Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 145501 |
| ensemblid | ENSG00000100593.18 |
| hgncid | 23176 |
| symbol | ISM2 |
| name | isthmin 2 |
| refseq_nuc | NM_199296.3 |
| refseq_prot | NP_954993.1 |
| ensembl_nuc | ENST00000342219.9 |
| ensembl_prot | ENSP00000341490.4 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 77474394 |
| end | 77498816 |
| strand | - |
| ver | v1.2 |
| region | chr14:77474394-77498816 |
| region5000 | chr14:77469394-77503816 |
| regionname0 | ISM2_chr14_77474394_77498816 |
| regionname5000 | ISM2_chr14_77469394_77503816 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 571 | 137 | 15 | 37 | 57 | 7 | 20 | 35 | ISM2_chr14_77469394_77503816 | ISM2 | MRALR others(566): Show |
chr14 | 77469394 | 77503816 |
| a0002 | 1/0 | 571 | 120 | 63 | 24 | 8 | 6 | 18 | 7 | ISM2_chr14_77469394_77503816 | ISM2 | MRALR others(566): Show |
chr14 | 77469394 | 77503816 |
| a0003 | 0/0 | 571 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | MRALR others(566): Show |
chr14 | 77469394 | 77503816 |
| a0004 | 0/0 | 571 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | MRALR others(566): Show |
chr14 | 77469394 | 77503816 |
| a0005 | 0/0 | 571 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | MRALR others(566): Show |
chr14 | 77469394 | 77503816 |
| a0006 | 0/0 | 571 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | MRALR others(566): Show |
chr14 | 77469394 | 77503816 |
| a0007 | 0/0 | 571 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | MRALR others(566): Show |
chr14 | 77469394 | 77503816 |
| a0008 | 0/0 | 571 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | MRALR others(566): Show |
chr14 | 77469394 | 77503816 |
| a0009 | 0/0 | 571 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | MRALR others(566): Show |
chr14 | 77469394 | 77503816 |
| a0010 | 0/0 | 571 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | MRALR others(566): Show |
chr14 | 77469394 | 77503816 |
| a0011 | 0/0 | 571 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | MRALR others(566): Show |
chr14 | 77469394 | 77503816 |
| a0012 | 0/0 | 571 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | MRALR others(566): Show |
chr14 | 77469394 | 77503816 |
| a0013 | 0/0 | 571 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | MRALR others(566): Show |
chr14 | 77469394 | 77503816 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1713 | 128 | 14 | 36 | 51 | 6 | 20 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0001c0005 | 0/0 | 1713 | 3 | 0 | 0 | 3 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0001c0009 | 0/0 | 1713 | 2 | 1 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0001c0010 | 0/0 | 1713 | 2 | 0 | 0 | 1 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0001c0012 | 0/0 | 1713 | 2 | 0 | 0 | 2 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0002c0002 | 1/0 | 1713 | 96 | 58 | 15 | 4 | 5 | 13 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0002c0003 | 0/0 | 1713 | 14 | 1 | 6 | 3 | 1 | 3 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0002c0007 | 0/0 | 1713 | 3 | 2 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0002c0008 | 0/0 | 1713 | 3 | 0 | 1 | 0 | 0 | 2 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0002c0015 | 0/0 | 1713 | 2 | 0 | 2 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0002c0021 | 0/0 | 1713 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0002c0023 | 0/0 | 1713 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0003c0004 | 0/0 | 1713 | 8 | 8 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0004c0006 | 0/0 | 1713 | 3 | 0 | 3 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0005c0014 | 0/0 | 1713 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0006c0011 | 0/0 | 1713 | 2 | 0 | 0 | 0 | 0 | 2 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0007c0013 | 0/0 | 1713 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0008c0017 | 0/0 | 1713 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0009c0016 | 0/0 | 1713 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0010c0022 | 0/0 | 1713 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0011c0018 | 0/0 | 1713 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0012c0019 | 0/0 | 1713 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 | ||
| a0013c0020 | 0/0 | 1713 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | ATGCG others(1708): Show |
chr14 | 77469394 | 77503816 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2950 | 120 | 11 | 35 | 48 | 6 | 19 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0001c0001t0002 | 0/0 | 2939 | 2 | 0 | 0 | 1 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2934): Show |
chr14 | 77469394 | 77503816 |
| a0001c0001t0004 | 0/0 | 2950 | 3 | 3 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0001c0001t0013 | 0/0 | 2950 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0001c0001t0016 | 0/0 | 2950 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0001c0001t0017 | 0/0 | 2950 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0001c0005t0001 | 0/0 | 2950 | 3 | 0 | 0 | 3 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0001c0009t0004 | 0/0 | 2950 | 2 | 1 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0001c0010t0001 | 0/0 | 2950 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0001c0010t0007 | 0/0 | 2950 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0001c0012t0001 | 0/0 | 2950 | 2 | 0 | 0 | 2 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0002c0002t0001 | 0/0 | 2950 | 44 | 24 | 9 | 3 | 3 | 5 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0002c0002t0002 | 0/0 | 2939 | 23 | 8 | 5 | 1 | 2 | 7 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2934): Show |
chr14 | 77469394 | 77503816 |
| a0002c0002t0003 | 1/0 | 2940 | 19 | 18 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2935): Show |
chr14 | 77469394 | 77503816 |
| a0002c0002t0005 | 0/0 | 2939 | 3 | 2 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2934): Show |
chr14 | 77469394 | 77503816 |
| a0002c0002t0006 | 0/0 | 2950 | 3 | 3 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0002c0002t0008 | 0/0 | 2950 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0002c0002t0009 | 0/0 | 2939 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2934): Show |
chr14 | 77469394 | 77503816 |
| a0002c0002t0011 | 0/0 | 2950 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0002c0003t0001 | 0/0 | 2950 | 13 | 1 | 6 | 2 | 1 | 3 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0002c0003t0007 | 0/0 | 2950 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0002c0007t0001 | 0/0 | 2950 | 2 | 1 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0002c0007t0015 | 0/0 | 2950 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0002c0008t0001 | 0/0 | 2950 | 3 | 0 | 1 | 0 | 0 | 2 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0002c0015t0001 | 0/0 | 2950 | 2 | 0 | 2 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0002c0021t0002 | 0/0 | 2939 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2934): Show |
chr14 | 77469394 | 77503816 |
| a0002c0023t0012 | 0/0 | 2950 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0003c0004t0001 | 0/0 | 2950 | 8 | 8 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0004c0006t0001 | 0/0 | 2950 | 3 | 0 | 3 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0005c0014t0001 | 0/0 | 2950 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0006c0011t0001 | 0/0 | 2950 | 2 | 0 | 0 | 0 | 0 | 2 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0007c0013t0001 | 0/0 | 2950 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0007c0013t0014 | 0/0 | 2950 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0008c0017t0001 | 0/0 | 2950 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0009c0016t0003 | 0/0 | 2940 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2935): Show |
chr14 | 77469394 | 77503816 |
| a0010c0022t0001 | 0/0 | 2950 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0011c0018t0001 | 0/0 | 2950 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| a0012c0019t0010 | 0/0 | 2939 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2934): Show |
chr14 | 77469394 | 77503816 |
| a0013c0020t0001 | 0/0 | 2950 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | AGAGC others(2945): Show |
chr14 | 77469394 | 77503816 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0068 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0013g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0016g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0001t0017g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0005t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0005t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0005t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0009t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0009t0004g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0010t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0010t0007g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0012t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0001c0012t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0003g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0003g0143 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0005g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0006g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0008g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0008g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0009g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0002t0011g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0003t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0003t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0003t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0003t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0003t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0003t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0003t0007g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0007t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0007t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0007t0015g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0008t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0008t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0008t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0015t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0021t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0002c0023t0012g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0003c0004t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0003c0004t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0003c0004t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0003c0004t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0003c0004t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0003c0004t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0003c0004t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0004c0006t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0004c0006t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0004c0006t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0005c0014t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0005c0014t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0006c0011t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0006c0011t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0007c0013t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0007c0013t0014g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0008c0017t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0009c0016t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0010c0022t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0011c0018t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0012c0019t0010g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| a0013c0020t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0010 | t0001 | g0219 | EUR | GBR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0131 | EUR | GBR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0048 | EUR | GBR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00140 | hp2 | a0008 | c0017 | t0001 | g0035 | EUR | GBR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0102 | EUR | FIN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00642 | hp1 | a0002 | c0015 | t0001 | g0022 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00735 | hp1 | a0002 | c0015 | t0001 | g0022 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00741 | hp1 | a0002 | c0003 | t0001 | g0245 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0236 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01069 | hp2 | a0001 | c0001 | t0013 | g0044 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01070 | hp1 | a0002 | c0008 | t0001 | g0233 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01070 | hp2 | a0004 | c0006 | t0001 | g0117 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01071 | hp2 | a0004 | c0006 | t0001 | g0121 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0129 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0185 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01109 | hp1 | a0001 | c0009 | t0004 | g0082 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0070 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0187 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01192 | hp1 | a0004 | c0006 | t0001 | g0126 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01243 | hp1 | a0002 | c0002 | t0005 | g0014 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01255 | hp1 | a0002 | c0003 | t0001 | g0241 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01257 | hp1 | a0002 | c0003 | t0001 | g0021 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0189 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0188 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0159 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0234 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0190 | EUR | IBS | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | IBS | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | IBS | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0179 | EUR | IBS | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0138 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0130 