Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3670 |
| ensemblid | ENSG00000016082.15 |
| hgncid | 6132 |
| symbol | ISL1 |
| name | ISL LIM homeobox 1 |
| refseq_nuc | NM_002202.3 |
| refseq_prot | NP_002193.2 |
| ensembl_nuc | ENST00000230658.12 |
| ensembl_prot | ENSP00000230658.7 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 51383448 |
| end | 51394730 |
| strand | + |
| ver | v1.2 |
| region | chr5:51383448-51394730 |
| region5000 | chr5:51378448-51399730 |
| regionname0 | ISL1_chr5_51383448_51394730 |
| regionname5000 | ISL1_chr5_51378448_51399730 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 349 | 341 | 87 | 64 | 144 | 14 | 30 | 110 | ISL1_chr5_51378448_51399730 | ISL1 | MGDMG others(344): Show |
chr5 | 51378448 | 51399730 |
| a0002 | 0/0 | 349 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | MGDMG others(344): Show |
chr5 | 51378448 | 51399730 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1047 | 200 | 32 | 37 | 100 | 10 | 19 | ISL1_chr5_51378448_51399730 | ISL1 | ATGGG others(1042): Show |
chr5 | 51378448 | 51399730 | ||
| a0001c0002 | 0/0 | 1047 | 138 | 55 | 27 | 44 | 3 | 9 | ISL1_chr5_51378448_51399730 | ISL1 | ATGGG others(1042): Show |
chr5 | 51378448 | 51399730 | ||
| a0001c0003 | 0/0 | 1047 | 2 | 0 | 0 | 0 | 0 | 2 | ISL1_chr5_51378448_51399730 | ISL1 | ATGGG others(1042): Show |
chr5 | 51378448 | 51399730 | ||
| a0001c0004 | 0/0 | 1047 | 1 | 0 | 0 | 0 | 1 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | ATGGG others(1042): Show |
chr5 | 51378448 | 51399730 | ||
| a0002c0005 | 0/0 | 1047 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | ATGGG others(1042): Show |
chr5 | 51378448 | 51399730 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2394 | 179 | 17 | 34 | 97 | 10 | 19 | ISL1_chr5_51378448_51399730 | ISL1 | GAGTC others(2389): Show |
chr5 | 51378448 | 51399730 |
| a0001c0001t0003 | 0/0 | 2395 | 10 | 9 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | GAGTC others(2390): Show |
chr5 | 51378448 | 51399730 |
| a0001c0001t0004 | 0/0 | 2396 | 3 | 3 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | GAGTC others(2391): Show |
chr5 | 51378448 | 51399730 |
| a0001c0001t0006 | 0/0 | 2395 | 2 | 0 | 1 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | GAGTC others(2390): Show |
chr5 | 51378448 | 51399730 |
| a0001c0001t0008 | 0/0 | 2394 | 2 | 1 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | GAGTC others(2389): Show |
chr5 | 51378448 | 51399730 |
| a0001c0001t0011 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | GAGTC others(2389): Show |
chr5 | 51378448 | 51399730 |
| a0001c0001t0012 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | GAGTC others(2389): Show |
chr5 | 51378448 | 51399730 |
| a0001c0001t0013 | 0/0 | 2394 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | GAGTC others(2389): Show |
chr5 | 51378448 | 51399730 |
| a0001c0001t0014 | 0/0 | 2394 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | GAGTC others(2389): Show |
chr5 | 51378448 | 51399730 |
| a0001c0002t0002 | 0/0 | 2396 | 120 | 46 | 24 | 41 | 2 | 7 | ISL1_chr5_51378448_51399730 | ISL1 | GAGTC others(2391): Show |
chr5 | 51378448 | 51399730 |
| a0001c0002t0003 | 0/0 | 2395 | 9 | 4 | 2 | 1 | 1 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | GAGTC others(2390): Show |
chr5 | 51378448 | 51399730 |
| a0001c0002t0005 | 0/0 | 2395 | 3 | 3 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | GAGTC others(2390): Show |
chr5 | 51378448 | 51399730 |
| a0001c0002t0007 | 0/0 | 2394 | 2 | 1 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | GAGTC others(2389): Show |
chr5 | 51378448 | 51399730 |
| a0001c0002t0009 | 0/0 | 2396 | 2 | 0 | 1 | 0 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | GAGTC others(2391): Show |
chr5 | 51378448 | 51399730 |
| a0001c0002t0010 | 0/0 | 2396 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | GAGTC others(2391): Show |
chr5 | 51378448 | 51399730 |
| a0001c0002t0015 | 0/0 | 2396 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | GAGTC others(2391): Show |
chr5 | 51378448 | 51399730 |
| a0001c0003t0002 | 0/0 | 2396 | 2 | 0 | 0 | 0 | 0 | 2 | ISL1_chr5_51378448_51399730 | ISL1 | GAGTC others(2391): Show |
chr5 | 51378448 | 51399730 |
| a0001c0004t0001 | 0/0 | 2394 | 1 | 0 | 0 | 0 | 1 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | GAGTC others(2389): Show |
chr5 | 51378448 | 51399730 |
| a0002c0005t0003 | 0/0 | 2395 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | GAGTC others(2390): Show |
chr5 | 51378448 | 51399730 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 10 | 0 | 5 | 5 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0004 | 0/0 | 8 | 1 | 1 | 5 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0008 | 1/0 | 5 | 0 | 1 | 2 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0015 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0016 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0025 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0043 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0142 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0003g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0003g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0006g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0008g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0008g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0011g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0012g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0013g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0001t0014g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0001 | 0/0 | 44 | 5 | 12 | 23 | 1 | 3 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0003 | 0/0 | 8 | 4 | 0 | 2 | 0 | 2 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0005 | 0/0 | 7 | 2 | 1 | 3 | 1 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0010 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0012 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0018 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0050 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0003g0029 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0005g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0007g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0009g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0009g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0002t0015g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0003t0002g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0001c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| a0002c0005t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | GBR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | GBR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00140 | hp1 | a0001 | c0004 | t0001 | g0126 | EUR | GBR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0005 | EUR | FIN | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | FIN | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0059 | EAS | CHS | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00558 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | CHS | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0077 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01069 | hp2 | a0001 | c0001 | t0006 | g0156 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01074 | hp2 | a0001 | c0001 | t0008 | g0166 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01099 | hp1 | a0001 | c0002 | t0003 | g0056 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0050 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01109 | hp1 | a0001 | c0002 | t0003 | g0146 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0018 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01168 | hp2 | a0001 | c0002 | t0009 | g0153 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0018 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0034 | AMR | PUR | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0046 | AMR | CLM | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | CLM | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | CLM | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0174 | AMR | CLM | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | CLM | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01516 | hp1 | a0001 | c0002 | t0002 | g0001 | EUR | IBS | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0069 | AFR | ACB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ACB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0018 | AFR | ACB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01891 | hp2 | a0001 | c0002 | t0002 | g0055 | AFR | ACB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01978 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | KHV | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02055 | hp1 | a0001 | c0002 | t0007 | g0005 | AFR | ACB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0022 | AFR | ACB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CDX | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CDX | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CDX | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CDX | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02280 | hp1 | a0001 | c0002 | t0002 | g0019 | AFR | ACB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02280 | hp2 | a0001 | c0002 | t0010 | g0034 | AFR | ACB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0030 | AFR | ACB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0046 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02615 | hp2 | a0001 | c0002 | t0003 | g0072 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02622 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0152 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0175 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02717 | hp1 | a0001 | c0001 | t0008 | g0167 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02717 | hp2 | a0001 | c0002 | t0003 | g0057 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02723 | hp2 | a0001 | c0002 | t0005 | g0020 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02735 | hp2 | a0001 | c0002 | t0002 | g0074 | SAS | PJL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0050 | SAS | PJL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02886 | hp1 | a0002 | c0005 | t0003 | g0017 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0021 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0148 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02896 | hp1 | a0001 | c0002 | t0003 | g0017 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02896 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0075 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ESN | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02922 | hp2 | a0001 | c0002 | t0005 | g0020 | AFR | ESN | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | ESN | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0022 | AFR | ESN | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0019 | AFR | ESN | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03041 | hp1 | a0001 | c0001 | t0011 | g0168 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0085 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | MSL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0062 | AFR | ESN | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | ESN | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0022 | AFR | ESN | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0054 | AFR | ESN | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03209 | hp1 | a0001 | c0002 | t0005 | g0020 | AFR | MSL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | MSL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0001 | AFR | MSL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | MSL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | MSL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | MSL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0012 | AFR | MSL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | PJL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03490 | hp2 | a0001 | c0003 | t0002 | g0028 | SAS | PJL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03492 | hp2 | a0001 | c0003 | t0002 | g0028 | SAS | PJL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0149 | AFR | ESN | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0182 | AFR | ESN | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0071 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0179 | AFR | GWD | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0084 | AFR | MSL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03579 | hp2 | a0001 | c0001 | t0014 | g0016 | AFR | MSL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03927 | hp2 | a0001 | c0002 | t0009 | g0021 | SAS | BEB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | STU | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG04204 | hp1 | a0001 | c0002 | t0003 | g0029 | SAS | STU | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | STU | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0030 | AFR | YRI | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | YRI | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18612 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0151 | AFR | YRI | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18946 | hp1 | a0001 | c0001 | t0013 | g0027 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18964 | hp1 | a0001 | c0002 | t0015 | g0001 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18993 