HG02622.hp1 HG02647.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2582+3141G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15976254 | |||||||
| chr4:15976357 | C | A | 62 | a0001c0001t0001g0042 a0001c0001t0001g0061 a0001c0001t0001g0094 others(59): Show |
63 | HG00323.hp1 HG00438.hp2 HG01071.hp2 others(60): Show |
intron_variant | MODIFIER | c.2582+3038G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15976357 | |||||||
| chr4:15976527 | C | T | 7 | a0001c0001t0004g0015 a0001c0001t0004g0031 a0001c0001t0004g0034 others(4): Show |
7 | HG01109.hp2 HG02559.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2582+2868G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15976527 | |||||||
| chr4:15976622 | A | G | 85 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0050 others(82): Show |
86 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.2582+2773T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15976622 | |||||||
| chr4:15976646 | G | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0350 a0001c0003t0001g0152 |
3 | HG02280.hp2 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2582+2749C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15976646 | |||||||
| chr4:15976796 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG02015.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.2582+2599C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15976796 | |||||||
| chr4:15976930 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0004g0053 a0001c0001t0004g0323 others(1): Show |
4 | HG02647.hp1 HG02976.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2582+2465G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15976930 | |||||||
| chr4:15976990 | A | C | 1 | a0001c0001t0001g0351 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2582+2405T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15976990 | |||||||
| chr4:15977091 | C | T | 7 | a0001c0001t0004g0015 a0001c0001t0004g0031 a0001c0001t0004g0034 others(4): Show |
7 | HG01109.hp2 HG02559.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.2582+2304G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15977091 | |||||||
| chr4:15977099 | C | A | 5 | a0001c0002t0001g0100 a0001c0002t0002g0058 a0001c0002t0002g0176 others(2): Show |
5 | NA18941.hp1 NA18982.hp2 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.2582+2296G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15977099 | |||||||
| chr4:15977194 | C | CGT | 197 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0033 others(194): Show |
198 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.2582+2200_2582+220 others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15977194 | |||||||
| chr4:15977195 | A | C | 197 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0033 others(194): Show |
198 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.2582+2200T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15977195 | |||||||
| chr4:15977195 | A | G | 134 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0042 others(131): Show |
135 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.2582+2200T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15977195 | |||||||
| chr4:15977220 | C | A | 4 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0002g0083 others(1): Show |
4 | HG01243.hp1 HG02630.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2582+2175G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15977220 | |||||||
| chr4:15977422 | C | T | 1 | a0001c0003t0011g0013 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2582+1973G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15977422 | |||||||
| chr4:15977439 | G | C | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | NA19002.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.2582+1956C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15977439 | |||||||
| chr4:15977493 | T | C | 1 | a0001c0001t0012g0223 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2582+1902A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15977493 | |||||||
| chr4:15977793 | T | C | 5 | a0001c0001t0001g0190 a0001c0001t0002g0258 a0001c0001t0002g0259 others(2): Show |
5 | HG00738.hp2 HG06807.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.2582+1602A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15977793 | |||||||
| chr4:15977800 | G | A | 5 | a0001c0001t0001g0188 a0001c0002t0001g0175 a0003c0007t0001g0174 others(2): Show |
5 | HG00438.hp1 HG01993.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.2582+1595C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15977800 | |||||||
| chr4:15977834 | G | A | 18 | a0001c0001t0001g0137 a0001c0001t0001g0288 a0001c0001t0001g0299 others(15): Show |
18 | HG03225.hp1 HG03453.hp1 HG03453.hp2 others(15): Show |
intron_variant | MODIFIER | c.2582+1561C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15977834 | |||||||
| chr4:15977850 | G | A | 4 | a0001c0001t0001g0067 a0001c0001t0001g0360 a0001c0001t0001g0361 others(1): Show |
4 | NA18949.hp2 NA18960.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.2582+1545C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15977850 | |||||||
| chr4:15977859 | A | T | 2 | a0001c0001t0004g0081 a0001c0001t0005g0036 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2582+1536T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15977859 | |||||||
| chr4:15977887 | C | T | 60 | a0001c0001t0001g0042 a0001c0001t0001g0061 a0001c0001t0001g0091 others(57): Show |
61 | HG00323.hp1 HG00438.hp2 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.2582+1508G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15977887 | |||||||
| chr4:15977998 | A | G | 70 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0056 others(67): Show |
71 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.2582+1397T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15977998 | |||||||
| chr4:15978717 | G | A | 4 | a0001c0001t0002g0297 a0001c0004t0001g0046 a0001c0004t0002g0047 others(1): Show |
4 | HG02145.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2582+678C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15978717 | |||||||
| chr4:15978831 | C | A | 127 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0024 others(124): Show |
129 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.2582+564G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15978831 | |||||||
| chr4:15978831 | C | T | 2 | a0001c0001t0002g0052 a0001c0003t0011g0013 |
2 | HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2582+564G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15978831 | |||||||
| chr4:15978953 | T | C | 4 | a0001c0001t0001g0333 a0001c0001t0002g0326 a0001c0001t0004g0123 others(1): Show |
4 | HG00323.hp2 HG01099.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.2582+442A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15978953 | |||||||
| chr4:15978990 | AAAAGGAA others(5): Show |
A | 2 | a0001c0001t0001g0035 a0001c0001t0002g0086 |
2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2582+393_2582+404d others(14): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15978990 | |||||||
| chr4:15978990 | AAAAGGAA others(9): Show |
A | 4 | a0001c0001t0001g0106 a0001c0001t0001g0350 a0001c0001t0002g0342 others(1): Show |
4 | HG02572.hp2 HG03486.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2582+389_2582+404d others(18): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15978990 | |||||||
| chr4:15978991 | A | G | 1 | a0001c0018t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2582+404T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15978991 | |||||||
| chr4:15979006 | G | A | 1 | a0001c0018t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2582+389C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15979006 | |||||||
| chr4:15979010 | A | AGAAG | 182 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0039 others(179): Show |
184 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.2582+381_2582+384d others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15979010 | |||||||
| chr4:15979010 | A | G | 7 | a0001c0001t0001g0035 a0001c0001t0001g0106 a0001c0001t0001g0350 others(4): Show |
7 | HG02572.hp2 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2582+385T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15979010 | |||||||
| chr4:15979038 | A | G | 4 | a0001c0001t0001g0307 a0001c0001t0002g0239 a0001c0001t0003g0225 others(1): Show |
4 | HG00323.hp1 HG01071.hp2 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.2582+357T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15979038 | |||||||
| chr4:15979210 | G | A | 1 | a0003c0007t0001g0174 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2582+185C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15979210 | |||||||
| chr4:15979262 | G | C | 1 | a0001c0001t0001g0042 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2582+133C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15979262 | |||||||
| chr4:15979283 | T | C | 1 | a0001c0001t0002g0289 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2582+112A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15979283 | |||||||
| chr4:15979352 | G | A | 52 | a0001c0001t0001g0042 a0001c0001t0001g0061 a0001c0001t0001g0094 others(49): Show |
53 | HG00323.hp1 HG00438.hp2 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.2582+43C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15979352 | |||||||
| chr4:15979366 | C | G | 4 | a0001c0001t0002g0297 a0001c0004t0001g0046 a0001c0004t0002g0047 others(1): Show |
4 | HG02145.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2582+29G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15979366 | |||||||
| chr4:15979367 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2582+28C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 26/27 | chr4 | 15979367 | |||||||
| chr4:15979706 | A | T | 1 | a0001c0001t0001g0188 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2513+175T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 25/27 | chr4 | 15979706 | |||||||
| chr4:15979709 | C | T | 129 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0043 others(126): Show |
130 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.2513+172G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 25/27 | chr4 | 15979709 | |||||||
| chr4:15979987 | TC | T | 6 | a0001c0001t0001g0050 a0001c0001t0004g0044 a0001c0001t0004g0298 others(3): Show |
6 | HG02559.hp2 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2490-84delG | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 24/27 | chr4 | 15979987 | |||||||
| chr4:15980120 | A | G | 1 | a0001c0001t0001g0299 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2490-216T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 24/27 | chr4 | 15980120 | |||||||
| chr4:15980251 | A | C | 4 | a0001c0001t0002g0258 a0001c0001t0002g0259 a0001c0002t0004g0268 others(1): Show |
4 | HG00738.hp2 HG03579.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.2489+171T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 24/27 | chr4 | 15980251 | |||||||
| chr4:15980262 | G | GA | 274 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0024 others(271): Show |
277 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(274): Show |
intron_variant | MODIFIER | c.2489+159dupT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 24/27 | chr4 | 15980262 | |||||||
| chr4:15980303 | T | TA | 84 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0035 others(81): Show |
85 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.2489+118dupT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 24/27 | chr4 | 15980303 | |||||||
| chr4:15980303 | TA | T | 180 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0043 others(177): Show |
182 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.2489+118delT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 24/27 | chr4 | 15980303 | |||||||
| chr4:15980540 | A | AG | 112 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0056 others(109): Show |
113 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(110): Show |
splice_region_variant&intron_variant | LOW | c.2374-4dupC | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980540 | |||||||
| chr4:15980543 | A | G | 68 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0051 others(65): Show |
69 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(66): Show |
splice_region_variant&intron_variant | LOW | c.2374-6T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980543 | |||||||
| chr4:15980553 | C | T | 2 | a0001c0001t0002g0052 a0001c0003t0011g0013 |
2 | HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2374-16G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980553 | |||||||
| chr4:15980606 | AT | A | 52 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0113 others(49): Show |
52 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.2374-70delA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980606 | |||||||
| chr4:15980606 | ATT | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0035 others(69): Show |
73 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.2374-71_2374-70del others(2): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980606 | |||||||
| chr4:15980606 | ATTT | A | 10 | a0001c0001t0001g0301 a0001c0001t0001g0357 a0001c0001t0004g0145 others(7): Show |
10 | HG01099.hp1 HG02145.hp1 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.2374-72_2374-70del others(3): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980606 | |||||||
| chr4:15980606 | ATTTT | A | 6 | a0001c0001t0001g0033 a0001c0001t0001g0085 a0001c0001t0001g0137 others(3): Show |
6 | HG02559.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2374-73_2374-70del others(4): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980606 | |||||||
| chr4:15980606 | ATTTTT | A | 9 | a0001c0001t0002g0297 a0001c0001t0004g0053 a0001c0001t0009g0076 others(6): Show |
9 | HG02109.hp1 HG02145.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.2374-74_2374-70del others(5): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980606 | |||||||
| chr4:15980606 | ATTTTTT | A | 82 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0050 others(79): Show |
83 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.2374-75_2374-70del others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980606 | |||||||
| chr4:15980606 | ATTTTTTT | A | 82 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0095 others(79): Show |
83 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.2374-76_2374-70del others(7): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980606 | |||||||
| chr4:15980606 | ATTTTTTT others(1): Show |
A | 8 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0004g0081 others(5): Show |
8 | HG02622.hp2 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2374-77_2374-70del others(8): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980606 | |||||||
| chr4:15980612 | T | A | 8 | a0001c0001t0002g0297 a0001c0001t0009g0076 a0001c0002t0001g0184 others(5): Show |
8 | HG02109.hp1 HG02145.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.2374-75A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980612 | |||||||
| chr4:15980613 | T | A | 82 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0050 others(79): Show |
83 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.2374-76A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980613 | |||||||
| chr4:15980614 | T | A | 82 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0001c0001t0001g0095 others(79): Show |
83 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.2374-77A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980614 | |||||||
| chr4:15980615 | T | A | 8 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0004g0081 others(5): Show |
8 | HG02622.hp2 HG02818.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2374-78A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980615 | |||||||
| chr4:15980639 | T | A | 5 | a0001c0001t0003g0148 a0001c0001t0003g0150 a0001c0001t0003g0291 others(2): Show |
5 | HG01106.hp1 HG01346.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.2374-102A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980639 | |||||||
| chr4:15980700 | T | C | 1 | a0001c0005t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2374-163A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980700 | |||||||
| chr4:15980759 | G | A | 11 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0002g0115 others(8): Show |
11 | HG01109.hp2 HG01243.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.2374-222C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980759 | |||||||
| chr4:15980857 | C | T | 91 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0056 others(88): Show |
92 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.2374-320G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980857 | |||||||
| chr4:15980882 | C | T | 1 | a0007c0017t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2374-345G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980882 | |||||||
| chr4:15980946 | G | GTTAT | 10 | a0001c0001t0001g0095 a0001c0001t0001g0179 a0001c0001t0001g0195 others(7): Show |
10 | HG00609.hp1 HG02055.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.2374-413_2374-410d others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980946 | |||||||
| chr4:15980946 | G | GTTATTTA others(1): Show |
88 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0035 others(85): Show |
89 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.2374-417_2374-410d others(10): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980946 | |||||||
| chr4:15980946 | G | GTTATTTA others(5): Show |
46 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0050 others(43): Show |
47 | HG00738.hp2 HG01074.hp2 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.2374-421_2374-410d others(14): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980946 | |||||||
| chr4:15980946 | G | GTTATTTA others(9): Show |
60 | a0001c0001t0001g0051 a0001c0001t0001g0054 a0001c0001t0001g0061 others(57): Show |
60 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.2374-425_2374-410d others(18): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980946 | |||||||
| chr4:15980946 | G | GTTATTTA others(13): Show |
6 | a0001c0001t0001g0165 a0001c0001t0001g0211 a0001c0002t0001g0062 others(3): Show |
6 | HG01256.hp2 HG01258.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.2374-429_2374-410d others(22): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15980946 | |||||||
| chr4:15981007 | G | T | 8 | a0001c0001t0001g0050 a0001c0001t0001g0351 a0001c0001t0004g0044 others(5): Show |
8 | HG02559.hp2 HG02630.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.2374-470C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15981007 | |||||||
| chr4:15981036 | A | T | 1 | a0007c0017t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2374-499T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15981036 | |||||||
| chr4:15981047 | C | T | 1 | a0001c0005t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2374-510G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15981047 | |||||||
| chr4:15981105 | G | A | 4 | a0001c0001t0001g0353 a0001c0003t0001g0006 a0001c0003t0001g0010 others(1): Show |
4 | HG02622.hp2 HG02886.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2374-568C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15981105 | |||||||
| chr4:15981205 | C | T | 1 | a0001c0018t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2374-668G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15981205 | |||||||
| chr4:15981270 | G | T | 17 | a0001c0001t0001g0188 a0001c0002t0001g0100 a0001c0002t0001g0184 others(14): Show |
17 | HG00423.hp1 HG00438.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.2374-733C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15981270 | |||||||
| chr4:15981273 | A | G | 3 | a0001c0001t0002g0146 a0001c0003t0002g0008 a0001c0003t0004g0007 |
3 | HG02451.hp2 HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2374-736T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15981273 | |||||||
| chr4:15981427 | C | T | 1 | a0001c0003t0004g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2374-890G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15981427 | |||||||
| chr4:15981488 | C | T | 57 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0067 others(54): Show |
57 | HG00423.hp1 HG00438.hp1 HG01993.hp1 others(54): Show |
intron_variant | MODIFIER | c.2374-951G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15981488 | |||||||
| chr4:15981521 | G | A | 1 | a0007c0017t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2374-984C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15981521 | |||||||
| chr4:15981580 | GA | G | 112 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0056 others(109): Show |
113 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.2374-1044delT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15981580 | |||||||
| chr4:15981583 | A | G | 1 | a0001c0018t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2374-1046T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15981583 | |||||||
| chr4:15981587 | A | C | 1 | a0001c0005t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2374-1050T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15981587 | |||||||
| chr4:15981623 | T | C | 13 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0002g0115 others(10): Show |
13 | HG01109.hp2 HG01243.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.2374-1086A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15981623 | |||||||
| chr4:15981694 | T | C | 184 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0043 others(181): Show |
186 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.2374-1157A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15981694 | |||||||
| chr4:15981712 | C | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0035 others(67): Show |
71 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.2374-1175G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15981712 | |||||||
| chr4:15981728 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2374-1191G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15981728 | |||||||
| chr4:15981995 | C | T | 125 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0043 others(122): Show |
126 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2374-1458G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15981995 | |||||||
| chr4:15982176 | A | G | 186 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0043 others(183): Show |
188 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.2374-1639T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15982176 | |||||||
| chr4:15982247 | C | A | 1 | a0001c0001t0002g0180 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2374-1710G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15982247 | |||||||
| chr4:15982276 | G | A | 1 | a0001c0001t0003g0130 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2374-1739C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15982276 | |||||||
| chr4:15982321 | C | T | 10 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0002g0115 others(7): Show |
10 | HG01109.hp2 HG01243.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.2374-1784G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15982321 | |||||||
| chr4:15982410 | A | G | 180 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0043 others(177): Show |
182 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.2373+1853T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15982410 | |||||||
| chr4:15982475 | T | C | 1 | a0001c0001t0004g0053 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2373+1788A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15982475 | |||||||
| chr4:15982529 | T | C | 112 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0056 others(109): Show |
113 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.2373+1734A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15982529 | |||||||
| chr4:15982553 | G | A | 1 | a0001c0001t0003g0203 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2373+1710C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15982553 | |||||||
| chr4:15982754 | T | C | 1 | a0001c0001t0004g0053 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2373+1509A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15982754 | |||||||
| chr4:15982758 | C | T | 72 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0051 others(69): Show |
73 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.2373+1505G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15982758 | |||||||
| chr4:15982849 | G | A | 1 | a0001c0001t0002g0292 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2373+1414C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15982849 | |||||||
| chr4:15982949 | G | T | 11 | a0001c0001t0001g0024 a0001c0001t0002g0146 a0001c0001t0004g0145 others(8): Show |
11 | HG01884.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2373+1314C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15982949 | |||||||
| chr4:15983253 | C | T | 1 | a0001c0019t0005g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2373+1010G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15983253 | |||||||
| chr4:15983275 | A | C | 1 | a0001c0001t0004g0053 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2373+988T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15983275 | |||||||
| chr4:15983357 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0002g0319 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2373+906G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15983357 | |||||||
| chr4:15983387 | CAA | C | 71 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0051 others(68): Show |
72 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.2373+874_2373+875d others(4): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15983387 | |||||||
| chr4:15983430 | C | T | 54 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0061 others(51): Show |
55 | HG00323.hp1 HG00438.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.2373+833G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15983430 | |||||||
| chr4:15983585 | C | T | 1 | a0003c0007t0003g0314 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2373+678G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15983585 | |||||||
| chr4:15983690 | G | A | 1 | a0001c0001t0002g0239 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2373+573C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15983690 | |||||||
| chr4:15983739 | C | A | 1 | a0001c0005t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2373+524G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15983739 | |||||||
| chr4:15983831 | G | C | 13 | a0001c0001t0001g0050 a0001c0001t0001g0351 a0001c0001t0002g0037 others(10): Show |
13 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.2373+432C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15983831 | |||||||
| chr4:15983919 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0035 others(147): Show |
152 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.2373+344A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15983919 | |||||||
| chr4:15983969 | A | C | 1 | a0001c0018t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2373+294T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15983969 | |||||||
| chr4:15983989 | C | T | 13 | a0001c0001t0001g0050 a0001c0001t0001g0351 a0001c0001t0002g0037 others(10): Show |
13 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.2373+274G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15983989 | |||||||
| chr4:15984069 | G | A | 5 | a0001c0001t0002g0037 a0001c0001t0002g0297 a0001c0004t0001g0046 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2373+194C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15984069 | |||||||
| chr4:15984079 | G | T | 16 | a0001c0002t0001g0100 a0001c0002t0001g0184 a0001c0002t0002g0058 others(13): Show |
16 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.2373+184C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15984079 | |||||||
| chr4:15984179 | A | C | 56 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0113 others(53): Show |
56 | HG00597.hp2 HG00609.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.2373+84T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 23/27 | chr4 | 15984179 | |||||||
| chr4:15984361 | G | C | 56 | a0001c0001t0001g0021 a0001c0001t0001g0056 a0001c0001t0001g0095 others(53): Show |
57 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(54): Show |
splice_region_variant&intron_variant | LOW | c.2281-6C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15984361 | |||||||
| chr4:15984378 | A | C | 6 | a0001c0001t0001g0084 a0001c0001t0002g0005 a0001c0001t0002g0358 others(3): Show |
6 | HG02257.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2281-23T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15984378 | |||||||
| chr4:15984419 | G | A | 363 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(360): Show |
366 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(363): Show |
intron_variant | MODIFIER | c.2281-64C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15984419 | |||||||
| chr4:15984490 | T | C | 367 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(364): Show |
370 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(367): Show |
intron_variant | MODIFIER | c.2281-135A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15984490 | |||||||
| chr4:15984490 | T | G | 1 | a0001c0001t0002g0244 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2281-135A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15984490 | |||||||
| chr4:15984519 | G | A | 2 | a0001c0001t0002g0115 a0001c0001t0004g0034 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.2281-164C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15984519 | |||||||
| chr4:15984545 | T | A | 1 | a0001c0001t0004g0141 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2281-190A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15984545 | |||||||
| chr4:15984563 | G | T | 365 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(362): Show |
368 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(365): Show |
intron_variant | MODIFIER | c.2281-208C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15984563 | |||||||
| chr4:15984616 | T | G | 4 | a0001c0001t0002g0343 a0001c0001t0002g0354 a0001c0001t0005g0346 others(1): Show |
4 | HG02258.hp2 HG02486.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2281-261A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15984616 | |||||||
| chr4:15984711 | A | C | 43 | a0001c0001t0001g0056 a0001c0001t0001g0095 a0001c0001t0001g0098 others(40): Show |
44 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.2281-356T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15984711 | |||||||
| chr4:15984985 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2281-630C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15984985 | |||||||
| chr4:15985026 | C | T | 75 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0051 others(72): Show |
76 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.2281-671G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15985026 | |||||||
| chr4:15985108 | G | A | 1 | a0001c0001t0003g0124 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2280+652C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15985108 | |||||||
| chr4:15985116 | A | G | 1 | a0001c0019t0005g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2280+644T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15985116 | |||||||
| chr4:15985328 | A | T | 1 | a0001c0018t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2280+432T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15985328 | |||||||
| chr4:15985334 | A | T | 1 | a0001c0001t0004g0069 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2280+426T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15985334 | |||||||
| chr4:15985337 | G | T | 4 | a0001c0001t0002g0343 a0001c0001t0002g0354 a0001c0001t0005g0346 others(1): Show |
4 | HG02258.hp2 HG02486.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2280+423C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15985337 | |||||||
| chr4:15985346 | A | G | 11 | a0001c0001t0002g0244 a0001c0001t0003g0040 a0001c0001t0003g0041 others(8): Show |
11 | HG01952.hp2 NA18944.hp1 NA18966.hp2 others(8): Show |
intron_variant | MODIFIER | c.2280+414T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15985346 | |||||||
| chr4:15985422 | C | T | 1 | a0001c0004t0002g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2280+338G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15985422 | |||||||
| chr4:15985472 | G | A | 1 | a0001c0001t0002g0303 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2280+288C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15985472 | |||||||
| chr4:15985489 | T | C | 13 | a0001c0001t0001g0050 a0001c0001t0001g0351 a0001c0001t0002g0037 others(10): Show |
13 | HG02145.hp2 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.2280+271A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15985489 | |||||||
| chr4:15985520 | G | C | 17 | a0001c0001t0002g0134 a0001c0002t0001g0100 a0001c0002t0001g0184 others(14): Show |
17 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.2280+240C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15985520 | |||||||
| chr4:15985527 | G | A | 3 | a0001c0001t0004g0081 a0001c0001t0005g0036 a0001c0019t0005g0018 |
3 | HG02818.hp2 NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2280+233C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15985527 | |||||||
| chr4:15985711 | A | G | 8 | a0001c0001t0001g0084 a0001c0001t0002g0005 a0001c0001t0002g0052 others(5): Show |
8 | HG02257.hp1 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2280+49T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15985711 | |||||||
| chr4:15985725 | C | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0151 others(24): Show |
28 | HG00544.hp2 HG01496.hp1 HG01993.hp2 others(25): Show |
intron_variant | MODIFIER | c.2280+35G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 22/27 | chr4 | 15985725 | |||||||
| chr4:15985886 | T | TTTAAGTA others(35): Show |
315 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0023 others(312): Show |
318 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(315): Show |
intron_variant | MODIFIER | c.2212-59_2212-58ins others(42): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 21/27 | chr4 | 15985886 | |||||||
| chr4:15985886 | T | TTTAAGTA others(72): Show |
1 | a0001c0003t0004g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2212-59_2212-58ins others(79): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 21/27 | chr4 | 15985886 | |||||||
| chr4:15985889 | T | A | 316 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0023 others(313): Show |
319 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(316): Show |
intron_variant | MODIFIER | c.2212-61A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 21/27 | chr4 | 15985889 | |||||||
| chr4:15985903 | G | A | 1 | a0001c0001t0002g0232 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2211+54C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 21/27 | chr4 | 15985903 | |||||||
| chr4:15985915 | T | A | 1 | a0010c0015t0003g0093 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.2211+42A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 21/27 | chr4 | 15985915 | |||||||
| chr4:15985927 | G | A | 2 | a0001c0001t0002g0111 a0004c0008t0002g0077 |
2 | HG01934.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.2211+30C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 21/27 | chr4 | 15985927 | |||||||
| chr4:15986085 | T | C | 1 | a0001c0001t0003g0305 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2131-48A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15986085 | |||||||
| chr4:15986112 | A | C | 5 | a0001c0001t0001g0084 a0001c0001t0002g0005 a0001c0001t0002g0358 others(2): Show |
5 | HG02257.hp1 HG02615.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2131-75T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15986112 | |||||||
| chr4:15986119 | G | A | 1 | a0009c0014t0002g0194 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2131-82C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15986119 | |||||||
| chr4:15986132 | G | C | 16 | a0001c0002t0001g0100 a0001c0002t0001g0184 a0001c0002t0002g0058 others(13): Show |
16 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.2131-95C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15986132 | |||||||
| chr4:15986184 | G | C | 367 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(364): Show |
370 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(367): Show |
intron_variant | MODIFIER | c.2131-147C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15986184 | |||||||
| chr4:15986302 | G | T | 29 | a0001c0001t0001g0024 a0001c0001t0001g0067 a0001c0001t0001g0288 others(26): Show |
29 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(26): Show |
intron_variant | MODIFIER | c.2131-265C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15986302 | |||||||
| chr4:15986385 | G | A | 1 | a0001c0001t0004g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2131-348C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15986385 | |||||||
| chr4:15986435 | A | T | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2131-398T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15986435 | |||||||
| chr4:15986465 | C | T | 4 | a0001c0001t0002g0343 a0001c0001t0002g0354 a0001c0001t0005g0346 others(1): Show |
4 | HG02258.hp2 HG02486.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2131-428G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15986465 | |||||||
| chr4:15986616 | C | T | 94 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0068 others(91): Show |
94 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.2131-579G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15986616 | |||||||
| chr4:15986856 | G | A | 1 | a0001c0001t0003g0150 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2130+807C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15986856 | |||||||
| chr4:15986874 | G | C | 367 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(364): Show |
370 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(367): Show |
intron_variant | MODIFIER | c.2130+789C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15986874 | |||||||
| chr4:15986927 | G | A | 1 | a0001c0001t0001g0299 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2130+736C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15986927 | |||||||
| chr4:15987026 | G | T | 2 | a0001c0001t0001g0084 a0011c0009t0004g0317 |
2 | HG02257.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2130+637C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15987026 | |||||||
| chr4:15987036 | T | C | 4 | a0001c0001t0002g0343 a0001c0001t0002g0354 a0001c0001t0005g0346 others(1): Show |
4 | HG02258.hp2 HG02486.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.2130+627A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15987036 | |||||||
| chr4:15987101 | C | G | 50 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0050 others(47): Show |
50 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(47): Show |
intron_variant | MODIFIER | c.2130+562G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15987101 | |||||||
| chr4:15987115 | A | C | 1 | a0001c0001t0001g0357 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2130+548T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15987115 | |||||||
| chr4:15987143 | C | T | 1 | a0007c0017t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2130+520G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15987143 | |||||||
| chr4:15987208 | T | C | 4 | a0001c0001t0001g0105 a0001c0001t0002g0083 a0001c0001t0004g0015 others(1): Show |
4 | HG02717.hp2 HG02897.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.2130+455A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15987208 | |||||||
| chr4:15987243 | C | A | 1 | a0001c0001t0004g0053 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2130+420G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15987243 | |||||||
| chr4:15987290 | T | C | 2 | a0001c0001t0003g0233 a0001c0001t0003g0318 |
2 | HG00735.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.2130+373A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15987290 | |||||||
| chr4:15987339 | C | T | 1 | a0001c0001t0002g0354 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2130+324G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15987339 | |||||||
| chr4:15987567 | TC | T | 56 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0061 others(53): Show |
57 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.2130+95delG | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15987567 | |||||||
| chr4:15987568 | C | T | 255 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(252): Show |
257 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(254): Show |
intron_variant | MODIFIER | c.2130+95G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15987568 | |||||||
| chr4:15987592 | C | G | 1 | a0007c0017t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2130+71G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15987592 | |||||||
| chr4:15987603 | C | G | 1 | a0003c0007t0002g0236 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2130+60G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 20/27 | chr4 | 15987603 | |||||||
| chr4:15987749 | T | C | 2 | a0001c0001t0006g0030 a0001c0001t0006g0032 |
2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2077-33A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15987749 | |||||||
| chr4:15987799 | T | C | 1 | a0001c0001t0002g0240 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2077-83A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15987799 | |||||||
| chr4:15987877 | C | CT | 168 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0024 others(165): Show |
170 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.2077-162dupA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15987877 | |||||||