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01891 | hp1 | a0002 | c0002 | t0008 | g0075 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01891 | hp2 | a0002 | c0002 | t0003 | g0142 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0154 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01981 | hp1 | a0010 | c0022 | t0001 | g0240 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01993 | hp1 | a0002 | c0003 | t0001 | g0246 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02074 | hp1 | a0011 | c0018 | t0001 | g0123 | EAS | KHV | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0178 | EAS | KHV | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0158 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0118 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02148 | hp2 | a0002 | c0003 | t0001 | g0248 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CDX | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | CDX | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02165 | hp2 | a0001 | c0001 | t0017 | g0164 | EAS | CDX | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02257 | hp2 | a0002 | c0002 | t0003 | g0152 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02280 | hp1 | a0003 | c0004 | t0001 | g0034 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | PEL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0105 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0137 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02615 | hp1 | a0002 | c0002 | t0003 | g0141 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0106 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0078 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02630 | hp2 | a0002 | c0002 | t0003 | g0026 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02647 | hp1 | a0002 | c0002 | t0003 | g0002 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0183 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02698 | hp1 | a0002 | c0003 | t0001 | g0243 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0013 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02717 | hp1 | a0005 | c0014 | t0001 | g0033 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02723 | hp1 | a0002 | c0002 | t0003 | g0015 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0115 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0132 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02735 | hp2 | a0002 | c0003 | t0001 | g0249 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02738 | hp2 | a0002 | c0002 | t0002 | g0071 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0177 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0101 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02818 | hp1 | a0002 | c0002 | t0008 | g0074 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02818 | hp2 | a0002 | c0002 | t0005 | g0014 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0232 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02886 | hp2 | a0002 | c0007 | t0015 | g0062 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02895 | hp2 | a0003 | c0004 | t0001 | g0006 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0238 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02922 | hp1 | a0002 | c0002 | t0005 | g0146 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02922 | hp2 | a0002 | c0002 | t0006 | g0079 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02965 | hp1 | a0002 | c0002 | t0006 | g0069 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02965 | hp2 | a0002 | c0023 | t0012 | g0253 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0184 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02970 | hp2 | a0003 | c0004 | t0001 | g0029 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0100 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0181 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0180 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0081 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0151 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03098 | hp1 | a0002 | c0002 | t0003 | g0139 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0239 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03130 | hp1 | a0003 | c0004 | t0001 | g0030 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03130 | hp2 | a0002 | c0002 | t0003 | g0015 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03139 | hp1 | a0002 | c0002 | t0003 | g0149 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03139 | hp2 | a0002 | c0007 | t0001 | g0024 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03195 | hp1 | a0002 | c0002 | t0002 | g0104 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03195 | hp2 | a0005 | c0014 | t0001 | g0032 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03209 | hp1 | a0002 | c0002 | t0003 | g0145 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03225 | hp1 | a0003 | c0004 | t0001 | g0028 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03225 | hp2 | a0003 | c0004 | t0001 | g0111 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03239 | hp2 | a0006 | c0011 | t0001 | g0162 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03486 | hp1 | a0007 | c0013 | t0014 | g0109 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03486 | hp2 | a0002 | c0002 | t0003 | g0150 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0231 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0192 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0116 | AFR | ESN | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03540 | hp1 | a0002 | c0002 | t0011 | g0237 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03540 | hp2 | a0002 | c0002 | t0003 | g0144 | AFR | GWD | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03579 | hp1 | a0003 | c0004 | t0001 | g0031 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0186 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0217 | SAS | STU | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | STU | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03704 | hp1 | a0002 | c0008 | t0001 | g0039 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0016 | SAS | PJL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0112 | SAS | BEB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0016 | SAS | BEB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0136 | SAS | BEB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0182 | SAS | STU | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | STU | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG04199 | hp2 | a0002 | c0002 | t0009 | g0156 | SAS | STU | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG04204 | hp1 | a0002 | c0003 | t0001 | g0250 | SAS | STU | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | STU | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | STU | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG04228 | hp2 | a0002 | c0008 | t0001 | g0235 | SAS | STU | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18522 | hp1 | a0002 | c0002 | t0003 | g0025 | AFR | YRI | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0001 | AFR | YRI | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | YRI | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0061 | AFR | YRI | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18946 | hp2 | a0002 | c0003 | t0001 | g0252 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18967 | hp1 | a0002 | c0003 | t0007 | g0244 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18969 | hp2 | a0002 | c0007 | t0001 | g0058 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0093 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18990 | hp1 | a0001 | c0010 | t0007 | g0113 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19000 | hp1 | a0001 | c0012 | t0001 | g0228 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19011 | hp2 | a0001 | c0005 | t0001 | g0216 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | LWK | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0176 | AFR | LWK | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19043 | hp1 | a0002 | c0002 | t0006 | g0107 | AFR | LWK | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19043 | hp2 | a0002 | c0002 | t0003 | g0148 | AFR | LWK | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19063 | hp2 | a0001 | c0005 | t0001 | g0210 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19066 | hp2 | a0001 | c0012 | t0001 | g0215 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19074 | hp2 | a0001 | c0001 | t0016 | g0196 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19081 | hp2 | a0002 | c0003 | t0001 | g0251 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19083 | hp2 | a0001 | c0005 | t0001 | g0206 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0076 | AFR | YRI | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0080 | AFR | YRI | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA20129 | hp1 | a0002 | c0002 | t0003 | g0140 | AFR | ASW | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ASW | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | TSI | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA20752 | hp2 | a0002 | c0003 | t0001 | g0247 | EUR | TSI | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0134 | EUR | TSI | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA20905 | hp1 | a0006 | c0011 | t0001 | g0204 | SAS | GIH | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | GIH | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01123 | hp1 | a0002 | c0003 | t0001 | g0242 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG01123 | hp2 | a0009 | c0016 | t0003 | g0153 | AMR | CLM | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02109 | hp1 | a0003 | c0004 | t0001 | g0006 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02109 | hp2 | a0002 | c0002 | t0003 | g0002 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02486 | hp1 | a0012 | c0019 | t0010 | g0155 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0103 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0135 | AFR | ACB | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0157 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG03471 | hp2 | a0002 | c0002 | t0003 | g0147 | AFR | MSL | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG06807 | hp1 | a0013 | c0020 | t0001 | g0108 | AFR | USA | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| HG06807 | hp2 | a0001 | c0009 | t0004 | g0072 | AFR | USA | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA20300 | hp1 | a0002 | c0003 | t0001 | g0021 | AFR | USA | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA20300 | hp2 | a0002 | c0002 | t0003 | g0002 | AFR | USA | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA21309 | hp1 | a0002 | c0021 | t0002 | g0023 | AFR | LWK | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| NA21309 | hp2 | a0007 | c0013 | t0001 | g0110 | AFR | LWK | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0068 | REF | REF | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0003 | g0143 | REF | REF | ISM2_chr14_77469394_77503816 | ISM2 | chr14 | 77469394 | 77503816 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77475696 | G | A | 1 | a0013 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1615C>T | p.Arg539Cys | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1638/2940 | 1615/1716 | 539/571 | chr14 | 77475696 | |||
| chr14:77475882 | G | A | 1 | a0007 | 2 | HG03486.hp1 NA21309.hp2 |
missense_variant | MODERATE | c.1429C>T | p.Arg477Cys | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1452/2940 | 1429/1716 | 477/571 | chr14 | 77475882 | |||
| chr14:77475929 | G | A | 1 | a0010 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.1382C>T | p.Pro461Leu | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1405/2940 | 1382/1716 | 461/571 | chr14 | 77475929 | |||
| chr14:77478253 | A | G | 1 | a0011 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.1187T>C | p.Met396Thr | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/7 | 1210/2940 | 1187/1716 | 396/571 | chr14 | 77478253 | |||
| chr14:77478281 | T | C | 1 | a0006 | 2 | HG03239.hp2 NA20905.hp1 |
missense_variant | MODERATE | c.1159A>G | p.Lys387Glu | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/7 | 1182/2940 | 1159/1716 | 387/571 | chr14 | 77478281 | |||
| chr14:77482494 | C | G | 1 | a0012 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.801G>C | p.Glu267Asp | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/7 | 824/2940 | 801/1716 | 267/571 | chr14 | 77482494 | |||
| chr14:77482498 | C | T | 1 | a0005 | 2 | HG02717.hp1 HG03195.hp2 |
missense_variant | MODERATE | c.797G>A | p.Gly266Glu | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/7 | 820/2940 | 797/1716 | 266/571 | chr14 | 77482498 | |||
| chr14:77482594 | G | A | 1 | a0004 | 3 | HG01070.hp2 HG01071.hp2 HG01192.hp1 |
missense_variant | MODERATE | c.701C>T | p.Pro234Leu | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/7 | 724/2940 | 701/1716 | 234/571 | chr14 | 77482594 | |||
| chr14:77484513 | A | T | 1 | a0008 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.437T>A | p.Leu146Gln | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/7 | 460/2940 | 437/1716 | 146/571 | chr14 | 77484513 | |||
| chr14:77484553 | G | C | 2 | a0003 a0005 |
10 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(7): Show |
missense_variant | MODERATE | c.397C>G | p.Pro133Ala | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/7 | 420/2940 | 397/1716 | 133/571 | chr14 | 77484553 | |||
| chr14:77484781 | C | T | 5 | a0001 a0004 a0006 others(2): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
missense_variant | MODERATE | c.280G>A | p.Ala94Thr | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 2/7 | 303/2940 | 280/1716 | 94/571 | chr14 | 77484781 | |||
| chr14:77484865 | G | T | 1 | a0009 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.196C>A | p.Leu66Ile | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 2/7 | 219/2940 | 196/1716 | 66/571 | chr14 | 77484865 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77475736 | G | A | 1 | a0001c0005 | 3 | NA19011.hp2 NA19063.hp2 NA19083.hp2 |
synonymous_variant | LOW | c.1575C>T | p.Phe525Phe | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1598/2940 | 1575/1716 | 525/571 | chr14 | 77475736 | |||