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18997 | hp1 | a0001 | c0001 | t0006 | g0087 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18999 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | LWK | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19043 | hp2 | a0001 | c0002 | t0003 | g0017 | AFR | LWK | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19056 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19076 | hp2 | a0001 | c0002 | t0002 | g0065 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19082 | hp2 | a0001 | c0001 | t0012 | g0108 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19084 | hp1 | a0001 | c0002 | t0007 | g0001 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19089 | hp1 | a0001 | c0002 | t0003 | g0177 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | YRI | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0060 | AFR | YRI | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ASW | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ASW | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0080 | EUR | TSI | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA20752 | hp2 | a0001 | c0002 | t0003 | g0029 | EUR | TSI | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | TSI | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0001 | SAS | GIH | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | GIH | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0033 | AMR | CLM | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0073 | AFR | ACB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0021 | AFR | ACB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0001 | AFR | ACB | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0019 | AFR | MSL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0083 | AFR | USA | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | USA | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | LWK | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0178 | AFR | LWK | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0142 | REF | REF | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0008 | REF | REF | ISL1_chr5_51378448_51399730 | ISL1 | chr5 | 51378448 | 51399730 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:51389922 | A | G | 1 | a0002 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.755A>G | p.Asn252Ser | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/6 | 979/2394 | 755/1050 | 252/349 | chr5 | 51389922 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:51389671 | A | G | 3 | a0001c0002 a0001c0003 a0002c0005 |
141 | HG00323.hp1 HG00408.hp1 HG00558.hp2 others(138): Show |
synonymous_variant | LOW | c.504A>G | p.Pro168Pro | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/6 | 728/2394 | 504/1050 | 168/349 | chr5 | 51389671 | |||
| chr5:51389680 | G | A | 1 | a0001c0003 | 2 | HG03490.hp2 HG03492.hp2 |
synonymous_variant | LOW | c.513G>A | p.Arg171Arg | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/6 | 737/2394 | 513/1050 | 171/349 | chr5 | 51389680 | |||
| chr5:51389882 | C | A | 1 | a0001c0004 | 1 | HG00140.hp1 | synonymous_variant | LOW | c.715C>A | p.Arg239Arg | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/6 | 939/2394 | 715/1050 | 239/349 | chr5 | 51389882 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:51383453 | T | C | 1 | a0001c0002t0010 | 1 | HG02280.hp2 | 5_prime_UTR_variant | MODIFIER | c.-219T>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 1/6 | 219 | chr5 | 51383453 | ||||||
| chr5:51383598 | A | G | 1 | a0001c0002t0015 | 1 | NA18964.hp1 | 5_prime_UTR_variant | MODIFIER | c.-74A>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 1/6 | 74 | chr5 | 51383598 | ||||||
| chr5:51383625 | A | G | 1 | a0001c0002t0009 | 2 | HG01168.hp2 HG03927.hp2 |
5_prime_UTR_variant | MODIFIER | c.-47A>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 1/6 | 47 | chr5 | 51383625 | ||||||
| chr5:51393888 | T | G | 1 | a0001c0001t0011 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*278T>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 6/6 | 278 | chr5 | 51393888 | ||||||
| chr5:51394074 | C | G | 1 | a0001c0001t0014 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*464C>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 6/6 | 464 | chr5 | 51394074 | ||||||
| chr5:51394111 | C | T | 1 | a0001c0001t0013 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*501C>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 6/6 | 501 | chr5 | 51394111 | ||||||
| chr5:51394149 | G | T | 2 | a0001c0001t0008 a0001c0002t0005 |
5 | HG01074.hp2 HG02717.hp1 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*539G>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 6/6 | 539 | chr5 | 51394149 | ||||||
| chr5:51394261 | A | T | 10 | a0001c0001t0003 a0001c0002t0002 a0001c0002t0003 others(7): Show |
151 | HG00323.hp1 HG00408.hp1 HG00558.hp2 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*651A>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 6/6 | 651 | chr5 | 51394261 | ||||||
| chr5:51394338 | G | A | 1 | a0001c0001t0012 | 1 | NA19082.hp2 | 3_prime_UTR_variant | MODIFIER | c.*728G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 6/6 | 728 | chr5 | 51394338 | ||||||
| chr5:51394444 | G | GA | 5 | a0001c0001t0003 a0001c0001t0006 a0001c0002t0003 others(2): Show |
25 | HG01069.hp2 HG01099.hp1 HG01109.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*845dupA | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 6/6 | 846 | INFO_REALIGN_3_PRIME | chr5 | 51394444 | |||||
| chr5:51394444 | G | GAA | 6 | a0001c0001t0004 a0001c0002t0002 a0001c0002t0009 others(3): Show |
129 | HG00323.hp1 HG00408.hp1 HG00558.hp2 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*844_*845dupAA | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 6/6 | 846 | INFO_REALIGN_3_PRIME | chr5 | 51394444 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:51383716 | C | T | 1 | a0001c0002t0002g0050 | 2 | HG01106.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.28+17C>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 1/5 | chr5 | 51383716 | |||||||
| chr5:51383770 | T | A | 1 | a0001c0001t0001g0051 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.28+71T>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 1/5 | chr5 | 51383770 | |||||||
| chr5:51384241 | G | A | 1 | a0001c0003t0002g0028 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.29-300G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 1/5 | chr5 | 51384241 | |||||||
| chr5:51384243 | A | AG | 34 | a0001c0001t0001g0009 a0001c0001t0001g0047 a0001c0001t0001g0048 others(31): Show |
42 | HG00438.hp1 HG00621.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.29-288dupG | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 51384243 | ||||||