| chr4:15987877 | C | CTT | 39 | a0001c0001t0001g0023 a0001c0001t0001g0068 a0001c0001t0001g0122 others(36): Show |
39 | HG00544.hp1 HG00597.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.2077-163_2077-162d others(4): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15987877 | |||||||
| chr4:15987877 | CT | C | 35 | a0001c0001t0001g0033 a0001c0001t0001g0050 a0001c0001t0001g0085 others(32): Show |
35 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.2077-162delA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15987877 | |||||||
| chr4:15988031 | C | A | 2 | a0001c0001t0001g0021 a0001c0001t0002g0319 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2077-315G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15988031 | |||||||
| chr4:15988037 | C | T | 56 | a0001c0001t0001g0021 a0001c0001t0001g0056 a0001c0001t0001g0095 others(53): Show |
57 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.2077-321G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15988037 | |||||||
| chr4:15988066 | CG | C | 5 | a0001c0001t0002g0037 a0001c0001t0002g0297 a0001c0004t0001g0046 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2077-351delC | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15988066 | |||||||
| chr4:15988167 | C | T | 8 | a0001c0001t0001g0084 a0001c0001t0002g0005 a0001c0001t0002g0052 others(5): Show |
8 | HG02257.hp1 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2077-451G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15988167 | |||||||
| chr4:15988168 | G | T | 1 | a0001c0001t0002g0172 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2077-452C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15988168 | |||||||
| chr4:15988377 | G | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0023 others(207): Show |
212 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.2077-661C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15988377 | |||||||
| chr4:15988401 | C | G | 315 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(312): Show |
318 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(315): Show |
intron_variant | MODIFIER | c.2077-685G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15988401 | |||||||
| chr4:15988432 | C | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0023 others(207): Show |
212 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.2077-716G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15988432 | |||||||
| chr4:15988433 | A | G | 315 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(312): Show |
318 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(315): Show |
intron_variant | MODIFIER | c.2077-717T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15988433 | |||||||
| chr4:15988484 | G | A | 1 | a0001c0002t0001g0336 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2077-768C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15988484 | |||||||
| chr4:15988586 | A | G | 1 | a0001c0003t0002g0012 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2077-870T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15988586 | |||||||
| chr4:15988793 | CA | C | 69 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0051 others(66): Show |
70 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.2076+938delT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15988793 | |||||||
| chr4:15988849 | C | T | 69 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0051 others(66): Show |
70 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.2076+883G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15988849 | |||||||
| chr4:15988852 | G | C | 1 | a0001c0001t0003g0313 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2076+880C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15988852 | |||||||
| chr4:15989160 | A | G | 1 | a0001c0001t0004g0145 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2076+572T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15989160 | |||||||
| chr4:15989392 | A | C | 60 | a0001c0001t0001g0021 a0001c0001t0001g0056 a0001c0001t0001g0095 others(57): Show |
61 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.2076+340T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15989392 | |||||||
| chr4:15989403 | G | A | 1 | a0001c0004t0004g0312 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2076+329C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15989403 | |||||||
| chr4:15989544 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2076+188C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15989544 | |||||||
| chr4:15989652 | G | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0023 others(202): Show |
207 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.2076+80C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 19/27 | chr4 | 15989652 | |||||||
| chr4:15989976 | T | C | 328 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(325): Show |
331 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(328): Show |
intron_variant | MODIFIER | c.1984-152A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15989976 | |||||||
| chr4:15990168 | T | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0023 others(250): Show |
256 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.1984-344A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15990168 | |||||||
| chr4:15990421 | G | A | 2 | a0001c0001t0002g0172 a0001c0001t0002g0371 |
2 | HG02165.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1984-597C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15990421 | |||||||
| chr4:15990460 | T | C | 1 | a0001c0002t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1984-636A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15990460 | |||||||
| chr4:15990499 | C | G | 4 | a0001c0001t0004g0081 a0001c0001t0005g0036 a0001c0018t0001g0215 others(1): Show |
4 | HG02818.hp2 HG03195.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1984-675G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15990499 | |||||||
| chr4:15990589 | T | C | 2 | a0001c0001t0002g0115 a0001c0001t0004g0034 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1983+633A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15990589 | |||||||
| chr4:15990677 | G | A | 4 | a0001c0001t0004g0081 a0001c0001t0005g0036 a0001c0018t0001g0215 others(1): Show |
4 | HG02818.hp2 HG03195.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1983+545C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15990677 | |||||||
| chr4:15990680 | C | A | 5 | a0001c0001t0002g0037 a0001c0001t0002g0297 a0001c0004t0001g0046 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1983+542G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15990680 | |||||||
| chr4:15990685 | C | T | 2 | a0001c0001t0002g0134 a0001c0002t0002g0181 |
2 | HG02080.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1983+537G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15990685 | |||||||
| chr4:15990727 | C | G | 1 | a0001c0001t0001g0307 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1983+495G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15990727 | |||||||
| chr4:15990793 | C | A | 17 | a0001c0001t0002g0134 a0001c0002t0001g0100 a0001c0002t0001g0184 others(14): Show |
17 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.1983+429G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15990793 | |||||||
| chr4:15990843 | A | T | 1 | a0001c0002t0003g0285 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1983+379T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15990843 | |||||||
| chr4:15990863 | C | T | 326 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(323): Show |
329 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(326): Show |
intron_variant | MODIFIER | c.1983+359G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15990863 | |||||||
| chr4:15990872 | A | G | 1 | a0001c0001t0003g0038 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1983+350T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15990872 | |||||||
| chr4:15990912 | C | T | 4 | a0001c0001t0002g0343 a0001c0001t0002g0354 a0001c0001t0005g0346 others(1): Show |
4 | HG02258.hp2 HG02486.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1983+310G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15990912 | |||||||
| chr4:15990915 | T | C | 320 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0023 others(317): Show |
323 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(320): Show |
intron_variant | MODIFIER | c.1983+307A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15990915 | |||||||
| chr4:15991031 | C | T | 43 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0068 others(40): Show |
43 | HG00544.hp1 HG00735.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.1983+191G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15991031 | |||||||
| chr4:15991079 | C | T | 48 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0068 others(45): Show |
48 | HG00544.hp1 HG00735.hp1 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.1983+143G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15991079 | |||||||
| chr4:15991160 | A | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1983+62T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15991160 | |||||||
| chr4:15991179 | A | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(47): Show |
51 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1983+43T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15991179 | |||||||
| chr4:15991208 | C | T | 50 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(47): Show |
51 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1983+14G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 18/27 | chr4 | 15991208 | |||||||
| chr4:15991490 | C | G | 1 | a0001c0001t0003g0266 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1912-197G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15991490 | |||||||
| chr4:15991524 | A | G | 1 | a0001c0001t0004g0031 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1912-231T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15991524 | |||||||
| chr4:15991526 | A | C | 13 | a0001c0001t0001g0054 a0001c0001t0001g0105 a0001c0001t0002g0083 others(10): Show |
13 | HG01109.hp2 HG01346.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1912-233T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15991526 | |||||||
| chr4:15991563 | A | G | 1 | a0001c0002t0003g0192 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1912-270T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15991563 | |||||||
| chr4:15991584 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1912-291A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15991584 | |||||||
| chr4:15991589 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1912-296G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15991589 | |||||||
| chr4:15991595 | CT | C | 9 | a0001c0001t0001g0084 a0001c0001t0002g0005 a0001c0001t0002g0052 others(6): Show |
9 | HG02257.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1912-303delA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15991595 | |||||||
| chr4:15991656 | C | T | 4 | a0001c0001t0002g0343 a0001c0001t0002g0354 a0001c0001t0005g0346 others(1): Show |
4 | HG02258.hp2 HG02486.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1912-363G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15991656 | |||||||
| chr4:15991768 | A | C | 1 | a0001c0016t0001g0143 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1912-475T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15991768 | |||||||
| chr4:15991809 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1911+439C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15991809 | |||||||
| chr4:15991865 | A | G | 325 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(322): Show |
328 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(325): Show |
intron_variant | MODIFIER | c.1911+383T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15991865 | |||||||
| chr4:15991875 | G | A | 1 | a0001c0002t0001g0336 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1911+373C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15991875 | |||||||
| chr4:15991884 | C | T | 1 | a0001c0004t0002g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1911+364G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15991884 | |||||||
| chr4:15991930 | G | A | 1 | a0001c0001t0004g0053 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1911+318C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15991930 | |||||||
| chr4:15991934 | C | CA | 29 | a0001c0001t0001g0050 a0001c0001t0001g0095 a0001c0001t0001g0109 others(26): Show |
29 | HG00423.hp1 HG00423.hp2 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.1911+313dupT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15991934 | |||||||
| chr4:15991934 | CA | C | 9 | a0001c0001t0001g0110 a0001c0001t0004g0053 a0001c0001t0004g0331 others(6): Show |
9 | HG01167.hp1 HG02015.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.1911+313delT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15991934 | |||||||
| chr4:15991934 | CAA | C | 31 | a0001c0001t0001g0068 a0001c0001t0001g0162 a0001c0001t0001g0170 others(28): Show |
31 | HG00438.hp2 HG00597.hp1 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.1911+312_1911+313d others(4): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15991934 | |||||||
| chr4:15991934 | CAAA | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0023 others(167): Show |
172 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.1911+311_1911+313d others(5): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15991934 | |||||||
| chr4:15991934 | CAAAA | C | 22 | a0001c0001t0001g0054 a0001c0001t0001g0084 a0001c0001t0001g0105 others(19): Show |
22 | HG00438.hp1 HG01109.hp2 HG01346.hp2 others(19): Show |
intron_variant | MODIFIER | c.1911+310_1911+313d others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15991934 | |||||||
| chr4:15991934 | CAAAAAAA others(3): Show |
C | 7 | a0001c0001t0002g0146 a0001c0002t0004g0026 a0001c0002t0004g0027 others(4): Show |
7 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1911+304_1911+313d others(12): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15991934 | |||||||
| chr4:15992119 | A | T | 29 | a0001c0001t0001g0024 a0001c0001t0001g0067 a0001c0001t0001g0288 others(26): Show |
29 | HG01884.hp2 HG02257.hp2 HG02451.hp2 others(26): Show |
intron_variant | MODIFIER | c.1911+129T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15992119 | |||||||
| chr4:15992234 | C | T | 5 | a0001c0001t0001g0351 a0001c0001t0001g0360 a0001c0001t0001g0361 others(2): Show |
5 | HG03453.hp2 HG03486.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.1911+14G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15992234 | |||||||
| chr4:15992241 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19079.hp2 | splice_region_variant&intron_variant | LOW | c.1911+7C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 17/27 | chr4 | 15992241 | |||||||
| chr4:15992396 | G | A | 3 | a0001c0001t0002g0258 a0001c0001t0002g0259 a0001c0002t0004g0268 |
3 | HG00738.hp2 HG06807.hp2 NA20752.hp1 |
splice_region_variant&intron_variant | LOW | c.1768-5C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15992396 | |||||||
| chr4:15992479 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1768-88C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15992479 | |||||||
| chr4:15992570 | T | C | 44 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0068 others(41): Show |
44 | HG00544.hp1 HG00597.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.1768-179A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15992570 | |||||||
| chr4:15992763 | C | T | 1 | a0001c0003t0011g0013 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1768-372G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15992763 | |||||||
| chr4:15992788 | G | A | 1 | a0001c0001t0002g0232 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1768-397C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15992788 | |||||||
| chr4:15992820 | G | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(319): Show |
325 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(322): Show |
intron_variant | MODIFIER | c.1768-429C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15992820 | |||||||
| chr4:15992822 | C | A | 221 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0023 others(218): Show |
223 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.1768-431G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15992822 | |||||||
| chr4:15992891 | T | G | 8 | a0001c0001t0001g0084 a0001c0001t0002g0005 a0001c0001t0002g0052 others(5): Show |
8 | HG02257.hp1 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1768-500A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15992891 | |||||||
| chr4:15993035 | G | A | 1 | a0002c0006t0002g0073 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1768-644C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15993035 | |||||||
| chr4:15993075 | G | A | 4 | a0001c0001t0004g0081 a0001c0001t0005g0036 a0001c0018t0001g0215 others(1): Show |
4 | HG02818.hp2 HG03195.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1768-684C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15993075 | |||||||
| chr4:15993085 | T | C | 1 | a0001c0001t0003g0254 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1768-694A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15993085 | |||||||
| chr4:15993087 | T | C | 1 | a0007c0017t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1768-696A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15993087 | |||||||
| chr4:15993138 | C | T | 45 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0043 others(42): Show |
45 | HG00423.hp1 HG01243.hp1 HG01993.hp1 others(42): Show |
intron_variant | MODIFIER | c.1768-747G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15993138 | |||||||
| chr4:15993296 | A | C | 1 | a0001c0004t0002g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1767+691T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15993296 | |||||||
| chr4:15993317 | G | A | 88 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0043 others(85): Show |
89 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1767+670C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15993317 | |||||||
| chr4:15993361 | G | A | 42 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0068 others(39): Show |
42 | HG00544.hp1 HG00735.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.1767+626C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15993361 | |||||||
| chr4:15993418 | G | A | 1 | a0007c0017t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1767+569C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15993418 | |||||||
| chr4:15993426 | C | T | 1 | a0001c0019t0005g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1767+561G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15993426 | |||||||
| chr4:15993464 | G | A | 1 | a0001c0001t0004g0053 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1767+523C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15993464 | |||||||
| chr4:15993502 | A | G | 13 | a0001c0001t0001g0054 a0001c0001t0001g0105 a0001c0001t0002g0083 others(10): Show |
13 | HG01109.hp2 HG01346.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1767+485T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15993502 | |||||||
| chr4:15993508 | T | C | 1 | a0001c0001t0007g0166 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1767+479A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15993508 | |||||||
| chr4:15993551 | TAAGG | T | 8 | a0001c0001t0001g0084 a0001c0001t0002g0005 a0001c0001t0002g0052 others(5): Show |
8 | HG02257.hp1 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1767+432_1767+435d others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15993551 | |||||||
| chr4:15993691 | C | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0035 others(156): Show |
161 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.1767+296G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15993691 | |||||||
| chr4:15993811 | G | A | 1 | a0001c0002t0002g0214 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1767+176C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15993811 | |||||||
| chr4:15993895 | C | T | 10 | a0001c0001t0002g0037 a0001c0001t0002g0297 a0001c0001t0004g0053 others(7): Show |
10 | HG02145.hp2 HG02258.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1767+92G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15993895 | |||||||
| chr4:15993960 | G | A | 6 | a0001c0001t0001g0033 a0001c0001t0001g0085 a0001c0001t0001g0137 others(3): Show |
6 | HG02559.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1767+27C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 16/27 | chr4 | 15993960 | |||||||
| chr4:15994074 | G | A | 1 | a0001c0001t0004g0025 | 1 | HG03516.hp2 | splice_region_variant&intron_variant | LOW | c.1683-3C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15994074 | |||||||
| chr4:15994243 | T | G | 2 | a0001c0001t0002g0115 a0001c0001t0004g0034 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1683-172A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15994243 | |||||||
| chr4:15994351 | C | T | 4 | a0001c0001t0004g0081 a0001c0001t0005g0036 a0001c0018t0001g0215 others(1): Show |
4 | HG02818.hp2 HG03195.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1683-280G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15994351 | |||||||
| chr4:15994365 | A | T | 1 | a0001c0001t0001g0280 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1683-294T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15994365 | |||||||
| chr4:15994498 | C | T | 8 | a0001c0001t0001g0084 a0001c0001t0002g0005 a0001c0001t0002g0052 others(5): Show |
8 | HG02257.hp1 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1683-427G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15994498 | |||||||
| chr4:15994527 | G | A | 1 | a0001c0001t0004g0031 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1683-456C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15994527 | |||||||
| chr4:15994807 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1683-736G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15994807 | |||||||
| chr4:15995137 | A | G | 17 | a0001c0001t0002g0134 a0001c0002t0001g0100 a0001c0002t0001g0184 others(14): Show |
17 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.1683-1066T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15995137 | |||||||
| chr4:15995150 | G | C | 7 | a0001c0001t0002g0146 a0001c0002t0004g0026 a0001c0002t0004g0027 others(4): Show |
7 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1683-1079C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15995150 | |||||||
| chr4:15995322 | AGAAGAAG others(2): Show |
A | 66 | a0001c0001t0001g0021 a0001c0001t0001g0043 a0001c0001t0001g0050 others(63): Show |
67 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.1683-1260_1683-125 others(13): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15995322 | |||||||
| chr4:15995341 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1683-1270C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15995341 | |||||||
| chr4:15995474 | G | A | 42 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0068 others(39): Show |
42 | HG00544.hp1 HG00735.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.1683-1403C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15995474 | |||||||
| chr4:15995718 | A | T | 23 | a0001c0001t0001g0091 a0001c0001t0001g0102 a0001c0001t0001g0161 others(20): Show |
23 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.1683-1647T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15995718 | |||||||
| chr4:15995917 | A | G | 2 | a0001c0001t0002g0224 a0001c0001t0002g0267 |
2 | NA18939.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1683-1846T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15995917 | |||||||
| chr4:15996023 | G | A | 5 | a0001c0001t0002g0037 a0001c0001t0002g0297 a0001c0004t0001g0046 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1683-1952C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15996023 | |||||||
| chr4:15996051 | G | C | 1 | a0007c0017t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1683-1980C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15996051 | |||||||
| chr4:15996101 | A | T | 325 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(322): Show |
328 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(325): Show |
intron_variant | MODIFIER | c.1683-2030T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15996101 | |||||||
| chr4:15996208 | G | T | 5 | a0001c0001t0002g0037 a0001c0001t0002g0297 a0001c0004t0001g0046 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1683-2137C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15996208 | |||||||
| chr4:15996312 | C | T | 1 | a0001c0002t0001g0336 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1682+2073G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15996312 | |||||||
| chr4:15996372 | T | G | 8 | a0001c0001t0001g0084 a0001c0001t0002g0005 a0001c0001t0002g0052 others(5): Show |
8 | HG02257.hp1 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1682+2013A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15996372 | |||||||
| chr4:15996496 | C | T | 3 | a0001c0002t0002g0153 a0001c0002t0002g0156 a0001c0002t0002g0214 |
3 | NA18966.hp1 NA18968.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1682+1889G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15996496 | |||||||
| chr4:15996512 | AAAAT | A | 270 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0024 others(267): Show |
273 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.1682+1869_1682+187 others(8): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15996512 | |||||||
| chr4:15996821 | A | G | 4 | a0001c0001t0004g0081 a0001c0001t0005g0036 a0001c0018t0001g0215 others(1): Show |
4 | HG02818.hp2 HG03195.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1682+1564T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15996821 | |||||||
| chr4:15996847 | C | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0035 others(171): Show |
176 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1682+1538G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15996847 | |||||||
| chr4:15996976 | C | T | 4 | a0001c0001t0001g0071 a0001c0004t0002g0349 a0001c0005t0001g0216 others(1): Show |
4 | HG02622.hp1 HG02970.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1682+1409G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15996976 | |||||||
| chr4:15997175 | G | T | 1 | a0001c0001t0003g0291 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1682+1210C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15997175 | |||||||
| chr4:15997219 | CAT | C | 8 | a0001c0001t0001g0084 a0001c0001t0002g0005 a0001c0001t0002g0052 others(5): Show |
8 | HG02257.hp1 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1682+1164_1682+116 others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15997219 | |||||||
| chr4:15997282 | C | CAT | 136 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(133): Show |
138 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1682+1101_1682+110 others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15997282 | |||||||
| chr4:15997282 | C | CATAT | 26 | a0001c0001t0001g0024 a0001c0001t0001g0067 a0001c0001t0001g0106 others(23): Show |
26 | HG02257.hp2 HG02622.hp2 HG02886.hp2 others(23): Show |
intron_variant | MODIFIER | c.1682+1099_1682+110 others(8): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15997282 | |||||||
| chr4:15997309 | CAT | C | 74 | a0001c0001t0001g0021 a0001c0001t0001g0056 a0001c0001t0001g0095 others(71): Show |
75 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.1682+1074_1682+107 others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15997309 | |||||||
| chr4:15997309 | CATAT | C | 235 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0023 others(232): Show |
237 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.1682+1072_1682+107 others(8): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15997309 | |||||||
| chr4:15997374 | C | CA | 3 | a0001c0001t0002g0258 a0001c0001t0002g0259 a0001c0002t0004g0268 |
3 | HG00738.hp2 HG06807.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1682+1010dupT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15997374 | |||||||
| chr4:15997437 | T | TTA | 51 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(48): Show |
52 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1682+946_1682+947d others(4): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15997437 | |||||||
| chr4:15997587 | G | A | 65 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0054 others(62): Show |
66 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.1682+798C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15997587 | |||||||
| chr4:15997652 | A | G | 1 | a0001c0001t0002g0086 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1682+733T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15997652 | |||||||
| chr4:15997778 | T | C | 8 | a0001c0001t0001g0084 a0001c0001t0002g0005 a0001c0001t0002g0052 others(5): Show |
8 | HG02257.hp1 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.1682+607A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15997778 | |||||||
| chr4:15997792 | T | C | 1 | a0001c0001t0002g0358 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1682+593A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15997792 | |||||||
| chr4:15998043 | C | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(46): Show |
50 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.1682+342G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 15/27 | chr4 | 15998043 | |||||||
| chr4:15998494 | A | G | 1 | a0001c0001t0001g0350 | 1 | NA18906.hp2 | splice_region_variant&intron_variant | LOW | c.1579-6T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15998494 | |||||||
| chr4:15998513 | C | T | 1 | a0001c0004t0002g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1579-25G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15998513 | |||||||
| chr4:15998570 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1579-82C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15998570 | |||||||
| chr4:15998612 | G | A | 1 | a0001c0002t0002g0294 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1579-124C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15998612 | |||||||
| chr4:15998624 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1579-136T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15998624 | |||||||
| chr4:15998711 | T | C | 43 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0068 others(40): Show |
43 | HG00544.hp1 HG00597.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1579-223A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15998711 | |||||||
| chr4:15998769 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0035 others(105): Show |
109 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.1579-281C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15998769 | |||||||
| chr4:15998803 | C | G | 1 | a0001c0001t0002g0066 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1579-315G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15998803 | |||||||
| chr4:15998809 | G | A | 1 | a0001c0001t0004g0031 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1579-321C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15998809 | |||||||
| chr4:15998828 | G | A | 66 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0054 others(63): Show |
67 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1579-340C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15998828 | |||||||
| chr4:15998919 | A | G | 325 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(322): Show |
328 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(325): Show |
intron_variant | MODIFIER | c.1579-431T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15998919 | |||||||
| chr4:15999057 | T | G | 6 | a0001c0001t0001g0084 a0001c0001t0002g0005 a0001c0001t0002g0358 others(3): Show |
6 | HG02257.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1579-569A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999057 | |||||||
| chr4:15999200 | T | G | 7 | a0001c0001t0002g0343 a0001c0001t0002g0354 a0001c0001t0004g0031 others(4): Show |
7 | HG02258.hp2 HG02486.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1579-712A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999200 | |||||||
| chr4:15999264 | G | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(44): Show |
48 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.1579-776C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999264 | |||||||
| chr4:15999267 | C | T | 1 | a0001c0001t0002g0120 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1579-779G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999267 | |||||||
| chr4:15999270 | G | A | 11 | a0001c0001t0002g0037 a0001c0001t0002g0297 a0001c0001t0004g0053 others(8): Show |
11 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1579-782C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999270 | |||||||
| chr4:15999286 | G | A | 1 | a0001c0004t0004g0312 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1579-798C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999286 | |||||||
| chr4:15999287 | T | C | 8 | a0001c0001t0002g0146 a0001c0002t0004g0026 a0001c0002t0004g0027 others(5): Show |
8 | HG01884.hp2 HG02451.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1579-799A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999287 | |||||||
| chr4:15999328 | G | A | 19 | a0001c0001t0002g0037 a0001c0001t0002g0146 a0001c0001t0002g0297 others(16): Show |
19 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1579-840C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999328 | |||||||
| chr4:15999395 | C | T | 1 | a0001c0001t0003g0003 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1579-907G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999395 | |||||||
| chr4:15999457 | T | A | 2 | a0001c0001t0004g0031 a0001c0004t0004g0312 |
2 | HG03130.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1579-969A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999457 | |||||||
| chr4:15999470 | T | TA | 7 | a0001c0001t0001g0039 a0001c0001t0001g0310 a0001c0001t0001g0337 others(4): Show |
7 | HG00735.hp2 HG03017.hp1 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.1579-983dupT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999470 | |||||||
| chr4:15999470 | TA | T | 7 | a0001c0001t0001g0162 a0001c0001t0002g0146 a0001c0001t0003g0124 others(4): Show |
7 | HG01099.hp2 HG01496.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.1579-983delT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999470 | |||||||
| chr4:15999487 | TCA | T | 6 | a0001c0001t0001g0033 a0001c0001t0001g0085 a0001c0001t0001g0137 others(3): Show |
6 | HG02559.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1579-1001_1579-100 others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999487 | |||||||
| chr4:15999512 | T | C | 1 | a0001c0001t0001g0248 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1578+984A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999512 | |||||||
| chr4:15999517 | A | T | 1 | a0001c0001t0003g0254 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1578+979T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999517 | |||||||
| chr4:15999526 | G | T | 11 | a0001c0001t0002g0037 a0001c0001t0002g0297 a0001c0001t0004g0053 others(8): Show |
11 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1578+970C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999526 | |||||||
| chr4:15999552 | G | A | 44 | a0001c0001t0001g0023 a0001c0001t0001g0068 a0001c0001t0001g0122 others(41): Show |
44 | HG00544.hp1 HG00735.hp1 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.1578+944C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999552 | |||||||
| chr4:15999584 | C | T | 21 | a0001c0001t0001g0091 a0001c0001t0001g0102 a0001c0001t0001g0161 others(18): Show |
21 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.1578+912G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999584 | |||||||
| chr4:15999616 | G | A | 6 | a0001c0001t0001g0113 a0001c0001t0002g0240 a0001c0001t0003g0241 others(3): Show |
6 | HG02056.hp2 NA18950.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1578+880C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999616 | |||||||
| chr4:15999660 | T | C | 5 | a0001c0001t0002g0037 a0001c0001t0002g0297 a0001c0004t0001g0046 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1578+836A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999660 | |||||||
| chr4:15999680 | G | A | 1 | a0001c0002t0002g0237 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1578+816C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999680 | |||||||
| chr4:15999705 | A | C | 4 | a0001c0001t0004g0081 a0001c0001t0005g0036 a0001c0018t0001g0215 others(1): Show |
4 | HG02818.hp2 HG03195.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1578+791T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999705 | |||||||
| chr4:15999755 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(55): Show |
59 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1578+741T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999755 | |||||||
| chr4:15999847 | G | GA | 56 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(53): Show |
57 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.1578+648dupT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999847 | |||||||
| chr4:15999848 | A | G | 37 | a0001c0001t0001g0023 a0001c0001t0001g0068 a0001c0001t0001g0122 others(34): Show |
37 | HG00544.hp1 HG00735.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1578+648T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999848 | |||||||
| chr4:15999867 | G | A | 1 | a0001c0001t0001g0363 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1578+629C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999867 | |||||||
| chr4:15999943 | G | A | 47 | a0001c0001t0001g0056 a0001c0001t0001g0095 a0001c0001t0001g0098 others(44): Show |
48 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.1578+553C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999943 | |||||||
| chr4:15999964 | G | C | 1 | a0001c0001t0004g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1578+532C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999964 | |||||||
| chr4:15999968 | G | A | 111 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0035 others(108): Show |
113 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.1578+528C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 15999968 | |||||||
| chr4:16000048 | G | A | 6 | a0001c0001t0001g0033 a0001c0001t0001g0085 a0001c0001t0001g0137 others(3): Show |
6 | HG02559.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1578+448C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 16000048 | |||||||
| chr4:16000283 | G | A | 1 | a0002c0006t0002g0362 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1578+213C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 16000283 | |||||||
| chr4:16000290 | T | C | 37 | a0001c0001t0001g0023 a0001c0001t0001g0068 a0001c0001t0001g0122 others(34): Show |
37 | HG00544.hp1 HG00735.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1578+206A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 16000290 | |||||||
| chr4:16000300 | T | C | 1 | a0001c0001t0001g0328 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1578+196A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 16000300 | |||||||
| chr4:16000328 | A | G | 23 | a0001c0001t0001g0024 a0001c0001t0001g0067 a0001c0001t0001g0288 others(20): Show |
23 | HG02622.hp2 HG02886.hp2 HG02922.hp2 others(20): Show |
intron_variant | MODIFIER | c.1578+168T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 16000328 | |||||||
| chr4:16000389 | A | G | 1 | a0001c0003t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1578+107T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 16000389 | |||||||
| chr4:16000427 | T | C | 329 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(326): Show |
332 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(329): Show |
intron_variant | MODIFIER | c.1578+69A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 14/27 | chr4 | 16000427 | |||||||
| chr4:16000665 | T | C | 53 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0061 others(50): Show |
54 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.1455-46A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16000665 | |||||||
| chr4:16000694 | C | T | 37 | a0001c0001t0001g0023 a0001c0001t0001g0068 a0001c0001t0001g0122 others(34): Show |
37 | HG00544.hp1 HG00735.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.1455-75G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16000694 | |||||||
| chr4:16000790 | G | C | 3 | a0001c0001t0001g0050 a0001c0001t0004g0298 a0001c0003t0002g0009 |
3 | HG02559.hp2 HG02630.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1455-171C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16000790 | |||||||
| chr4:16000850 | G | T | 1 | a0001c0001t0004g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1455-231C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16000850 | |||||||
| chr4:16000919 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1455-300G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16000919 | |||||||
| chr4:16000958 | G | T | 1 | a0001c0001t0001g0278 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1455-339C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16000958 | |||||||
| chr4:16000984 | C | T | 1 | a0001c0005t0002g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1455-365G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16000984 | |||||||
| chr4:16001060 | A | G | 1 | a0007c0017t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1455-441T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16001060 | |||||||
| chr4:16001098 | C | A | 1 | a0007c0017t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1455-479G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16001098 | |||||||