| chr14:77475766 | G | A | 1 | a0001c0009 | 2 | HG01109.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.1545C>T | p.Thr515Thr | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1568/2940 | 1545/1716 | 515/571 | chr14 | 77475766 | |||
| chr14:77475973 | G | A | 4 | a0001c0010 a0002c0003 a0002c0007 others(1): Show |
20 | HG00099.hp1 HG00741.hp1 HG01123.hp1 others(17): Show |
synonymous_variant | LOW | c.1338C>T | p.Asp446Asp | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1361/2940 | 1338/1716 | 446/571 | chr14 | 77475973 | |||
| chr14:77478609 | G | A | 1 | a0001c0012 | 2 | NA19000.hp1 NA19066.hp2 |
synonymous_variant | LOW | c.1080C>T | p.Thr360Thr | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 5/7 | 1103/2940 | 1080/1716 | 360/571 | chr14 | 77478609 | |||
| chr14:77482323 | G | A | 1 | a0002c0021 | 1 | NA21309.hp1 | splice_region_variant&synonymous_variant | LOW | c.972C>T | p.Tyr324Tyr | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/7 | 995/2940 | 972/1716 | 324/571 | chr14 | 77482323 | |||
| chr14:77484800 | T | C | 1 | a0002c0008 | 3 | HG01070.hp1 HG03704.hp1 HG04228.hp2 |
synonymous_variant | LOW | c.261A>G | p.Ala87Ala | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 2/7 | 284/2940 | 261/1716 | 87/571 | chr14 | 77484800 | |||
| chr14:77498751 | G | A | 3 | a0002c0003 a0002c0015 a0010c0022 |
17 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(14): Show |
synonymous_variant | LOW | c.43C>T | p.Leu15Leu | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/7 | 66/2940 | 43/1716 | 15/571 | chr14 | 77498751 | |||
| chr14:77498758 | G | A | 1 | a0002c0023 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.36C>T | p.Leu12Leu | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/7 | 59/2940 | 36/1716 | 12/571 | chr14 | 77498758 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77474403 | A | T | 1 | a0012c0019t0010 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1192T>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1192 | chr14 | 77474403 | ||||||
| chr14:77474484 | G | A | 2 | a0001c0001t0004 a0001c0009t0004 |
5 | HG01109.hp1 HG02145.hp2 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1111C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1111 | chr14 | 77474484 | ||||||
| chr14:77474517 | T | C | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(34): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*1078A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1078 | chr14 | 77474517 | ||||||
| chr14:77474526 | C | A | 1 | a0002c0007t0015 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1069G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1069 | chr14 | 77474526 | ||||||
| chr14:77474590 | C | T | 1 | a0002c0002t0009 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1005G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 1005 | chr14 | 77474590 | ||||||
| chr14:77474623 | C | G | 1 | a0007c0013t0014 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*972G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 972 | chr14 | 77474623 | ||||||
| chr14:77474831 | C | T | 1 | a0001c0001t0013 | 1 | HG01069.hp2 | 3_prime_UTR_variant | MODIFIER | c.*764G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 764 | chr14 | 77474831 | ||||||
| chr14:77474947 | G | A | 2 | a0001c0010t0007 a0002c0003t0007 |
2 | NA18967.hp1 NA18990.hp1 |
3_prime_UTR_variant | MODIFIER | c.*648C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 648 | chr14 | 77474947 | ||||||
| chr14:77475099 | A | T | 1 | a0002c0002t0011 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*496T>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 496 | chr14 | 77475099 | ||||||
| chr14:77475102 | C | T | 2 | a0002c0002t0011 a0002c0023t0012 |
2 | HG02965.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*493G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 493 | chr14 | 77475102 | ||||||
| chr14:77475103 | A | G | 32 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0013 others(29): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
3_prime_UTR_variant | MODIFIER | c.*492T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 492 | chr14 | 77475103 | ||||||
| chr14:77475111 | T | C | 1 | a0001c0001t0016 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*484A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 484 | chr14 | 77475111 | ||||||
| chr14:77475112 | GC | G | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(34): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*482delG | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 482 | chr14 | 77475112 | ||||||
| chr14:77475120 | C | A | 1 | a0002c0002t0008 | 2 | HG01891.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*475G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 475 | chr14 | 77475120 | ||||||
| chr14:77475445 | G | A | 1 | a0012c0019t0010 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*150C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 150 | chr14 | 77475445 | ||||||
| chr14:77475480 | C | T | 2 | a0002c0002t0011 a0002c0023t0012 |
2 | HG02965.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*115G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 115 | chr14 | 77475480 | ||||||
| chr14:77475522 | G | GAGGGCCC others(4): Show |
31 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0013 others(28): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*72_*73insGGTAGGGC others(3): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 72 | chr14 | 77475522 | ||||||
| chr14:77475537 | G | A | 1 | a0001c0001t0017 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*58C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 58 | chr14 | 77475537 | ||||||
| chr14:77475551 | G | A | 1 | a0002c0002t0006 | 3 | HG02922.hp2 HG02965.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*44C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 7/7 | 44 | chr14 | 77475551 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:77476163 | C | T | 17 | a0001c0010t0001g0219 a0001c0010t0007g0113 a0002c0003t0001g0021 others(14): Show |
18 | HG00099.hp1 HG00741.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.1199-51G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476163 | |||||||
| chr14:77476164 | G | A | 2 | a0002c0007t0001g0024 a0002c0007t0015g0062 |
2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1199-52C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476164 | |||||||
| chr14:77476172 | C | T | 6 | a0003c0004t0001g0006 a0003c0004t0001g0028 a0003c0004t0001g0029 others(3): Show |
7 | HG02109.hp1 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1199-60G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476172 | |||||||
| chr14:77476199 | G | C | 1 | a0001c0001t0001g0201 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1199-87C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476199 | |||||||
| chr14:77476235 | G | A | 25 | a0001c0010t0001g0219 a0001c0010t0007g0113 a0002c0003t0001g0021 others(22): Show |
27 | HG00099.hp1 HG00741.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.1199-123C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476235 | |||||||
| chr14:77476267 | G | C | 1 | a0002c0002t0001g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1199-155C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476267 | |||||||
| chr14:77476269 | T | C | 1 | a0009c0016t0003g0153 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1199-157A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476269 | |||||||
| chr14:77476650 | C | T | 4 | a0002c0002t0003g0140 a0002c0002t0003g0142 a0002c0002t0003g0148 others(1): Show |
4 | HG01891.hp2 HG03486.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.1199-538G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476650 | |||||||
| chr14:77476664 | A | T | 233 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(230): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1199-552T>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476664 | |||||||
| chr14:77476727 | A | G | 1 | a0002c0002t0003g0148 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1199-615T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476727 | |||||||
| chr14:77476776 | G | A | 2 | a0002c0002t0011g0237 a0002c0023t0012g0253 |
2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1199-664C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476776 | |||||||
| chr14:77476779 | A | G | 2 | a0002c0002t0011g0237 a0002c0023t0012g0253 |
2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1199-667T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77476779 | |||||||
| chr14:77477089 | A | G | 6 | a0001c0001t0001g0133 a0002c0002t0001g0131 a0002c0002t0001g0136 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1199-977T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477089 | |||||||
| chr14:77477132 | A | G | 6 | a0002c0002t0001g0061 a0002c0002t0001g0103 a0002c0002t0001g0105 others(3): Show |
6 | HG02559.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1199-1020T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477132 | |||||||
| chr14:77477135 | G | A | 1 | a0001c0001t0001g0230 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1199-1023C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477135 | |||||||
| chr14:77477230 | T | C | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1198+1012A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477230 | |||||||
| chr14:77477273 | C | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(92): Show |
106 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.1198+969G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477273 | |||||||
| chr14:77477305 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1198+937G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477305 | |||||||
| chr14:77477326 | G | A | 6 | a0001c0001t0004g0118 a0001c0001t0004g0176 a0001c0001t0004g0177 others(3): Show |
6 | HG01109.hp1 HG02145.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1198+916C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477326 | |||||||
| chr14:77477370 | T | C | 203 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(200): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1198+872A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477370 | |||||||
| chr14:77477499 | G | A | 17 | a0001c0010t0001g0219 a0001c0010t0007g0113 a0002c0003t0001g0021 others(14): Show |
18 | HG00099.hp1 HG00741.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.1198+743C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477499 | |||||||
| chr14:77477726 | C | A | 1 | a0002c0002t0001g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1198+516G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477726 | |||||||
| chr14:77477815 | G | A | 2 | a0002c0002t0011g0237 a0002c0023t0012g0253 |
2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1198+427C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477815 | |||||||
| chr14:77477904 | G | T | 2 | a0002c0002t0011g0237 a0002c0023t0012g0253 |
2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1198+338C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477904 | |||||||
| chr14:77477918 | C | T | 2 | a0005c0014t0001g0032 a0005c0014t0001g0033 |
2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1198+324G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477918 | |||||||
| chr14:77477951 | C | T | 1 | a0002c0002t0001g0132 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1198+291G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 6/6 | chr14 | 77477951 | |||||||
| chr14:77478360 | G | C | 1 | a0003c0004t0001g0111 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1115-35C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 5/6 | chr14 | 77478360 | |||||||
| chr14:77478382 | A | G | 4 | a0001c0001t0001g0194 a0001c0001t0001g0200 a0001c0001t0001g0223 others(1): Show |
4 | HG02015.hp2 HG02523.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1115-57T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 5/6 | chr14 | 77478382 | |||||||
| chr14:77478395 | C | T | 1 | a0002c0007t0015g0062 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1115-70G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 5/6 | chr14 | 77478395 | |||||||
| chr14:77478428 | C | T | 6 | a0001c0001t0001g0120 a0001c0001t0001g0165 a0001c0001t0001g0207 others(3): Show |
6 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.1115-103G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 5/6 | chr14 | 77478428 | |||||||
| chr14:77478728 | A | G | 2 | a0002c0002t0011g0237 a0002c0023t0012g0253 |
2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.974-13T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77478728 | |||||||
| chr14:77478744 | G | C | 1 | a0002c0003t0001g0247 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.974-29C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77478744 | |||||||
| chr14:77478803 | T | A | 1 | a0002c0023t0012g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.974-88A>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77478803 | |||||||
| chr14:77478848 | G | A | 2 | a0002c0002t0011g0237 a0002c0023t0012g0253 |
2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.974-133C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77478848 | |||||||
| chr14:77478946 | C | T | 2 | a0002c0002t0011g0237 a0002c0023t0012g0253 |
2 | HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.974-231G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77478946 | |||||||
| chr14:77478976 | T | C | 233 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(230): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.974-261A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77478976 | |||||||
| chr14:77479157 | C | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0173 a0001c0001t0001g0175 |
3 | HG02071.hp1 NA18612.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.974-442G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77479157 | |||||||
| chr14:77479157 | C | T | 1 | a0002c0023t0012g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.974-442G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77479157 | |||||||
| chr14:77479347 | C | T | 203 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(200): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.974-632G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77479347 | |||||||
| chr14:77479385 | A | AT | 25 | a0001c0010t0001g0219 a0001c0010t0007g0113 a0002c0002t0003g0139 others(22): Show |