| chr5:51384243 | A | AGG | 11 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0003g0174 others(8): Show |
21 | HG00323.hp1 HG01167.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.29-289_29-288dupGG | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 51384243 | ||||||
| chr5:51384251 | G | T | 1 | a0001c0002t0002g0182 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.29-290G>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 1/5 | chr5 | 51384251 | |||||||
| chr5:51384299 | T | C | 1 | a0001c0002t0002g0052 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.29-242T>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 1/5 | chr5 | 51384299 | |||||||
| chr5:51384310 | C | A | 1 | a0001c0001t0001g0053 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.29-231C>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 1/5 | chr5 | 51384310 | |||||||
| chr5:51384399 | G | A | 67 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0058 others(64): Show |
151 | HG00323.hp1 HG00408.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.29-142G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 1/5 | chr5 | 51384399 | |||||||
| chr5:51384403 | T | TA | 11 | a0001c0001t0001g0078 a0001c0002t0002g0018 a0001c0002t0002g0030 others(8): Show |
16 | HG01099.hp1 HG01109.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.29-123dupA | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 51384403 | ||||||
| chr5:51384403 | TA | T | 8 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0144 others(5): Show |
9 | HG01168.hp2 HG02040.hp2 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.29-123delA | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 51384403 | ||||||
| chr5:51384415 | A | G | 2 | a0001c0002t0002g0050 a0001c0002t0002g0077 |
3 | HG00735.hp2 HG01106.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.29-126A>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 1/5 | chr5 | 51384415 | |||||||
| chr5:51384415 | AAAAG | A | 6 | a0001c0001t0001g0154 a0001c0001t0003g0058 a0001c0002t0002g0019 others(3): Show |
10 | HG00408.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.29-106_29-103delGA others(2): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 51384415 | ||||||
| chr5:51384416 | AAAG | A | 7 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0061 others(4): Show |
9 | HG01433.hp2 HG02572.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.29-122_29-120delGA others(1): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 51384416 | ||||||
| chr5:51384439 | A | G | 1 | a0001c0002t0002g0076 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.29-102A>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 1/5 | chr5 | 51384439 | |||||||
| chr5:51384508 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.29-33G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 1/5 | chr5 | 51384508 | |||||||
| chr5:51384874 | T | TA | 8 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0058 others(5): Show |
10 | HG01433.hp2 HG02572.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.218+151dupA | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 51384874 | ||||||
| chr5:51384954 | G | C | 1 | a0001c0001t0001g0080 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.218+224G>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51384954 | |||||||
| chr5:51385025 | C | G | 1 | a0001c0001t0001g0143 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.218+295C>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51385025 | |||||||
| chr5:51385082 | G | A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | NA18985.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.218+352G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51385082 | |||||||
| chr5:51385107 | G | C | 1 | a0001c0002t0002g0065 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.218+377G>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51385107 | |||||||
| chr5:51385198 | A | G | 34 | a0001c0002t0002g0003 a0001c0002t0002g0005 a0001c0002t0002g0010 others(31): Show |
63 | HG00323.hp1 HG01099.hp1 HG01109.hp1 others(60): Show |
intron_variant | MODIFIER | c.218+468A>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51385198 | |||||||
| chr5:51385203 | G | A | 3 | a0001c0001t0004g0083 a0001c0001t0004g0084 a0001c0001t0004g0085 |
3 | HG03041.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.218+473G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51385203 | |||||||
| chr5:51385264 | A | T | 2 | a0001c0002t0002g0018 a0001c0002t0002g0030 |
5 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+534A>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51385264 | |||||||
| chr5:51385632 | T | C | 1 | a0001c0001t0001g0078 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.218+902T>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51385632 | |||||||
| chr5:51385781 | A | G | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG00323.hp2 HG00738.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.218+1051A>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51385781 | |||||||
| chr5:51386231 | G | A | 32 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0058 others(29): Show |
87 | HG00408.hp1 HG00558.hp2 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.219-1259G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51386231 | |||||||
| chr5:51386339 | C | A | 14 | a0001c0001t0001g0035 a0001c0001t0001g0079 a0001c0001t0001g0086 others(11): Show |
15 | HG00673.hp1 HG01069.hp2 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.219-1151C>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51386339 | |||||||
| chr5:51386363 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.219-1127C>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51386363 | |||||||
| chr5:51386376 | C | CTG | 26 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0001g0041 others(23): Show |
31 | HG00140.hp1 HG00673.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.219-1078_219-1077d others(4): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 51386376 | ||||||
| chr5:51386376 | C | CTGTG | 16 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(13): Show |
19 | HG00099.hp1 HG01099.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.219-1080_219-1077d others(6): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 51386376 | ||||||
| chr5:51386376 | CTG | C | 21 | a0001c0001t0001g0036 a0001c0001t0001g0099 a0001c0001t0001g0100 others(18): Show |
30 | HG00735.hp2 HG00738.hp2 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.219-1078_219-1077d others(4): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 51386376 | ||||||
| chr5:51386376 | CTGTG | C | 22 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(19): Show |