| chr4:16001184 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1455-565A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16001184 | |||||||
| chr4:16001218 | G | A | 1 | a0001c0001t0005g0045 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1455-599C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16001218 | |||||||
| chr4:16001430 | C | T | 1 | a0001c0001t0004g0053 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1455-811G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16001430 | |||||||
| chr4:16001506 | G | C | 27 | a0001c0001t0001g0033 a0001c0001t0001g0085 a0001c0001t0001g0137 others(24): Show |
27 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.1455-887C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16001506 | |||||||
| chr4:16001528 | T | C | 74 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0061 others(71): Show |
75 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.1455-909A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16001528 | |||||||
| chr4:16001552 | T | C | 328 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(325): Show |
331 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(328): Show |
intron_variant | MODIFIER | c.1455-933A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16001552 | |||||||
| chr4:16001615 | C | G | 17 | a0001c0001t0002g0134 a0001c0002t0001g0100 a0001c0002t0001g0184 others(14): Show |
17 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.1455-996G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16001615 | |||||||
| chr4:16001730 | A | G | 1 | a0007c0017t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1455-1111T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16001730 | |||||||
| chr4:16002019 | C | A | 16 | a0001c0002t0001g0100 a0001c0002t0001g0184 a0001c0002t0002g0058 others(13): Show |
16 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.1455-1400G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16002019 | |||||||
| chr4:16002163 | C | T | 7 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0004g0044 others(4): Show |
7 | HG01243.hp1 HG02559.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1455-1544G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16002163 | |||||||
| chr4:16002208 | G | A | 14 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0165 others(11): Show |
14 | HG00597.hp2 HG00621.hp1 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.1455-1589C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16002208 | |||||||
| chr4:16002226 | A | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0035 others(108): Show |
113 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.1455-1607T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16002226 | |||||||
| chr4:16002336 | C | T | 2 | a0001c0001t0004g0031 a0001c0004t0004g0312 |
2 | HG03130.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1455-1717G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16002336 | |||||||
| chr4:16002465 | G | T | 2 | a0001c0001t0004g0031 a0001c0004t0004g0312 |
2 | HG03130.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1455-1846C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16002465 | |||||||
| chr4:16002481 | G | A | 1 | a0001c0002t0002g0153 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1455-1862C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16002481 | |||||||
| chr4:16002579 | A | G | 3 | a0001c0001t0001g0248 a0001c0002t0001g0245 a0001c0002t0001g0246 |
3 | HG01074.hp2 HG01975.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1455-1960T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16002579 | |||||||
| chr4:16002661 | AAAG | A | 9 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0351 others(6): Show |
9 | HG01243.hp1 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1455-2045_1455-204 others(7): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16002661 | |||||||
| chr4:16002782 | T | C | 1 | a0001c0001t0002g0048 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1455-2163A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16002782 | |||||||
| chr4:16002797 | G | T | 16 | a0001c0002t0001g0100 a0001c0002t0001g0184 a0001c0002t0002g0058 others(13): Show |
16 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.1455-2178C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16002797 | |||||||
| chr4:16002965 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(49): Show |
53 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1455-2346C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16002965 | |||||||
| chr4:16003194 | T | G | 6 | a0001c0001t0002g0037 a0001c0001t0002g0297 a0001c0004t0001g0046 others(3): Show |
6 | HG02109.hp1 HG02145.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1455-2575A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16003194 | |||||||
| chr4:16003352 | A | G | 1 | a0007c0017t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1455-2733T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16003352 | |||||||
| chr4:16003371 | T | G | 1 | a0001c0001t0004g0053 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1455-2752A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16003371 | |||||||
| chr4:16003427 | A | G | 1 | a0001c0019t0005g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1455-2808T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16003427 | |||||||
| chr4:16003438 | T | C | 74 | a0001c0001t0001g0021 a0001c0001t0001g0043 a0001c0001t0001g0050 others(71): Show |
75 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.1455-2819A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16003438 | |||||||
| chr4:16003487 | C | A | 1 | a0001c0001t0001g0113 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1455-2868G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16003487 | |||||||
| chr4:16003515 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1455-2896T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16003515 | |||||||
| chr4:16003531 | G | C | 1 | a0001c0001t0002g0164 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1455-2912C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16003531 | |||||||
| chr4:16003723 | G | A | 1 | a0001c0001t0003g0154 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1454+2815C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16003723 | |||||||
| chr4:16003751 | G | C | 45 | a0001c0001t0001g0056 a0001c0001t0001g0095 a0001c0001t0001g0098 others(42): Show |
46 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.1454+2787C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16003751 | |||||||
| chr4:16003786 | A | C | 17 | a0001c0001t0002g0134 a0001c0002t0001g0100 a0001c0002t0001g0184 others(14): Show |
17 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.1454+2752T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16003786 | |||||||
| chr4:16003803 | A | T | 7 | a0001c0001t0001g0033 a0001c0001t0001g0085 a0001c0001t0001g0137 others(4): Show |
7 | HG02559.hp1 HG02647.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1454+2735T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16003803 | |||||||
| chr4:16003824 | G | A | 1 | a0007c0017t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1454+2714C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16003824 | |||||||
| chr4:16004012 | C | T | 2 | a0001c0002t0001g0062 a0001c0002t0001g0121 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1454+2526G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004012 | |||||||
| chr4:16004073 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1454+2465C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004073 | |||||||
| chr4:16004076 | T | C | 38 | a0001c0001t0001g0023 a0001c0001t0001g0122 a0001c0001t0001g0213 others(35): Show |
38 | HG00544.hp1 HG00597.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1454+2462A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004076 | |||||||
| chr4:16004111 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1454+2427G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004111 | |||||||
| chr4:16004182 | C | T | 1 | a0001c0004t0002g0349 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1454+2356G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004182 | |||||||
| chr4:16004203 | T | C | 1 | a0001c0011t0003g0356 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1454+2335A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004203 | |||||||
| chr4:16004654 | G | A | 1 | a0001c0001t0003g0305 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1454+1884C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004654 | |||||||
| chr4:16004681 | T | A | 2 | a0001c0001t0001g0127 a0001c0001t0002g0289 |
2 | HG01978.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1454+1857A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004681 | |||||||
| chr4:16004685 | C | T | 1 | a0001c0002t0002g0207 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1454+1853G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004685 | |||||||
| chr4:16004805 | ATCTT | A | 45 | a0001c0001t0001g0023 a0001c0001t0001g0043 a0001c0001t0001g0050 others(42): Show |
45 | HG00544.hp1 HG00735.hp1 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.1454+1729_1454+173 others(8): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004805 | |||||||
| chr4:16004828 | T | C | 6 | a0001c0001t0002g0037 a0001c0001t0002g0297 a0001c0004t0001g0046 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1454+1710A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004828 | |||||||
| chr4:16004829 | T | TTCTTTCT others(11): Show |
1 | a0001c0001t0004g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1454+1708_1454+170 others(22): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004829 | |||||||
| chr4:16004829 | T | TTCTTTCT others(21): Show |
3 | a0001c0002t0002g0176 a0001c0002t0002g0177 a0001c0002t0002g0201 |
3 | HG00423.hp1 NA18982.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1454+1708_1454+170 others(32): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004829 | |||||||
| chr4:16004829 | T | TTCTTTCT others(17): Show |
13 | a0001c0002t0001g0100 a0001c0002t0001g0184 a0001c0002t0002g0058 others(10): Show |
13 | HG01993.hp1 HG02056.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1454+1708_1454+170 others(28): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004829 | |||||||
| chr4:16004829 | T | TTCTTTCT others(14): Show |
7 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0193 others(4): Show |
8 | HG02074.hp2 HG02135.hp1 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.1454+1708_1454+170 others(25): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004829 | |||||||
| chr4:16004829 | T | TTCTTTCT others(6): Show |
3 | a0001c0001t0002g0220 a0001c0001t0002g0309 a0001c0001t0003g0097 |
3 | HG01175.hp2 HG01515.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.1454+1708_1454+170 others(17): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004829 | |||||||
| chr4:16004829 | T | TTCTTTCT others(10): Show |
33 | a0001c0001t0001g0068 a0001c0001t0001g0151 a0001c0001t0001g0159 others(30): Show |
33 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1454+1708_1454+170 others(21): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004829 | |||||||
| chr4:16004829 | T | TTCTTTCT others(14): Show |
5 | a0001c0001t0001g0035 a0001c0001t0001g0106 a0001c0001t0001g0350 others(2): Show |
5 | HG02717.hp1 HG02723.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1454+1708_1454+170 others(25): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004829 | |||||||
| chr4:16004829 | T | TTCTTTCT others(18): Show |
1 | a0001c0001t0002g0086 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1454+1708_1454+170 others(29): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004829 | |||||||
| chr4:16004829 | T | TTCTTTTT others(2): Show |
5 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0315 others(2): Show |
5 | NA18952.hp1 NA18970.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1454+1708_1454+170 others(13): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004829 | |||||||
| chr4:16004829 | T | TTCTTTTT others(6): Show |
2 | a0001c0001t0001g0195 a0001c0001t0002g0048 |
2 | HG00738.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1454+1708_1454+170 others(17): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004829 | |||||||
| chr4:16004829 | T | TTTCTTTC others(33): Show |
5 | a0001c0001t0002g0037 a0001c0001t0002g0297 a0001c0004t0001g0046 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1454+1708_1454+170 others(44): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004829 | |||||||
| chr4:16004829 | T | TTTCTTTC others(26): Show |
1 | a0001c0019t0005g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1454+1708_1454+170 others(37): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004829 | |||||||
| chr4:16004830 | T | C | 21 | a0001c0001t0001g0091 a0001c0001t0001g0102 a0001c0001t0001g0161 others(18): Show |
21 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.1454+1708A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004830 | |||||||
| chr4:16004830 | T | TCTTTCTT others(5): Show |
1 | a0001c0001t0001g0257 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1454+1707_1454+170 others(16): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004830 | |||||||
| chr4:16004832 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(75): Show |
79 | HG00423.hp1 HG00544.hp2 HG00597.hp2 others(76): Show |
intron_variant | MODIFIER | c.1454+1706A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004832 | |||||||
| chr4:16004832 | T | TCTTC | 17 | a0001c0001t0001g0071 a0001c0001t0001g0107 a0001c0001t0001g0116 others(14): Show |
17 | HG00735.hp2 HG01192.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.1454+1702_1454+170 others(8): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004832 | |||||||
| chr4:16004832 | TCTTC | T | 103 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0042 others(100): Show |
104 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.1454+1702_1454+170 others(8): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004832 | |||||||
| chr4:16004836 | C | T | 4 | a0001c0001t0003g0150 a0001c0001t0004g0025 a0001c0001t0004g0031 others(1): Show |
4 | HG02109.hp2 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1454+1702G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004836 | |||||||
| chr4:16004840 | C | T | 3 | a0001c0001t0004g0031 a0001c0004t0004g0312 a0001c0018t0001g0215 |
3 | HG03130.hp1 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1454+1698G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004840 | |||||||
| chr4:16004844 | C | T | 2 | a0001c0001t0004g0031 a0001c0018t0001g0215 |
2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1454+1694G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004844 | |||||||
| chr4:16004862 | T | TTCCTTCC others(3): Show |
1 | a0001c0001t0004g0028 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1454+1675_1454+167 others(14): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004862 | |||||||
| chr4:16004869 | C | T | 22 | a0001c0001t0001g0091 a0001c0001t0001g0102 a0001c0001t0001g0161 others(19): Show |
22 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.1454+1669G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004869 | |||||||
| chr4:16004871 | C | T | 2 | a0001c0001t0004g0031 a0001c0018t0001g0215 |
2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1454+1667G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004871 | |||||||
| chr4:16004872 | C | T | 1 | a0001c0001t0004g0028 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1454+1666G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004872 | |||||||
| chr4:16004872 | CCTCT | C | 6 | a0001c0001t0001g0033 a0001c0001t0001g0085 a0001c0001t0001g0137 others(3): Show |
6 | HG02559.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1454+1662_1454+166 others(8): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004872 | |||||||
| chr4:16004874 | T | C | 1 | a0001c0001t0004g0028 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1454+1664A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004874 | |||||||
| chr4:16004890 | T | TC | 5 | a0001c0001t0001g0315 a0001c0001t0001g0360 a0001c0001t0002g0334 others(2): Show |
5 | HG02055.hp1 NA18977.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.1454+1647dupG | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004890 | |||||||
| chr4:16004905 | C | CCCTT | 4 | a0001c0001t0002g0343 a0001c0001t0002g0354 a0001c0001t0005g0346 others(1): Show |
4 | HG02258.hp2 HG02486.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1454+1629_1454+163 others(8): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004905 | |||||||
| chr4:16004905 | CCCTT | C | 81 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0024 others(78): Show |
81 | HG00423.hp1 HG00609.hp2 HG01109.hp2 others(78): Show |
intron_variant | MODIFIER | c.1454+1629_1454+163 others(8): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004905 | |||||||
| chr4:16004906 | C | CCTCCCCC others(25): Show |
2 | a0001c0001t0004g0031 a0001c0018t0001g0215 |
2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1454+1631_1454+163 others(36): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004906 | |||||||
| chr4:16004909 | T | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(61): Show |
65 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1454+1629A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004909 | |||||||
| chr4:16004910 | C | CCCCTCT | 62 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(59): Show |
63 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1454+1627_1454+162 others(10): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004910 | |||||||
| chr4:16004913 | T | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(59): Show |
63 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1454+1625A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004913 | |||||||
| chr4:16004914 | C | T | 62 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(59): Show |
63 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1454+1624G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004914 | |||||||
| chr4:16004917 | T | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(59): Show |
63 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1454+1621A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004917 | |||||||
| chr4:16004931 | CTCTT | C | 60 | a0001c0001t0001g0042 a0001c0001t0001g0051 a0001c0001t0001g0061 others(57): Show |
61 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.1454+1603_1454+160 others(8): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004931 | |||||||
| chr4:16004963 | C | CTT | 57 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(54): Show |
58 | HG00544.hp2 HG00597.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1454+1573_1454+157 others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004963 | |||||||
| chr4:16004963 | CT | C | 204 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(201): Show |
206 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.1454+1574delA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004963 | |||||||
| chr4:16004963 | CTT | C | 50 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0183 others(47): Show |
50 | HG00408.hp1 HG00423.hp1 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.1454+1573_1454+157 others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16004963 | |||||||
| chr4:16005031 | C | T | 3 | a0001c0001t0003g0148 a0001c0001t0003g0150 a0001c0001t0013g0366 |
3 | HG01346.hp1 HG01361.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1454+1507G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005031 | |||||||
| chr4:16005073 | G | A | 16 | a0001c0002t0001g0100 a0001c0002t0001g0184 a0001c0002t0002g0058 others(13): Show |
16 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.1454+1465C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005073 | |||||||
| chr4:16005149 | C | T | 16 | a0001c0002t0001g0100 a0001c0002t0001g0184 a0001c0002t0002g0058 others(13): Show |
16 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.1454+1389G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005149 | |||||||
| chr4:16005164 | T | C | 6 | a0001c0001t0001g0033 a0001c0001t0001g0085 a0001c0001t0001g0137 others(3): Show |
6 | HG02559.hp1 HG02647.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1454+1374A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005164 | |||||||
| chr4:16005206 | G | A | 1 | a0001c0002t0003g0302 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1454+1332C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005206 | |||||||
| chr4:16005276 | T | C | 2 | a0001c0001t0002g0146 a0001c0001t0004g0053 |
2 | HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1454+1262A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005276 | |||||||
| chr4:16005393 | A | G | 1 | a0001c0001t0002g0290 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1454+1145T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005393 | |||||||
| chr4:16005495 | GGT | G | 40 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0054 others(37): Show |
40 | HG00423.hp1 HG00544.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1454+1041_1454+104 others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005495 | |||||||
| chr4:16005495 | GGTGT | G | 29 | a0001c0001t0001g0021 a0001c0001t0001g0109 a0001c0001t0001g0361 others(26): Show |
29 | HG00673.hp1 HG01109.hp2 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.1454+1039_1454+104 others(8): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005495 | |||||||
| chr4:16005495 | GGTGTGT | G | 60 | a0001c0001t0001g0024 a0001c0001t0001g0043 a0001c0001t0001g0050 others(57): Show |
60 | HG00609.hp2 HG00621.hp2 HG01167.hp2 others(57): Show |
intron_variant | MODIFIER | c.1454+1037_1454+104 others(10): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005495 | |||||||
| chr4:16005495 | GGTGTGTG others(1): Show |
G | 57 | a0001c0001t0001g0033 a0001c0001t0001g0051 a0001c0001t0001g0067 others(54): Show |
58 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.1454+1035_1454+104 others(12): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005495 | |||||||
| chr4:16005495 | GGTGTGTG others(3): Show |
G | 92 | a0001c0001t0001g0042 a0001c0001t0001g0056 a0001c0001t0001g0061 others(89): Show |
93 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1454+1033_1454+104 others(14): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005495 | |||||||
| chr4:16005495 | GGTGTGTG others(5): Show |
G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0068 others(47): Show |
51 | HG00438.hp1 HG00597.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1454+1031_1454+104 others(16): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005495 | |||||||
| chr4:16005495 | GGTGTGTG others(7): Show |
G | 12 | a0001c0001t0001g0035 a0001c0001t0001g0251 a0001c0001t0001g0252 others(9): Show |
12 | HG00544.hp2 HG02015.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1454+1029_1454+104 others(18): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005495 | |||||||
| chr4:16005495 | GGTGTGTG others(9): Show |
G | 8 | a0001c0001t0001g0127 a0001c0001t0001g0193 a0001c0001t0001g0204 others(5): Show |
8 | HG00639.hp1 HG01978.hp1 HG02004.hp1 others(5): Show |
intron_variant | MODIFIER | c.1454+1027_1454+104 others(20): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005495 | |||||||
| chr4:16005495 | GGTGTGTG others(15): Show |
G | 1 | a0001c0001t0002g0326 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1454+1021_1454+104 others(26): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005495 | |||||||
| chr4:16005505 | T | G | 1 | a0001c0001t0002g0052 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1454+1033A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005505 | |||||||
| chr4:16005541 | T | A | 5 | a0001c0001t0002g0037 a0001c0001t0002g0297 a0001c0004t0001g0046 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1454+997A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005541 | |||||||
| chr4:16005607 | C | T | 16 | a0001c0002t0001g0100 a0001c0002t0001g0184 a0001c0002t0002g0058 others(13): Show |
16 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.1454+931G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005607 | |||||||
| chr4:16005617 | C | T | 1 | a0001c0001t0003g0209 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1454+921G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005617 | |||||||
| chr4:16005618 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1454+920C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005618 | |||||||
| chr4:16005697 | A | G | 1 | a0001c0004t0004g0312 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1454+841T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005697 | |||||||
| chr4:16005956 | G | C | 2 | a0001c0001t0004g0031 a0001c0018t0001g0215 |
2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1454+582C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005956 | |||||||
| chr4:16005977 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(60): Show |
64 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1454+561C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16005977 | |||||||
| chr4:16006025 | G | C | 1 | a0001c0001t0004g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1454+513C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16006025 | |||||||
| chr4:16006066 | G | T | 1 | a0001c0001t0001g0091 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1454+472C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16006066 | |||||||
| chr4:16006154 | A | G | 46 | a0001c0001t0001g0023 a0001c0001t0001g0043 a0001c0001t0001g0050 others(43): Show |
46 | HG00544.hp1 HG00735.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.1454+384T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16006154 | |||||||
| chr4:16006313 | GTGT | G | 20 | a0001c0002t0001g0100 a0001c0002t0001g0175 a0001c0002t0001g0184 others(17): Show |
20 | HG00423.hp1 HG00438.hp2 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.1454+222_1454+224d others(5): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16006313 | |||||||
| chr4:16006404 | C | G | 16 | a0001c0002t0001g0100 a0001c0002t0001g0184 a0001c0002t0002g0058 others(13): Show |
16 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.1454+134G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16006404 | |||||||
| chr4:16006413 | G | A | 1 | a0001c0001t0004g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1454+125C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16006413 | |||||||
| chr4:16006416 | C | G | 16 | a0001c0002t0001g0100 a0001c0002t0001g0184 a0001c0002t0002g0058 others(13): Show |
16 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.1454+122G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16006416 | |||||||
| chr4:16006456 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1454+82C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16006456 | |||||||
| chr4:16006517 | CAG | C | 16 | a0001c0002t0001g0100 a0001c0002t0001g0184 a0001c0002t0002g0058 others(13): Show |
16 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.1454+19_1454+20del others(2): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 13/27 | chr4 | 16006517 | |||||||
| chr4:16006773 | C | T | 2 | a0001c0001t0004g0031 a0001c0018t0001g0215 |
2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1302-83G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16006773 | |||||||
| chr4:16006834 | T | C | 11 | a0001c0001t0001g0021 a0001c0001t0001g0084 a0001c0001t0001g0299 others(8): Show |
11 | HG02257.hp1 HG02572.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1302-144A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16006834 | |||||||
| chr4:16006883 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1302-193G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16006883 | |||||||
| chr4:16006963 | T | G | 1 | a0001c0001t0002g0308 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1302-273A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16006963 | |||||||
| chr4:16007086 | A | G | 3 | a0001c0001t0002g0005 a0001c0001t0002g0358 a0001c0005t0002g0338 |
3 | HG02615.hp2 HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1302-396T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16007086 | |||||||
| chr4:16007198 | C | T | 16 | a0001c0002t0001g0100 a0001c0002t0001g0184 a0001c0002t0002g0058 others(13): Show |
16 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.1302-508G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16007198 | |||||||
| chr4:16007409 | G | A | 1 | a0001c0001t0002g0308 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1302-719C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16007409 | |||||||
| chr4:16007533 | T | C | 1 | a0001c0004t0004g0312 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1302-843A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16007533 | |||||||
| chr4:16007587 | T | C | 1 | a0001c0001t0004g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1302-897A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16007587 | |||||||
| chr4:16007670 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0023 others(185): Show |
190 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.1302-980A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16007670 | |||||||
| chr4:16007742 | C | T | 5 | a0001c0001t0002g0037 a0001c0001t0002g0297 a0001c0004t0001g0046 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1302-1052G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16007742 | |||||||
| chr4:16007749 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1302-1059C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16007749 | |||||||
| chr4:16007930 | A | G | 1 | a0001c0001t0001g0023 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1301+1019T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16007930 | |||||||
| chr4:16007939 | G | A | 50 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0043 others(47): Show |
50 | HG00544.hp1 HG00735.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.1301+1010C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16007939 | |||||||
| chr4:16007977 | T | C | 7 | a0001c0001t0002g0244 a0001c0001t0003g0060 a0001c0001t0003g0104 others(4): Show |
7 | NA18944.hp1 NA18972.hp2 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1301+972A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16007977 | |||||||
| chr4:16008156 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1301+793G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16008156 | |||||||
| chr4:16008172 | C | T | 10 | a0001c0001t0001g0071 a0001c0002t0004g0026 a0001c0002t0004g0027 others(7): Show |
10 | HG01884.hp2 HG02451.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1301+777G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16008172 | |||||||
| chr4:16008187 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1301+762C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16008187 | |||||||
| chr4:16008256 | C | G | 45 | a0001c0001t0001g0023 a0001c0001t0001g0043 a0001c0001t0001g0050 others(42): Show |
45 | HG00544.hp1 HG00735.hp1 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.1301+693G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16008256 | |||||||
| chr4:16008327 | C | T | 29 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0288 others(26): Show |
29 | HG01884.hp2 HG02451.hp2 HG02622.hp1 others(26): Show |
intron_variant | MODIFIER | c.1301+622G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16008327 | |||||||
| chr4:16008425 | C | G | 1 | a0001c0001t0002g0308 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1301+524G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16008425 | |||||||
| chr4:16008530 | T | C | 1 | a0001c0019t0005g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1301+419A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16008530 | |||||||
| chr4:16008646 | G | A | 1 | a0001c0001t0002g0292 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1301+303C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16008646 | |||||||
| chr4:16008729 | C | T | 1 | a0001c0001t0003g0147 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1301+220G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16008729 | |||||||
| chr4:16008815 | G | T | 1 | a0001c0004t0002g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1301+134C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16008815 | |||||||
| chr4:16008819 | A | G | 9 | a0001c0001t0001g0021 a0001c0001t0001g0084 a0001c0001t0001g0299 others(6): Show |
9 | HG02257.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1301+130T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16008819 | |||||||
| chr4:16008836 | G | A | 1 | a0001c0001t0004g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1301+113C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 12/27 | chr4 | 16008836 | |||||||
| chr4:16009125 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1142-17G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16009125 | |||||||
| chr4:16009361 | C | T | 1 | a0001c0001t0003g0313 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1142-253G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16009361 | |||||||
| chr4:16009575 | T | C | 1 | a0001c0001t0002g0308 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1142-467A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16009575 | |||||||
| chr4:16009581 | A | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(57): Show |
61 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.1142-473T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16009581 | |||||||
| chr4:16009586 | A | G | 1 | a0001c0001t0004g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1142-478T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16009586 | |||||||
| chr4:16009588 | C | A | 189 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0023 others(186): Show |
191 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.1142-480G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16009588 | |||||||
| chr4:16009841 | G | C | 2 | a0001c0001t0001g0137 a0001c0004t0004g0312 |
2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1142-733C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16009841 | |||||||
| chr4:16009847 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1142-739G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16009847 | |||||||
| chr4:16009929 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1142-821C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16009929 | |||||||
| chr4:16009934 | C | CA | 7 | a0001c0001t0001g0363 a0001c0001t0002g0182 a0001c0001t0003g0079 others(4): Show |
7 | HG02965.hp2 NA18949.hp2 NA18995.hp1 others(4): Show |
intron_variant | MODIFIER | c.1142-827dupT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16009934 | |||||||
| chr4:16009934 | CA | C | 56 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0033 others(53): Show |
57 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.1142-827delT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16009934 | |||||||
| chr4:16009934 | CAA | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0023 others(143): Show |
147 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.1142-828_1142-827d others(4): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16009934 | |||||||
| chr4:16009999 | C | A | 9 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0351 others(6): Show |
9 | HG01243.hp1 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1142-891G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16009999 | |||||||
| chr4:16010026 | G | A | 2 | a0001c0001t0001g0339 a0008c0013t0003g0335 |
2 | HG03710.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1142-918C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16010026 | |||||||
| chr4:16010259 | C | T | 1 | a0001c0002t0001g0245 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1142-1151G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16010259 | |||||||
| chr4:16010317 | G | A | 1 | a0001c0001t0003g0124 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1142-1209C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16010317 | |||||||
| chr4:16010323 | C | T | 1 | a0001c0001t0004g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1142-1215G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16010323 | |||||||
| chr4:16010337 | A | AT | 16 | a0001c0002t0001g0100 a0001c0002t0001g0184 a0001c0002t0002g0058 others(13): Show |
16 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.1142-1230dupA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16010337 | |||||||
| chr4:16010501 | G | A | 1 | a0001c0001t0002g0157 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1142-1393C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16010501 | |||||||
| chr4:16010573 | G | C | 26 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0278 others(23): Show |
26 | HG02135.hp2 HG02451.hp2 HG02622.hp1 others(23): Show |
intron_variant | MODIFIER | c.1142-1465C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16010573 | |||||||
| chr4:16010680 | T | G | 2 | a0001c0001t0001g0137 a0001c0004t0004g0312 |
2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1142-1572A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16010680 | |||||||
| chr4:16010717 | C | CATGTTGC others(13): Show |
1 | a0001c0001t0004g0053 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1142-1629_1142-161 others(24): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16010717 | |||||||
| chr4:16010934 | T | C | 16 | a0001c0002t0001g0100 a0001c0002t0001g0184 a0001c0002t0002g0058 others(13): Show |
16 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(13): Show |
intron_variant | MODIFIER | c.1142-1826A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16010934 | |||||||
| chr4:16011025 | C | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0023 others(192): Show |
197 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(194): Show |
intron_variant | MODIFIER | c.1142-1917G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16011025 | |||||||
| chr4:16011038 | T | G | 1 | a0001c0001t0004g0123 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1142-1930A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16011038 | |||||||
| chr4:16011163 | C | T | 3 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0334 |
3 | HG01081.hp1 HG01106.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1142-2055G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16011163 | |||||||
| chr4:16011251 | T | G | 1 | a0010c0015t0003g0093 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1141+2024A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16011251 | |||||||
| chr4:16011292 | C | T | 1 | a0001c0001t0003g0090 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1141+1983G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16011292 | |||||||
| chr4:16011425 | C | T | 24 | a0001c0001t0001g0091 a0001c0001t0001g0102 a0001c0001t0001g0161 others(21): Show |
24 | HG00323.hp2 HG00408.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.1141+1850G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16011425 | |||||||
| chr4:16011517 | C | A | 1 | a0001c0001t0001g0333 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1141+1758G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16011517 | |||||||
| chr4:16011553 | C | T | 3 | a0001c0001t0001g0165 a0001c0001t0001g0198 a0001c0001t0001g0211 |
3 | NA18949.hp1 NA18950.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1141+1722G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16011553 | |||||||
| chr4:16012015 | GT | G | 25 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0351 others(22): Show |
25 | HG00423.hp1 HG01243.hp1 HG01993.hp1 others(22): Show |
intron_variant | MODIFIER | c.1141+1259delA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012015 | |||||||
| chr4:16012110 | C | G | 1 | a0001c0001t0002g0052 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1141+1165G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012110 | |||||||
| chr4:16012113 | C | T | 1 | a0001c0001t0002g0052 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1141+1162G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012113 | |||||||
| chr4:16012171 | AT | A | 3 | a0001c0001t0004g0029 a0001c0001t0004g0145 a0001c0001t0004g0348 |
3 | HG02145.hp1 HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1141+1103delA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012171 | |||||||
| chr4:16012277 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1141+998C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012277 | |||||||
| chr4:16012360 | C | G | 3 | a0001c0001t0004g0025 a0001c0001t0004g0031 a0001c0018t0001g0215 |
3 | HG03130.hp1 HG03195.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1141+915G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012360 | |||||||
| chr4:16012420 | T | C | 2 | a0001c0001t0002g0146 a0001c0001t0004g0053 |
2 | HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1141+855A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012420 | |||||||
| chr4:16012531 | C | A | 2 | a0001c0001t0003g0147 a0001c0001t0003g0273 |
2 | HG01361.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1141+744G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012531 | |||||||
| chr4:16012588 | T | G | 62 | a0001c0001t0001g0021 a0001c0001t0001g0056 a0001c0001t0001g0084 others(59): Show |
63 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.1141+687A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012588 | |||||||
| chr4:16012621 | A | T | 2 | a0001c0001t0004g0025 a0001c0001t0004g0031 |
2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1141+654T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012621 | |||||||
| chr4:16012624 | A | C | 2 | a0001c0001t0004g0025 a0001c0001t0004g0031 |
2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1141+651T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012624 | |||||||