27 | HG00099.hp1 HG00741.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.974-671dupA | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77479385 | |||||||
| chr14:77479426 | C | G | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(93): Show |
107 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.974-711G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77479426 | |||||||
| chr14:77479550 | A | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(93): Show |
107 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.974-835T>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77479550 | |||||||
| chr14:77479596 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(93): Show |
107 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.974-881G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77479596 | |||||||
| chr14:77479706 | C | T | 1 | a0001c0001t0004g0118 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.974-991G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77479706 | |||||||
| chr14:77480295 | A | C | 204 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(201): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.974-1580T>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480295 | |||||||
| chr14:77480302 | CAA | C | 67 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(64): Show |
73 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(70): Show |
intron_variant | MODIFIER | c.974-1589_974-1588d others(4): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480302 | |||||||
| chr14:77480402 | G | C | 233 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(230): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.974-1687C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480402 | |||||||
| chr14:77480441 | C | T | 2 | a0002c0002t0006g0069 a0002c0002t0006g0079 |
2 | HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.974-1726G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480441 | |||||||
| chr14:77480444 | A | G | 1 | a0002c0002t0003g0147 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.974-1729T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480444 | |||||||
| chr14:77480491 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.974-1776C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480491 | |||||||
| chr14:77480547 | CCT | C | 5 | a0001c0001t0004g0176 a0001c0001t0004g0177 a0001c0009t0004g0072 others(2): Show |
5 | HG01109.hp1 HG02809.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.973+1773_973+1774d others(4): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480547 | |||||||
| chr14:77480548 | CT | C | 21 | a0002c0002t0001g0076 a0002c0002t0001g0103 a0002c0002t0001g0136 others(18): Show |
24 | HG01070.hp1 HG01243.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.973+1773delA | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480548 | |||||||
| chr14:77480548 | CTT | C | 41 | a0001c0001t0001g0060 a0001c0001t0001g0064 a0001c0001t0001g0066 others(38): Show |
46 | HG00099.hp2 HG00323.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.973+1772_973+1773d others(4): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480548 | |||||||
| chr14:77480548 | CTTT | C | 147 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(144): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.973+1771_973+1773d others(5): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480548 | |||||||
| chr14:77480548 | CTTTT | C | 31 | a0001c0005t0001g0210 a0001c0010t0001g0219 a0001c0010t0007g0113 others(28): Show |
34 | HG00099.hp1 HG00741.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.973+1770_973+1773d others(6): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480548 | |||||||
| chr14:77480595 | T | TCACC | 26 | a0001c0001t0001g0133 a0002c0002t0001g0001 a0002c0002t0001g0004 others(23): Show |
30 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.973+1723_973+1726d others(6): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480595 | |||||||
| chr14:77480633 | C | G | 1 | a0002c0002t0001g0102 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.973+1689G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480633 | |||||||
| chr14:77480695 | C | CTACA | 61 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(58): Show |
66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.973+1623_973+1626d others(6): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480695 | |||||||
| chr14:77480713 | G | A | 174 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(171): Show |
192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.973+1609C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480713 | |||||||
| chr14:77480734 | T | G | 25 | a0001c0010t0001g0219 a0001c0010t0007g0113 a0002c0003t0001g0021 others(22): Show |
27 | HG00099.hp1 HG00741.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.973+1588A>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480734 | |||||||
| chr14:77480769 | A | G | 237 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(234): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.973+1553T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480769 | |||||||
| chr14:77480834 | A | C | 1 | a0002c0002t0011g0237 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.973+1488T>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480834 | |||||||
| chr14:77480855 | G | A | 2 | a0002c0002t0001g0005 a0002c0002t0001g0239 |
4 | HG02451.hp1 HG02572.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.973+1467C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480855 | |||||||
| chr14:77480901 | G | A | 1 | a0002c0002t0001g0151 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.973+1421C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480901 | |||||||
| chr14:77480955 | A | G | 30 | a0001c0001t0001g0133 a0002c0002t0001g0001 a0002c0002t0001g0004 others(27): Show |
34 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.973+1367T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77480955 | |||||||
| chr14:77481005 | T | A | 1 | a0002c0002t0011g0237 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.973+1317A>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481005 | |||||||
| chr14:77481156 | C | T | 49 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(46): Show |
54 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.973+1166G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481156 | |||||||
| chr14:77481189 | A | C | 1 | a0002c0002t0006g0107 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.973+1133T>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481189 | |||||||
| chr14:77481339 | C | CA | 37 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(34): Show |
40 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(37): Show |
intron_variant | MODIFIER | c.973+982dupT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481339 | |||||||
| chr14:77481342 | A | C | 1 | a0001c0001t0001g0064 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.973+980T>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481342 | |||||||
| chr14:77481348 | T | A | 1 | a0001c0001t0001g0050 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.973+974A>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481348 | |||||||
| chr14:77481363 | T | C | 6 | a0001c0001t0004g0118 a0001c0001t0004g0176 a0001c0001t0004g0177 others(3): Show |
6 | HG01109.hp1 HG02145.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.973+959A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481363 | |||||||
| chr14:77481488 | A | G | 6 | a0001c0001t0004g0118 a0001c0001t0004g0176 a0001c0001t0004g0177 others(3): Show |
6 | HG01109.hp1 HG02145.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.973+834T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481488 | |||||||
| chr14:77481509 | ACT | A | 6 | a0001c0001t0004g0118 a0001c0001t0004g0176 a0001c0001t0004g0177 others(3): Show |
6 | HG01109.hp1 HG02145.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.973+811_973+812del others(2): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481509 | |||||||
| chr14:77481582 | G | A | 12 | a0001c0001t0001g0049 a0001c0001t0001g0205 a0002c0002t0001g0013 others(9): Show |
14 | HG00642.hp1 HG00735.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.973+740C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481582 | |||||||
| chr14:77481807 | G | GAA | 98 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(95): Show |
109 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.973+513_973+514dup others(2): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481807 | |||||||
| chr14:77481943 | T | TA | 6 | a0001c0001t0001g0027 a0001c0001t0001g0059 a0001c0001t0001g0086 others(3): Show |
6 | HG00544.hp1 HG00544.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.973+378dupT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481943 | |||||||
| chr14:77481987 | C | G | 15 | a0001c0010t0001g0219 a0002c0003t0001g0021 a0002c0003t0001g0241 others(12): Show |
16 | HG00099.hp1 HG00741.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.973+335G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77481987 | |||||||
| chr14:77482008 | A | T | 1 | a0003c0004t0001g0111 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.973+314T>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77482008 | |||||||
| chr14:77482071 | C | G | 64 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(61): Show |
71 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.973+251G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77482071 | |||||||
| chr14:77482125 | T | TA | 20 | a0001c0001t0001g0133 a0002c0002t0001g0001 a0002c0002t0001g0004 others(17): Show |
24 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.973+196dupT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77482125 | |||||||
| chr14:77482125 | TA | T | 12 | a0001c0001t0001g0089 a0001c0001t0001g0094 a0001c0001t0001g0096 others(9): Show |
12 | HG01256.hp2 HG01515.hp1 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.973+196delT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77482125 | |||||||
| chr14:77482223 | A | G | 22 | a0001c0001t0001g0133 a0002c0002t0001g0001 a0002c0002t0001g0004 others(19): Show |
26 | HG00099.hp2 HG00323.hp1 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.973+99T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77482223 | |||||||
| chr14:77482284 | G | A | 1 | a0002c0002t0001g0138 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.973+38C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 4/6 | chr14 | 77482284 | |||||||
| chr14:77482682 | C | T | 1 | a0001c0001t0001g0009 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.628-15G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77482682 | |||||||
| chr14:77482894 | C | T | 6 | a0003c0004t0001g0006 a0003c0004t0001g0028 a0003c0004t0001g0029 others(3): Show |
7 | HG02109.hp1 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.628-227G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77482894 | |||||||
| chr14:77482924 | TG | T | 128 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(125): Show |
140 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.628-258delC | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77482924 | |||||||
| chr14:77483470 | C | T | 125 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(122): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.628-803G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77483470 | |||||||
| chr14:77483544 | T | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(127): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.627+779A>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77483544 | |||||||
| chr14:77483547 | C | CA | 50 | a0001c0001t0001g0133 a0002c0002t0001g0013 a0002c0002t0001g0070 others(47): Show |
52 | HG00099.hp2 HG01081.hp2 HG01099.hp1 others(49): Show |
intron_variant | MODIFIER | c.627+775dupT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77483547 | |||||||
| chr14:77483547 | CA | C | 12 | a0001c0001t0001g0043 a0001c0001t0001g0091 a0002c0003t0001g0246 others(9): Show |
13 | HG01515.hp2 HG01993.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.627+775delT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77483547 | |||||||
| chr14:77483643 | C | CGT | 8 | a0003c0004t0001g0006 a0003c0004t0001g0028 a0003c0004t0001g0029 others(5): Show |
9 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.627+678_627+679dup others(2): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77483643 | |||||||
| chr14:77483652 | G | C | 1 | a0002c0002t0001g0061 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.627+671C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77483652 | |||||||
| chr14:77483780 | A | G | 237 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(234): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.627+543T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77483780 | |||||||
| chr14:77483862 | C | T | 16 | a0002c0003t0001g0021 a0002c0003t0001g0241 a0002c0003t0001g0242 others(13): Show |
18 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.627+461G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77483862 | |||||||
| chr14:77483965 | C | A | 1 | a0002c0023t0012g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.627+358G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77483965 | |||||||
| chr14:77484073 | C | T | 2 | a0005c0014t0001g0032 a0005c0014t0001g0033 |
2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.627+250G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77484073 | |||||||
| chr14:77484127 | G | A | 1 | a0002c0003t0001g0247 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.627+196C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77484127 | |||||||
| chr14:77484242 | A | G | 45 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0061 others(42): Show |
52 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.627+81T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77484242 | |||||||
| chr14:77484273 | C | T | 2 | a0001c0001t0001g0175 a0002c0002t0001g0088 |
2 | NA18612.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.627+50G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77484273 | |||||||
| chr14:77484297 | G | A | 9 | a0003c0004t0001g0006 a0003c0004t0001g0028 a0003c0004t0001g0029 others(6): Show |