71 | HG00408.hp1 HG00558.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.219-1080_219-1077d others(6): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 51386376 | ||||||
| chr5:51386376 | CTGTGTG | C | 16 | a0001c0001t0004g0083 a0001c0002t0002g0003 a0001c0002t0002g0005 others(13): Show |
32 | HG00323.hp1 HG01123.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.219-1082_219-1077d others(8): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 51386376 | ||||||
| chr5:51386376 | CTGTGTGT others(1): Show |
C | 12 | a0001c0002t0002g0021 a0001c0002t0002g0022 a0001c0002t0002g0073 others(9): Show |
19 | HG01099.hp1 HG01109.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.219-1084_219-1077d others(10): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 51386376 | ||||||
| chr5:51386376 | CTGTGTGT others(3): Show |
C | 4 | a0001c0002t0002g0010 a0001c0002t0002g0149 a0001c0002t0002g0182 others(1): Show |
8 | HG01884.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.219-1086_219-1077d others(12): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 51386376 | ||||||
| chr5:51386480 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.219-1010A>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51386480 | |||||||
| chr5:51386647 | A | G | 4 | a0001c0002t0003g0017 a0001c0002t0003g0057 a0001c0002t0003g0146 others(1): Show |
5 | HG01109.hp1 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.219-843A>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51386647 | |||||||
| chr5:51386770 | T | A | 2 | a0001c0002t0002g0151 a0001c0002t0002g0152 |
2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.219-720T>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51386770 | |||||||
| chr5:51386794 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.219-696A>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51386794 | |||||||
| chr5:51386798 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.219-692G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51386798 | |||||||
| chr5:51386945 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.219-545G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51386945 | |||||||
| chr5:51386947 | G | A | 7 | a0001c0002t0003g0017 a0001c0002t0003g0029 a0001c0002t0003g0056 others(4): Show |
11 | HG01099.hp1 HG01109.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.219-543G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51386947 | |||||||
| chr5:51387046 | G | T | 1 | a0001c0002t0002g0148 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.219-444G>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51387046 | |||||||
| chr5:51387168 | A | G | 1 | a0001c0002t0002g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.219-322A>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51387168 | |||||||
| chr5:51387243 | C | T | 2 | a0001c0002t0002g0022 a0001c0002t0002g0073 |
4 | HG02055.hp2 HG02109.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.219-247C>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51387243 | |||||||
| chr5:51387475 | C | G | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0100 others(4): Show |
9 | HG02074.hp2 HG02080.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.219-15C>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 2/5 | chr5 | 51387475 | |||||||
| chr5:51387765 | G | A | 1 | a0001c0002t0002g0148 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.478+16G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 3/5 | chr5 | 51387765 | |||||||
| chr5:51387821 | T | C | 67 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0058 others(64): Show |
151 | HG00323.hp1 HG00408.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.478+72T>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 3/5 | chr5 | 51387821 | |||||||
| chr5:51387973 | C | A | 8 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0058 others(5): Show |
10 | HG01433.hp2 HG02572.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.478+224C>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 3/5 | chr5 | 51387973 | |||||||
| chr5:51388242 | A | T | 1 | a0001c0003t0002g0028 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.478+493A>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 3/5 | chr5 | 51388242 | |||||||
| chr5:51388243 | A | T | 5 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(2): Show |
5 | HG02647.hp1 NA18906.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.478+494A>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 3/5 | chr5 | 51388243 | |||||||
| chr5:51388243 | AT | A | 6 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(3): Show |
6 | HG00099.hp1 HG00099.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.478+504delT | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 51388243 | ||||||
| chr5:51388253 | T | A | 2 | a0001c0002t0002g0176 a0001c0002t0003g0177 |
2 | NA19011.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.478+504T>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 3/5 | chr5 | 51388253 | |||||||
| chr5:51388404 | T | G | 1 | a0001c0002t0002g0150 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.478+655T>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 3/5 | chr5 | 51388404 | |||||||
| chr5:51388617 | C | T | 23 | a0001c0002t0002g0001 a0001c0002t0002g0011 a0001c0002t0002g0012 others(20): Show |
76 | HG00408.hp1 HG00558.hp2 HG00733.hp1 others(73): Show |
intron_variant | MODIFIER | c.478+868C>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 3/5 | chr5 | 51388617 | |||||||
| chr5:51388646 | C | T | 1 | a0001c0002t0002g0071 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.478+897C>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 3/5 | chr5 | 51388646 | |||||||
| chr5:51388674 | A | C | 1 | a0001c0002t0005g0020 | 3 | HG02723.hp2 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.478+925A>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 3/5 | chr5 | 51388674 | |||||||
| chr5:51388736 | A | G | 2 | a0001c0002t0002g0068 a0001c0002t0002g0070 |
2 | NA18962.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.479-910A>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 3/5 | chr5 | 51388736 | |||||||
| chr5:51388774 | C | A | 1 | a0001c0002t0002g0148 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.479-872C>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 3/5 | chr5 | 51388774 | |||||||
| chr5:51388780 | A | T | 1 | a0001c0001t0001g0036 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.479-866A>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 3/5 | chr5 | 51388780 | |||||||
| chr5:51389223 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.479-423A>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 3/5 | chr5 | 51389223 | |||||||
| chr5:51389334 | C | T | 1 | a0001c0002t0003g0177 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.479-312C>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 3/5 | chr5 | 51389334 | |||||||