| chr4:16012667 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1141+608C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012667 | |||||||
| chr4:16012689 | T | C | 1 | a0001c0001t0001g0287 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1141+586A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012689 | |||||||
| chr4:16012768 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1141+507C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012768 | |||||||
| chr4:16012784 | T | A | 59 | a0001c0001t0001g0021 a0001c0001t0001g0056 a0001c0001t0001g0084 others(56): Show |
60 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.1141+491A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012784 | |||||||
| chr4:16012796 | G | A | 2 | a0001c0001t0002g0258 a0001c0001t0002g0259 |
2 | HG06807.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1141+479C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012796 | |||||||
| chr4:16012820 | G | A | 6 | a0001c0001t0001g0033 a0001c0001t0001g0085 a0001c0001t0002g0120 others(3): Show |
6 | HG02280.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1141+455C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012820 | |||||||
| chr4:16012843 | C | G | 20 | a0001c0001t0001g0067 a0001c0001t0001g0278 a0001c0001t0001g0288 others(17): Show |
20 | HG02135.hp2 HG02622.hp2 HG02886.hp2 others(17): Show |
intron_variant | MODIFIER | c.1141+432G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012843 | |||||||
| chr4:16012865 | T | C | 91 | a0001c0001t0001g0021 a0001c0001t0001g0043 a0001c0001t0001g0050 others(88): Show |
92 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1141+410A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012865 | |||||||
| chr4:16012866 | G | A | 1 | a0001c0001t0002g0308 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1141+409C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012866 | |||||||
| chr4:16012867 | T | C | 1 | a0001c0001t0002g0173 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1141+408A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012867 | |||||||
| chr4:16012870 | C | CA | 90 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0043 others(87): Show |
91 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.1141+404dupT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012870 | |||||||
| chr4:16012870 | C | CAA | 21 | a0001c0001t0001g0159 a0001c0001t0001g0257 a0001c0001t0001g0370 others(18): Show |
21 | HG00621.hp1 HG00738.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.1141+403_1141+404d others(4): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012870 | |||||||
| chr4:16012870 | CAA | C | 6 | a0001c0001t0002g0244 a0001c0001t0002g0334 a0001c0001t0003g0040 others(3): Show |
6 | HG02055.hp1 HG02602.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.1141+403_1141+404d others(4): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012870 | |||||||
| chr4:16012870 | CAAA | C | 30 | a0001c0001t0001g0023 a0001c0001t0001g0122 a0001c0001t0001g0275 others(27): Show |
30 | HG00544.hp1 HG00735.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.1141+402_1141+404d others(5): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012870 | |||||||
| chr4:16012889 | A | AC | 3 | a0001c0001t0002g0115 a0001c0001t0004g0034 a0011c0009t0004g0317 |
3 | HG01109.hp2 HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1141+385_1141+386i others(3): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012889 | |||||||
| chr4:16012889 | A | C | 3 | a0001c0001t0001g0024 a0001c0001t0001g0352 a0001c0005t0001g0219 |
3 | HG02922.hp2 HG03516.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1141+386T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012889 | |||||||
| chr4:16012891 | A | AAAAAC | 12 | a0001c0002t0001g0100 a0001c0002t0001g0184 a0001c0002t0002g0058 others(9): Show |
12 | HG02056.hp1 HG02080.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1141+383_1141+384i others(7): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012891 | |||||||
| chr4:16012892 | C | A | 26 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0351 others(23): Show |
26 | HG00423.hp1 HG01243.hp1 HG01993.hp1 others(23): Show |
intron_variant | MODIFIER | c.1141+383G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012892 | |||||||
| chr4:16012895 | C | A | 9 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0351 others(6): Show |
9 | HG01243.hp1 HG02559.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1141+380G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16012895 | |||||||
| chr4:16013113 | C | A | 77 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0056 others(74): Show |
78 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.1141+162G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16013113 | |||||||
| chr4:16013115 | G | A | 1 | a0001c0001t0002g0144 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1141+160C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16013115 | |||||||
| chr4:16013115 | G | C | 25 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0351 others(22): Show |
25 | HG00423.hp1 HG01243.hp1 HG01993.hp1 others(22): Show |
intron_variant | MODIFIER | c.1141+160C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16013115 | |||||||
| chr4:16013229 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1141+46C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 11/27 | chr4 | 16013229 | |||||||
| chr4:16013388 | A | T | 4 | a0001c0002t0001g0283 a0001c0002t0002g0072 a0001c0002t0002g0074 others(1): Show |
4 | NA18952.hp2 NA18954.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078-50T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16013388 | |||||||
| chr4:16013420 | CGAGTA | C | 17 | a0001c0001t0001g0179 a0001c0002t0001g0100 a0001c0002t0001g0184 others(14): Show |
17 | HG00423.hp1 HG00609.hp1 HG01993.hp1 others(14): Show |
intron_variant | MODIFIER | c.1078-87_1078-83del others(5): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16013420 | |||||||
| chr4:16013568 | G | C | 17 | a0001c0001t0002g0180 a0001c0002t0001g0100 a0001c0002t0001g0184 others(14): Show |
17 | HG00423.hp1 HG01993.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.1078-230C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16013568 | |||||||
| chr4:16013618 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1078-280A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16013618 | |||||||
| chr4:16013659 | G | A | 2 | a0001c0001t0002g0115 a0001c0001t0004g0034 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1078-321C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16013659 | |||||||
| chr4:16013720 | AGTTGTGG others(3): Show |
A | 1 | a0001c0001t0003g0082 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1078-392_1078-383d others(12): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16013720 | |||||||
| chr4:16013853 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1078-515G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16013853 | |||||||
| chr4:16013866 | C | T | 1 | a0001c0001t0002g0354 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1078-528G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16013866 | |||||||
| chr4:16013894 | A | C | 1 | a0001c0001t0005g0036 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1078-556T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16013894 | |||||||
| chr4:16013946 | GA | G | 282 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(279): Show |
284 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.1078-609delT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16013946 | |||||||
| chr4:16014193 | CA | C | 3 | a0001c0001t0004g0145 a0001c0005t0004g0075 a0011c0009t0004g0317 |
3 | HG02451.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1078-856delT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16014193 | |||||||
| chr4:16014217 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0039 others(45): Show |
49 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.1078-879G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16014217 | |||||||
| chr4:16014224 | T | C | 1 | a0001c0001t0003g0082 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1078-886A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16014224 | |||||||
| chr4:16014303 | C | T | 1 | a0001c0019t0005g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1078-965G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16014303 | |||||||
| chr4:16014617 | T | C | 2 | a0001c0004t0002g0004 a0001c0019t0005g0018 |
2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1078-1279A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16014617 | |||||||
| chr4:16015048 | A | G | 4 | a0001c0001t0002g0066 a0001c0001t0003g0090 a0001c0001t0003g0316 others(1): Show |
4 | HG00621.hp2 NA18977.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1077+1118T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16015048 | |||||||
| chr4:16015067 | C | T | 64 | a0001c0001t0001g0113 a0001c0001t0002g0240 a0001c0001t0003g0203 others(61): Show |
64 | HG00423.hp1 HG00438.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1077+1099G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16015067 | |||||||
| chr4:16015067 | CG | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0035 others(59): Show |
63 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1077+1098delC | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16015067 | |||||||
| chr4:16015100 | C | T | 24 | a0001c0001t0001g0033 a0001c0001t0001g0061 a0001c0001t0001g0084 others(21): Show |
24 | HG01081.hp1 HG01106.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.1077+1066G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16015100 | |||||||
| chr4:16015102 | T | C | 1 | a0001c0001t0002g0274 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1077+1064A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16015102 | |||||||
| chr4:16015215 | G | A | 1 | a0001c0005t0004g0217 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1077+951C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16015215 | |||||||
| chr4:16015330 | C | T | 2 | a0001c0001t0002g0277 a0001c0001t0003g0149 |
2 | HG02055.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.1077+836G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16015330 | |||||||
| chr4:16015331 | G | A | 3 | a0001c0001t0001g0105 a0001c0001t0002g0083 a0001c0001t0004g0015 |
3 | HG02717.hp2 HG02897.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1077+835C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16015331 | |||||||
| chr4:16015345 | C | CA | 165 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0023 others(162): Show |
167 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.1077+820dupT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16015345 | |||||||
| chr4:16015345 | C | CAA | 9 | a0001c0001t0001g0188 a0001c0001t0001g0204 a0001c0001t0002g0052 others(6): Show |
9 | HG00438.hp1 HG01884.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.1077+819_1077+820d others(4): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16015345 | |||||||
| chr4:16015345 | C | CAAA | 13 | a0001c0001t0001g0071 a0001c0001t0001g0288 a0001c0001t0001g0330 others(10): Show |
13 | HG01943.hp2 HG02622.hp1 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.1077+818_1077+820d others(5): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16015345 | |||||||
| chr4:16015345 | C | CAAAA | 102 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0054 others(99): Show |
103 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(100): Show |
intron_variant | MODIFIER | c.1077+817_1077+820d others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16015345 | |||||||
| chr4:16015345 | C | CAAAAA | 10 | a0001c0001t0001g0151 a0001c0001t0001g0310 a0001c0001t0001g0363 others(7): Show |
10 | HG00639.hp1 HG00735.hp2 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.1077+816_1077+820d others(7): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16015345 | |||||||
| chr4:16015345 | CA | C | 6 | a0001c0002t0001g0283 a0001c0002t0002g0176 a0001c0002t0004g0344 others(3): Show |
6 | HG01993.hp1 HG02074.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077+820delT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16015345 | |||||||
| chr4:16015631 | A | G | 83 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0056 others(80): Show |
84 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1077+535T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16015631 | |||||||
| chr4:16015639 | G | A | 1 | a0001c0001t0001g0039 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1077+527C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16015639 | |||||||
| chr4:16015718 | A | G | 111 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0054 others(108): Show |
112 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.1077+448T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16015718 | |||||||
| chr4:16015908 | G | C | 25 | a0001c0001t0001g0033 a0001c0001t0001g0061 a0001c0001t0001g0084 others(22): Show |
25 | HG01081.hp1 HG01106.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.1077+258C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 10/27 | chr4 | 16015908 | |||||||
| chr4:16016275 | T | G | 84 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0050 others(81): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1003-35A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16016275 | |||||||
| chr4:16016316 | G | A | 2 | a0001c0001t0001g0021 a0001c0003t0002g0020 |
2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1003-76C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16016316 | |||||||
| chr4:16016337 | A | G | 83 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0050 others(80): Show |
84 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.1003-97T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16016337 | |||||||
| chr4:16016358 | C | T | 16 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0288 others(13): Show |
16 | HG02622.hp1 HG02965.hp1 HG02970.hp2 others(13): Show |
intron_variant | MODIFIER | c.1003-118G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16016358 | |||||||
| chr4:16016381 | G | A | 2 | a0001c0001t0002g0224 a0001c0001t0002g0267 |
2 | NA18939.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1003-141C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16016381 | |||||||
| chr4:16016434 | T | G | 2 | a0001c0001t0001g0021 a0001c0003t0002g0020 |
2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1003-194A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16016434 | |||||||
| chr4:16016519 | C | T | 258 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0023 others(255): Show |
260 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(257): Show |
intron_variant | MODIFIER | c.1003-279G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16016519 | |||||||
| chr4:16016593 | G | C | 88 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0050 others(85): Show |
89 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.1003-353C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16016593 | |||||||
| chr4:16016621 | C | T | 30 | a0001c0001t0001g0014 a0001c0001t0001g0054 a0001c0001t0001g0275 others(27): Show |
30 | HG00639.hp1 HG01099.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1003-381G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16016621 | |||||||
| chr4:16016659 | T | G | 282 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0024 others(279): Show |
284 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.1003-419A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16016659 | |||||||
| chr4:16016701 | C | T | 282 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0024 others(279): Show |
284 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.1003-461G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16016701 | |||||||
| chr4:16016740 | G | A | 25 | a0001c0001t0001g0033 a0001c0001t0001g0061 a0001c0001t0001g0084 others(22): Show |
25 | HG01081.hp1 HG01106.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.1003-500C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16016740 | |||||||
| chr4:16016775 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0035 others(124): Show |
128 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.1003-535T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16016775 | |||||||
| chr4:16016826 | G | T | 1 | a0001c0001t0002g0267 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1003-586C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16016826 | |||||||
| chr4:16016904 | C | T | 278 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0024 others(275): Show |
280 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.1003-664G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16016904 | |||||||
| chr4:16016911 | T | C | 278 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0024 others(275): Show |
280 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.1003-671A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16016911 | |||||||
| chr4:16017000 | C | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0024 others(277): Show |
282 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(279): Show |
intron_variant | MODIFIER | c.1003-760G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16017000 | |||||||
| chr4:16017128 | T | C | 3 | a0001c0001t0001g0351 a0001c0001t0004g0044 a0001c0003t0002g0070 |
3 | HG03098.hp1 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1003-888A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16017128 | |||||||
| chr4:16017132 | C | T | 61 | a0001c0001t0001g0262 a0001c0001t0003g0203 a0001c0002t0001g0062 others(58): Show |
61 | HG00423.hp1 HG00438.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.1003-892G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16017132 | |||||||
| chr4:16017158 | C | G | 1 | a0001c0018t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1003-918G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16017158 | |||||||
| chr4:16017297 | G | A | 278 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0024 others(275): Show |
280 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(277): Show |
intron_variant | MODIFIER | c.1002+1026C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16017297 | |||||||
| chr4:16017317 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1002+1006T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16017317 | |||||||
| chr4:16017354 | C | A | 1 | a0001c0002t0003g0192 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1002+969G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16017354 | |||||||
| chr4:16017490 | A | G | 286 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(283): Show |
288 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.1002+833T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16017490 | |||||||
| chr4:16017642 | G | A | 2 | a0001c0001t0001g0021 a0001c0003t0002g0020 |
2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1002+681C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16017642 | |||||||
| chr4:16017690 | G | A | 5 | a0001c0001t0001g0101 a0001c0001t0001g0107 a0001c0001t0001g0169 others(2): Show |
5 | HG02129.hp1 HG02165.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002+633C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16017690 | |||||||
| chr4:16017745 | C | T | 1 | a0007c0017t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1002+578G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16017745 | |||||||
| chr4:16017752 | T | C | 3 | a0001c0001t0001g0360 a0001c0001t0001g0361 a0001c0001t0001g0363 |
3 | NA18949.hp2 NA19058.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1002+571A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16017752 | |||||||
| chr4:16017882 | C | G | 25 | a0001c0001t0001g0033 a0001c0001t0001g0061 a0001c0001t0001g0084 others(22): Show |
25 | HG01081.hp1 HG01106.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.1002+441G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16017882 | |||||||
| chr4:16017910 | T | C | 6 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0002g0086 others(3): Show |
6 | HG01243.hp1 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1002+413A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16017910 | |||||||
| chr4:16017974 | A | G | 3 | a0001c0001t0001g0021 a0001c0001t0001g0137 a0001c0003t0002g0020 |
3 | HG02559.hp1 HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1002+349T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16017974 | |||||||
| chr4:16018011 | T | TA | 5 | a0001c0001t0001g0183 a0001c0001t0001g0230 a0001c0001t0001g0279 others(2): Show |
5 | HG00408.hp1 HG01496.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002+311dupT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16018011 | |||||||
| chr4:16018016 | A | AT | 280 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(277): Show |
282 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(279): Show |
intron_variant | MODIFIER | c.1002+306dupA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16018016 | |||||||
| chr4:16018112 | A | G | 1 | a0001c0001t0005g0080 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1002+211T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16018112 | |||||||
| chr4:16018201 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1002+122C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 9/27 | chr4 | 16018201 | |||||||
| chr4:16018557 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.785-17G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16018557 | |||||||
| chr4:16018558 | G | A | 1 | a0001c0001t0003g0266 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.785-18C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16018558 | |||||||
| chr4:16018695 | G | A | 24 | a0001c0001t0001g0033 a0001c0001t0001g0061 a0001c0001t0001g0084 others(21): Show |
24 | HG01081.hp1 HG01106.hp2 HG01346.hp2 others(21): Show |
intron_variant | MODIFIER | c.785-155C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16018695 | |||||||
| chr4:16018813 | T | C | 33 | a0001c0001t0001g0014 a0001c0001t0001g0054 a0001c0001t0001g0137 others(30): Show |
33 | HG00639.hp1 HG01099.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.785-273A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16018813 | |||||||
| chr4:16019035 | G | C | 1 | a0001c0001t0002g0277 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.785-495C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16019035 | |||||||
| chr4:16019041 | T | C | 25 | a0001c0001t0001g0033 a0001c0001t0001g0061 a0001c0001t0001g0084 others(22): Show |
25 | HG01081.hp1 HG01106.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.785-501A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16019041 | |||||||
| chr4:16019201 | C | G | 25 | a0001c0001t0001g0033 a0001c0001t0001g0061 a0001c0001t0001g0084 others(22): Show |
25 | HG01081.hp1 HG01106.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.785-661G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16019201 | |||||||
| chr4:16019293 | C | T | 2 | a0001c0001t0001g0021 a0001c0003t0002g0020 |
2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.785-753G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16019293 | |||||||
| chr4:16019599 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.785-1059G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16019599 | |||||||
| chr4:16019600 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.785-1060T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16019600 | |||||||
| chr4:16019688 | T | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(282): Show |
287 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.785-1148A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16019688 | |||||||
| chr4:16019864 | T | C | 1 | a0001c0002t0003g0285 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.785-1324A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16019864 | |||||||
| chr4:16019871 | T | TAC | 61 | a0001c0001t0002g0146 a0001c0001t0002g0205 a0001c0002t0001g0062 others(58): Show |
61 | HG00423.hp1 HG00438.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.785-1333_785-1332d others(4): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16019871 | |||||||
| chr4:16019871 | T | TACAC | 35 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0054 others(32): Show |
35 | HG01993.hp1 HG02074.hp1 HG02280.hp2 others(32): Show |
intron_variant | MODIFIER | c.785-1335_785-1332d others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16019871 | |||||||
| chr4:16019871 | T | TACACAC | 3 | a0001c0003t0011g0013 a0001c0018t0001g0215 a0001c0019t0005g0018 |
3 | HG02717.hp1 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.785-1337_785-1332d others(8): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16019871 | |||||||
| chr4:16019871 | T | TACACACA others(1): Show |
73 | a0001c0001t0001g0042 a0001c0001t0001g0091 a0001c0001t0001g0094 others(70): Show |
74 | HG00323.hp2 HG00544.hp2 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.785-1339_785-1332d others(10): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16019871 | |||||||
| chr4:16019871 | T | TACACACA others(3): Show |
8 | a0001c0001t0001g0116 a0001c0001t0001g0137 a0001c0001t0001g0307 others(5): Show |
8 | HG00323.hp1 HG00735.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.785-1341_785-1332d others(12): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16019871 | |||||||
| chr4:16019871 | T | TACACACA others(5): Show |
1 | a0001c0001t0003g0065 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.785-1343_785-1332d others(14): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16019871 | |||||||
| chr4:16019871 | TAC | T | 81 | a0001c0001t0001g0023 a0001c0001t0001g0050 a0001c0001t0001g0051 others(78): Show |
82 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.785-1333_785-1332d others(4): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16019871 | |||||||
| chr4:16019871 | TACACAC | T | 31 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0061 others(28): Show |
31 | HG01081.hp1 HG01106.hp2 HG01346.hp2 others(28): Show |
intron_variant | MODIFIER | c.785-1337_785-1332d others(8): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16019871 | |||||||
| chr4:16019891 | C | CACACACA others(1): Show |
24 | a0001c0001t0001g0275 a0001c0001t0001g0299 a0001c0001t0001g0330 others(21): Show |
24 | HG00639.hp1 HG01099.hp1 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.785-1359_785-1352d others(10): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16019891 | |||||||
| chr4:16019915 | G | A | 282 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(279): Show |
284 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(281): Show |
intron_variant | MODIFIER | c.785-1375C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16019915 | |||||||
| chr4:16019968 | C | G | 3 | a0001c0001t0001g0351 a0001c0001t0004g0044 a0001c0003t0002g0070 |
3 | HG03098.hp1 HG03453.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.785-1428G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16019968 | |||||||
| chr4:16020031 | G | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(46): Show |
50 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.785-1491C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16020031 | |||||||
| chr4:16020093 | T | C | 3 | a0001c0001t0001g0165 a0001c0001t0001g0198 a0001c0001t0001g0211 |
3 | NA18949.hp1 NA18950.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.785-1553A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16020093 | |||||||
| chr4:16020106 | C | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0035 others(130): Show |
135 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.785-1566G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16020106 | |||||||
| chr4:16020155 | C | A | 1 | a0001c0004t0004g0049 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.785-1615G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16020155 | |||||||
| chr4:16020185 | C | T | 1 | a0001c0001t0004g0123 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.785-1645G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16020185 | |||||||
| chr4:16020349 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0004g0053 a0001c0001t0004g0323 others(3): Show |
6 | HG02451.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.785-1809G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16020349 | |||||||
| chr4:16020473 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(282): Show |
287 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.785-1933C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16020473 | |||||||
| chr4:16020655 | AACC | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0024 others(231): Show |
236 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.785-2118_785-2116d others(5): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16020655 | |||||||
| chr4:16020655 | AACCACC | A | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0016t0001g0143 |
3 | HG01516.hp2 HG01517.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.785-2121_785-2116d others(8): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16020655 | |||||||
| chr4:16020672 | C | A | 14 | a0001c0001t0001g0014 a0001c0001t0002g0114 a0001c0001t0002g0146 others(11): Show |
14 | HG02055.hp2 HG02071.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.785-2132G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16020672 | |||||||
| chr4:16020672 | C | CCAA | 234 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0024 others(231): Show |
236 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.785-2135_785-2133d others(5): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16020672 | |||||||
| chr4:16020672 | C | CCAACAA | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0016t0001g0143 |
3 | HG01516.hp2 HG01517.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.785-2138_785-2133d others(8): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16020672 | |||||||
| chr4:16020828 | A | C | 59 | a0001c0002t0001g0062 a0001c0002t0001g0100 a0001c0002t0001g0121 others(56): Show |
59 | HG00423.hp1 HG00438.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.785-2288T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16020828 | |||||||
| chr4:16020917 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(282): Show |
287 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.785-2377C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16020917 | |||||||
| chr4:16020944 | T | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(282): Show |
287 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.784+2382A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16020944 | |||||||
| chr4:16021098 | C | CA | 96 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(93): Show |
97 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.784+2227dupT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16021098 | |||||||
| chr4:16021098 | C | CAA | 133 | a0001c0001t0001g0024 a0001c0001t0001g0042 a0001c0001t0001g0091 others(130): Show |
134 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.784+2226_784+2227d others(4): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16021098 | |||||||
| chr4:16021098 | C | CAAA | 10 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0061 others(7): Show |
10 | HG02293.hp2 HG02559.hp1 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.784+2225_784+2227d others(5): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16021098 | |||||||
| chr4:16021098 | C | CAAAA | 21 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0105 others(18): Show |
21 | HG01081.hp1 HG01106.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.784+2224_784+2227d others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16021098 | |||||||
| chr4:16021187 | G | A | 257 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(254): Show |
259 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.784+2139C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16021187 | |||||||
| chr4:16021202 | CA | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(282): Show |
287 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(284): Show |
intron_variant | MODIFIER | c.784+2123delT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16021202 | |||||||
| chr4:16021525 | T | A | 106 | a0001c0001t0001g0042 a0001c0001t0001g0091 a0001c0001t0001g0094 others(103): Show |
107 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(104): Show |
intron_variant | MODIFIER | c.784+1801A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16021525 | |||||||
| chr4:16021804 | G | A | 1 | a0007c0017t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.784+1522C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16021804 | |||||||
| chr4:16021813 | A | T | 1 | a0001c0004t0002g0322 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.784+1513T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16021813 | |||||||
| chr4:16021880 | G | A | 15 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0288 others(12): Show |
15 | HG02622.hp1 HG02970.hp2 NA18944.hp2 others(12): Show |
intron_variant | MODIFIER | c.784+1446C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16021880 | |||||||
| chr4:16022382 | T | C | 1 | a0001c0003t0004g0011 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.784+944A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16022382 | |||||||
| chr4:16022513 | G | A | 40 | a0001c0001t0001g0033 a0001c0001t0001g0061 a0001c0001t0001g0067 others(37): Show |
40 | HG01081.hp1 HG01106.hp2 HG01346.hp2 others(37): Show |
intron_variant | MODIFIER | c.784+813C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16022513 | |||||||
| chr4:16022525 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.784+801T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16022525 | |||||||
| chr4:16022554 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.784+772T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16022554 | |||||||
| chr4:16022573 | C | G | 1 | a0001c0018t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.784+753G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16022573 | |||||||
| chr4:16022592 | A | AG | 41 | a0001c0001t0001g0033 a0001c0001t0001g0061 a0001c0001t0001g0067 others(38): Show |
41 | HG01081.hp1 HG01106.hp2 HG01346.hp2 others(38): Show |
intron_variant | MODIFIER | c.784+733dupC | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16022592 | |||||||
| chr4:16022748 | T | C | 1 | a0001c0001t0001g0315 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.784+578A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16022748 | |||||||
| chr4:16022786 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.784+540T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16022786 | |||||||
| chr4:16022857 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.784+469A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16022857 | |||||||
| chr4:16022861 | C | T | 4 | a0001c0001t0002g0066 a0001c0001t0003g0090 a0001c0001t0003g0316 others(1): Show |
4 | HG00621.hp2 NA18977.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.784+465G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16022861 | |||||||
| chr4:16022942 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(258): Show |
263 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.784+384G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16022942 | |||||||
| chr4:16023262 | A | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(243): Show |
248 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.784+64T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 8/27 | chr4 | 16023262 | |||||||
| chr4:16023516 | A | G | 1 | a0001c0001t0003g0090 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.695-101T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 7/27 | chr4 | 16023516 | |||||||
| chr4:16023518 | C | G | 6 | a0001c0001t0001g0014 a0001c0001t0001g0054 a0001c0001t0004g0053 others(3): Show |
6 | HG02451.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.695-103G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 7/27 | chr4 | 16023518 | |||||||
| chr4:16023547 | G | T | 1 | a0001c0001t0003g0060 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.695-132C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 7/27 | chr4 | 16023547 | |||||||
| chr4:16023555 | C | T | 1 | a0001c0004t0002g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.695-140G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 7/27 | chr4 | 16023555 | |||||||
| chr4:16023704 | G | A | 1 | a0001c0004t0002g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.695-289C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 7/27 | chr4 | 16023704 | |||||||
| chr4:16023758 | G | T | 1 | a0001c0001t0001g0310 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.695-343C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 7/27 | chr4 | 16023758 | |||||||
| chr4:16023829 | C | A | 1 | a0007c0017t0001g0019 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.695-414G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 7/27 | chr4 | 16023829 | |||||||
| chr4:16023829 | C | T | 1 | a0001c0001t0009g0076 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.695-414G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 7/27 | chr4 | 16023829 | |||||||
| chr4:16023873 | C | T | 3 | a0001c0001t0002g0354 a0001c0001t0005g0080 a0001c0003t0002g0017 |
3 | HG02257.hp2 HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.694+422G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 7/27 | chr4 | 16023873 | |||||||
| chr4:16024013 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(45): Show |
49 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.694+282G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 7/27 | chr4 | 16024013 | |||||||
| chr4:16024214 | C | T | 70 | a0001c0001t0001g0042 a0001c0001t0001g0091 a0001c0001t0001g0094 others(67): Show |
71 | HG00323.hp1 HG00323.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.694+81G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 7/27 | chr4 | 16024214 | |||||||
| chr4:16024230 | A | G | 76 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0113 others(73): Show |
76 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.694+65T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 7/27 | chr4 | 16024230 | |||||||
| chr4:16024372 | A | G | 6 | a0001c0001t0001g0014 a0001c0001t0001g0054 a0001c0001t0004g0053 others(3): Show |
6 | HG02451.hp2 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.631-14T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 6/27 | chr4 | 16024372 | |||||||
| chr4:16024408 | A | G | 1 | a0001c0001t0004g0028 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.631-50T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 6/27 | chr4 | 16024408 | |||||||
| chr4:16024700 | C | T | 2 | a0001c0004t0002g0004 a0001c0019t0005g0018 |
2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.631-342G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 6/27 | chr4 | 16024700 | |||||||
| chr4:16024835 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(241): Show |
246 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.630+357T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 6/27 | chr4 | 16024835 | |||||||
| chr4:16024858 | A | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(140): Show |
145 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.630+334T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 6/27 | chr4 | 16024858 | |||||||
| chr4:16024896 | C | T | 284 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(281): Show |
286 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.630+296G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 6/27 | chr4 | 16024896 | |||||||
| chr4:16024904 | T | A | 1 | a0001c0003t0002g0012 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.630+288A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 6/27 | chr4 | 16024904 | |||||||
| chr4:16025073 | C | T | 2 | a0001c0001t0003g0147 a0001c0001t0003g0273 |
2 | HG01361.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.630+119G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 6/27 | chr4 | 16025073 | |||||||
| chr4:16025112 | T | C | 2 | a0001c0001t0002g0146 a0011c0009t0004g0317 |
2 | HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.630+80A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 6/27 | chr4 | 16025112 | |||||||
| chr4:16025160 | G | A | 1 | a0001c0001t0002g0292 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.630+32C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 6/27 | chr4 | 16025160 | |||||||
| chr4:16025360 | T | C | 29 | a0001c0001t0001g0024 a0001c0001t0001g0043 a0001c0001t0001g0050 others(26): Show |
30 | HG00735.hp2 HG01192.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.510-48A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16025360 | |||||||
| chr4:16025466 | G | A | 1 | a0001c0001t0002g0112 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.510-154C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16025466 | |||||||
| chr4:16025494 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.510-182C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16025494 | |||||||
| chr4:16025602 | T | C | 1 | a0001c0001t0003g0209 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.510-290A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16025602 | |||||||
| chr4:16025719 | G | GCA | 30 | a0001c0001t0001g0137 a0001c0001t0001g0275 a0001c0001t0001g0278 others(27): Show |
30 | HG00423.hp1 HG00597.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.510-409_510-408dup others(2): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16025719 | |||||||
| chr4:16025719 | GCA | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(176): Show |
182 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.510-409_510-408del others(2): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16025719 | |||||||
| chr4:16025726 | C | T | 11 | a0001c0001t0001g0288 a0001c0001t0001g0310 a0001c0001t0002g0037 others(8): Show |