10 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.627+26C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 3/6 | chr14 | 77484297 | |||||||
| chr14:77485021 | G | A | 51 | a0002c0002t0001g0013 a0002c0002t0001g0070 a0002c0002t0001g0078 others(48): Show |
53 | HG00099.hp2 HG01081.hp2 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.142-102C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485021 | |||||||
| chr14:77485022 | G | A | 2 | a0002c0002t0001g0102 a0002c0002t0001g0234 |
2 | HG00323.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.142-103C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485022 | |||||||
| chr14:77485088 | C | G | 29 | a0002c0002t0001g0088 a0002c0002t0001g0092 a0002c0002t0001g0093 others(26): Show |
30 | HG01099.hp1 HG01175.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.142-169G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485088 | |||||||
| chr14:77485110 | C | T | 8 | a0002c0002t0001g0004 a0002c0002t0001g0102 a0002c0002t0001g0231 others(5): Show |
10 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-191G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485110 | |||||||
| chr14:77485111 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.142-192C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485111 | |||||||
| chr14:77485149 | A | G | 3 | a0003c0004t0001g0111 a0005c0014t0001g0032 a0005c0014t0001g0033 |
3 | HG02717.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.142-230T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485149 | |||||||
| chr14:77485159 | T | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(233): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.142-240A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485159 | |||||||
| chr14:77485225 | A | G | 3 | a0003c0004t0001g0111 a0005c0014t0001g0032 a0005c0014t0001g0033 |
3 | HG02717.hp1 HG03195.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.142-306T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485225 | |||||||
| chr14:77485253 | G | T | 36 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0061 others(33): Show |
42 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.142-334C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485253 | |||||||
| chr14:77485254 | A | G | 36 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0061 others(33): Show |
42 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.142-335T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485254 | |||||||
| chr14:77485322 | C | T | 2 | a0002c0007t0001g0024 a0002c0007t0015g0062 |
2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.142-403G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485322 | |||||||
| chr14:77485570 | A | G | 2 | a0001c0001t0001g0223 a0001c0001t0001g0225 |
2 | NA19065.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.142-651T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485570 | |||||||
| chr14:77485786 | C | T | 3 | a0002c0002t0003g0025 a0002c0002t0003g0026 a0002c0002t0011g0237 |
3 | HG02630.hp2 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.142-867G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77485786 | |||||||
| chr14:77486080 | A | G | 19 | a0002c0002t0001g0013 a0002c0002t0001g0070 a0002c0002t0001g0078 others(16): Show |
20 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.142-1161T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486080 | |||||||
| chr14:77486267 | T | TACTG | 180 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(177): Show |
199 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.142-1349_142-1348i others(6): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486267 | |||||||
| chr14:77486271 | T | C | 2 | a0005c0014t0001g0032 a0005c0014t0001g0033 |
2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.142-1352A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486271 | |||||||
| chr14:77486373 | C | A | 1 | a0003c0004t0001g0111 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142-1454G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486373 | |||||||
| chr14:77486378 | C | T | 1 | a0002c0002t0002g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.142-1459G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486378 | |||||||
| chr14:77486389 | A | G | 3 | a0002c0002t0003g0140 a0002c0002t0003g0142 a0002c0002t0003g0148 |
3 | HG01891.hp2 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.142-1470T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486389 | |||||||
| chr14:77486412 | G | A | 1 | a0009c0016t0003g0153 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.142-1493C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486412 | |||||||
| chr14:77486619 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.142-1700C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486619 | |||||||
| chr14:77486685 | G | T | 3 | a0002c0002t0006g0069 a0002c0002t0006g0079 a0002c0002t0006g0107 |
3 | HG02922.hp2 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.142-1766C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486685 | |||||||
| chr14:77486847 | C | G | 2 | a0001c0001t0001g0055 a0002c0008t0001g0039 |
2 | HG02055.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.142-1928G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486847 | |||||||
| chr14:77486864 | G | C | 1 | a0009c0016t0003g0153 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.142-1945C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486864 | |||||||
| chr14:77486969 | C | T | 1 | a0001c0001t0001g0052 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.142-2050G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486969 | |||||||
| chr14:77486979 | C | T | 1 | a0009c0016t0003g0153 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.142-2060G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77486979 | |||||||
| chr14:77487032 | G | A | 1 | a0002c0023t0012g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142-2113C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487032 | |||||||
| chr14:77487061 | G | A | 1 | a0003c0004t0001g0111 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142-2142C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487061 | |||||||
| chr14:77487103 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.142-2184C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487103 | |||||||
| chr14:77487140 | G | T | 1 | a0003c0004t0001g0111 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142-2221C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487140 | |||||||
| chr14:77487159 | C | T | 60 | a0001c0001t0001g0133 a0002c0002t0001g0013 a0002c0002t0001g0070 others(57): Show |
63 | HG00099.hp2 HG01081.hp2 HG01099.hp1 others(60): Show |
intron_variant | MODIFIER | c.142-2240G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487159 | |||||||
| chr14:77487206 | T | C | 1 | a0002c0002t0001g0134 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.142-2287A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487206 | |||||||
| chr14:77487243 | T | TTAAA | 21 | a0001c0001t0001g0007 a0001c0001t0001g0036 a0001c0001t0001g0038 others(18): Show |
22 | HG00140.hp2 HG00621.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.142-2328_142-2325d others(6): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487243 | |||||||
| chr14:77487243 | T | TTAAATAA others(1): Show |
13 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0002c0002t0001g0061 others(10): Show |
13 | HG00140.hp1 HG00738.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.142-2332_142-2325d others(10): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487243 | |||||||
| chr14:77487243 | T | TTAAATAA others(5): Show |
11 | a0002c0002t0001g0004 a0002c0002t0001g0005 a0002c0002t0001g0102 others(8): Show |
15 | HG00323.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.142-2336_142-2325d others(14): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487243 | |||||||
| chr14:77487243 | T | TTAAATAA others(9): Show |
7 | a0002c0002t0001g0001 a0002c0002t0001g0076 a0002c0002t0001g0234 others(4): Show |
9 | HG01358.hp2 HG02717.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.142-2340_142-2325d others(18): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487243 | |||||||
| chr14:77487243 | TTAAA | T | 102 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(99): Show |
113 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.142-2328_142-2325d others(6): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487243 | |||||||
| chr14:77487243 | TTAAATAA others(1): Show |
T | 9 | a0001c0001t0001g0197 a0001c0010t0007g0113 a0002c0002t0003g0147 others(6): Show |
10 | HG02109.hp1 HG02280.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-2332_142-2325d others(10): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487243 | |||||||
| chr14:77487243 | TTAAATAA others(5): Show |
T | 1 | a0002c0002t0002g0115 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.142-2336_142-2325d others(14): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487243 | |||||||
| chr14:77487255 | A | G | 16 | a0002c0003t0001g0021 a0002c0003t0001g0241 a0002c0003t0001g0242 others(13): Show |
18 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.142-2336T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487255 | |||||||
| chr14:77487260 | TA | T | 6 | a0001c0001t0001g0120 a0001c0001t0001g0165 a0001c0001t0001g0207 others(3): Show |
6 | HG01070.hp2 HG01071.hp2 HG01081.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-2342delT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487260 | |||||||
| chr14:77487440 | C | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(128): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.142-2521G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487440 | |||||||
| chr14:77487466 | A | C | 13 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0076 others(10): Show |
17 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.142-2547T>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487466 | |||||||
| chr14:77487496 | C | A | 2 | a0002c0002t0003g0025 a0002c0002t0003g0026 |
2 | HG02630.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.142-2577G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487496 | |||||||
| chr14:77487498 | C | A | 1 | a0002c0002t0003g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.142-2579G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487498 | |||||||
| chr14:77487524 | T | C | 2 | a0002c0002t0001g0061 a0002c0002t0003g0139 |
2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142-2605A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487524 | |||||||
| chr14:77487532 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.142-2613C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487532 | |||||||
| chr14:77487549 | T | C | 243 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(240): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.142-2630A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487549 | |||||||
| chr14:77487663 | G | T | 2 | a0005c0014t0001g0032 a0005c0014t0001g0033 |
2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.142-2744C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487663 | |||||||
| chr14:77487676 | C | T | 4 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0002g0180 others(1): Show |
4 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.142-2757G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487676 | |||||||
| chr14:77487778 | C | A | 7 | a0002c0002t0001g0004 a0002c0002t0001g0102 a0002c0002t0001g0231 others(4): Show |
9 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.142-2859G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487778 | |||||||
| chr14:77487793 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.142-2874C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487793 | |||||||
| chr14:77487799 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.142-2880C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487799 | |||||||
| chr14:77487836 | C | T | 1 | a0002c0002t0001g0130 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.142-2917G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487836 | |||||||
| chr14:77487876 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(100): Show |
113 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.142-2957C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487876 | |||||||
| chr14:77487938 | G | C | 1 | a0002c0002t0001g0061 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.142-3019C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487938 | |||||||
| chr14:77487982 | G | A | 1 | a0002c0002t0001g0080 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.142-3063C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77487982 | |||||||
| chr14:77488208 | G | A | 2 | a0002c0002t0001g0061 a0002c0002t0003g0139 |
2 | HG03098.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.142-3289C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77488208 | |||||||
| chr14:77488256 | C | T | 1 | a0002c0002t0003g0152 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.142-3337G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77488256 | |||||||
| chr14:77488510 | T | C | 15 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0076 others(12): Show |
19 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.142-3591A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77488510 | |||||||
| chr14:77488693 | C | T | 2 | a0002c0002t0005g0014 a0002c0002t0005g0146 |
3 | HG01243.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.142-3774G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77488693 | |||||||
| chr14:77488896 | G | A | 236 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(233): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.142-3977C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77488896 | |||||||
| chr14:77489042 | C | T | 1 | a0002c0002t0001g0061 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.142-4123G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489042 | |||||||
| chr14:77489084 | C | T | 236 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(233): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.142-4165G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489084 | |||||||
| chr14:77489332 | T | C | 1 | a0003c0004t0001g0111 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142-4413A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489332 | |||||||