| chr5:51389365 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.479-281G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 3/5 | chr5 | 51389365 | |||||||
| chr5:51389429 | T | G | 8 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0058 others(5): Show |
10 | HG01433.hp2 HG02572.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.479-217T>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 3/5 | chr5 | 51389429 | |||||||
| chr5:51389554 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.479-92C>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 3/5 | chr5 | 51389554 | |||||||
| chr5:51389642 | G | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0023 others(10): Show |
23 | HG00621.hp2 HG02027.hp2 HG02074.hp1 others(20): Show |
splice_region_variant&intron_variant | LOW | c.479-4G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 3/5 | chr5 | 51389642 | |||||||
| chr5:51389978 | C | A | 1 | a0001c0001t0001g0117 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.765+46C>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51389978 | |||||||
| chr5:51390158 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.765+226G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390158 | |||||||
| chr5:51390159 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.765+227G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390159 | |||||||
| chr5:51390228 | G | A | 4 | a0001c0001t0001g0123 a0001c0001t0001g0132 a0001c0001t0001g0169 others(1): Show |
4 | HG02965.hp1 HG03098.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.765+296G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390228 | |||||||
| chr5:51390258 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.765+326G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390258 | |||||||
| chr5:51390313 | C | T | 8 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0058 others(5): Show |
10 | HG01433.hp2 HG02572.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.765+381C>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390313 | |||||||
| chr5:51390394 | C | T | 1 | a0001c0002t0002g0179 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.765+462C>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390394 | |||||||
| chr5:51390415 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.765+483A>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390415 | |||||||
| chr5:51390507 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0132 |
2 | HG03098.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.765+575C>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390507 | |||||||
| chr5:51390632 | CTTTCTTT others(19): Show |
C | 1 | a0001c0002t0002g0148 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.766-638_766-613del others(26): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390632 | ||||||
| chr5:51390636 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.766-638C>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390636 | |||||||
| chr5:51390636 | CTTTTT | C | 2 | a0001c0001t0003g0032 a0001c0001t0003g0058 |
3 | HG02895.hp1 HG02897.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.766-637_766-633del others(5): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390636 | |||||||
| chr5:51390636 | CTTTTTCT others(2): Show |
C | 11 | a0001c0002t0002g0011 a0001c0002t0002g0018 a0001c0002t0002g0022 others(8): Show |
19 | HG00408.hp1 HG01167.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.766-632_766-624del others(9): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390636 | ||||||
| chr5:51390636 | CTTTTTCT others(3): Show |
C | 38 | a0001c0001t0003g0174 a0001c0002t0002g0001 a0001c0002t0002g0003 others(35): Show |
110 | HG00323.hp1 HG00558.hp2 HG00733.hp1 others(107): Show |
intron_variant | MODIFIER | c.766-632_766-623del others(10): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390636 | ||||||
| chr5:51390636 | CTTTTTCT others(4): Show |
C | 3 | a0001c0002t0002g0067 a0001c0002t0002g0075 a0001c0002t0002g0179 |
3 | HG02897.hp2 HG03540.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.766-632_766-622del others(11): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390636 | ||||||
| chr5:51390636 | CTTTTTCT others(6): Show |
C | 2 | a0001c0002t0003g0056 a0001c0002t0003g0057 |
2 | HG01099.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.766-632_766-620del others(13): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390636 | ||||||
| chr5:51390636 | CTTTTTCT others(7): Show |
C | 4 | a0001c0002t0003g0017 a0001c0002t0003g0029 a0001c0002t0003g0146 others(1): Show |
6 | HG01109.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-632_766-619del others(14): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390636 | ||||||
| chr5:51390636 | CTTTTTCT others(8): Show |
C | 1 | a0001c0001t0003g0064 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.766-632_766-618del others(15): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390636 | ||||||
| chr5:51390642 | C | CT | 8 | a0001c0001t0001g0016 a0001c0001t0001g0025 a0001c0001t0001g0135 others(5): Show |
12 | HG01069.hp2 HG01981.hp1 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.766-594dupT | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390642 | ||||||
| chr5:51390642 | C | CTT | 7 | a0001c0001t0001g0035 a0001c0001t0001g0049 a0001c0001t0001g0088 others(4): Show |
9 | HG01516.hp2 HG01517.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.766-595_766-594dup others(2): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390642 | ||||||
| chr5:51390642 | C | CTTT | 6 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0091 others(3): Show |
9 | HG01167.hp1 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.766-596_766-594dup others(3): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390642 | ||||||
| chr5:51390642 | C | CTTTTT | 6 | a0001c0001t0001g0027 a0001c0001t0001g0044 a0001c0001t0001g0092 others(3): Show |
8 | HG00438.hp2 HG02109.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.766-598_766-594dup others(5): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390642 | ||||||
| chr5:51390642 | C | CTTTTTT | 8 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0045 others(5): Show |
18 | HG00673.hp2 HG02015.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.766-599_766-594dup others(6): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390642 | ||||||
| chr5:51390642 | C | CTTTTTTT | 19 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0036 others(16): Show |
32 | HG00741.hp2 HG01106.hp2 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.766-600_766-594dup others(7): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390642 | ||||||
| chr5:51390642 | C | CTTTTTTT others(1): Show |