11 | HG00735.hp2 HG01192.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.510-414G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16025726 | |||||||
| chr4:16025740 | C | T | 22 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0061 others(19): Show |
22 | HG02145.hp1 HG02257.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.510-428G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16025740 | |||||||
| chr4:16025784 | C | T | 1 | a0001c0002t0004g0344 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.510-472G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16025784 | |||||||
| chr4:16025792 | T | C | 11 | a0001c0001t0001g0288 a0001c0001t0001g0310 a0001c0001t0002g0037 others(8): Show |
11 | HG00735.hp2 HG01192.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.510-480A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16025792 | |||||||
| chr4:16025855 | C | A | 1 | a0003c0007t0003g0314 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.510-543G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16025855 | |||||||
| chr4:16025917 | A | G | 1 | a0001c0001t0002g0267 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.510-605T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16025917 | |||||||
| chr4:16025932 | T | G | 367 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(364): Show |
370 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(367): Show |
intron_variant | MODIFIER | c.510-620A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16025932 | |||||||
| chr4:16025980 | G | A | 1 | a0001c0019t0005g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.510-668C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16025980 | |||||||
| chr4:16026066 | T | G | 2 | a0001c0001t0002g0078 a0001c0001t0003g0079 |
2 | NA18995.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.510-754A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16026066 | |||||||
| chr4:16026095 | T | G | 1 | a0011c0009t0004g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.510-783A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16026095 | |||||||
| chr4:16026127 | C | T | 5 | a0001c0001t0001g0068 a0001c0001t0001g0263 a0001c0001t0001g0311 others(2): Show |
5 | HG00544.hp2 HG01934.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-815G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16026127 | |||||||
| chr4:16026151 | G | C | 37 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0165 others(34): Show |
37 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.510-839C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16026151 | |||||||
| chr4:16026160 | C | G | 21 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0061 others(18): Show |
21 | HG02145.hp1 HG02257.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.510-848G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16026160 | |||||||
| chr4:16026182 | G | A | 1 | a0001c0002t0004g0027 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.510-870C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16026182 | |||||||
| chr4:16026190 | T | C | 1 | a0001c0001t0002g0220 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.510-878A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16026190 | |||||||
| chr4:16026202 | A | T | 1 | a0001c0003t0011g0013 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.510-890T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16026202 | |||||||
| chr4:16026390 | G | A | 1 | a0001c0001t0002g0210 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.510-1078C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16026390 | |||||||
| chr4:16026415 | G | A | 1 | a0001c0001t0009g0076 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.510-1103C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16026415 | |||||||
| chr4:16026473 | TA | T | 172 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0035 others(169): Show |
174 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.510-1162delT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16026473 | |||||||
| chr4:16026531 | C | T | 14 | a0001c0001t0001g0071 a0001c0001t0001g0288 a0001c0001t0001g0310 others(11): Show |
14 | HG00735.hp2 HG01192.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.510-1219G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16026531 | |||||||
| chr4:16026646 | C | T | 14 | a0001c0001t0001g0071 a0001c0001t0001g0288 a0001c0001t0001g0310 others(11): Show |
14 | HG00735.hp2 HG01192.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.510-1334G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16026646 | |||||||
| chr4:16026656 | G | A | 2 | a0001c0001t0002g0037 a0001c0002t0004g0344 |
2 | HG02258.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.510-1344C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16026656 | |||||||
| chr4:16026858 | G | A | 1 | a0001c0001t0002g0173 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.510-1546C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16026858 | |||||||
| chr4:16027116 | T | C | 8 | a0001c0001t0001g0288 a0001c0001t0001g0310 a0001c0001t0002g0059 others(5): Show |
8 | HG00735.hp2 HG01192.hp1 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.510-1804A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16027116 | |||||||
| chr4:16027243 | T | G | 148 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0043 others(145): Show |
150 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.510-1931A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16027243 | |||||||
| chr4:16027265 | A | C | 1 | a0001c0002t0002g0058 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.510-1953T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16027265 | |||||||
| chr4:16027297 | A | AAC | 32 | a0001c0001t0001g0035 a0001c0001t0001g0054 a0001c0001t0001g0071 others(29): Show |
32 | HG00735.hp2 HG01099.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.510-1987_510-1986d others(4): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16027297 | |||||||
| chr4:16027297 | A | AACACACA others(3): Show |
15 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0091 others(12): Show |
15 | HG00408.hp2 HG00621.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.510-1995_510-1986d others(12): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16027297 | |||||||
| chr4:16027297 | A | AACACACA others(5): Show |
70 | a0001c0001t0001g0024 a0001c0001t0001g0043 a0001c0001t0001g0095 others(67): Show |
72 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.510-1997_510-1986d others(14): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16027297 | |||||||
| chr4:16027297 | A | AACACACA others(7): Show |
51 | a0001c0001t0001g0021 a0001c0001t0001g0109 a0001c0001t0001g0159 others(48): Show |
51 | HG00438.hp1 HG00609.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.510-1999_510-1986d others(16): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16027297 | |||||||
| chr4:16027297 | A | AACACACA others(9): Show |
7 | a0001c0001t0002g0103 a0001c0001t0002g0196 a0001c0001t0002g0210 others(4): Show |
7 | HG00597.hp2 HG02723.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.510-2001_510-1986d others(18): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16027297 | |||||||
| chr4:16027297 | A | AACACACA others(11): Show |
1 | a0001c0001t0001g0197 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.510-2003_510-1986d others(20): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16027297 | |||||||
| chr4:16027297 | A | AACACACA others(13): Show |
7 | a0001c0001t0001g0042 a0001c0001t0002g0303 a0001c0001t0003g0065 others(4): Show |
7 | HG01109.hp1 HG01978.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.510-2005_510-1986d others(22): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16027297 | |||||||
| chr4:16027297 | A | AACACACA others(15): Show |
1 | a0004c0008t0002g0119 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.510-2007_510-1986d others(24): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16027297 | |||||||
| chr4:16027297 | A | AACACACA others(17): Show |
1 | a0011c0009t0004g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.510-2009_510-1986d others(26): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16027297 | |||||||
| chr4:16027297 | A | ACACACAC others(6): Show |
1 | a0001c0001t0001g0284 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.510-1986_510-1985i others(15): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16027297 | |||||||
| chr4:16027319 | C | CACACACA others(5): Show |
2 | a0001c0001t0001g0350 a0001c0001t0005g0346 |
2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.510-2008_510-2007i others(14): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16027319 | |||||||
| chr4:16027324 | A | ACACACAC others(6): Show |
1 | a0001c0001t0001g0068 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.510-2013_510-2012i others(15): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16027324 | |||||||
| chr4:16027441 | T | C | 4 | a0001c0001t0001g0054 a0001c0003t0001g0006 a0001c0003t0001g0010 others(1): Show |
4 | HG02886.hp2 HG03041.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-2129A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16027441 | |||||||
| chr4:16027495 | T | C | 1 | a0001c0003t0002g0009 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.510-2183A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16027495 | |||||||
| chr4:16027915 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.510-2603T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16027915 | |||||||
| chr4:16027935 | C | T | 1 | a0001c0002t0003g0192 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.510-2623G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16027935 | |||||||
| chr4:16028019 | A | T | 160 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0043 others(157): Show |
162 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.510-2707T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16028019 | |||||||
| chr4:16028078 | CACCGACA | C | 10 | a0001c0001t0001g0035 a0001c0001t0002g0052 a0001c0001t0002g0086 others(7): Show |
10 | HG02258.hp2 HG02630.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.510-2773_510-2767d others(9): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16028078 | |||||||
| chr4:16028351 | GA | G | 4 | a0001c0001t0004g0029 a0001c0001t0004g0031 a0001c0001t0006g0030 others(1): Show |
4 | HG02615.hp1 HG03130.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-3040delT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16028351 | |||||||
| chr4:16028394 | A | G | 1 | a0011c0009t0004g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.510-3082T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16028394 | |||||||
| chr4:16028421 | A | T | 1 | a0001c0001t0001g0310 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.510-3109T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16028421 | |||||||
| chr4:16028451 | A | G | 1 | a0011c0009t0004g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.510-3139T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16028451 | |||||||
| chr4:16028497 | T | A | 1 | a0001c0003t0002g0020 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.510-3185A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16028497 | |||||||
| chr4:16028580 | A | T | 1 | a0011c0009t0004g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.510-3268T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16028580 | |||||||
| chr4:16028624 | C | G | 9 | a0001c0001t0001g0035 a0001c0001t0002g0052 a0001c0001t0002g0086 others(6): Show |
9 | HG02258.hp2 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.510-3312G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16028624 | |||||||
| chr4:16028689 | AT | A | 149 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0043 others(146): Show |
151 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.510-3378delA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16028689 | |||||||
| chr4:16028693 | T | G | 1 | a0001c0001t0004g0331 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.510-3381A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16028693 | |||||||
| chr4:16028774 | T | C | 2 | a0001c0002t0001g0329 a0001c0016t0001g0143 |
2 | HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.510-3462A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16028774 | |||||||
| chr4:16028803 | C | T | 1 | a0001c0003t0011g0013 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.510-3491G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16028803 | |||||||
| chr4:16028899 | T | C | 1 | a0001c0001t0002g0205 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.510-3587A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16028899 | |||||||
| chr4:16028917 | C | T | 4 | a0001c0001t0004g0029 a0001c0001t0004g0031 a0001c0001t0006g0030 others(1): Show |
4 | HG02615.hp1 HG03130.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-3605G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16028917 | |||||||
| chr4:16029005 | C | T | 18 | a0001c0001t0001g0054 a0001c0001t0004g0053 a0001c0002t0004g0026 others(15): Show |
18 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-3693G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16029005 | |||||||
| chr4:16029360 | G | GT | 126 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0033 others(123): Show |
127 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(124): Show |
intron_variant | MODIFIER | c.509+3943dupA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16029360 | |||||||
| chr4:16029360 | G | GTT | 18 | a0001c0001t0001g0054 a0001c0001t0004g0053 a0001c0002t0004g0026 others(15): Show |
18 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.509+3942_509+3943d others(4): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16029360 | |||||||
| chr4:16029380 | A | G | 5 | a0001c0001t0002g0005 a0001c0001t0002g0342 a0001c0001t0002g0343 others(2): Show |
5 | HG02615.hp2 HG02809.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+3924T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16029380 | |||||||
| chr4:16029445 | C | A | 1 | a0001c0001t0001g0051 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.509+3859G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16029445 | |||||||
| chr4:16029488 | G | T | 1 | a0001c0001t0001g0116 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.509+3816C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16029488 | |||||||
| chr4:16029516 | C | T | 9 | a0001c0001t0001g0056 a0001c0001t0001g0113 a0001c0001t0001g0213 others(6): Show |
9 | HG00597.hp1 HG02523.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.509+3788G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16029516 | |||||||
| chr4:16029760 | G | C | 2 | a0001c0001t0002g0103 a0001c0001t0003g0104 |
2 | NA19002.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.509+3544C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16029760 | |||||||
| chr4:16029785 | T | C | 8 | a0001c0001t0001g0042 a0001c0001t0002g0303 a0001c0001t0003g0065 others(5): Show |
8 | HG01109.hp1 HG01978.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.509+3519A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16029785 | |||||||
| chr4:16029825 | C | T | 205 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0023 others(202): Show |
206 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(203): Show |
intron_variant | MODIFIER | c.509+3479G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16029825 | |||||||
| chr4:16029898 | AAG | A | 4 | a0001c0001t0001g0071 a0001c0001t0002g0297 a0001c0001t0005g0036 others(1): Show |
4 | HG02622.hp1 HG02970.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+3404_509+3405d others(4): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16029898 | |||||||
| chr4:16030111 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.509+3193A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16030111 | |||||||
| chr4:16030189 | G | T | 72 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0067 others(69): Show |
72 | HG00438.hp2 HG00609.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.509+3115C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16030189 | |||||||
| chr4:16030194 | C | T | 7 | a0001c0001t0001g0042 a0001c0001t0002g0303 a0001c0001t0003g0065 others(4): Show |
7 | HG01109.hp1 HG01978.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+3110G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16030194 | |||||||
| chr4:16030195 | G | A | 31 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0061 others(28): Show |
31 | HG01099.hp1 HG02145.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.509+3109C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16030195 | |||||||
| chr4:16030358 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.509+2946A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16030358 | |||||||
| chr4:16030427 | G | A | 1 | a0001c0005t0002g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.509+2877C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16030427 | |||||||
| chr4:16030430 | GA | G | 7 | a0001c0001t0001g0042 a0001c0001t0002g0303 a0001c0001t0003g0065 others(4): Show |
7 | HG01109.hp1 HG01978.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+2873delT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16030430 | |||||||
| chr4:16030570 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0094 others(71): Show |
75 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.509+2734G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16030570 | |||||||
| chr4:16030572 | G | A | 9 | a0001c0001t0001g0179 a0001c0001t0002g0180 a0001c0002t0001g0100 others(6): Show |
9 | HG00609.hp1 HG02080.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.509+2732C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16030572 | |||||||
| chr4:16030629 | A | T | 1 | a0001c0001t0003g0203 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.509+2675T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16030629 | |||||||
| chr4:16030646 | G | C | 4 | a0001c0001t0002g0037 a0001c0002t0004g0344 a0001c0003t0001g0152 others(1): Show |
4 | HG02258.hp1 HG02280.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+2658C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16030646 | |||||||
| chr4:16030915 | G | A | 1 | a0001c0002t0002g0237 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.509+2389C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16030915 | |||||||
| chr4:16030947 | G | A | 1 | a0003c0007t0001g0174 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.509+2357C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16030947 | |||||||
| chr4:16031017 | A | G | 263 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0023 others(260): Show |
264 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.509+2287T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16031017 | |||||||
| chr4:16031046 | A | G | 1 | a0001c0001t0001g0333 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.509+2258T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16031046 | |||||||
| chr4:16031069 | A | G | 1 | a0001c0001t0002g0244 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.509+2235T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16031069 | |||||||
| chr4:16031071 | T | C | 9 | a0001c0001t0001g0024 a0001c0001t0001g0352 a0001c0001t0001g0353 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.509+2233A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16031071 | |||||||
| chr4:16031258 | G | A | 1 | a0001c0003t0002g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.509+2046C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16031258 | |||||||
| chr4:16031325 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0023 others(217): Show |
221 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(218): Show |
intron_variant | MODIFIER | c.509+1979A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16031325 | |||||||
| chr4:16031326 | G | A | 1 | a0001c0002t0001g0227 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.509+1978C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16031326 | |||||||
| chr4:16031443 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0094 others(62): Show |
66 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.509+1861T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16031443 | |||||||
| chr4:16031528 | T | A | 2 | a0001c0001t0001g0350 a0001c0001t0005g0346 |
2 | HG02976.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.509+1776A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16031528 | |||||||
| chr4:16031711 | A | G | 5 | a0001c0001t0001g0071 a0001c0001t0002g0297 a0001c0001t0002g0354 others(2): Show |
5 | HG02486.hp1 HG02622.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+1593T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16031711 | |||||||
| chr4:16031747 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.509+1557G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16031747 | |||||||
| chr4:16031812 | G | A | 2 | a0001c0001t0001g0235 a0001c0001t0003g0003 |
3 | HG01515.hp1 HG01517.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.509+1492C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16031812 | |||||||
| chr4:16031947 | T | C | 1 | a0001c0018t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.509+1357A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16031947 | |||||||
| chr4:16031964 | G | A | 1 | a0001c0001t0001g0351 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.509+1340C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16031964 | |||||||
| chr4:16031980 | CAA | C | 14 | a0001c0001t0004g0053 a0001c0002t0004g0026 a0001c0002t0004g0027 others(11): Show |
14 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.509+1322_509+1323d others(4): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16031980 | |||||||
| chr4:16032086 | C | T | 1 | a0001c0001t0004g0347 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.509+1218G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16032086 | |||||||
| chr4:16032150 | C | CT | 102 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0035 others(99): Show |
102 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.509+1153dupA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16032150 | |||||||
| chr4:16032150 | C | CTT | 79 | a0001c0001t0001g0023 a0001c0001t0001g0054 a0001c0001t0001g0056 others(76): Show |
79 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.509+1152_509+1153d others(4): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16032150 | |||||||
| chr4:16032150 | CT | C | 7 | a0001c0001t0001g0275 a0001c0001t0002g0146 a0001c0001t0002g0290 others(4): Show |
7 | HG01074.hp1 HG01175.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+1153delA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16032150 | |||||||
| chr4:16032169 | GTT | G | 3 | a0001c0001t0002g0037 a0001c0002t0004g0344 a0001c0003t0001g0152 |
3 | HG02258.hp1 HG02280.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.509+1133_509+1134d others(4): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16032169 | |||||||
| chr4:16032260 | C | T | 5 | a0001c0001t0001g0054 a0001c0003t0001g0006 a0001c0003t0001g0010 others(2): Show |
5 | HG02717.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+1044G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16032260 | |||||||
| chr4:16032758 | T | C | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0003t0002g0012 |
3 | HG03225.hp2 HG03579.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.509+546A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16032758 | |||||||
| chr4:16032902 | A | T | 117 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(114): Show |
117 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(114): Show |
intron_variant | MODIFIER | c.509+402T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16032902 | |||||||
| chr4:16032966 | C | T | 198 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0035 others(195): Show |
199 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(196): Show |
intron_variant | MODIFIER | c.509+338G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16032966 | |||||||
| chr4:16033002 | G | T | 1 | a0011c0009t0004g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.509+302C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16033002 | |||||||
| chr4:16033011 | G | A | 192 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0035 others(189): Show |
193 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(190): Show |
intron_variant | MODIFIER | c.509+293C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16033011 | |||||||
| chr4:16033097 | C | CT | 76 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0067 others(73): Show |
76 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.509+206dupA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16033097 | |||||||
| chr4:16033110 | C | T | 1 | a0001c0001t0002g0182 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.509+194G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16033110 | |||||||
| chr4:16033186 | G | GT | 8 | a0001c0001t0001g0042 a0001c0001t0003g0065 a0001c0001t0003g0163 others(5): Show |
8 | HG01109.hp1 HG01993.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.509+117dupA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 5/27 | chr4 | 16033186 | |||||||
| chr4:16033586 | C | CT | 58 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0061 others(55): Show |
58 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.304-78dupA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16033586 | |||||||
| chr4:16033586 | C | CTT | 213 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(210): Show |
215 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.304-79_304-78dupAA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16033586 | |||||||
| chr4:16033586 | C | CTTT | 18 | a0001c0001t0001g0262 a0001c0001t0002g0005 a0001c0001t0002g0048 others(15): Show |
18 | HG00738.hp1 HG01167.hp1 HG01993.hp1 others(15): Show |
intron_variant | MODIFIER | c.304-80_304-78dupAA others(1): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16033586 | |||||||
| chr4:16033586 | C | CTTTT | 74 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0050 others(71): Show |
75 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.304-81_304-78dupAA others(2): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16033586 | |||||||
| chr4:16033643 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.304-134C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16033643 | |||||||
| chr4:16033672 | C | A | 78 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0050 others(75): Show |
79 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.304-163G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16033672 | |||||||
| chr4:16033715 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.304-206C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16033715 | |||||||
| chr4:16033741 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.304-232C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16033741 | |||||||
| chr4:16033902 | C | CAT | 6 | a0001c0001t0001g0071 a0001c0001t0002g0297 a0001c0001t0002g0354 others(3): Show |
6 | HG02486.hp1 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-395_304-394dup others(2): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16033902 | |||||||
| chr4:16033902 | CAT | C | 116 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(113): Show |
116 | HG00438.hp2 HG00609.hp1 HG00738.hp2 others(113): Show |
intron_variant | MODIFIER | c.304-395_304-394del others(2): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16033902 | |||||||
| chr4:16033919 | A | G | 23 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0061 others(20): Show |
23 | HG01081.hp2 HG02145.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.304-410T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16033919 | |||||||
| chr4:16033981 | A | T | 138 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0033 others(135): Show |
138 | HG00438.hp2 HG00609.hp1 HG00738.hp2 others(135): Show |
intron_variant | MODIFIER | c.304-472T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16033981 | |||||||
| chr4:16033989 | A | G | 2 | a0001c0002t0002g0153 a0001c0002t0002g0156 |
2 | NA18968.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.304-480T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16033989 | |||||||
| chr4:16034172 | A | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0023 others(219): Show |
223 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(220): Show |
intron_variant | MODIFIER | c.304-663T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16034172 | |||||||
| chr4:16034220 | T | C | 1 | a0001c0001t0001g0351 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.304-711A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16034220 | |||||||
| chr4:16034290 | C | G | 5 | a0001c0001t0001g0024 a0001c0001t0001g0352 a0001c0001t0001g0353 others(2): Show |
5 | HG02622.hp2 HG02922.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-781G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16034290 | |||||||
| chr4:16034373 | C | T | 285 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(282): Show |
287 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(284): Show |
intron_variant | MODIFIER | c.304-864G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16034373 | |||||||
| chr4:16034489 | C | G | 140 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0033 others(137): Show |
140 | HG00438.hp2 HG00609.hp1 HG00738.hp2 others(137): Show |
intron_variant | MODIFIER | c.304-980G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16034489 | |||||||
| chr4:16034513 | C | T | 1 | a0001c0004t0002g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.304-1004G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16034513 | |||||||
| chr4:16034597 | G | A | 1 | a0001c0018t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.304-1088C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16034597 | |||||||
| chr4:16034614 | G | A | 1 | a0001c0001t0001g0351 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.304-1105C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16034614 | |||||||
| chr4:16034656 | C | T | 3 | a0001c0001t0003g0057 a0001c0001t0003g0316 a0001c0001t0003g0341 |
3 | HG00408.hp2 NA18993.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.303+1079G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16034656 | |||||||
| chr4:16034829 | A | G | 5 | a0001c0001t0001g0071 a0001c0001t0002g0297 a0001c0001t0002g0354 others(2): Show |
5 | HG02486.hp1 HG02622.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.303+906T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16034829 | |||||||
| chr4:16035074 | G | A | 5 | a0001c0001t0001g0054 a0001c0003t0001g0006 a0001c0003t0001g0010 others(2): Show |
5 | HG02717.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.303+661C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16035074 | |||||||
| chr4:16035217 | A | G | 1 | a0001c0001t0002g0052 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.303+518T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16035217 | |||||||
| chr4:16035427 | T | C | 1 | a0001c0004t0002g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.303+308A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16035427 | |||||||
| chr4:16035461 | C | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0023 others(218): Show |
222 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(219): Show |
intron_variant | MODIFIER | c.303+274G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16035461 | |||||||
| chr4:16035489 | G | A | 9 | a0001c0001t0001g0035 a0001c0001t0001g0351 a0001c0001t0002g0052 others(6): Show |
9 | HG02630.hp2 HG02723.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.303+246C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16035489 | |||||||
| chr4:16035526 | T | C | 1 | a0001c0018t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.303+209A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16035526 | |||||||
| chr4:16035695 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.303+40G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16035695 | |||||||
| chr4:16035725 | A | C | 1 | a0001c0001t0003g0128 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.303+10T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16035725 | |||||||
| chr4:16035729 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0094 others(70): Show |
74 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(71): Show |
splice_region_variant&intron_variant | LOW | c.303+6G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 4/27 | chr4 | 16035729 | |||||||
| chr4:16036041 | G | A | 1 | a0001c0001t0003g0341 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.277-280C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16036041 | |||||||
| chr4:16036077 | C | T | 6 | a0001c0001t0001g0042 a0001c0001t0003g0065 a0001c0001t0003g0222 others(3): Show |
6 | HG01109.hp1 HG01993.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.277-316G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16036077 | |||||||
| chr4:16036443 | T | C | 1 | a0001c0001t0001g0351 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.277-682A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16036443 | |||||||
| chr4:16036501 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.277-740G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16036501 | |||||||
| chr4:16036502 | G | A | 1 | a0001c0018t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.277-741C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16036502 | |||||||
| chr4:16036528 | C | T | 53 | a0001c0001t0001g0122 a0001c0001t0001g0159 a0001c0001t0001g0160 others(50): Show |
53 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(50): Show |
intron_variant | MODIFIER | c.277-767G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16036528 | |||||||
| chr4:16036719 | T | C | 77 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0067 others(74): Show |
77 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.277-958A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16036719 | |||||||
| chr4:16036743 | G | C | 4 | a0001c0001t0001g0107 a0001c0001t0001g0169 a0001c0001t0002g0108 others(1): Show |
4 | HG02165.hp1 NA18988.hp2 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.277-982C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16036743 | |||||||
| chr4:16036915 | G | T | 7 | a0001c0001t0001g0024 a0001c0001t0001g0352 a0001c0001t0001g0353 others(4): Show |
7 | HG02622.hp2 HG02723.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.277-1154C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16036915 | |||||||
| chr4:16037038 | C | T | 2 | a0001c0002t0001g0329 a0001c0016t0001g0143 |
2 | HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.277-1277G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16037038 | |||||||
| chr4:16037129 | G | T | 76 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0067 others(73): Show |
76 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.277-1368C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16037129 | |||||||
| chr4:16037177 | T | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0035 others(252): Show |
256 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.277-1416A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16037177 | |||||||
| chr4:16037272 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.277-1511G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16037272 | |||||||
| chr4:16037474 | T | A | 172 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(169): Show |
172 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.276+1472A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16037474 | |||||||
| chr4:16037920 | A | C | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.276+1026T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16037920 | |||||||
| chr4:16038201 | A | G | 6 | a0001c0001t0001g0042 a0001c0001t0003g0065 a0001c0001t0003g0222 others(3): Show |
6 | HG01109.hp1 HG01993.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.276+745T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16038201 | |||||||
| chr4:16038260 | A | G | 2 | a0001c0001t0003g0154 a0001c0002t0002g0055 |
2 | HG02015.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.276+686T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16038260 | |||||||
| chr4:16038343 | T | G | 69 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0067 others(66): Show |
69 | HG00438.hp2 HG00609.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.276+603A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16038343 | |||||||
| chr4:16038389 | A | T | 1 | a0001c0001t0004g0081 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.276+557T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16038389 | |||||||
| chr4:16038451 | G | A | 17 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0084 others(14): Show |
17 | HG02257.hp1 HG02280.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.276+495C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16038451 | |||||||
| chr4:16038471 | C | T | 66 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0067 others(63): Show |
66 | HG00438.hp2 HG00609.hp1 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.276+475G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16038471 | |||||||
| chr4:16038547 | C | T | 1 | a0001c0001t0003g0003 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.276+399G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16038547 | |||||||
| chr4:16038680 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.276+266G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 3/27 | chr4 | 16038680 | |||||||
| chr4:16039348 | A | G | 6 | a0001c0001t0001g0042 a0001c0001t0003g0065 a0001c0001t0003g0222 others(3): Show |
6 | HG01109.hp1 HG01993.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.221-347T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16039348 | |||||||
| chr4:16039455 | C | T | 1 | a0001c0002t0002g0072 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.221-454G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16039455 | |||||||
| chr4:16039456 | G | A | 1 | a0001c0018t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.221-455C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16039456 | |||||||
| chr4:16039606 | C | T | 5 | a0001c0001t0001g0054 a0001c0003t0001g0006 a0001c0003t0001g0010 others(2): Show |
5 | HG02717.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.221-605G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16039606 | |||||||
| chr4:16039715 | C | CA | 127 | a0001c0001t0001g0023 a0001c0001t0001g0054 a0001c0001t0001g0056 others(124): Show |
128 | HG00323.hp2 HG00438.hp2 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.221-715dupT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16039715 | |||||||
| chr4:16039715 | C | CAA | 84 | a0001c0001t0001g0042 a0001c0001t0001g0122 a0001c0001t0001g0127 others(81): Show |
84 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.221-716_221-715dup others(2): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16039715 | |||||||
| chr4:16039732 | T | A | 1 | a0001c0002t0001g0336 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.221-731A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16039732 | |||||||
| chr4:16039749 | C | A | 1 | a0001c0002t0002g0181 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.221-748G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16039749 | |||||||
| chr4:16039864 | G | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(192): Show |
196 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.221-863C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16039864 | |||||||
| chr4:16039943 | T | C | 1 | a0004c0008t0002g0077 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.221-942A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16039943 | |||||||
| chr4:16039996 | A | T | 266 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0035 others(263): Show |
267 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.221-995T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16039996 | |||||||
| chr4:16040013 | G | A | 1 | a0001c0001t0001g0330 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.221-1012C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16040013 | |||||||
| chr4:16040085 | A | G | 2 | a0001c0004t0002g0349 a0001c0004t0004g0312 |
2 | HG02970.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.221-1084T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16040085 | |||||||
| chr4:16040107 | G | C | 4 | a0001c0001t0001g0116 a0001c0001t0001g0333 a0001c0001t0002g0220 others(1): Show |
4 | HG00323.hp2 HG01515.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-1106C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16040107 | |||||||
| chr4:16040112 | G | C | 1 | a0001c0018t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.221-1111C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16040112 | |||||||
| chr4:16040152 | A | G | 1 | a0001c0001t0002g0342 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.221-1151T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16040152 | |||||||
| chr4:16040277 | A | G | 1 | a0011c0009t0004g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.221-1276T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16040277 | |||||||
| chr4:16040278 | G | GA | 266 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0035 others(263): Show |
267 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.221-1278dupT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16040278 | |||||||
| chr4:16040356 | G | T | 70 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0067 others(67): Show |
70 | HG00438.hp2 HG00609.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.221-1355C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16040356 | |||||||
| chr4:16040438 | T | C | 11 | a0001c0001t0003g0147 a0001c0004t0001g0046 a0001c0004t0002g0004 others(8): Show |