| chr14:77489416 | T | C | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.142-4497A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489416 | |||||||
| chr14:77489429 | C | T | 1 | a0002c0023t0012g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142-4510G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489429 | |||||||
| chr14:77489552 | C | CT | 134 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): Show |
146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.142-4634dupA | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489552 | |||||||
| chr14:77489719 | A | G | 1 | a0009c0016t0003g0153 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.142-4800T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489719 | |||||||
| chr14:77489903 | G | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): Show |
146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.142-4984C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489903 | |||||||
| chr14:77489948 | A | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(233): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.142-5029T>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489948 | |||||||
| chr14:77489949 | A | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(233): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.142-5030T>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489949 | |||||||
| chr14:77489965 | G | A | 2 | a0005c0014t0001g0032 a0005c0014t0001g0033 |
2 | HG02717.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.142-5046C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489965 | |||||||
| chr14:77489990 | A | G | 1 | a0002c0002t0006g0107 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.142-5071T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77489990 | |||||||
| chr14:77490009 | G | A | 1 | a0002c0002t0001g0138 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.142-5090C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490009 | |||||||
| chr14:77490021 | G | A | 4 | a0002c0002t0001g0001 a0002c0002t0001g0076 a0002c0002t0008g0074 others(1): Show |
6 | HG01891.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-5102C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490021 | |||||||
| chr14:77490064 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.142-5145G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490064 | |||||||
| chr14:77490098 | C | T | 1 | a0002c0002t0003g0140 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.142-5179G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490098 | |||||||
| chr14:77490110 | T | TCCTCGGC others(127): Show |
1 | a0002c0002t0003g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.142-5192_142-5191i others(136): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490110 | |||||||
| chr14:77490145 | G | T | 1 | a0002c0002t0003g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.142-5226C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490145 | |||||||
| chr14:77490149 | C | T | 3 | a0002c0002t0003g0025 a0002c0002t0003g0026 a0002c0002t0011g0237 |
3 | HG02630.hp2 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.142-5230G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490149 | |||||||
| chr14:77490155 | G | A | 3 | a0002c0002t0006g0069 a0002c0002t0006g0079 a0002c0002t0006g0107 |
3 | HG02922.hp2 HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.142-5236C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490155 | |||||||
| chr14:77490159 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.142-5240C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490159 | |||||||
| chr14:77490199 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.142-5280T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490199 | |||||||
| chr14:77490213 | G | A | 3 | a0002c0002t0002g0071 a0002c0002t0002g0182 a0002c0002t0002g0186 |
3 | HG02738.hp2 HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.142-5294C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490213 | |||||||
| chr14:77490222 | C | CTCTTGAC others(7): Show |
1 | a0002c0023t0012g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.142-5317_142-5304d others(16): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490222 | |||||||
| chr14:77490390 | G | GAAAAGTA others(9): Show |
235 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(232): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.142-5472_142-5471i others(18): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490390 | |||||||
| chr14:77490390 | G | GAAAAGTA others(10): Show |
1 | a0001c0001t0001g0230 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.142-5472_142-5471i others(19): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490390 | |||||||
| chr14:77490393 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.142-5474G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490393 | |||||||
| chr14:77490434 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0195 others(1): Show |
6 | HG01256.hp2 HG01361.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-5515A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490434 | |||||||
| chr14:77490498 | C | T | 13 | a0001c0001t0001g0133 a0002c0002t0001g0013 a0002c0002t0001g0070 others(10): Show |
14 | HG00099.hp2 HG01167.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.142-5579G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490498 | |||||||
| chr14:77490518 | T | A | 16 | a0002c0003t0001g0021 a0002c0003t0001g0241 a0002c0003t0001g0242 others(13): Show |
18 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.142-5599A>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490518 | |||||||
| chr14:77490520 | A | T | 1 | a0002c0002t0001g0151 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.142-5601T>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490520 | |||||||
| chr14:77490622 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.142-5703C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490622 | |||||||
| chr14:77490760 | C | T | 3 | a0002c0002t0001g0061 a0003c0004t0001g0111 a0009c0016t0003g0153 |
3 | HG01123.hp2 HG03225.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.142-5841G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77490760 | |||||||
| chr14:77491011 | G | A | 54 | a0001c0001t0001g0133 a0002c0002t0001g0013 a0002c0002t0001g0061 others(51): Show |
56 | HG00099.hp2 HG01081.hp2 HG01099.hp1 others(53): Show |
intron_variant | MODIFIER | c.142-6092C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491011 | |||||||
| chr14:77491034 | G | A | 79 | a0001c0001t0001g0133 a0002c0002t0001g0005 a0002c0002t0001g0013 others(76): Show |
85 | HG00099.hp2 HG00642.hp1 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.142-6115C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491034 | |||||||
| chr14:77491107 | G | A | 2 | a0001c0001t0001g0125 a0012c0019t0010g0155 |
2 | HG00621.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.142-6188C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491107 | |||||||
| chr14:77491169 | G | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(233): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.142-6250C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491169 | |||||||
| chr14:77491170 | G | A | 1 | a0003c0004t0001g0111 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.142-6251C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491170 | |||||||
| chr14:77491214 | G | A | 2 | a0002c0002t0002g0154 a0002c0002t0002g0159 |
2 | HG01358.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.142-6295C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491214 | |||||||
| chr14:77491348 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.142-6429G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491348 | |||||||
| chr14:77491390 | T | G | 1 | a0001c0001t0001g0170 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.142-6471A>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491390 | |||||||
| chr14:77491414 | G | T | 6 | a0003c0004t0001g0006 a0003c0004t0001g0028 a0003c0004t0001g0029 others(3): Show |
7 | HG02109.hp1 HG02280.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-6495C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491414 | |||||||
| chr14:77491550 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.142-6631C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491550 | |||||||
| chr14:77491590 | C | T | 1 | a0002c0002t0002g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.142-6671G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491590 | |||||||
| chr14:77491685 | T | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(174): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.142-6766A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491685 | |||||||
| chr14:77491685 | T | G | 59 | a0001c0001t0001g0133 a0002c0002t0001g0013 a0002c0002t0001g0061 others(56): Show |
61 | HG00099.hp2 HG01081.hp2 HG01099.hp1 others(58): Show |
intron_variant | MODIFIER | c.142-6766A>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491685 | |||||||
| chr14:77491691 | C | CT | 30 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0095 others(27): Show |
30 | HG00621.hp2 HG00735.hp2 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.142-6773dupA | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491691 | |||||||
| chr14:77491691 | CT | C | 11 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0002c0002t0001g0189 others(8): Show |
11 | HG01123.hp2 HG01167.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.142-6773delA | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491691 | |||||||
| chr14:77491691 | CTT | C | 17 | a0002c0002t0001g0005 a0002c0002t0001g0238 a0002c0002t0001g0239 others(14): Show |
21 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.142-6774_142-6773d others(4): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491691 | |||||||
| chr14:77491717 | G | A | 16 | a0002c0003t0001g0021 a0002c0003t0001g0241 a0002c0003t0001g0242 others(13): Show |
18 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.142-6798C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491717 | |||||||
| chr14:77491747 | G | A | 1 | a0002c0002t0001g0151 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.142-6828C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491747 | |||||||
| chr14:77491820 | C | T | 1 | a0001c0001t0017g0164 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.141+6833G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491820 | |||||||
| chr14:77491859 | C | T | 51 | a0001c0001t0001g0133 a0002c0002t0001g0013 a0002c0002t0001g0070 others(48): Show |
53 | HG00099.hp2 HG01081.hp2 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.141+6794G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77491859 | |||||||
| chr14:77492000 | C | CT | 22 | a0001c0001t0001g0066 a0002c0002t0001g0005 a0002c0002t0001g0238 others(19): Show |
26 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.141+6652dupA | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492000 | |||||||
| chr14:77492013 | T | A | 1 | a0001c0001t0001g0199 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.141+6640A>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492013 | |||||||
| chr14:77492032 | A | G | 55 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(52): Show |
61 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.141+6621T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492032 | |||||||
| chr14:77492361 | C | T | 21 | a0001c0001t0001g0089 a0001c0001t0001g0094 a0001c0001t0016g0196 others(18): Show |
23 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.141+6292G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492361 | |||||||
| chr14:77492362 | G | C | 1 | a0002c0007t0015g0062 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.141+6291C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492362 | |||||||
| chr14:77492415 | G | A | 2 | a0002c0007t0001g0024 a0002c0007t0015g0062 |
2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.141+6238C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492415 | |||||||
| chr14:77492443 | C | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0227 |
2 | HG04115.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.141+6210G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492443 | |||||||
| chr14:77492472 | G | A | 19 | a0001c0001t0001g0133 a0002c0002t0001g0013 a0002c0002t0001g0070 others(16): Show |
20 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.141+6181C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492472 | |||||||
| chr14:77492516 | CT | C | 191 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(188): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.141+6136delA | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492516 | |||||||
| chr14:77492516 | CTT | C | 7 | a0001c0001t0001g0052 a0002c0002t0001g0061 a0002c0002t0001g0088 others(4): Show |
7 | HG01123.hp2 HG02630.hp2 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+6135_141+6136d others(4): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492516 | |||||||
| chr14:77492536 | T | C | 1 | a0002c0021t0002g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.141+6117A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492536 | |||||||
| chr14:77492580 | T | C | 3 | a0002c0002t0001g0005 a0002c0002t0001g0238 a0002c0002t0001g0239 |
5 | HG02451.hp1 HG02572.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+6073A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492580 | |||||||
| chr14:77492605 | G | A | 1 | a0002c0023t0012g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+6048C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492605 | |||||||
| chr14:77492614 | G | T | 16 | a0002c0003t0001g0021 a0002c0003t0001g0241 a0002c0003t0001g0242 others(13): Show |
18 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.141+6039C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492614 | |||||||
| chr14:77492633 | T | G | 1 | a0003c0004t0001g0111 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.141+6020A>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492633 | |||||||
| chr14:77492705 | T | A | 14 | a0001c0001t0001g0060 a0001c0001t0001g0122 a0001c0001t0001g0124 others(11): Show |