10 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0040 others(7): Show |
23 | HG00099.hp2 HG00408.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.766-601_766-594dup others(8): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390642 | ||||||
| chr5:51390642 | C | CTTTTTTT others(2): Show |
8 | a0001c0001t0001g0098 a0001c0001t0001g0101 a0001c0001t0001g0105 others(5): Show |
8 | HG00558.hp1 HG02027.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.766-602_766-594dup others(9): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390642 | ||||||
| chr5:51390642 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0001g0094 a0001c0001t0001g0120 |
2 | HG00733.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.766-603_766-594dup others(10): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390642 | ||||||
| chr5:51390642 | C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0106 others(1): Show |
8 | HG00621.hp1 HG01256.hp1 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.766-604_766-594dup others(11): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390642 | ||||||
| chr5:51390642 | C | CTTTTTTT others(5): Show |
3 | a0001c0001t0001g0015 a0001c0001t0001g0051 a0001c0001t0001g0082 |
6 | HG01123.hp2 NA18945.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-605_766-594dup others(12): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390642 | ||||||
| chr5:51390642 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0001g0107 a0001c0001t0001g0113 a0001c0001t0001g0172 |
3 | HG00621.hp2 HG01433.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.766-606_766-594dup others(13): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390642 | ||||||
| chr5:51390642 | C | CTTTTTTT others(7): Show |
3 | a0001c0001t0001g0038 a0001c0001t0001g0163 a0001c0001t0001g0180 |
4 | HG01261.hp1 NA18961.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-607_766-594dup others(14): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390642 | ||||||
| chr5:51390642 | C | CTTTTTTT others(8): Show |
2 | a0001c0001t0001g0048 a0001c0001t0001g0124 |
3 | HG03491.hp2 NA18983.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.766-608_766-594dup others(15): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390642 | ||||||
| chr5:51390642 | C | CTTTTTTT others(9): Show |
2 | a0001c0001t0001g0125 a0001c0001t0001g0164 |
2 | HG03492.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.766-609_766-594dup others(16): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390642 | ||||||
| chr5:51390642 | C | T | 2 | a0001c0001t0001g0154 a0001c0001t0003g0031 |
3 | HG02257.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.766-632C>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390642 | |||||||
| chr5:51390642 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0001g0037 a0001c0001t0001g0080 a0001c0001t0004g0083 others(1): Show |
5 | HG00140.hp2 HG03041.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-603_766-594del others(10): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390642 | ||||||
| chr5:51390642 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0024 a0001c0001t0004g0084 |
4 | HG01109.hp2 HG01517.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-604_766-594del others(11): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390642 | ||||||
| chr5:51390642 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0012g0108 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.766-605_766-594del others(12): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390642 | ||||||
| chr5:51390642 | CTTTTTTT others(17): Show |
C | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0004t0001g0126 |
3 | HG00099.hp1 HG00140.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.766-617_766-594del others(24): Show |
ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr5 | 51390642 | ||||||
| chr5:51390643 | T | C | 1 | a0001c0001t0003g0061 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.766-631T>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390643 | |||||||
| chr5:51390644 | T | C | 1 | a0001c0001t0003g0062 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.766-630T>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390644 | |||||||
| chr5:51390645 | T | C | 1 | a0001c0001t0003g0063 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.766-629T>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390645 | |||||||
| chr5:51390647 | T | C | 1 | a0001c0001t0003g0174 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.766-627T>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390647 | |||||||
| chr5:51390650 | T | G | 1 | a0001c0002t0002g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.766-624T>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390650 | |||||||
| chr5:51390651 | T | G | 13 | a0001c0002t0002g0011 a0001c0002t0002g0018 a0001c0002t0002g0022 others(10): Show |
21 | HG00408.hp1 HG01099.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.766-623T>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390651 | |||||||
| chr5:51390652 | T | C | 1 | a0001c0001t0003g0064 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.766-622T>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390652 | |||||||
| chr5:51390652 | T | G | 41 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0005 others(38): Show |
115 | HG00323.hp1 HG00558.hp2 HG00733.hp1 others(112): Show |
intron_variant | MODIFIER | c.766-622T>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390652 | |||||||
| chr5:51390653 | T | G | 3 | a0001c0002t0002g0067 a0001c0002t0002g0075 a0001c0002t0002g0179 |
3 | HG02897.hp2 HG03540.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.766-621T>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390653 | |||||||
| chr5:51390660 | T | C | 1 | a0001c0002t0002g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.766-614T>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390660 | |||||||
| chr5:51390661 | T | C | 12 | a0001c0002t0002g0011 a0001c0002t0002g0018 a0001c0002t0002g0022 others(9): Show |
20 | HG00408.hp1 HG01099.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.766-613T>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390661 | |||||||
| chr5:51390662 | T | C | 43 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0005 others(40): Show |
117 | HG00323.hp1 HG00558.hp2 HG00733.hp1 others(114): Show |
intron_variant | MODIFIER | c.766-612T>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390662 | |||||||
| chr5:51390663 | T | C | 2 | a0001c0002t0002g0067 a0001c0002t0002g0075 |
2 | HG02897.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.766-611T>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390663 | |||||||