11 | HG01099.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-1437A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16040438 | |||||||
| chr4:16040664 | A | T | 1 | a0001c0011t0003g0356 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.221-1663T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16040664 | |||||||
| chr4:16040728 | A | T | 8 | a0001c0001t0002g0052 a0001c0001t0002g0115 a0001c0001t0004g0025 others(5): Show |
8 | HG01109.hp2 HG01884.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-1727T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16040728 | |||||||
| chr4:16040832 | G | A | 1 | a0001c0001t0004g0331 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.221-1831C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16040832 | |||||||
| chr4:16040891 | T | C | 3 | a0001c0001t0002g0052 a0001c0005t0001g0327 a0001c0005t0002g0022 |
3 | NA19043.hp2 NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.221-1890A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16040891 | |||||||
| chr4:16040971 | T | C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | NA18612.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.221-1970A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16040971 | |||||||
| chr4:16041003 | C | T | 1 | a0001c0001t0002g0240 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.221-2002G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041003 | |||||||
| chr4:16041030 | G | A | 68 | a0001c0001t0001g0122 a0001c0001t0001g0159 a0001c0001t0001g0160 others(65): Show |
68 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.221-2029C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041030 | |||||||
| chr4:16041083 | T | A | 1 | a0001c0018t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.221-2082A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041083 | |||||||
| chr4:16041153 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0002g0086 |
2 | HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.221-2152C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041153 | |||||||
| chr4:16041243 | C | T | 120 | a0001c0001t0001g0023 a0001c0001t0001g0042 a0001c0001t0001g0054 others(117): Show |
120 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.221-2242G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041243 | |||||||
| chr4:16041349 | T | TA | 10 | a0001c0001t0001g0137 a0001c0001t0003g0147 a0001c0004t0001g0046 others(7): Show |
10 | HG01099.hp1 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.221-2349dupT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041349 | |||||||
| chr4:16041501 | G | A | 1 | a0001c0003t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.221-2500C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041501 | |||||||
| chr4:16041567 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.221-2566T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041567 | |||||||
| chr4:16041646 | G | C | 3 | a0001c0001t0003g0147 a0001c0004t0002g0322 a0001c0004t0004g0321 |
3 | HG01099.hp1 NA18952.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.221-2645C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041646 | |||||||
| chr4:16041734 | C | T | 3 | a0001c0001t0001g0351 a0001c0003t0002g0008 a0001c0003t0004g0007 |
3 | HG02451.hp2 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.221-2733G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041734 | |||||||
| chr4:16041735 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.221-2734C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041735 | |||||||
| chr4:16041747 | CAAATAAA others(1): Show |
C | 21 | a0001c0001t0001g0014 a0001c0001t0001g0033 a0001c0001t0001g0042 others(18): Show |
21 | HG01109.hp1 HG01993.hp1 HG02148.hp2 others(18): Show |
intron_variant | MODIFIER | c.221-2754_221-2747d others(10): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041747 | |||||||
| chr4:16041747 | CAAATAAA others(5): Show |
C | 75 | a0001c0001t0001g0021 a0001c0001t0001g0054 a0001c0001t0001g0122 others(72): Show |
75 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.221-2758_221-2747d others(14): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041747 | |||||||
| chr4:16041747 | CAAATAAA others(9): Show |
C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(68): Show |
72 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.221-2762_221-2747d others(18): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041747 | |||||||
| chr4:16041763 | T | A | 71 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0067 others(68): Show |
71 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.221-2762A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041763 | |||||||
| chr4:16041767 | TAAATAAA others(3): Show |
T | 3 | a0001c0001t0001g0350 a0001c0001t0002g0048 a0001c0001t0003g0254 |
3 | HG00738.hp1 NA18906.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.221-2776_221-2767d others(12): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041767 | |||||||
| chr4:16041767 | TAAATAAA others(7): Show |
T | 10 | a0001c0001t0001g0071 a0001c0001t0001g0118 a0001c0001t0001g0360 others(7): Show |
10 | HG01884.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.221-2780_221-2767d others(16): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041767 | |||||||
| chr4:16041771 | TAAATAAA others(3): Show |
T | 1 | a0001c0001t0002g0297 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.221-2780_221-2771d others(12): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041771 | |||||||
| chr4:16041771 | TAAATAAA others(7): Show |
T | 2 | a0001c0004t0002g0004 a0001c0004t0004g0049 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.221-2784_221-2771d others(16): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041771 | |||||||
| chr4:16041773 | A | T | 1 | a0001c0018t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.221-2772T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041773 | |||||||
| chr4:16041773 | AATAAATA others(9): Show |
A | 10 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0051 others(7): Show |
11 | HG01243.hp1 HG01515.hp1 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-2788_221-2773d others(18): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041773 | |||||||
| chr4:16041775 | TAAATAAA others(3): Show |
T | 6 | a0001c0001t0002g0016 a0001c0001t0004g0015 a0001c0001t0004g0029 others(3): Show |
6 | HG02280.hp1 HG02615.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-2784_221-2775d others(12): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041775 | |||||||
| chr4:16041777 | A | T | 3 | a0001c0003t0002g0008 a0001c0003t0004g0007 a0001c0018t0001g0215 |
3 | HG02451.hp2 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.221-2776T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041777 | |||||||
| chr4:16041777 | AATAAATA others(5): Show |
A | 7 | a0001c0001t0001g0248 a0001c0001t0002g0037 a0001c0001t0002g0111 others(4): Show |
7 | HG01074.hp2 HG01934.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-2788_221-2777d others(14): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041777 | |||||||
| chr4:16041777 | AATAAATA others(7): Show |
A | 1 | a0011c0009t0004g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.221-2790_221-2777d others(16): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041777 | |||||||
| chr4:16041777 | AATAAATA others(9): Show |
A | 3 | a0001c0001t0004g0145 a0001c0001t0004g0348 a0001c0003t0002g0020 |
3 | HG02145.hp1 HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.221-2792_221-2777d others(18): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041777 | |||||||
| chr4:16041781 | A | T | 12 | a0001c0001t0001g0350 a0001c0001t0002g0048 a0001c0001t0002g0220 others(9): Show |
12 | HG00738.hp1 HG01515.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.221-2780T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041781 | |||||||
| chr4:16041781 | AATAAATA others(1): Show |
A | 7 | a0001c0001t0001g0024 a0001c0001t0001g0352 a0001c0001t0001g0353 others(4): Show |
7 | HG02622.hp2 HG02922.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-2788_221-2781d others(10): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041781 | |||||||
| chr4:16041781 | AATAAATA others(3): Show |
A | 71 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0067 others(68): Show |
71 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.221-2790_221-2781d others(12): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041781 | |||||||
| chr4:16041781 | AATAAATA others(5): Show |
A | 5 | a0001c0001t0002g0115 a0001c0001t0004g0025 a0001c0001t0004g0034 others(2): Show |
5 | HG01109.hp2 HG01884.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.221-2792_221-2781d others(14): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041781 | |||||||
| chr4:16041785 | A | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(116): Show |
120 | HG00323.hp1 HG00323.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.221-2784T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041785 | |||||||
| chr4:16041789 | T | A | 1 | a0001c0001t0002g0052 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.221-2788A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041789 | |||||||
| chr4:16041791 | T | A | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.221-2790A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041791 | |||||||
| chr4:16041793 | T | A | 2 | a0001c0001t0002g0052 a0001c0005t0001g0327 |
2 | NA20129.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.221-2792A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041793 | |||||||
| chr4:16041849 | T | C | 75 | a0001c0001t0001g0023 a0001c0001t0001g0056 a0001c0001t0001g0067 others(72): Show |
75 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.221-2848A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041849 | |||||||
| chr4:16041871 | G | A | 8 | a0001c0001t0001g0275 a0001c0001t0001g0299 a0001c0001t0003g0148 others(5): Show |
8 | HG01106.hp1 HG01346.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-2870C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041871 | |||||||
| chr4:16041874 | G | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0039 others(76): Show |
80 | HG00323.hp1 HG00323.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.221-2873C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041874 | |||||||
| chr4:16041912 | T | C | 67 | a0001c0001t0001g0054 a0001c0001t0001g0122 a0001c0001t0001g0159 others(64): Show |
67 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.221-2911A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041912 | |||||||
| chr4:16041960 | C | T | 1 | a0001c0002t0002g0276 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.221-2959G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041960 | |||||||
| chr4:16041985 | T | C | 76 | a0001c0001t0001g0122 a0001c0001t0001g0159 a0001c0001t0001g0160 others(73): Show |
76 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.221-2984A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16041985 | |||||||
| chr4:16042051 | C | T | 5 | a0001c0001t0001g0054 a0001c0003t0001g0006 a0001c0003t0001g0010 others(2): Show |
5 | HG02717.hp1 HG02886.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.221-3050G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16042051 | |||||||
| chr4:16042201 | T | C | 1 | a0001c0001t0003g0060 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.221-3200A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16042201 | |||||||
| chr4:16042283 | T | C | 72 | a0001c0001t0001g0122 a0001c0001t0001g0159 a0001c0001t0001g0160 others(69): Show |
72 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.221-3282A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16042283 | |||||||
| chr4:16042404 | G | T | 11 | a0001c0001t0002g0115 a0001c0001t0003g0065 a0001c0001t0003g0222 others(8): Show |
11 | HG01109.hp2 HG01884.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.221-3403C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16042404 | |||||||
| chr4:16042409 | C | A | 2 | a0001c0001t0003g0254 a0001c0001t0003g0281 |
2 | HG01934.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.221-3408G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16042409 | |||||||
| chr4:16042424 | A | T | 1 | a0001c0001t0001g0288 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.221-3423T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16042424 | |||||||
| chr4:16042460 | A | G | 2 | a0001c0001t0003g0065 a0001c0001t0003g0286 |
2 | NA18969.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.221-3459T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16042460 | |||||||
| chr4:16042478 | A | T | 13 | a0001c0001t0001g0189 a0001c0001t0001g0279 a0001c0001t0002g0320 others(10): Show |
13 | HG00673.hp1 HG01099.hp1 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.221-3477T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16042478 | |||||||
| chr4:16042860 | C | T | 2 | a0001c0001t0002g0048 a0001c0002t0002g0276 |
2 | HG00738.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.221-3859G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16042860 | |||||||
| chr4:16042866 | G | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0039 others(81): Show |
87 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.221-3865C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16042866 | |||||||
| chr4:16042888 | T | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0003g0038 |
4 | NA18953.hp2 NA19011.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-3887A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16042888 | |||||||
| chr4:16043036 | G | A | 1 | a0001c0001t0002g0111 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.221-4035C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16043036 | |||||||
| chr4:16043061 | A | G | 1 | a0001c0005t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.221-4060T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16043061 | |||||||
| chr4:16043221 | C | A | 1 | a0001c0001t0002g0255 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.221-4220G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16043221 | |||||||
| chr4:16043293 | A | T | 2 | a0001c0003t0001g0152 a0001c0018t0001g0215 |
2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.221-4292T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16043293 | |||||||
| chr4:16043356 | T | C | 1 | a0001c0011t0003g0356 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.221-4355A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16043356 | |||||||
| chr4:16043391 | T | A | 1 | a0001c0001t0001g0339 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.221-4390A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16043391 | |||||||
| chr4:16043409 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.221-4408G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16043409 | |||||||
| chr4:16043474 | C | T | 1 | a0001c0005t0004g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.221-4473G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16043474 | |||||||
| chr4:16043481 | C | G | 307 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0023 others(304): Show |
309 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.221-4480G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16043481 | |||||||
| chr4:16043743 | A | G | 307 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0023 others(304): Show |
309 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(306): Show |
intron_variant | MODIFIER | c.221-4742T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16043743 | |||||||
| chr4:16043979 | C | T | 1 | a0001c0001t0004g0081 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.221-4978G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16043979 | |||||||
| chr4:16044012 | G | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0023 others(305): Show |
310 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(307): Show |
intron_variant | MODIFIER | c.221-5011C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16044012 | |||||||
| chr4:16044066 | G | A | 2 | a0001c0001t0001g0361 a0002c0006t0002g0362 |
2 | NA19088.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.221-5065C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16044066 | |||||||
| chr4:16044109 | C | T | 10 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0351 others(7): Show |
11 | HG01109.hp1 HG01243.hp1 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.221-5108G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16044109 | |||||||
| chr4:16044373 | C | T | 3 | a0001c0001t0001g0351 a0001c0003t0002g0008 a0001c0003t0004g0007 |
3 | HG02451.hp2 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.221-5372G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16044373 | |||||||
| chr4:16044510 | C | A | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0004g0044 |
3 | HG01109.hp1 HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.221-5509G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16044510 | |||||||
| chr4:16044519 | G | A | 1 | a0001c0019t0005g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.221-5518C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16044519 | |||||||
| chr4:16044684 | G | A | 3 | a0001c0001t0002g0115 a0001c0001t0004g0034 a0001c0003t0002g0017 |
3 | HG01109.hp2 HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.221-5683C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16044684 | |||||||
| chr4:16044836 | CA | C | 3 | a0001c0001t0002g0115 a0001c0001t0004g0034 a0001c0005t0001g0218 |
3 | HG01109.hp2 HG01884.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.221-5836delT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16044836 | |||||||
| chr4:16044846 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.221-5845A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16044846 | |||||||
| chr4:16044854 | C | A | 1 | a0001c0005t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.221-5853G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16044854 | |||||||
| chr4:16044952 | T | C | 308 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0023 others(305): Show |
310 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(307): Show |
intron_variant | MODIFIER | c.221-5951A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16044952 | |||||||
| chr4:16045069 | G | A | 2 | a0001c0001t0001g0071 a0001c0005t0002g0022 |
2 | HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.221-6068C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16045069 | |||||||
| chr4:16045081 | T | A | 1 | a0001c0001t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.221-6080A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16045081 | |||||||
| chr4:16045091 | C | A | 2 | a0001c0001t0001g0021 a0001c0003t0002g0020 |
2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.221-6090G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16045091 | |||||||
| chr4:16045092 | C | T | 7 | a0001c0001t0001g0021 a0001c0001t0002g0115 a0001c0001t0004g0034 others(4): Show |
7 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-6091G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16045092 | |||||||
| chr4:16045094 | G | C | 2 | a0001c0001t0001g0021 a0001c0003t0002g0020 |
2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.221-6093C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16045094 | |||||||
| chr4:16045095 | C | T | 2 | a0001c0001t0001g0021 a0001c0003t0002g0020 |
2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.221-6094G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16045095 | |||||||
| chr4:16045096 | C | G | 2 | a0001c0001t0001g0021 a0001c0003t0002g0020 |
2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.221-6095G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16045096 | |||||||
| chr4:16045097 | G | T | 2 | a0001c0001t0001g0021 a0001c0003t0002g0020 |
2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.221-6096C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16045097 | |||||||
| chr4:16045163 | A | T | 3 | a0001c0002t0002g0207 a0002c0006t0001g0206 a0002c0006t0001g0208 |
3 | NA18970.hp1 NA18984.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.221-6162T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16045163 | |||||||
| chr4:16045346 | T | A | 3 | a0001c0001t0002g0297 a0001c0005t0001g0216 a0001c0005t0001g0327 |
3 | HG02970.hp1 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.221-6345A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16045346 | |||||||
| chr4:16045589 | T | C | 1 | a0001c0004t0002g0322 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.221-6588A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16045589 | |||||||
| chr4:16045616 | C | G | 2 | a0001c0003t0001g0152 a0011c0009t0004g0317 |
2 | HG02280.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.221-6615G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16045616 | |||||||
| chr4:16045709 | A | C | 1 | a0001c0001t0002g0320 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.221-6708T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16045709 | |||||||
| chr4:16045802 | C | T | 1 | a0001c0005t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.221-6801G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16045802 | |||||||
| chr4:16045806 | T | G | 1 | a0001c0005t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.221-6805A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16045806 | |||||||
| chr4:16045836 | T | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0054 others(66): Show |
71 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.221-6835A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16045836 | |||||||
| chr4:16045902 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.221-6901G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16045902 | |||||||
| chr4:16045984 | C | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0151 a0001c0001t0001g0263 others(1): Show |
4 | HG00544.hp2 NA18960.hp2 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.221-6983G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16045984 | |||||||
| chr4:16046048 | C | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0003g0038 others(2): Show |
6 | NA18953.hp2 NA18966.hp2 NA19009.hp1 others(3): Show |
intron_variant | MODIFIER | c.221-7047G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16046048 | |||||||
| chr4:16046110 | C | T | 1 | a0001c0005t0004g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.221-7109G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16046110 | |||||||
| chr4:16046198 | T | C | 1 | a0001c0002t0003g0256 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.221-7197A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16046198 | |||||||
| chr4:16046349 | T | G | 3 | a0001c0001t0001g0014 a0001c0001t0002g0016 a0001c0001t0004g0015 |
3 | HG02280.hp1 HG03540.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.221-7348A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16046349 | |||||||
| chr4:16046631 | A | T | 241 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(238): Show |
242 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.221-7630T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16046631 | |||||||
| chr4:16046640 | A | G | 1 | a0001c0005t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.221-7639T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16046640 | |||||||
| chr4:16046790 | T | G | 52 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0054 others(49): Show |
54 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.221-7789A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16046790 | |||||||
| chr4:16047117 | A | T | 1 | a0001c0001t0002g0173 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.221-8116T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16047117 | |||||||
| chr4:16047156 | T | C | 12 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(9): Show |
12 | HG01952.hp1 HG02015.hp2 HG03927.hp1 others(9): Show |
intron_variant | MODIFIER | c.221-8155A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16047156 | |||||||
| chr4:16047231 | G | C | 2 | a0001c0001t0001g0361 a0002c0006t0002g0362 |
2 | NA19088.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.221-8230C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16047231 | |||||||
| chr4:16047476 | A | G | 1 | a0001c0004t0004g0049 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.221-8475T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16047476 | |||||||
| chr4:16047520 | T | C | 5 | a0001c0001t0002g0115 a0001c0001t0004g0034 a0001c0001t0004g0145 others(2): Show |
5 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-8519A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16047520 | |||||||
| chr4:16047575 | T | TGTTACAA others(8): Show |
21 | a0001c0001t0001g0024 a0001c0001t0001g0189 a0001c0001t0001g0330 others(18): Show |
21 | HG01099.hp1 HG01167.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.221-8589_221-8575d others(17): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16047575 | |||||||
| chr4:16047756 | C | T | 315 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0023 others(312): Show |
318 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(315): Show |
intron_variant | MODIFIER | c.221-8755G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16047756 | |||||||
| chr4:16047757 | C | A | 1 | a0001c0005t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.221-8756G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16047757 | |||||||
| chr4:16047824 | C | G | 1 | a0001c0002t0001g0185 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.221-8823G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16047824 | |||||||
| chr4:16047962 | A | C | 1 | a0001c0018t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.221-8961T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16047962 | |||||||
| chr4:16048047 | G | A | 1 | a0001c0019t0005g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.221-9046C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16048047 | |||||||
| chr4:16048059 | G | T | 1 | a0011c0009t0004g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.221-9058C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16048059 | |||||||
| chr4:16048106 | C | T | 1 | a0001c0001t0001g0014 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.221-9105G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16048106 | |||||||
| chr4:16048364 | A | G | 5 | a0001c0001t0001g0360 a0001c0001t0001g0361 a0001c0001t0001g0363 others(2): Show |
5 | NA18949.hp2 NA18989.hp2 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-9363T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16048364 | |||||||
| chr4:16048526 | C | T | 47 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0091 others(44): Show |
48 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.221-9525G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16048526 | |||||||
| chr4:16048684 | G | A | 1 | a0001c0005t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.221-9683C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16048684 | |||||||
| chr4:16048759 | A | G | 2 | a0001c0001t0003g0087 a0010c0015t0003g0093 |
2 | NA19003.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.221-9758T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16048759 | |||||||
| chr4:16049068 | T | G | 21 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0137 others(18): Show |
21 | HG01109.hp2 HG01884.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.221-10067A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16049068 | |||||||
| chr4:16049082 | C | A | 1 | a0001c0001t0001g0095 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.221-10081G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16049082 | |||||||
| chr4:16049290 | G | A | 15 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0137 others(12): Show |
15 | HG01952.hp1 HG02015.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.221-10289C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16049290 | |||||||
| chr4:16049410 | T | C | 47 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0091 others(44): Show |
48 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.221-10409A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16049410 | |||||||
| chr4:16049507 | C | T | 315 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0023 others(312): Show |
318 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(315): Show |
intron_variant | MODIFIER | c.221-10506G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16049507 | |||||||
| chr4:16049724 | T | C | 5 | a0001c0001t0002g0115 a0001c0001t0004g0034 a0001c0001t0004g0145 others(2): Show |
5 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-10723A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16049724 | |||||||
| chr4:16049735 | T | C | 4 | a0001c0001t0002g0297 a0001c0001t0005g0036 a0001c0005t0001g0216 others(1): Show |
4 | HG02970.hp1 NA19030.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-10734A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16049735 | |||||||
| chr4:16049880 | A | G | 67 | a0001c0001t0001g0113 a0001c0001t0001g0118 a0001c0001t0001g0151 others(64): Show |
67 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.221-10879T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16049880 | |||||||
| chr4:16049968 | A | G | 58 | a0001c0001t0001g0023 a0001c0001t0001g0161 a0001c0001t0001g0162 others(55): Show |
58 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.221-10967T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16049968 | |||||||
| chr4:16050258 | C | CA | 26 | a0001c0001t0001g0021 a0001c0001t0001g0098 a0001c0001t0001g0102 others(23): Show |
26 | HG01952.hp1 HG01978.hp1 HG02015.hp2 others(23): Show |
intron_variant | MODIFIER | c.221-11258dupT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16050258 | |||||||
| chr4:16050402 | A | G | 70 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0091 others(67): Show |
71 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.221-11401T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16050402 | |||||||
| chr4:16050434 | T | C | 1 | a0001c0001t0001g0287 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.221-11433A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16050434 | |||||||
| chr4:16050438 | T | G | 68 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0091 others(65): Show |
69 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.221-11437A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16050438 | |||||||
| chr4:16050542 | T | C | 1 | a0001c0001t0002g0092 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.221-11541A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16050542 | |||||||
| chr4:16050796 | T | C | 2 | a0001c0001t0001g0357 a0001c0001t0002g0292 |
2 | HG03491.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.221-11795A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16050796 | |||||||
| chr4:16050971 | A | G | 1 | a0001c0001t0003g0233 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.221-11970T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16050971 | |||||||
| chr4:16051226 | A | G | 3 | a0001c0001t0001g0357 a0001c0001t0001g0364 a0001c0001t0002g0292 |
3 | HG03491.hp1 HG03834.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.221-12225T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16051226 | |||||||
| chr4:16051291 | T | C | 2 | a0001c0003t0001g0152 a0001c0018t0001g0215 |
2 | HG02280.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.221-12290A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16051291 | |||||||
| chr4:16051556 | C | A | 49 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0091 others(46): Show |
50 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.221-12555G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16051556 | |||||||
| chr4:16051556 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.221-12555G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16051556 | |||||||
| chr4:16051717 | T | C | 5 | a0001c0001t0002g0239 a0001c0001t0002g0258 a0001c0001t0002g0259 others(2): Show |
5 | HG00735.hp1 HG01255.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.221-12716A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16051717 | |||||||
| chr4:16051780 | G | C | 12 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(9): Show |
12 | HG01952.hp1 HG02015.hp2 HG03927.hp1 others(9): Show |
intron_variant | MODIFIER | c.221-12779C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16051780 | |||||||
| chr4:16051863 | G | A | 56 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0091 others(53): Show |
57 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.221-12862C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16051863 | |||||||
| chr4:16051903 | A | G | 1 | a0001c0003t0004g0007 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.221-12902T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16051903 | |||||||
| chr4:16051911 | A | G | 56 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0091 others(53): Show |
57 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.221-12910T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16051911 | |||||||
| chr4:16052073 | A | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG00621.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.221-13072T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16052073 | |||||||
| chr4:16052113 | C | T | 1 | a0001c0002t0001g0283 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.221-13112G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16052113 | |||||||
| chr4:16052276 | G | A | 12 | a0001c0001t0001g0021 a0001c0001t0002g0146 a0001c0001t0004g0025 others(9): Show |
12 | HG02559.hp1 HG02630.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.221-13275C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16052276 | |||||||
| chr4:16052439 | T | A | 1 | a0001c0001t0003g0079 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.221-13438A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16052439 | |||||||
| chr4:16052600 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0050 others(142): Show |
146 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.221-13599G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16052600 | |||||||
| chr4:16052763 | G | A | 1 | a0001c0002t0001g0184 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.221-13762C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16052763 | |||||||
| chr4:16052952 | C | G | 1 | a0001c0002t0003g0202 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.221-13951G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16052952 | |||||||
| chr4:16052988 | C | T | 1 | a0001c0002t0001g0187 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.221-13987G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16052988 | |||||||
| chr4:16053303 | G | A | 70 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0091 others(67): Show |
71 | HG00408.hp2 HG00423.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.221-14302C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16053303 | |||||||
| chr4:16053329 | T | G | 1 | a0001c0001t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.221-14328A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16053329 | |||||||
| chr4:16053383 | C | T | 7 | a0001c0001t0002g0115 a0001c0001t0004g0034 a0001c0001t0004g0145 others(4): Show |
7 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-14382G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16053383 | |||||||
| chr4:16053602 | C | T | 12 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(9): Show |
12 | HG01952.hp1 HG02015.hp2 HG03927.hp1 others(9): Show |
intron_variant | MODIFIER | c.221-14601G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16053602 | |||||||
| chr4:16053614 | G | A | 5 | a0001c0001t0002g0115 a0001c0001t0004g0034 a0001c0001t0004g0145 others(2): Show |
5 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-14613C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16053614 | |||||||
| chr4:16053735 | C | T | 5 | a0001c0001t0002g0005 a0001c0001t0002g0342 a0001c0001t0002g0343 others(2): Show |
5 | HG02615.hp2 HG02809.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-14734G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16053735 | |||||||
| chr4:16053863 | T | C | 12 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(9): Show |
12 | HG01952.hp1 HG02015.hp2 HG03927.hp1 others(9): Show |
intron_variant | MODIFIER | c.221-14862A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16053863 | |||||||
| chr4:16053893 | A | G | 305 | a0001c0001t0001g0001 a0001c0001t0001g0023 a0001c0001t0001g0024 others(302): Show |
308 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(305): Show |
intron_variant | MODIFIER | c.221-14892T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16053893 | |||||||
| chr4:16053900 | G | T | 1 | a0001c0001t0003g0212 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.221-14899C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16053900 | |||||||
| chr4:16053959 | T | C | 3 | a0001c0001t0001g0330 a0001c0001t0004g0331 a0001c0002t0001g0329 |
3 | HG01167.hp1 HG03491.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.221-14958A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16053959 | |||||||
| chr4:16054221 | C | T | 1 | a0001c0001t0003g0065 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.221-15220G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16054221 | |||||||
| chr4:16054237 | C | T | 16 | a0001c0001t0001g0021 a0001c0001t0001g0071 a0001c0001t0002g0297 others(13): Show |
16 | HG02559.hp1 HG02622.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.221-15236G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16054237 | |||||||
| chr4:16054453 | A | C | 57 | a0001c0001t0001g0023 a0001c0001t0001g0161 a0001c0001t0001g0162 others(54): Show |
57 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.221-15452T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16054453 | |||||||
| chr4:16054455 | C | T | 14 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(11): Show |
14 | HG00609.hp2 HG01952.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.221-15454G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16054455 | |||||||
| chr4:16054495 | A | C | 14 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(11): Show |
14 | HG00609.hp2 HG01952.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.221-15494T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16054495 | |||||||
| chr4:16054524 | C | T | 14 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(11): Show |
14 | HG00609.hp2 HG01952.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.221-15523G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16054524 | |||||||
| chr4:16054612 | A | G | 1 | a0001c0002t0003g0304 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.221-15611T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16054612 | |||||||
| chr4:16054731 | C | A | 5 | a0001c0001t0001g0098 a0001c0001t0003g0096 a0001c0001t0003g0097 others(2): Show |
5 | NA18612.hp2 NA18945.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.221-15730G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16054731 | |||||||
| chr4:16054784 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.221-15783G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16054784 | |||||||
| chr4:16054847 | C | T | 14 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(11): Show |
14 | HG00609.hp2 HG01952.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.221-15846G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16054847 | |||||||
| chr4:16054862 | A | G | 1 | a0001c0002t0002g0276 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.221-15861T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16054862 | |||||||
| chr4:16054888 | T | TA | 14 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(11): Show |
14 | HG00609.hp2 HG01952.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.221-15888dupT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16054888 | |||||||
| chr4:16054891 | ATGTGAGG others(3): Show |
A | 1 | a0001c0001t0003g0041 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.221-15900_221-1589 others(14): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16054891 | |||||||
| chr4:16055001 | C | T | 1 | a0001c0001t0003g0332 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.221-16000G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16055001 | |||||||
| chr4:16055002 | G | A | 8 | a0001c0001t0002g0115 a0001c0001t0004g0034 a0001c0001t0004g0145 others(5): Show |
8 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.221-16001C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16055002 | |||||||
| chr4:16055063 | C | T | 1 | a0001c0005t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.221-16062G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16055063 | |||||||
| chr4:16055173 | A | G | 2 | a0001c0005t0004g0075 a0011c0009t0004g0317 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.221-16172T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16055173 | |||||||
| chr4:16055187 | C | G | 14 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(11): Show |
14 | HG00609.hp2 HG01952.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.221-16186G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16055187 | |||||||
| chr4:16055253 | G | T | 14 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(11): Show |
14 | HG00609.hp2 HG01952.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.221-16252C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16055253 | |||||||
| chr4:16055258 | G | C | 7 | a0001c0001t0002g0115 a0001c0001t0004g0034 a0001c0001t0004g0145 others(4): Show |
7 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.221-16257C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16055258 | |||||||
| chr4:16055372 | C | T | 1 | a0001c0005t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.221-16371G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16055372 | |||||||