14 | HG00408.hp1 HG01981.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.141+5948A>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492705 | |||||||
| chr14:77492725 | C | T | 16 | a0002c0003t0001g0021 a0002c0003t0001g0241 a0002c0003t0001g0242 others(13): Show |
18 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.141+5928G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492725 | |||||||
| chr14:77492746 | G | A | 1 | a0005c0014t0001g0033 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.141+5907C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492746 | |||||||
| chr14:77492766 | G | C | 2 | a0002c0002t0001g0061 a0009c0016t0003g0153 |
2 | HG01123.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.141+5887C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492766 | |||||||
| chr14:77492781 | A | G | 1 | a0002c0002t0006g0107 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.141+5872T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77492781 | |||||||
| chr14:77493017 | A | G | 16 | a0002c0003t0001g0021 a0002c0003t0001g0241 a0002c0003t0001g0242 others(13): Show |
18 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.141+5636T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493017 | |||||||
| chr14:77493147 | C | T | 16 | a0002c0003t0001g0021 a0002c0003t0001g0241 a0002c0003t0001g0242 others(13): Show |
18 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.141+5506G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493147 | |||||||
| chr14:77493344 | T | C | 2 | a0002c0002t0001g0001 a0002c0002t0001g0076 |
4 | HG02717.hp2 HG03579.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+5309A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493344 | |||||||
| chr14:77493380 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.141+5273A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493380 | |||||||
| chr14:77493521 | G | C | 1 | a0006c0011t0001g0204 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.141+5132C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493521 | |||||||
| chr14:77493556 | A | C | 150 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(147): Show |
166 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.141+5097T>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493556 | |||||||
| chr14:77493595 | G | A | 2 | a0002c0002t0001g0116 a0002c0002t0001g0157 |
2 | HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.141+5058C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493595 | |||||||
| chr14:77493762 | G | A | 1 | a0002c0002t0002g0158 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.141+4891C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493762 | |||||||
| chr14:77493835 | G | A | 1 | a0002c0002t0003g0139 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.141+4818C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493835 | |||||||
| chr14:77493875 | C | T | 1 | a0002c0002t0002g0129 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.141+4778G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493875 | |||||||
| chr14:77493876 | G | A | 1 | a0002c0023t0012g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+4777C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493876 | |||||||
| chr14:77493938 | A | AT | 5 | a0001c0001t0001g0230 a0002c0002t0001g0005 a0002c0002t0001g0238 others(2): Show |
7 | HG02451.hp1 HG02572.hp2 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+4714dupA | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493938 | |||||||
| chr14:77493979 | G | A | 1 | a0002c0023t0012g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+4674C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493979 | |||||||
| chr14:77493988 | A | G | 1 | a0002c0007t0001g0024 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.141+4665T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77493988 | |||||||
| chr14:77494024 | G | A | 1 | a0002c0023t0012g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+4629C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77494024 | |||||||
| chr14:77494059 | G | C | 1 | a0002c0023t0012g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+4594C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77494059 | |||||||
| chr14:77494716 | C | T | 1 | a0002c0002t0006g0079 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.141+3937G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77494716 | |||||||
| chr14:77494745 | G | A | 1 | a0012c0019t0010g0155 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.141+3908C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77494745 | |||||||
| chr14:77494826 | T | C | 1 | a0003c0004t0001g0111 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.141+3827A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77494826 | |||||||
| chr14:77494884 | TTTTA | T | 16 | a0002c0003t0001g0021 a0002c0003t0001g0241 a0002c0003t0001g0242 others(13): Show |
18 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.141+3765_141+3768d others(6): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77494884 | |||||||
| chr14:77494916 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0057 |
3 | HG00140.hp1 HG00642.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.141+3737G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77494916 | |||||||
| chr14:77495024 | C | T | 15 | a0002c0003t0001g0021 a0002c0003t0001g0241 a0002c0003t0001g0242 others(12): Show |
17 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.141+3629G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77495024 | |||||||
| chr14:77495067 | G | A | 1 | a0002c0007t0001g0024 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.141+3586C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77495067 | |||||||
| chr14:77495120 | G | C | 1 | a0002c0023t0012g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+3533C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77495120 | |||||||
| chr14:77495206 | G | A | 2 | a0001c0001t0001g0223 a0001c0001t0001g0225 |
2 | NA19065.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.141+3447C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77495206 | |||||||
| chr14:77495266 | G | C | 168 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(165): Show |
188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.141+3387C>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77495266 | |||||||
| chr14:77495669 | G | A | 8 | a0003c0004t0001g0006 a0003c0004t0001g0028 a0003c0004t0001g0029 others(5): Show |
9 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+2984C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77495669 | |||||||
| chr14:77495703 | G | A | 15 | a0002c0003t0001g0021 a0002c0003t0001g0241 a0002c0003t0001g0242 others(12): Show |
17 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.141+2950C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77495703 | |||||||
| chr14:77495934 | C | T | 1 | a0002c0002t0003g0141 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.141+2719G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77495934 | |||||||
| chr14:77496184 | G | GT | 91 | a0001c0001t0001g0027 a0001c0001t0001g0047 a0001c0001t0001g0056 others(88): Show |
101 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.141+2468_141+2469i others(3): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496184 | |||||||
| chr14:77496185 | C | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(142): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.141+2468G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496185 | |||||||
| chr14:77496186 | C | A | 91 | a0001c0001t0001g0027 a0001c0001t0001g0047 a0001c0001t0001g0056 others(88): Show |
101 | HG00099.hp2 HG00323.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.141+2467G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496186 | |||||||
| chr14:77496247 | G | T | 1 | a0002c0023t0012g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+2406C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496247 | |||||||
| chr14:77496248 | G | T | 1 | a0001c0001t0004g0177 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.141+2405C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496248 | |||||||
| chr14:77496298 | GACCAACA others(7): Show |
G | 1 | a0002c0023t0012g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+2341_141+2354d others(16): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496298 | |||||||
| chr14:77496353 | T | A | 3 | a0002c0003t0001g0251 a0002c0003t0001g0252 a0002c0003t0007g0244 |
3 | NA18946.hp2 NA18967.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.141+2300A>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496353 | |||||||
| chr14:77496381 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.141+2272C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496381 | |||||||
| chr14:77496420 | G | A | 19 | a0001c0001t0001g0133 a0002c0002t0001g0013 a0002c0002t0001g0070 others(16): Show |
20 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.141+2233C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496420 | |||||||
| chr14:77496594 | C | A | 2 | a0002c0007t0001g0024 a0002c0007t0015g0062 |
2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.141+2059G>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496594 | |||||||
| chr14:77496660 | G | T | 15 | a0002c0003t0001g0021 a0002c0003t0001g0241 a0002c0003t0001g0242 others(12): Show |
17 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.141+1993C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496660 | |||||||
| chr14:77496751 | T | C | 20 | a0002c0002t0001g0005 a0002c0002t0001g0238 a0002c0002t0001g0239 others(17): Show |
24 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.141+1902A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496751 | |||||||
| chr14:77496799 | G | GA | 20 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0036 others(17): Show |
23 | HG00140.hp2 HG00738.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.141+1853dupT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | |||||||
| chr14:77496799 | G | GAA | 14 | a0001c0001t0001g0007 a0001c0001t0001g0037 a0001c0001t0001g0038 others(11): Show |
15 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.141+1852_141+1853d others(4): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | |||||||
| chr14:77496799 | G | GAAA | 6 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0055 others(3): Show |
6 | HG01361.hp2 HG02055.hp2 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+1851_141+1853d others(5): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | |||||||
| chr14:77496799 | G | GAAAAAAA others(3): Show |
1 | a0002c0023t0012g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+1844_141+1853d others(12): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | |||||||
| chr14:77496799 | G | GAAAAAAA others(6): Show |
1 | a0001c0001t0004g0177 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.141+1841_141+1853d others(15): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | |||||||
| chr14:77496799 | GA | G | 43 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0065 others(40): Show |
46 | HG00099.hp1 HG00408.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.141+1853delT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | |||||||
| chr14:77496799 | GAA | G | 53 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(50): Show |
62 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.141+1852_141+1853d others(4): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | |||||||
| chr14:77496799 | GAAA | G | 7 | a0001c0001t0001g0059 a0001c0001t0001g0194 a0001c0001t0001g0195 others(4): Show |
7 | HG00544.hp1 HG01069.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+1851_141+1853d others(5): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | |||||||
| chr14:77496799 | GAAAA | G | 9 | a0002c0002t0001g0001 a0002c0002t0001g0061 a0002c0002t0001g0076 others(6): Show |
11 | HG00323.hp1 HG01070.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.141+1850_141+1853d others(6): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | |||||||
| chr14:77496799 | GAAAAA | G | 9 | a0002c0002t0001g0080 a0002c0002t0001g0100 a0002c0002t0001g0101 others(6): Show |
9 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.141+1849_141+1853d others(7): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | |||||||
| chr14:77496799 | GAAAAAA | G | 25 | a0001c0001t0001g0124 a0002c0002t0001g0105 a0002c0002t0001g0135 others(22): Show |
26 | HG01099.hp1 HG02071.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.141+1848_141+1853d others(8): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | |||||||
| chr14:77496799 | GAAAAAAA | G | 22 | a0001c0001t0001g0133 a0002c0002t0001g0013 a0002c0002t0001g0070 others(19): Show |
23 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.141+1847_141+1853d others(9): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | |||||||
| chr14:77496799 | GAAAAAAA others(3): Show |
G | 2 | a0001c0001t0001g0193 a0002c0002t0001g0232 |
2 | HG02071.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.141+1844_141+1853d others(12): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | |||||||
| chr14:77496799 | GAAAAAAA others(9): Show |
G | 1 | a0002c0003t0001g0243 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.141+1838_141+1853d others(18): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | |||||||
| chr14:77496799 | GAAAAAAA others(10): Show |
G | 14 | a0002c0002t0008g0074 a0002c0003t0001g0021 a0002c0003t0001g0242 others(11): Show |
16 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.141+1837_141+1853d others(19): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | |||||||
| chr14:77496799 | GAAAAAAA others(11): Show |
G | 1 | a0002c0003t0001g0241 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.141+1836_141+1853d others(20): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | |||||||
| chr14:77496799 | GAAAAAAA others(12): Show |
G | 2 | a0001c0009t0004g0072 a0001c0009t0004g0082 |
2 | HG01109.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.141+1835_141+1853d others(21): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496799 | |||||||
| chr14:77496804 | A | G | 1 | a0002c0002t0001g0231 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.141+1849T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496804 | |||||||
| chr14:77496929 | A | C | 54 | a0001c0001t0001g0133 a0002c0002t0001g0013 a0002c0002t0001g0061 others(51): Show |