| chr5:51390664 | T | C | 1 | a0001c0002t0002g0148 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.766-610T>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390664 | |||||||
| chr5:51390667 | T | C | 1 | a0001c0002t0002g0030 | 2 | HG02451.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.766-607T>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390667 | |||||||
| chr5:51390748 | T | C | 67 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0058 others(64): Show |
151 | HG00323.hp1 HG00408.hp1 HG00558.hp2 others(148): Show |
intron_variant | MODIFIER | c.766-526T>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390748 | |||||||
| chr5:51390974 | G | A | 8 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0058 others(5): Show |
10 | HG01433.hp2 HG02572.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.766-300G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390974 | |||||||
| chr5:51390982 | G | A | 2 | a0001c0002t0002g0034 a0001c0002t0010g0034 |
2 | HG01243.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.766-292G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51390982 | |||||||
| chr5:51391000 | G | C | 4 | a0001c0001t0001g0181 a0001c0001t0004g0083 a0001c0001t0004g0084 others(1): Show |
4 | HG01167.hp1 HG03041.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-274G>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51391000 | |||||||
| chr5:51391057 | C | G | 1 | a0001c0001t0001g0099 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.766-217C>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51391057 | |||||||
| chr5:51391072 | AG | A | 8 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0058 others(5): Show |
10 | HG01433.hp2 HG02572.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.766-201delG | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51391072 | |||||||
| chr5:51391129 | G | A | 1 | a0001c0002t0002g0148 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.766-145G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51391129 | |||||||
| chr5:51391140 | G | A | 2 | a0001c0002t0002g0034 a0001c0002t0010g0034 |
2 | HG01243.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.766-134G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51391140 | |||||||
| chr5:51391173 | A | G | 1 | a0001c0001t0006g0156 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.766-101A>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51391173 | |||||||
| chr5:51391203 | C | A | 1 | a0001c0001t0001g0160 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.766-71C>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 4/5 | chr5 | 51391203 | |||||||
| chr5:51391504 | C | T | 4 | a0001c0002t0002g0010 a0001c0002t0002g0149 a0001c0002t0002g0182 others(1): Show |
8 | HG01884.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.933+63C>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51391504 | |||||||
| chr5:51391534 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.933+93C>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51391534 | |||||||
| chr5:51391546 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.933+105C>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51391546 | |||||||
| chr5:51391567 | G | A | 1 | a0001c0002t0002g0178 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.933+126G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51391567 | |||||||
| chr5:51391585 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.933+144A>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51391585 | |||||||
| chr5:51391711 | T | C | 8 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0058 others(5): Show |
10 | HG01433.hp2 HG02572.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.933+270T>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51391711 | |||||||
| chr5:51391875 | C | T | 1 | a0001c0002t0002g0071 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.933+434C>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51391875 | |||||||
| chr5:51391925 | T | C | 2 | a0001c0001t0003g0062 a0001c0001t0003g0063 |
2 | HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.933+484T>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51391925 | |||||||
| chr5:51392297 | T | C | 1 | a0001c0002t0002g0148 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.933+856T>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51392297 | |||||||
| chr5:51392402 | A | C | 1 | a0001c0002t0002g0074 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.933+961A>C | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51392402 | |||||||
| chr5:51392429 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.933+988C>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51392429 | |||||||
| chr5:51392589 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.934-905G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51392589 | |||||||
| chr5:51392664 | C | T | 1 | a0001c0001t0012g0108 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.934-830C>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51392664 | |||||||
| chr5:51392699 | C | G | 59 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0005 others(56): Show |
141 | HG00323.hp1 HG00408.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.934-795C>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51392699 | |||||||
| chr5:51392824 | G | T | 1 | a0001c0001t0006g0087 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.934-670G>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51392824 | |||||||
| chr5:51392940 | T | G | 1 | a0001c0002t0002g0066 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.934-554T>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51392940 | |||||||
| chr5:51392967 | G | A | 59 | a0001c0002t0002g0001 a0001c0002t0002g0003 a0001c0002t0002g0005 others(56): Show |
141 | HG00323.hp1 HG00408.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.934-527G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51392967 | |||||||
| chr5:51393102 | A | G | 6 | a0001c0002t0003g0017 a0001c0002t0003g0029 a0001c0002t0003g0056 others(3): Show |
8 | HG01099.hp1 HG01109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.934-392A>G | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51393102 | |||||||
| chr5:51393175 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.934-319C>T | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51393175 | |||||||
| chr5:51393176 | G | A | 2 | a0001c0002t0002g0022 a0001c0002t0002g0073 |
4 | HG02055.hp2 HG02109.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.934-318G>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51393176 | |||||||
| chr5:51393389 | T | A | 1 | a0001c0001t0003g0031 | 2 | HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.934-105T>A | ISL1 | ENSG00000016082.15 | transcript | ENST00000230658.12 | protein_coding | 5/5 | chr5 | 51393389 |