| chr4:16055499 | T | C | 1 | a0001c0003t0002g0012 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.221-16498A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16055499 | |||||||
| chr4:16055589 | C | T | 1 | a0002c0006t0001g0206 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.221-16588G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16055589 | |||||||
| chr4:16055702 | G | A | 1 | a0001c0005t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.221-16701C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16055702 | |||||||
| chr4:16055854 | CT | C | 8 | a0001c0001t0004g0025 a0001c0003t0001g0006 a0001c0003t0001g0010 others(5): Show |
8 | HG02630.hp2 HG02717.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.221-16854delA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16055854 | |||||||
| chr4:16055993 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.221-16992T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16055993 | |||||||
| chr4:16056071 | G | T | 57 | a0001c0001t0001g0023 a0001c0001t0001g0161 a0001c0001t0001g0162 others(54): Show |
57 | HG00408.hp1 HG00438.hp2 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.221-17070C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16056071 | |||||||
| chr4:16056123 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.221-17122C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16056123 | |||||||
| chr4:16056182 | A | G | 1 | a0001c0002t0002g0072 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.221-17181T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16056182 | |||||||
| chr4:16056201 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0122 others(64): Show |
68 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.221-17200C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16056201 | |||||||
| chr4:16056368 | C | A | 1 | a0001c0001t0003g0231 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.221-17367G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16056368 | |||||||
| chr4:16056552 | C | T | 1 | a0001c0004t0002g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.221-17551G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16056552 | |||||||
| chr4:16056573 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.221-17572C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16056573 | |||||||
| chr4:16056693 | T | C | 2 | a0001c0005t0001g0216 a0001c0005t0004g0217 |
2 | NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.221-17692A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16056693 | |||||||
| chr4:16056721 | T | C | 51 | a0001c0001t0001g0056 a0001c0001t0001g0091 a0001c0001t0001g0094 others(48): Show |
52 | HG00408.hp2 HG00423.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.221-17720A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16056721 | |||||||
| chr4:16056723 | G | C | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0235 others(4): Show |
8 | HG01109.hp1 HG01243.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.221-17722C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16056723 | |||||||
| chr4:16057017 | G | A | 13 | a0001c0001t0001g0021 a0001c0001t0004g0025 a0001c0003t0001g0006 others(10): Show |
13 | HG02559.hp1 HG02630.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.221-18016C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16057017 | |||||||
| chr4:16057123 | A | T | 1 | a0001c0001t0003g0041 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.221-18122T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16057123 | |||||||
| chr4:16057218 | A | C | 4 | a0001c0003t0001g0006 a0001c0003t0001g0010 a0001c0003t0002g0070 others(1): Show |
4 | HG02717.hp1 HG02886.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.221-18217T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16057218 | |||||||
| chr4:16057310 | A | G | 1 | a0001c0001t0002g0324 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.221-18309T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16057310 | |||||||
| chr4:16057316 | C | A | 2 | a0001c0001t0002g0052 a0001c0005t0001g0218 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.221-18315G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16057316 | |||||||
| chr4:16057420 | T | C | 7 | a0001c0001t0002g0297 a0001c0001t0005g0036 a0001c0005t0001g0216 others(4): Show |
7 | HG02895.hp1 HG02970.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+18267A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16057420 | |||||||
| chr4:16057727 | T | A | 1 | a0001c0001t0003g0041 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.220+17960A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16057727 | |||||||
| chr4:16057822 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.220+17865C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16057822 | |||||||
| chr4:16057837 | C | G | 1 | a0001c0001t0002g0120 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.220+17850G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16057837 | |||||||
| chr4:16057894 | C | T | 14 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(11): Show |
14 | HG00609.hp2 HG01952.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.220+17793G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16057894 | |||||||
| chr4:16057942 | A | G | 7 | a0001c0001t0004g0145 a0001c0001t0004g0348 a0001c0001t0005g0045 others(4): Show |
7 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.220+17745T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16057942 | |||||||
| chr4:16057963 | C | T | 1 | a0001c0003t0002g0020 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.220+17724G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16057963 | |||||||
| chr4:16057982 | T | C | 1 | a0001c0001t0002g0319 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.220+17705A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16057982 | |||||||
| chr4:16058006 | C | A | 4 | a0001c0004t0001g0046 a0001c0004t0002g0047 a0001c0004t0002g0135 others(1): Show |
4 | HG02145.hp2 HG03139.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+17681G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16058006 | |||||||
| chr4:16058226 | C | A | 2 | a0001c0002t0001g0185 a0001c0002t0001g0186 |
2 | HG00438.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.220+17461G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16058226 | |||||||
| chr4:16058326 | A | T | 1 | a0001c0002t0002g0058 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.220+17361T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16058326 | |||||||
| chr4:16058424 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.220+17263C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16058424 | |||||||
| chr4:16058566 | G | T | 2 | a0001c0001t0002g0063 a0001c0001t0002g0064 |
2 | NA19000.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.220+17121C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16058566 | |||||||
| chr4:16058650 | G | GA | 20 | a0001c0001t0001g0021 a0001c0001t0001g0137 a0001c0001t0001g0198 others(17): Show |
20 | HG01071.hp2 HG02080.hp2 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.220+17036dupT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16058650 | |||||||
| chr4:16058766 | T | C | 1 | a0001c0001t0002g0205 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.220+16921A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16058766 | |||||||
| chr4:16058930 | AG | A | 14 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(11): Show |
14 | HG00609.hp2 HG01952.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.220+16756delC | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16058930 | |||||||
| chr4:16058936 | G | T | 1 | a0001c0001t0003g0241 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.220+16751C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16058936 | |||||||
| chr4:16059184 | G | A | 1 | a0001c0004t0002g0322 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.220+16503C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16059184 | |||||||
| chr4:16059267 | G | A | 3 | a0001c0001t0005g0045 a0001c0003t0002g0017 a0001c0004t0004g0049 |
3 | HG02257.hp2 HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.220+16420C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16059267 | |||||||
| chr4:16059293 | T | A | 1 | a0001c0001t0003g0041 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.220+16394A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16059293 | |||||||
| chr4:16059294 | A | T | 1 | a0001c0001t0003g0041 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.220+16393T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16059294 | |||||||
| chr4:16059473 | G | A | 1 | a0001c0005t0002g0338 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.220+16214C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16059473 | |||||||
| chr4:16059528 | A | G | 14 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(11): Show |
14 | HG00609.hp2 HG01952.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.220+16159T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16059528 | |||||||
| chr4:16059600 | A | T | 1 | a0001c0001t0003g0241 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.220+16087T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16059600 | |||||||
| chr4:16059757 | T | A | 13 | a0001c0001t0001g0021 a0001c0001t0004g0025 a0001c0003t0001g0006 others(10): Show |
13 | HG02451.hp2 HG02559.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.220+15930A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16059757 | |||||||
| chr4:16059799 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.220+15888G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16059799 | |||||||
| chr4:16059892 | T | C | 1 | a0001c0001t0001g0280 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.220+15795A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16059892 | |||||||
| chr4:16059927 | G | T | 37 | a0001c0001t0001g0021 a0001c0001t0001g0109 a0001c0001t0001g0110 others(34): Show |
37 | HG00609.hp2 HG01952.hp1 HG02015.hp2 others(34): Show |
intron_variant | MODIFIER | c.220+15760C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16059927 | |||||||
| chr4:16060059 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.220+15628C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16060059 | |||||||
| chr4:16060108 | T | A | 4 | a0001c0001t0002g0005 a0001c0001t0002g0342 a0001c0001t0002g0343 others(1): Show |
4 | HG02615.hp2 HG02809.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.220+15579A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16060108 | |||||||
| chr4:16060156 | A | G | 3 | a0001c0001t0001g0333 a0001c0001t0002g0220 a0001c0001t0002g0326 |
3 | HG00323.hp2 HG01515.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.220+15531T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16060156 | |||||||
| chr4:16060310 | C | CT | 317 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(314): Show |
320 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(317): Show |
intron_variant | MODIFIER | c.220+15376dupA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16060310 | |||||||
| chr4:16060333 | A | G | 1 | a0001c0005t0004g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.220+15354T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16060333 | |||||||
| chr4:16060345 | T | G | 7 | a0001c0001t0002g0297 a0001c0001t0005g0036 a0001c0005t0001g0216 others(4): Show |
7 | HG02895.hp1 HG02970.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+15342A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16060345 | |||||||
| chr4:16060472 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0002g0016 a0001c0001t0004g0015 others(2): Show |
5 | HG02257.hp2 HG02258.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.220+15215G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16060472 | |||||||
| chr4:16060652 | T | A | 1 | a0001c0001t0003g0281 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.220+15035A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16060652 | |||||||
| chr4:16060868 | T | G | 1 | a0001c0002t0003g0192 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.220+14819A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16060868 | |||||||
| chr4:16060880 | C | T | 2 | a0001c0001t0002g0319 a0001c0001t0004g0323 |
2 | HG02723.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.220+14807G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16060880 | |||||||
| chr4:16060882 | C | A | 1 | a0001c0001t0003g0318 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.220+14805G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16060882 | |||||||
| chr4:16060981 | C | A | 1 | a0001c0001t0003g0057 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.220+14706G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16060981 | |||||||
| chr4:16061043 | A | C | 1 | a0001c0001t0003g0041 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.220+14644T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16061043 | |||||||
| chr4:16061200 | G | GC | 131 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0113 others(128): Show |
131 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.220+14486dupG | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16061200 | |||||||
| chr4:16061207 | A | C | 1 | a0001c0001t0003g0041 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.220+14480T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16061207 | |||||||
| chr4:16061343 | G | A | 1 | a0001c0005t0002g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.220+14344C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16061343 | |||||||
| chr4:16061432 | A | G | 244 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(241): Show |
245 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.220+14255T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16061432 | |||||||
| chr4:16061484 | G | C | 232 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(229): Show |
233 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.220+14203C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16061484 | |||||||
| chr4:16061769 | T | C | 1 | a0001c0002t0002g0156 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.220+13918A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16061769 | |||||||
| chr4:16061777 | C | T | 1 | a0001c0001t0003g0041 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.220+13910G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16061777 | |||||||
| chr4:16061778 | T | C | 1 | a0001c0001t0003g0041 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.220+13909A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16061778 | |||||||
| chr4:16061883 | A | T | 1 | a0001c0001t0003g0041 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.220+13804T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16061883 | |||||||
| chr4:16061888 | CT | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0039 others(72): Show |
77 | HG00408.hp2 HG00609.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.220+13798delA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16061888 | |||||||
| chr4:16061888 | CTT | C | 240 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(237): Show |
241 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.220+13797_220+1379 others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16061888 | |||||||
| chr4:16061931 | G | A | 1 | a0001c0001t0003g0209 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.220+13756C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16061931 | |||||||
| chr4:16061946 | C | T | 244 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(241): Show |
245 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.220+13741G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16061946 | |||||||
| chr4:16061947 | A | G | 19 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0002g0016 others(16): Show |
19 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.220+13740T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16061947 | |||||||
| chr4:16061952 | C | T | 1 | a0001c0001t0003g0124 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.220+13735G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16061952 | |||||||
| chr4:16061978 | G | A | 244 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(241): Show |
245 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.220+13709C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16061978 | |||||||
| chr4:16061994 | C | T | 244 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(241): Show |
245 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.220+13693G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16061994 | |||||||
| chr4:16062029 | C | T | 14 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(11): Show |
14 | HG00609.hp2 HG01952.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.220+13658G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16062029 | |||||||
| chr4:16062036 | C | A | 14 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(11): Show |
14 | HG00609.hp2 HG01952.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.220+13651G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16062036 | |||||||
| chr4:16062036 | C | T | 1 | a0001c0019t0005g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.220+13651G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16062036 | |||||||
| chr4:16062038 | C | G | 14 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(11): Show |
14 | HG00609.hp2 HG01952.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.220+13649G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16062038 | |||||||
| chr4:16062123 | A | C | 1 | a0001c0001t0003g0163 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.220+13564T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16062123 | |||||||
| chr4:16062136 | C | G | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.220+13551G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16062136 | |||||||
| chr4:16062138 | G | A | 244 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(241): Show |
245 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.220+13549C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16062138 | |||||||
| chr4:16062176 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.220+13511G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16062176 | |||||||
| chr4:16062181 | G | A | 238 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(235): Show |
239 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(236): Show |
intron_variant | MODIFIER | c.220+13506C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16062181 | |||||||
| chr4:16062184 | C | T | 153 | a0001c0001t0001g0035 a0001c0001t0001g0050 a0001c0001t0001g0051 others(150): Show |
153 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.220+13503G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16062184 | |||||||
| chr4:16062186 | C | A | 2 | a0001c0001t0001g0021 a0001c0003t0002g0020 |
2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.220+13501G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16062186 | |||||||
| chr4:16062211 | G | A | 244 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(241): Show |
245 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.220+13476C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16062211 | |||||||
| chr4:16062222 | T | C | 60 | a0001c0001t0001g0023 a0001c0001t0001g0161 a0001c0001t0001g0162 others(57): Show |
60 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.220+13465A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16062222 | |||||||
| chr4:16062282 | A | G | 1 | a0001c0005t0001g0219 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.220+13405T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16062282 | |||||||
| chr4:16062283 | C | A | 1 | a0001c0005t0001g0219 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.220+13404G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16062283 | |||||||
| chr4:16062404 | T | G | 269 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(266): Show |
270 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.220+13283A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16062404 | |||||||
| chr4:16062568 | G | T | 239 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(236): Show |
240 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.220+13119C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16062568 | |||||||
| chr4:16062660 | C | A | 2 | a0004c0008t0002g0077 a0004c0008t0002g0119 |
2 | HG01943.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.220+13027G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16062660 | |||||||
| chr4:16062697 | T | C | 266 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(263): Show |
267 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(264): Show |
intron_variant | MODIFIER | c.220+12990A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16062697 | |||||||
| chr4:16062815 | T | A | 1 | a0001c0002t0001g0187 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.220+12872A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16062815 | |||||||
| chr4:16063025 | C | T | 236 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0035 others(233): Show |
237 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.220+12662G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16063025 | |||||||
| chr4:16063097 | T | C | 9 | a0001c0003t0001g0006 a0001c0003t0001g0010 a0001c0003t0002g0008 others(6): Show |
9 | HG02451.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.220+12590A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16063097 | |||||||
| chr4:16063323 | C | T | 239 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(236): Show |
240 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.220+12364G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16063323 | |||||||
| chr4:16063398 | C | T | 219 | a0001c0001t0001g0023 a0001c0001t0001g0035 a0001c0001t0001g0042 others(216): Show |
220 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.220+12289G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16063398 | |||||||
| chr4:16063668 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.220+12019A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16063668 | |||||||
| chr4:16063669 | C | G | 1 | a0001c0001t0001g0068 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.220+12018G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16063669 | |||||||
| chr4:16063704 | C | T | 2 | a0001c0001t0001g0021 a0001c0003t0002g0020 |
2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.220+11983G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16063704 | |||||||
| chr4:16063727 | C | A | 235 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0035 others(232): Show |
236 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(233): Show |
intron_variant | MODIFIER | c.220+11960G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16063727 | |||||||
| chr4:16063921 | TG | T | 14 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(11): Show |
14 | HG00609.hp2 HG01952.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.220+11765delC | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16063921 | |||||||
| chr4:16063955 | A | T | 1 | a0001c0001t0003g0041 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.220+11732T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16063955 | |||||||
| chr4:16063957 | C | T | 263 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(260): Show |
264 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.220+11730G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16063957 | |||||||
| chr4:16064100 | G | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0056 others(47): Show |
52 | HG00408.hp2 HG00639.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.220+11587C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16064100 | |||||||
| chr4:16064192 | C | T | 1 | a0001c0002t0001g0227 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.220+11495G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16064192 | |||||||
| chr4:16064233 | T | A | 1 | a0001c0001t0003g0041 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.220+11454A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16064233 | |||||||
| chr4:16064395 | A | T | 1 | a0001c0003t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.220+11292T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16064395 | |||||||
| chr4:16064425 | C | T | 1 | a0001c0001t0003g0332 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.220+11262G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16064425 | |||||||
| chr4:16064459 | G | A | 1 | a0001c0019t0005g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.220+11228C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16064459 | |||||||
| chr4:16064531 | C | T | 6 | a0001c0001t0005g0036 a0001c0005t0001g0216 a0001c0005t0001g0327 others(3): Show |
6 | HG02895.hp1 HG03195.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.220+11156G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16064531 | |||||||
| chr4:16064545 | T | C | 1 | a0001c0005t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.220+11142A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16064545 | |||||||
| chr4:16064724 | C | T | 1 | a0001c0001t0002g0240 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.220+10963G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16064724 | |||||||
| chr4:16064761 | C | T | 60 | a0001c0001t0001g0122 a0001c0001t0001g0159 a0001c0001t0001g0160 others(57): Show |
60 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.220+10926G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16064761 | |||||||
| chr4:16064766 | G | A | 5 | a0001c0001t0001g0021 a0001c0003t0001g0152 a0001c0003t0002g0020 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.220+10921C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16064766 | |||||||
| chr4:16064854 | T | C | 7 | a0001c0001t0001g0033 a0001c0001t0002g0200 a0001c0001t0004g0028 others(4): Show |
7 | HG02572.hp2 HG02615.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+10833A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16064854 | |||||||
| chr4:16064943 | G | A | 1 | a0001c0004t0002g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.220+10744C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16064943 | |||||||
| chr4:16065149 | G | A | 7 | a0001c0001t0005g0036 a0001c0004t0004g0049 a0001c0005t0001g0216 others(4): Show |
7 | HG02258.hp2 HG02895.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+10538C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16065149 | |||||||
| chr4:16065202 | A | G | 1 | a0001c0005t0004g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.220+10485T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16065202 | |||||||
| chr4:16065221 | T | G | 1 | a0001c0001t0003g0079 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.220+10466A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16065221 | |||||||
| chr4:16065270 | C | T | 1 | a0001c0005t0002g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.220+10417G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16065270 | |||||||
| chr4:16065330 | A | C | 14 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(11): Show |
14 | HG00609.hp2 HG01952.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.220+10357T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16065330 | |||||||
| chr4:16065573 | A | G | 239 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0035 others(236): Show |
240 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.220+10114T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16065573 | |||||||
| chr4:16065643 | G | A | 154 | a0001c0001t0001g0035 a0001c0001t0001g0050 a0001c0001t0001g0051 others(151): Show |
154 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.220+10044C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16065643 | |||||||
| chr4:16065795 | G | A | 1 | a0001c0004t0002g0349 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.220+9892C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16065795 | |||||||
| chr4:16065796 | A | T | 1 | a0001c0004t0002g0349 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.220+9891T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16065796 | |||||||
| chr4:16065933 | A | G | 2 | a0001c0001t0002g0146 a0001c0004t0002g0004 |
2 | HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.220+9754T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16065933 | |||||||
| chr4:16066011 | G | A | 1 | a0004c0008t0002g0077 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.220+9676C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16066011 | |||||||
| chr4:16066140 | G | A | 1 | a0001c0005t0004g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.220+9547C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16066140 | |||||||
| chr4:16066208 | C | A | 1 | a0001c0001t0003g0281 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.220+9479G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16066208 | |||||||
| chr4:16066247 | CAT | C | 3 | a0001c0001t0001g0024 a0001c0003t0002g0017 a0001c0003t0011g0013 |
3 | HG02257.hp2 HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.220+9438_220+9439d others(4): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16066247 | |||||||
| chr4:16066250 | G | T | 3 | a0001c0001t0001g0024 a0001c0003t0002g0017 a0001c0003t0011g0013 |
3 | HG02257.hp2 HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.220+9437C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16066250 | |||||||
| chr4:16066252 | C | A | 3 | a0001c0001t0001g0024 a0001c0003t0002g0017 a0001c0003t0011g0013 |
3 | HG02257.hp2 HG02717.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.220+9435G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16066252 | |||||||
| chr4:16066477 | A | G | 234 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0035 others(231): Show |
235 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.220+9210T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16066477 | |||||||
| chr4:16066494 | G | A | 1 | a0001c0002t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.220+9193C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16066494 | |||||||
| chr4:16066528 | C | T | 1 | a0001c0001t0002g0324 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.220+9159G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16066528 | |||||||
| chr4:16066617 | T | C | 7 | a0001c0001t0005g0036 a0001c0004t0004g0049 a0001c0005t0001g0216 others(4): Show |
7 | HG02258.hp2 HG02895.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+9070A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16066617 | |||||||
| chr4:16066674 | T | G | 1 | a0001c0005t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.220+9013A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16066674 | |||||||
| chr4:16066742 | T | C | 9 | a0001c0001t0001g0067 a0001c0001t0001g0288 a0001c0001t0002g0059 others(6): Show |
9 | HG00621.hp2 NA18944.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.220+8945A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16066742 | |||||||
| chr4:16066787 | A | C | 1 | a0001c0005t0004g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.220+8900T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16066787 | |||||||
| chr4:16066907 | C | T | 1 | a0001c0001t0003g0149 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.220+8780G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16066907 | |||||||
| chr4:16066912 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.220+8775G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16066912 | |||||||
| chr4:16066913 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.220+8774C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16066913 | |||||||
| chr4:16066943 | A | T | 1 | a0001c0001t0002g0144 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.220+8744T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16066943 | |||||||
| chr4:16067022 | C | T | 234 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0035 others(231): Show |
235 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.220+8665G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16067022 | |||||||
| chr4:16067125 | C | T | 15 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(12): Show |
15 | HG00609.hp2 HG01952.hp1 HG02015.hp2 others(12): Show |
intron_variant | MODIFIER | c.220+8562G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16067125 | |||||||
| chr4:16067126 | G | A | 6 | a0001c0001t0001g0033 a0001c0001t0004g0028 a0001c0001t0004g0029 others(3): Show |
6 | HG02572.hp2 HG02615.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+8561C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16067126 | |||||||
| chr4:16067166 | G | A | 1 | a0001c0001t0003g0313 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.220+8521C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16067166 | |||||||
| chr4:16067187 | G | A | 1 | a0001c0001t0002g0282 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.220+8500C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16067187 | |||||||
| chr4:16067344 | C | A | 1 | a0001c0004t0004g0049 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.220+8343G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16067344 | |||||||
| chr4:16067394 | G | A | 1 | a0001c0002t0001g0131 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.220+8293C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16067394 | |||||||
| chr4:16067442 | G | T | 57 | a0001c0001t0001g0023 a0001c0001t0001g0161 a0001c0001t0001g0162 others(54): Show |
57 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.220+8245C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16067442 | |||||||
| chr4:16067704 | G | A | 1 | a0001c0005t0001g0219 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.220+7983C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16067704 | |||||||
| chr4:16067727 | C | T | 1 | a0001c0019t0005g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.220+7960G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16067727 | |||||||
| chr4:16067747 | C | T | 1 | a0011c0009t0004g0317 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.220+7940G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16067747 | |||||||
| chr4:16067797 | T | TCTTTCCT others(5): Show |
1 | a0001c0005t0002g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.220+7889_220+7890i others(14): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16067797 | |||||||
| chr4:16067813 | T | C | 1 | a0001c0002t0003g0285 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.220+7874A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16067813 | |||||||
| chr4:16067851 | G | C | 1 | a0001c0003t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.220+7836C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16067851 | |||||||
| chr4:16067860 | G | A | 1 | a0001c0002t0002g0369 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.220+7827C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16067860 | |||||||
| chr4:16067866 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.220+7821C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16067866 | |||||||
| chr4:16067870 | C | T | 9 | a0001c0003t0001g0006 a0001c0003t0001g0010 a0001c0003t0002g0008 others(6): Show |
9 | HG02451.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.220+7817G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16067870 | |||||||
| chr4:16067927 | T | C | 3 | a0001c0001t0004g0145 a0001c0001t0004g0348 a0001c0001t0005g0045 |
3 | HG02145.hp1 HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.220+7760A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16067927 | |||||||
| chr4:16068060 | G | C | 1 | a0001c0005t0002g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.220+7627C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16068060 | |||||||
| chr4:16068156 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.220+7531G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16068156 | |||||||
| chr4:16068175 | C | A | 58 | a0001c0001t0001g0023 a0001c0001t0001g0161 a0001c0001t0001g0162 others(55): Show |
58 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.220+7512G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16068175 | |||||||
| chr4:16068383 | G | A | 1 | a0001c0005t0002g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.220+7304C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16068383 | |||||||
| chr4:16068699 | T | C | 1 | a0001c0018t0001g0215 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.220+6988A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16068699 | |||||||
| chr4:16068708 | T | G | 1 | a0001c0001t0007g0166 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.220+6979A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16068708 | |||||||
| chr4:16068759 | T | C | 1 | a0001c0001t0004g0069 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.220+6928A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16068759 | |||||||
| chr4:16068925 | C | T | 2 | a0001c0002t0002g0237 a0001c0002t0002g0300 |
2 | HG02083.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.220+6762G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16068925 | |||||||
| chr4:16069127 | C | T | 14 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0165 others(11): Show |
14 | HG00609.hp2 HG01952.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.220+6560G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16069127 | |||||||
| chr4:16069131 | A | G | 5 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0235 others(2): Show |
6 | HG01109.hp1 HG01243.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+6556T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16069131 | |||||||
| chr4:16069135 | T | G | 3 | a0001c0001t0001g0284 a0001c0002t0001g0283 a0003c0007t0003g0314 |
3 | NA18953.hp1 NA18954.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.220+6552A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16069135 | |||||||
| chr4:16069229 | T | C | 28 | a0001c0001t0001g0021 a0001c0001t0001g0109 a0001c0001t0001g0110 others(25): Show |
28 | HG00609.hp2 HG01952.hp1 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.220+6458A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16069229 | |||||||
| chr4:16069320 | G | A | 4 | a0001c0002t0002g0207 a0001c0002t0002g0214 a0002c0006t0001g0206 others(1): Show |
4 | NA18966.hp1 NA18970.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.220+6367C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16069320 | |||||||
| chr4:16069552 | T | C | 1 | a0001c0005t0004g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.220+6135A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16069552 | |||||||
| chr4:16069702 | C | T | 14 | a0001c0001t0001g0107 a0001c0001t0001g0127 a0001c0001t0002g0108 others(11): Show |
15 | HG00639.hp2 HG01071.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.220+5985G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16069702 | |||||||
| chr4:16070175 | G | A | 1 | a0001c0005t0001g0219 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.220+5512C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16070175 | |||||||
| chr4:16070395 | T | C | 280 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(277): Show |
281 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(278): Show |
intron_variant | MODIFIER | c.220+5292A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16070395 | |||||||
| chr4:16070410 | A | G | 1 | a0003c0007t0002g0236 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.220+5277T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16070410 | |||||||
| chr4:16070412 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.220+5275G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16070412 | |||||||
| chr4:16070492 | C | T | 7 | a0001c0001t0005g0036 a0001c0004t0004g0049 a0001c0005t0001g0216 others(4): Show |
7 | HG02258.hp2 HG02895.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+5195G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16070492 | |||||||
| chr4:16070598 | A | T | 6 | a0001c0001t0001g0095 a0001c0001t0001g0098 a0001c0001t0003g0096 others(3): Show |
6 | NA18612.hp2 NA18945.hp2 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.220+5089T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16070598 | |||||||
| chr4:16070633 | G | T | 2 | a0001c0001t0001g0021 a0001c0003t0002g0020 |
2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.220+5054C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16070633 | |||||||
| chr4:16070658 | C | A | 1 | a0001c0005t0004g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.220+5029G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16070658 | |||||||
| chr4:16070683 | T | G | 246 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0024 others(243): Show |
247 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.220+5004A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16070683 | |||||||
| chr4:16070727 | T | A | 29 | a0001c0001t0001g0021 a0001c0001t0001g0061 a0001c0001t0001g0067 others(26): Show |
29 | HG00621.hp2 HG01192.hp1 HG01256.hp2 others(26): Show |
intron_variant | MODIFIER | c.220+4960A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16070727 | |||||||
| chr4:16070864 | C | T | 262 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(259): Show |
263 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(260): Show |
intron_variant | MODIFIER | c.220+4823G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16070864 | |||||||
| chr4:16070875 | G | A | 1 | a0001c0001t0002g0157 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.220+4812C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16070875 | |||||||
| chr4:16071002 | C | A | 2 | a0001c0005t0001g0216 a0001c0005t0004g0217 |
2 | NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.220+4685G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16071002 | |||||||
| chr4:16071068 | A | G | 3 | a0001c0001t0001g0299 a0001c0001t0004g0298 a0005c0012t0003g0340 |
3 | HG01106.hp1 HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.220+4619T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16071068 | |||||||