56 | HG00099.hp2 HG01081.hp2 HG01099.hp1 others(53): Show |
intron_variant | MODIFIER | c.141+1724T>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496929 | |||||||
| chr14:77496933 | C | T | 2 | a0001c0001t0001g0191 a0002c0002t0002g0129 |
2 | HG01081.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.141+1720G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77496933 | |||||||
| chr14:77497020 | T | G | 1 | a0001c0001t0001g0175 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.141+1633A>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497020 | |||||||
| chr14:77497045 | C | G | 3 | a0001c0001t0004g0118 a0001c0001t0004g0176 a0001c0001t0004g0177 |
3 | HG02145.hp2 HG02809.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.141+1608G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497045 | |||||||
| chr14:77497351 | C | G | 228 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(225): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.141+1302G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497351 | |||||||
| chr14:77497367 | C | CA | 54 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(51): Show |
59 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.141+1285dupT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497367 | |||||||
| chr14:77497367 | C | CAA | 65 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0018 others(62): Show |
72 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.141+1284_141+1285d others(4): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497367 | |||||||
| chr14:77497367 | C | CAAA | 9 | a0001c0001t0001g0099 a0001c0001t0001g0226 a0001c0001t0001g0227 others(6): Show |
9 | HG01978.hp1 HG01978.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+1283_141+1285d others(5): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497367 | |||||||
| chr14:77497367 | CA | C | 27 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0036 others(24): Show |
29 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.141+1285delT | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497367 | |||||||
| chr14:77497493 | T | A | 1 | a0010c0022t0001g0240 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.141+1160A>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497493 | |||||||
| chr14:77497733 | A | AGGAAGTA others(1): Show |
18 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(15): Show |
18 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.141+919_141+920ins others(8): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497733 | |||||||
| chr14:77497733 | AGGAAGGA others(5): Show |
A | 5 | a0002c0003t0001g0021 a0002c0003t0001g0245 a0002c0003t0001g0246 others(2): Show |
6 | HG00741.hp1 HG01257.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+908_141+919del others(12): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497733 | |||||||
| chr14:77497733 | AGGAAGGA others(9): Show |
A | 5 | a0002c0003t0001g0249 a0002c0003t0001g0250 a0002c0003t0001g0251 others(2): Show |
6 | HG00642.hp1 HG00735.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+904_141+919del others(16): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497733 | |||||||
| chr14:77497737 | A | AGGAGGGA others(1): Show |
5 | a0002c0002t0006g0107 a0003c0004t0001g0111 a0007c0013t0001g0110 others(2): Show |
5 | HG03225.hp2 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+908_141+915dup others(8): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497737 | |||||||
| chr14:77497737 | A | AGGAGGGA others(5): Show |
3 | a0002c0002t0001g0105 a0002c0002t0001g0106 a0002c0002t0002g0104 |
3 | HG02572.hp1 HG02615.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.141+904_141+915dup others(12): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497737 | |||||||
| chr14:77497737 | A | AGGAGGGA others(9): Show |
1 | a0002c0002t0001g0103 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.141+900_141+915dup others(16): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497737 | |||||||
| chr14:77497737 | A | AGTAG | 24 | a0001c0001t0001g0007 a0001c0001t0001g0160 a0001c0001t0001g0161 others(21): Show |
25 | HG00408.hp1 HG00621.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.141+915_141+916ins others(4): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497737 | |||||||
| chr14:77497737 | A | AGTAGGGA others(5): Show |
3 | a0001c0001t0001g0114 a0001c0010t0007g0113 a0002c0002t0002g0112 |
3 | HG03834.hp2 NA18990.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.141+915_141+916ins others(12): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497737 | |||||||
| chr14:77497737 | A | G | 6 | a0002c0002t0011g0237 a0002c0003t0001g0241 a0002c0003t0001g0242 others(3): Show |
6 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+916T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497737 | |||||||
| chr14:77497739 | G | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(113): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.141+914C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497739 | |||||||
| chr14:77497741 | G | A | 24 | a0001c0001t0001g0007 a0001c0001t0001g0160 a0001c0001t0001g0161 others(21): Show |
25 | HG00408.hp1 HG00621.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.141+912C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497741 | |||||||
| chr14:77497745 | G | A | 130 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(127): Show |
146 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(143): Show |
intron_variant | MODIFIER | c.141+908C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497745 | |||||||
| chr14:77497749 | GGGAGGGA others(17): Show |
G | 1 | a0002c0002t0001g0005 | 2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.141+880_141+903del others(24): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497749 | |||||||
| chr14:77497749 | GGGAGGGA others(21): Show |
G | 3 | a0002c0002t0001g0005 a0002c0002t0001g0238 a0002c0002t0001g0239 |
3 | HG02897.hp2 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.141+876_141+903del others(28): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497749 | |||||||
| chr14:77497756 | A | T | 1 | a0002c0023t0012g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+897T>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497756 | |||||||
| chr14:77497757 | GGGAGGGA others(13): Show |
G | 3 | a0002c0003t0001g0241 a0002c0003t0001g0242 a0002c0003t0001g0243 |
3 | HG01123.hp1 HG01255.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.141+876_141+895del others(20): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497757 | |||||||
| chr14:77497757 | GGGAGGGA others(21): Show |
G | 1 | a0010c0022t0001g0240 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.141+868_141+895del others(28): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497757 | |||||||
| chr14:77497761 | GGGAGGGA others(9): Show |
G | 3 | a0002c0002t0001g0135 a0002c0002t0011g0237 a0002c0007t0001g0024 |
3 | HG02559.hp2 HG03139.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.141+876_141+891del others(16): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497761 | |||||||
| chr14:77497761 | GGGAGGGA others(41): Show |
G | 8 | a0003c0004t0001g0006 a0003c0004t0001g0028 a0003c0004t0001g0029 others(5): Show |
9 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+844_141+891del others(48): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497761 | |||||||
| chr14:77497765 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0004g0118 a0001c0010t0007g0113 |
3 | HG02145.hp2 NA18990.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.141+888C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497765 | |||||||
| chr14:77497765 | GGGAGGGA others(9): Show |
G | 1 | a0002c0002t0001g0134 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.141+872_141+887del others(16): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497765 | |||||||
| chr14:77497769 | G | A | 20 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(17): Show |
20 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.141+884C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497769 | |||||||
| chr14:77497769 | G | GGGAAGGA others(5): Show |
1 | a0001c0001t0004g0176 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.141+872_141+883dup others(12): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497769 | |||||||
| chr14:77497769 | G | GGGAGGGA others(9): Show |
1 | a0001c0001t0001g0020 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.141+883_141+884ins others(16): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497769 | |||||||
| chr14:77497769 | GGGAA | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(42): Show |
50 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.141+880_141+883del others(4): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497769 | |||||||
| chr14:77497769 | GGGAAGGA others(1): Show |
G | 39 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(36): Show |
43 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.141+876_141+883del others(8): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497769 | |||||||
| chr14:77497769 | GGGAAGGA others(5): Show |
G | 12 | a0001c0001t0001g0073 a0001c0009t0004g0072 a0002c0002t0001g0001 others(9): Show |
14 | HG01167.hp2 HG01891.hp1 HG02293.hp2 others(11): Show |
intron_variant | MODIFIER | c.141+872_141+883del others(12): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497769 | |||||||
| chr14:77497769 | GGGAAGGA others(9): Show |
G | 9 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(6): Show |
9 | HG00099.hp2 HG01099.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+868_141+883del others(16): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497769 | |||||||
| chr14:77497769 | GGGAAGGA others(17): Show |
G | 1 | a0002c0002t0003g0002 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.141+860_141+883del others(24): Show |
ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497769 | |||||||
| chr14:77497771 | G | A | 1 | a0002c0023t0012g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+882C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497771 | |||||||
| chr14:77497772 | A | G | 1 | a0002c0023t0012g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+881T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497772 | |||||||
| chr14:77497773 | A | G | 70 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0027 others(67): Show |
74 | HG00408.hp2 HG00544.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.141+880T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497773 | |||||||
| chr14:77497777 | A | G | 51 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(48): Show |
56 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.141+876T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497777 | |||||||
| chr14:77497781 | A | G | 32 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(29): Show |
35 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.141+872T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497781 | |||||||
| chr14:77497782 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.141+871C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497782 | |||||||
| chr14:77497785 | A | G | 10 | a0001c0001t0001g0073 a0001c0009t0004g0072 a0002c0002t0001g0001 others(7): Show |
12 | HG01167.hp2 HG01891.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.141+868T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497785 | |||||||
| chr14:77497786 | G | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0067 |
3 | HG02486.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.141+867C>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497786 | |||||||
| chr14:77497789 | A | G | 6 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(3): Show |
6 | HG01099.hp2 HG02055.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+864T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497789 | |||||||
| chr14:77497794 | G | A | 4 | a0002c0002t0003g0025 a0002c0002t0003g0026 a0002c0002t0011g0237 others(1): Show |
4 | HG02630.hp2 HG03139.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+859C>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497794 | |||||||
| chr14:77497832 | A | G | 1 | a0002c0023t0012g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.141+821T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497832 | |||||||
| chr14:77497834 | A | G | 1 | a0001c0001t0001g0060 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.141+819T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497834 | |||||||
| chr14:77497973 | T | A | 3 | a0002c0002t0001g0005 a0002c0002t0001g0238 a0002c0002t0001g0239 |
5 | HG02451.hp1 HG02572.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+680A>T | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77497973 | |||||||
| chr14:77498117 | A | G | 2 | a0001c0001t0001g0059 a0002c0007t0001g0058 |
2 | HG00544.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.141+536T>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77498117 | |||||||
| chr14:77498157 | C | T | 25 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0036 others(22): Show |
27 | HG00140.hp1 HG00140.hp2 HG00621.hp1 others(24): Show |
intron_variant | MODIFIER | c.141+496G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77498157 | |||||||
| chr14:77498318 | T | C | 15 | a0002c0003t0001g0021 a0002c0003t0001g0241 a0002c0003t0001g0242 others(12): Show |
17 | HG00642.hp1 HG00735.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.141+335A>G | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77498318 | |||||||
| chr14:77498323 | A | T | 8 | a0003c0004t0001g0006 a0003c0004t0001g0028 a0003c0004t0001g0029 others(5): Show |
9 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+330T>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77498323 | |||||||
| chr14:77498425 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.141+228G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77498425 | |||||||
| chr14:77498614 | C | G | 3 | a0002c0002t0003g0025 a0002c0002t0003g0026 a0002c0007t0001g0024 |
3 | HG02630.hp2 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.141+39G>C | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77498614 | |||||||
| chr14:77498643 | C | T | 1 | a0002c0021t0002g0023 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.141+10G>A | ISM2 | ENSG00000100593.18 | transcript | ENST00000342219.9 | protein_coding | 1/6 | chr14 | 77498643 |