| chr4:16071131 | C | G | 1 | a0003c0007t0002g0236 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.220+4556G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16071131 | |||||||
| chr4:16071137 | C | G | 9 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0002g0016 others(6): Show |
9 | HG02145.hp1 HG02257.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.220+4550G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16071137 | |||||||
| chr4:16071469 | C | T | 233 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(230): Show |
234 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.220+4218G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16071469 | |||||||
| chr4:16071514 | G | A | 239 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(236): Show |
240 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.220+4173C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16071514 | |||||||
| chr4:16071544 | G | T | 1 | a0001c0011t0003g0356 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.220+4143C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16071544 | |||||||
| chr4:16071558 | G | C | 1 | a0001c0001t0001g0188 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.220+4129C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16071558 | |||||||
| chr4:16071590 | G | A | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
2 | HG00609.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.220+4097C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16071590 | |||||||
| chr4:16071595 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.220+4092C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16071595 | |||||||
| chr4:16071598 | A | C | 283 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(280): Show |
284 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(281): Show |
intron_variant | MODIFIER | c.220+4089T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16071598 | |||||||
| chr4:16071798 | C | T | 239 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(236): Show |
240 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(237): Show |
intron_variant | MODIFIER | c.220+3889G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16071798 | |||||||
| chr4:16071932 | G | C | 1 | a0001c0005t0004g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.220+3755C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16071932 | |||||||
| chr4:16072011 | A | C | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.220+3676T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16072011 | |||||||
| chr4:16072240 | G | T | 7 | a0001c0001t0001g0169 a0001c0001t0001g0288 a0001c0001t0002g0167 others(4): Show |
7 | HG02056.hp1 HG02132.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.220+3447C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16072240 | |||||||
| chr4:16072248 | A | G | 1 | a0001c0001t0002g0319 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.220+3439T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16072248 | |||||||
| chr4:16072479 | T | C | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
2 | HG00609.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.220+3208A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16072479 | |||||||
| chr4:16072558 | G | A | 264 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(261): Show |
265 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(262): Show |
intron_variant | MODIFIER | c.220+3129C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16072558 | |||||||
| chr4:16072886 | C | T | 241 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(238): Show |
242 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(239): Show |
intron_variant | MODIFIER | c.220+2801G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16072886 | |||||||
| chr4:16073017 | A | C | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
2 | HG00609.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.220+2670T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16073017 | |||||||
| chr4:16073039 | G | A | 2 | a0001c0001t0002g0115 a0001c0001t0004g0034 |
2 | HG01109.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.220+2648C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16073039 | |||||||
| chr4:16073099 | A | G | 1 | a0001c0001t0003g0147 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.220+2588T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16073099 | |||||||
| chr4:16073138 | C | T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0136 |
2 | NA18944.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.220+2549G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16073138 | |||||||
| chr4:16073145 | A | G | 1 | a0001c0004t0002g0004 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.220+2542T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16073145 | |||||||
| chr4:16073155 | C | A | 19 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0095 others(16): Show |
20 | HG00323.hp2 HG01515.hp2 NA18612.hp1 others(17): Show |
intron_variant | MODIFIER | c.220+2532G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16073155 | |||||||
| chr4:16073165 | G | A | 2 | a0001c0001t0001g0287 a0001c0001t0004g0323 |
2 | HG03471.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.220+2522C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16073165 | |||||||
| chr4:16073249 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.220+2438C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16073249 | |||||||
| chr4:16073316 | C | A | 264 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(261): Show |
265 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(262): Show |
intron_variant | MODIFIER | c.220+2371G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16073316 | |||||||
| chr4:16073376 | G | C | 1 | a0001c0001t0001g0213 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.220+2311C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16073376 | |||||||
| chr4:16073410 | T | C | 21 | a0001c0001t0001g0330 a0001c0001t0001g0350 a0001c0001t0001g0351 others(18): Show |
21 | HG01099.hp1 HG01167.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.220+2277A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16073410 | |||||||
| chr4:16073452 | T | C | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
2 | HG00609.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.220+2235A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16073452 | |||||||
| chr4:16073466 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.220+2221G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16073466 | |||||||
| chr4:16073557 | T | TTCATCTG others(21): Show |
1 | a0001c0001t0001g0370 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.220+2102_220+2129d others(30): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16073557 | |||||||
| chr4:16073636 | T | A | 2 | a0001c0001t0002g0103 a0001c0001t0003g0104 |
2 | NA19002.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.220+2051A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16073636 | |||||||
| chr4:16073652 | GT | G | 137 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(134): Show |
137 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.220+2034delA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16073652 | |||||||
| chr4:16074090 | C | A | 3 | a0001c0003t0001g0152 a0001c0003t0002g0017 a0001c0019t0005g0018 |
3 | HG02257.hp2 HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.220+1597G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16074090 | |||||||
| chr4:16074120 | T | C | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
2 | HG00609.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.220+1567A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16074120 | |||||||
| chr4:16074253 | GGAGA | G | 76 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0159 others(73): Show |
76 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.220+1430_220+1433d others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16074253 | |||||||
| chr4:16074289 | A | G | 1 | a0001c0001t0001g0193 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.220+1398T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16074289 | |||||||
| chr4:16074297 | C | T | 1 | a0001c0019t0005g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.220+1390G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16074297 | |||||||
| chr4:16074328 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG02717.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.220+1359C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16074328 | |||||||
| chr4:16074353 | C | T | 1 | a0001c0019t0005g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.220+1334G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16074353 | |||||||
| chr4:16074467 | C | T | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
2 | HG00609.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.220+1220G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16074467 | |||||||
| chr4:16074475 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.220+1212C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16074475 | |||||||
| chr4:16074530 | AT | A | 267 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(264): Show |
268 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.220+1156delA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16074530 | |||||||
| chr4:16074684 | T | C | 1 | a0001c0003t0002g0020 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.220+1003A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16074684 | |||||||
| chr4:16074718 | T | A | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
2 | HG00609.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.220+969A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16074718 | |||||||
| chr4:16074917 | G | A | 22 | a0001c0003t0001g0006 a0001c0003t0001g0010 a0001c0003t0001g0152 others(19): Show |
22 | HG02257.hp2 HG02280.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.220+770C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16074917 | |||||||
| chr4:16074992 | G | C | 22 | a0001c0003t0001g0006 a0001c0003t0001g0010 a0001c0003t0001g0152 others(19): Show |
22 | HG02257.hp2 HG02280.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.220+695C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16074992 | |||||||
| chr4:16075040 | C | T | 2 | a0001c0001t0001g0235 a0001c0001t0003g0003 |
3 | HG01515.hp1 HG01517.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.220+647G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16075040 | |||||||
| chr4:16075081 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.220+606A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16075081 | |||||||
| chr4:16075103 | C | A | 1 | a0001c0001t0001g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.220+584G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16075103 | |||||||
| chr4:16075161 | C | A | 267 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(264): Show |
268 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.220+526G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16075161 | |||||||
| chr4:16075214 | A | T | 243 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(240): Show |
244 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.220+473T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16075214 | |||||||
| chr4:16075269 | A | G | 167 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0043 others(164): Show |
168 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.220+418T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16075269 | |||||||
| chr4:16075300 | C | A | 242 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(239): Show |
243 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(240): Show |
intron_variant | MODIFIER | c.220+387G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16075300 | |||||||
| chr4:16075571 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0190 |
2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.220+116C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16075571 | |||||||
| chr4:16075641 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.220+46C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 2/27 | chr4 | 16075641 | |||||||
| chr4:16076185 | G | A | 267 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(264): Show |
268 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-212-67C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16076185 | |||||||
| chr4:16076194 | G | A | 1 | a0001c0005t0002g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-212-76C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16076194 | |||||||
| chr4:16076284 | T | C | 265 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0042 others(262): Show |
266 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.-212-166A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16076284 | |||||||
| chr4:16076374 | A | G | 267 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(264): Show |
268 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-212-256T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16076374 | |||||||
| chr4:16076391 | T | C | 1 | a0001c0005t0004g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-212-273A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16076391 | |||||||
| chr4:16076429 | A | G | 245 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(242): Show |
246 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.-212-311T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16076429 | |||||||
| chr4:16076758 | G | C | 267 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(264): Show |
268 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-212-640C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16076758 | |||||||
| chr4:16076765 | A | G | 1 | a0001c0001t0002g0297 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-212-647T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16076765 | |||||||
| chr4:16076830 | C | T | 1 | a0001c0005t0004g0075 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-212-712G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16076830 | |||||||
| chr4:16076831 | G | C | 17 | a0001c0001t0001g0107 a0001c0001t0001g0109 a0001c0001t0001g0110 others(14): Show |
18 | HG00639.hp2 HG01071.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.-212-713C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16076831 | |||||||
| chr4:16076878 | GCTTGAAG others(21): Show |
G | 1 | a0001c0001t0001g0370 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-212-788_-212-761d others(30): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16076878 | |||||||
| chr4:16076929 | T | G | 1 | a0001c0005t0001g0219 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-212-811A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16076929 | |||||||
| chr4:16076964 | A | G | 267 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(264): Show |
268 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-212-846T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16076964 | |||||||
| chr4:16077053 | A | G | 7 | a0001c0005t0001g0216 a0001c0005t0001g0218 a0001c0005t0001g0219 others(4): Show |
7 | HG02895.hp1 HG03195.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-212-935T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16077053 | |||||||
| chr4:16077075 | G | A | 1 | a0001c0001t0002g0048 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-212-957C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16077075 | |||||||
| chr4:16077111 | A | G | 1 | a0001c0001t0003g0233 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-212-993T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16077111 | |||||||
| chr4:16077170 | G | A | 2 | a0001c0001t0003g0117 a0001c0001t0004g0069 |
2 | HG01192.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-212-1052C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16077170 | |||||||
| chr4:16077266 | C | T | 9 | a0001c0003t0001g0006 a0001c0003t0001g0010 a0001c0003t0002g0008 others(6): Show |
9 | HG02451.hp2 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-212-1148G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16077266 | |||||||
| chr4:16077453 | A | G | 1 | a0001c0001t0002g0232 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-212-1335T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16077453 | |||||||
| chr4:16077538 | T | C | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
2 | HG00609.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-212-1420A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16077538 | |||||||
| chr4:16077635 | T | G | 6 | a0001c0005t0001g0216 a0001c0005t0001g0218 a0001c0005t0001g0327 others(3): Show |
6 | HG02895.hp1 HG03195.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.-212-1517A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16077635 | |||||||
| chr4:16077758 | C | T | 244 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(241): Show |
245 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.-212-1640G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16077758 | |||||||
| chr4:16077770 | T | G | 246 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(243): Show |
247 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.-212-1652A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16077770 | |||||||
| chr4:16077973 | A | G | 269 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(266): Show |
270 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(267): Show |
intron_variant | MODIFIER | c.-212-1855T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16077973 | |||||||
| chr4:16077976 | A | T | 216 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(213): Show |
217 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.-212-1858T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16077976 | |||||||
| chr4:16078043 | C | A | 1 | a0001c0001t0001g0337 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-212-1925G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16078043 | |||||||
| chr4:16078047 | T | G | 247 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(244): Show |
248 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.-212-1929A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16078047 | |||||||
| chr4:16078057 | G | C | 239 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(236): Show |
240 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-212-1939C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16078057 | |||||||
| chr4:16078086 | G | A | 1 | a0001c0001t0002g0326 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-212-1968C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16078086 | |||||||
| chr4:16078112 | C | T | 238 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0042 others(235): Show |
239 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(236): Show |
intron_variant | MODIFIER | c.-212-1994G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16078112 | |||||||
| chr4:16078113 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-212-1995C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16078113 | |||||||
| chr4:16078475 | G | A | 1 | a0001c0003t0002g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-212-2357C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16078475 | |||||||
| chr4:16078480 | A | G | 4 | a0001c0001t0002g0157 a0001c0001t0003g0155 a0001c0002t0002g0153 others(1): Show |
4 | NA18959.hp1 NA18968.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.-212-2362T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16078480 | |||||||
| chr4:16078726 | A | G | 268 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(265): Show |
269 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(266): Show |
intron_variant | MODIFIER | c.-212-2608T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16078726 | |||||||
| chr4:16078829 | C | T | 1 | a0001c0001t0002g0005 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-212-2711G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16078829 | |||||||
| chr4:16078983 | C | T | 1 | a0001c0003t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-212-2865G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16078983 | |||||||
| chr4:16078988 | A | T | 267 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(264): Show |
268 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.-212-2870T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16078988 | |||||||
| chr4:16079023 | G | A | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
2 | HG00609.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-212-2905C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16079023 | |||||||
| chr4:16079089 | GT | G | 63 | a0001c0001t0001g0023 a0001c0001t0001g0159 a0001c0001t0001g0160 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.-212-2972delA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16079089 | |||||||
| chr4:16079089 | GTT | G | 198 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0024 others(195): Show |
199 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(196): Show |
intron_variant | MODIFIER | c.-212-2973_-212-297 others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16079089 | |||||||
| chr4:16079198 | A | G | 19 | a0001c0001t0001g0061 a0001c0001t0001g0067 a0001c0001t0001g0068 others(16): Show |
19 | HG00609.hp2 HG00621.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-212-3080T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16079198 | |||||||
| chr4:16079254 | C | T | 2 | a0001c0001t0005g0045 a0001c0004t0004g0049 |
2 | HG02258.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-212-3136G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16079254 | |||||||
| chr4:16079402 | A | G | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
2 | HG00609.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-212-3284T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16079402 | |||||||
| chr4:16079416 | T | C | 1 | a0001c0001t0002g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-212-3298A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16079416 | |||||||
| chr4:16079488 | T | G | 1 | a0001c0001t0003g0291 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-212-3370A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16079488 | |||||||
| chr4:16079561 | C | G | 1 | a0001c0001t0002g0133 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-212-3443G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16079561 | |||||||
| chr4:16079659 | A | G | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0146 |
3 | HG00609.hp2 HG02965.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-212-3541T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16079659 | |||||||
| chr4:16079698 | G | A | 2 | a0001c0001t0004g0145 a0001c0019t0005g0018 |
2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-212-3580C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16079698 | |||||||
| chr4:16079775 | G | A | 1 | a0001c0001t0002g0292 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-212-3657C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16079775 | |||||||
| chr4:16079810 | C | A | 3 | a0001c0005t0001g0216 a0001c0005t0004g0217 a0001c0018t0001g0215 |
3 | HG03195.hp1 NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-212-3692G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16079810 | |||||||
| chr4:16079827 | T | C | 1 | a0001c0002t0003g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-212-3709A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16079827 | |||||||
| chr4:16079840 | C | G | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0146 |
3 | HG00609.hp2 HG02965.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-212-3722G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16079840 | |||||||
| chr4:16079842 | T | A | 1 | a0001c0005t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-212-3724A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16079842 | |||||||
| chr4:16079862 | A | C | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0146 |
3 | HG00609.hp2 HG02965.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-212-3744T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16079862 | |||||||
| chr4:16079917 | T | A | 5 | a0001c0005t0001g0216 a0001c0005t0001g0218 a0001c0005t0001g0219 others(2): Show |
5 | HG03195.hp1 HG03516.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.-212-3799A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16079917 | |||||||
| chr4:16079932 | T | A | 1 | a0001c0001t0003g0163 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-212-3814A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16079932 | |||||||
| chr4:16080011 | C | CA | 13 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0002g0120 others(10): Show |
13 | HG01192.hp1 HG02148.hp1 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.-212-3894dupT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080011 | |||||||
| chr4:16080011 | C | CAA | 10 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0002g0224 others(7): Show |
10 | HG01167.hp2 HG01256.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.-212-3895_-212-389 others(6): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080011 | |||||||
| chr4:16080011 | C | CAAA | 97 | a0001c0001t0001g0014 a0001c0001t0001g0122 a0001c0001t0001g0230 others(94): Show |
98 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.-212-3896_-212-389 others(7): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080011 | |||||||
| chr4:16080011 | C | CAAAA | 59 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0137 others(56): Show |
59 | HG00323.hp1 HG00597.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.-212-3897_-212-389 others(8): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080011 | |||||||
| chr4:16080011 | C | CAAAAA | 11 | a0001c0001t0001g0054 a0001c0001t0001g0165 a0001c0001t0001g0333 others(8): Show |
11 | HG00323.hp2 HG02055.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.-212-3898_-212-389 others(9): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080011 | |||||||
| chr4:16080011 | C | CAAAAAA | 39 | a0001c0001t0001g0023 a0001c0001t0001g0169 a0001c0001t0001g0170 others(36): Show |
39 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.-212-3899_-212-389 others(10): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080011 | |||||||
| chr4:16080011 | C | CAAAAAAA | 16 | a0001c0001t0001g0204 a0001c0001t0001g0211 a0001c0001t0002g0133 others(13): Show |
16 | HG00423.hp1 HG00609.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.-212-3900_-212-389 others(11): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080011 | |||||||
| chr4:16080011 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0003g0147 a0001c0001t0003g0148 |
2 | HG01361.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-212-3903_-212-389 others(14): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080011 | |||||||
| chr4:16080011 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0003g0149 a0001c0001t0003g0150 |
2 | HG02055.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-212-3904_-212-389 others(15): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080011 | |||||||
| chr4:16080011 | CA | C | 11 | a0001c0001t0001g0056 a0001c0001t0002g0146 a0001c0001t0002g0157 others(8): Show |
11 | HG00408.hp2 HG01255.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.-212-3894delT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080011 | |||||||
| chr4:16080052 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0002g0005 others(1): Show |
4 | HG02615.hp2 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-213+3926G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080052 | |||||||
| chr4:16080191 | C | G | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0146 |
3 | HG00609.hp2 HG02965.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-213+3787G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080191 | |||||||
| chr4:16080243 | G | A | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0146 |
3 | HG00609.hp2 HG02965.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-213+3735C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080243 | |||||||
| chr4:16080247 | G | A | 1 | a0001c0001t0003g0341 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-213+3731C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080247 | |||||||
| chr4:16080295 | C | A | 1 | a0001c0019t0005g0018 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-213+3683G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080295 | |||||||
| chr4:16080302 | C | A | 1 | a0001c0001t0003g0212 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-213+3676G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080302 | |||||||
| chr4:16080317 | G | A | 4 | a0001c0001t0002g0342 a0001c0001t0002g0343 a0001c0001t0002g0358 others(1): Show |
4 | HG02809.hp1 HG02976.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-213+3661C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080317 | |||||||
| chr4:16080325 | C | A | 1 | a0001c0001t0001g0345 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-213+3653G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080325 | |||||||
| chr4:16080337 | G | A | 10 | a0001c0001t0001g0350 a0001c0001t0001g0351 a0001c0001t0001g0352 others(7): Show |
10 | HG02145.hp1 HG02486.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-213+3641C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080337 | |||||||
| chr4:16080453 | C | T | 1 | a0001c0003t0002g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-213+3525G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080453 | |||||||
| chr4:16080478 | T | C | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0146 |
3 | HG00609.hp2 HG02965.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-213+3500A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080478 | |||||||
| chr4:16080564 | C | T | 1 | a0001c0002t0002g0055 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-213+3414G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080564 | |||||||
| chr4:16080575 | CT | C | 5 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(2): Show |
5 | HG02647.hp1 HG03225.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.-213+3402delA | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080575 | |||||||
| chr4:16080587 | T | A | 1 | a0001c0005t0001g0219 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-213+3391A>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080587 | |||||||
| chr4:16080589 | A | T | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0146 |
3 | HG00609.hp2 HG02965.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-213+3389T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080589 | |||||||
| chr4:16080618 | A | C | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0146 |
3 | HG00609.hp2 HG02965.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-213+3360T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080618 | |||||||
| chr4:16080665 | G | A | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0146 |
3 | HG00609.hp2 HG02965.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-213+3313C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080665 | |||||||
| chr4:16080670 | T | C | 1 | a0001c0001t0004g0123 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-213+3308A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080670 | |||||||
| chr4:16080685 | A | T | 255 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0023 others(252): Show |
256 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.-213+3293T>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080685 | |||||||
| chr4:16080752 | G | A | 1 | a0001c0001t0002g0146 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-213+3226C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080752 | |||||||
| chr4:16080824 | G | A | 2 | a0001c0001t0001g0357 a0001c0011t0003g0356 |
2 | HG03017.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.-213+3154C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080824 | |||||||
| chr4:16080832 | A | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0004g0044 |
3 | HG01109.hp1 HG01243.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-213+3146T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080832 | |||||||
| chr4:16080950 | A | G | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0146 |
3 | HG00609.hp2 HG02965.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-213+3028T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16080950 | |||||||
| chr4:16081037 | A | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0003g0038 others(3): Show |
7 | HG02257.hp2 NA18953.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.-213+2941T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16081037 | |||||||
| chr4:16081050 | T | C | 5 | a0001c0005t0001g0216 a0001c0005t0001g0218 a0001c0005t0001g0219 others(2): Show |
5 | HG03195.hp1 HG03516.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.-213+2928A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16081050 | |||||||
| chr4:16081111 | T | C | 1 | a0001c0001t0002g0358 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-213+2867A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16081111 | |||||||
| chr4:16081122 | G | A | 10 | a0001c0001t0001g0127 a0001c0001t0003g0002 a0001c0001t0003g0124 others(7): Show |
11 | HG01071.hp1 HG01099.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.-213+2856C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16081122 | |||||||
| chr4:16081148 | C | T | 2 | a0001c0001t0002g0133 a0001c0001t0002g0134 |
2 | HG00609.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-213+2830G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16081148 | |||||||
| chr4:16081218 | G | A | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0146 |
3 | HG00609.hp2 HG02965.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-213+2760C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16081218 | |||||||
| chr4:16081224 | T | C | 3 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0146 |
3 | HG00609.hp2 HG02965.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-213+2754A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16081224 | |||||||
| chr4:16081320 | A | G | 1 | a0001c0005t0002g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-213+2658T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16081320 | |||||||
| chr4:16081400 | T | C | 1 | a0001c0004t0002g0135 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-213+2578A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16081400 | |||||||
| chr4:16081455 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-213+2523T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16081455 | |||||||
| chr4:16081573 | T | C | 69 | a0001c0001t0001g0023 a0001c0001t0001g0159 a0001c0001t0001g0160 others(66): Show |
69 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.-213+2405A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16081573 | |||||||
| chr4:16081662 | A | G | 1 | a0001c0001t0002g0037 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-213+2316T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16081662 | |||||||
| chr4:16081664 | C | T | 1 | a0001c0001t0003g0154 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-213+2314G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16081664 | |||||||
| chr4:16081699 | C | T | 1 | a0001c0001t0005g0036 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-213+2279G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16081699 | |||||||
| chr4:16081713 | T | G | 1 | a0001c0001t0002g0136 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-213+2265A>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16081713 | |||||||
| chr4:16081828 | C | T | 2 | a0001c0001t0004g0145 a0001c0019t0005g0018 |
2 | HG02451.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-213+2150G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16081828 | |||||||
| chr4:16081901 | T | C | 5 | a0001c0001t0001g0360 a0001c0001t0001g0361 a0001c0001t0001g0363 others(2): Show |
5 | NA18949.hp2 NA18989.hp2 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.-213+2077A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16081901 | |||||||
| chr4:16081911 | GA | G | 8 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0004g0028 others(5): Show |
8 | HG01109.hp2 HG02572.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-213+2066delT | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16081911 | |||||||
| chr4:16081922 | CAAG | C | 239 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0050 others(236): Show |
240 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-213+2053_-213+205 others(7): Show |
PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16081922 | |||||||
| chr4:16081925 | G | C | 3 | a0001c0001t0001g0364 a0001c0001t0002g0365 a0001c0001t0013g0366 |
3 | HG01346.hp1 HG03834.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.-213+2053C>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16081925 | |||||||
| chr4:16082076 | G | A | 5 | a0001c0005t0001g0216 a0001c0005t0001g0218 a0001c0005t0001g0219 others(2): Show |
5 | HG03195.hp1 HG03516.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.-213+1902C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16082076 | |||||||
| chr4:16082080 | G | T | 1 | a0001c0005t0002g0022 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-213+1898C>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16082080 | |||||||
| chr4:16082085 | C | T | 1 | a0001c0002t0002g0153 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-213+1893G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16082085 | |||||||
| chr4:16082093 | T | C | 1 | a0001c0001t0003g0368 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-213+1885A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16082093 | |||||||
| chr4:16082227 | T | C | 157 | a0001c0001t0001g0014 a0001c0001t0001g0151 a0001c0001t0001g0213 others(154): Show |
158 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.-213+1751A>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16082227 | |||||||
| chr4:16082503 | C | T | 10 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0137 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.-213+1475G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16082503 | |||||||
| chr4:16082505 | G | A | 2 | a0001c0003t0002g0020 a0007c0017t0001g0019 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-213+1473C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16082505 | |||||||
| chr4:16082636 | A | G | 68 | a0001c0001t0001g0023 a0001c0001t0001g0159 a0001c0001t0001g0160 others(65): Show |
68 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.-213+1342T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16082636 | |||||||
| chr4:16082669 | G | A | 1 | a0001c0002t0002g0369 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-213+1309C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16082669 | |||||||
| chr4:16082717 | C | T | 5 | a0001c0003t0002g0017 a0001c0003t0002g0020 a0001c0005t0002g0022 others(2): Show |
5 | HG02109.hp1 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-213+1261G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16082717 | |||||||
| chr4:16082784 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-213+1194T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16082784 | |||||||
| chr4:16082966 | C | T | 1 | a0001c0003t0001g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-213+1012G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16082966 | |||||||
| chr4:16083303 | C | G | 5 | a0001c0001t0001g0151 a0001c0001t0003g0147 a0001c0001t0003g0148 others(2): Show |
5 | HG01361.hp2 HG02055.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.-213+675G>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16083303 | |||||||
| chr4:16083310 | C | T | 3 | a0001c0003t0002g0020 a0001c0019t0005g0018 a0007c0017t0001g0019 |
3 | HG02109.hp1 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-213+668G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16083310 | |||||||
| chr4:16083551 | C | T | 1 | a0001c0001t0002g0005 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-213+427G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16083551 | |||||||
| chr4:16083569 | A | C | 2 | a0001c0003t0002g0017 a0001c0004t0002g0004 |
2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-213+409T>G | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16083569 | |||||||
| chr4:16083735 | A | G | 239 | a0001c0001t0001g0014 a0001c0001t0001g0151 a0001c0001t0001g0159 others(236): Show |
240 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.-213+243T>C | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16083735 | |||||||
| chr4:16083844 | C | T | 3 | a0001c0001t0002g0146 a0001c0001t0004g0145 a0001c0004t0002g0004 |
3 | HG02451.hp1 HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-213+134G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16083844 | |||||||
| chr4:16083857 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-213+121C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16083857 | |||||||
| chr4:16083877 | G | A | 1 | a0001c0001t0001g0370 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-213+101C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16083877 | |||||||
| chr4:16083899 | C | T | 363 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0021 others(360): Show |
366 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(363): Show |
intron_variant | MODIFIER | c.-213+79G>A | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16083899 | |||||||
| chr4:16083904 | C | A | 1 | a0001c0001t0002g0371 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-213+74G>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16083904 | |||||||
| chr4:16083940 | G | A | 227 | a0001c0001t0001g0151 a0001c0001t0001g0159 a0001c0001t0001g0160 others(224): Show |
228 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.-213+38C>T | PROM1 | ENSG00000007062.12 | transcript | ENST00000447510.7 | protein_coding | 1/27 | chr4 | 16083940 |