Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 90525 |
| ensemblid | ENSG00000138606.20 |
| hgncid | 25116 |
| symbol | SHF |
| name | Src homology 2 domain containing F |
| refseq_nuc | NM_001394037.1 |
| refseq_prot | NP_001380966.1 |
| ensembl_nuc | ENST00000690270.1 |
| ensembl_prot | ENSP00000508579.1 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 45167214 |
| end | 45187966 |
| strand | - |
| ver | v1.2 |
| region | chr15:45167214-45187966 |
| region5000 | chr15:45162214-45192966 |
| regionname0 | SHF_chr15_45167214_45187966 |
| regionname5000 | SHF_chr15_45162214_45192966 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 488 | 338 | 91 | 66 | 130 | 10 | 40 | 94 | SHF_chr15_45162214_45192966 | SHF | MLLSG others(483): Show |
chr15 | 45162214 | 45192966 |
| a0002 | 1/0 | 488 | 56 | 1 | 5 | 49 | 0 | 0 | 39 | SHF_chr15_45162214_45192966 | SHF | MLLSG others(483): Show |
chr15 | 45162214 | 45192966 |
| a0003 | 0/0 | 488 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | MLLSG others(483): Show |
chr15 | 45162214 | 45192966 |
| a0004 | 0/0 | 488 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | MLLSG others(483): Show |
chr15 | 45162214 | 45192966 |
| a0005 | 0/0 | 434 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | MLLSG others(429): Show |
chr15 | 45162214 | 45192966 |
| a0006 | 0/0 | 488 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | MLLSG others(483): Show |
chr15 | 45162214 | 45192966 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1464 | 336 | 89 | 66 | 130 | 10 | 40 | SHF_chr15_45162214_45192966 | SHF | ATGTT others(1459): Show |
chr15 | 45162214 | 45192966 | ||
| a0001c0004 | 0/0 | 1464 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | ATGTT others(1459): Show |
chr15 | 45162214 | 45192966 | ||
| a0002c0002 | 1/0 | 1464 | 42 | 1 | 5 | 35 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | ATGTT others(1459): Show |
chr15 | 45162214 | 45192966 | ||
| a0002c0003 | 0/0 | 1464 | 14 | 0 | 0 | 14 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | ATGTT others(1459): Show |
chr15 | 45162214 | 45192966 | ||
| a0003c0005 | 0/0 | 1464 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | ATGTT others(1459): Show |
chr15 | 45162214 | 45192966 | ||
| a0004c0007 | 0/0 | 1464 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | ATGTT others(1459): Show |
chr15 | 45162214 | 45192966 | ||
| a0005c0006 | 0/0 | 1463 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | ATGTT others(1458): Show |
chr15 | 45162214 | 45192966 | ||
| a0006c0008 | 0/0 | 1464 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | ATGTT others(1459): Show |
chr15 | 45162214 | 45192966 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2215 | 109 | 48 | 9 | 41 | 0 | 11 | SHF_chr15_45162214_45192966 | SHF | AGTCT others(2210): Show |
chr15 | 45162214 | 45192966 |
| a0001c0001t0002 | 0/1 | 2215 | 156 | 22 | 50 | 57 | 9 | 17 | SHF_chr15_45162214_45192966 | SHF | AGTCT others(2210): Show |
chr15 | 45162214 | 45192966 |
| a0001c0001t0003 | 0/0 | 2215 | 60 | 16 | 3 | 30 | 1 | 10 | SHF_chr15_45162214_45192966 | SHF | AGTCT others(2210): Show |
chr15 | 45162214 | 45192966 |
| a0001c0001t0004 | 0/0 | 2215 | 4 | 2 | 2 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | AGTCT others(2210): Show |
chr15 | 45162214 | 45192966 |
| a0001c0001t0005 | 0/0 | 2215 | 2 | 0 | 2 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | ATTCT others(2210): Show |
chr15 | 45162214 | 45192966 |
| a0001c0001t0006 | 0/0 | 2215 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | AGTCT others(2210): Show |
chr15 | 45162214 | 45192966 |
| a0001c0001t0007 | 0/0 | 2215 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | AGTCT others(2210): Show |
chr15 | 45162214 | 45192966 |
| a0001c0001t0008 | 0/0 | 2215 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | AGTCT others(2210): Show |
chr15 | 45162214 | 45192966 |
| a0001c0001t0009 | 0/0 | 2215 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | AGTCT others(2210): Show |
chr15 | 45162214 | 45192966 |
| a0001c0001t0010 | 0/0 | 2215 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | AGTCT others(2210): Show |
chr15 | 45162214 | 45192966 |
| a0001c0004t0002 | 0/0 | 2215 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | AGTCT others(2210): Show |
chr15 | 45162214 | 45192966 |
| a0002c0002t0001 | 1/0 | 2215 | 42 | 1 | 5 | 35 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | AGTCT others(2210): Show |
chr15 | 45162214 | 45192966 |
| a0002c0003t0001 | 0/0 | 2215 | 14 | 0 | 0 | 14 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | AGTCT others(2210): Show |
chr15 | 45162214 | 45192966 |
| a0003c0005t0002 | 0/0 | 2215 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | AGTCT others(2210): Show |
chr15 | 45162214 | 45192966 |
| a0004c0007t0002 | 0/0 | 2215 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | AGTCT others(2210): Show |
chr15 | 45162214 | 45192966 |
| a0005c0006t0002 | 0/0 | 2214 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | AGTCT others(2209): Show |
chr15 | 45162214 | 45192966 |
| a0006c0008t0002 | 0/0 | 2215 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | AGTCT others(2210): Show |
chr15 | 45162214 | 45192966 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 34 | 0 | 4 | 27 | 0 | 3 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0011 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0003 | 0/0 | 28 | 1 | 9 | 15 | 1 | 2 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0005 | 0/0 | 23 | 0 | 1 | 22 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0006 | 0/1 | 16 | 0 | 7 | 4 | 1 | 3 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0008 | 0/0 | 10 | 10 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0009 | 0/0 | 8 | 2 | 2 | 0 | 1 | 3 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0010 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0012 | 0/0 | 5 | 1 | 3 | 0 | 1 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0021 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0004 | 0/0 | 28 | 2 | 3 | 18 | 1 | 4 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0045 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0004g0018 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0005g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0007g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0008g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0001t0010g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0001c0004t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0002c0002t0001g0002 | 0/0 | 28 | 0 | 4 | 24 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0002c0002t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0002c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0002c0002t0001g0062 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0002c0003t0001g0007 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0002c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0002c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0003c0005t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0004c0007t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0005c0006t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| a0006c0008t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0043 | EUR | GBR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0009 | EUR | GBR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0127 | EUR | GBR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0126 | EUR | GBR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | FIN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0020 | EUR | FIN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00558 | hp2 | a0001 | c0001 | t0008 | g0130 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00639 | hp1 | a0003 | c0005 | t0002 | g0091 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0048 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0073 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0018 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0018 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0048 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0058 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0078 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0114 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0133 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0135 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0080 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02735 | hp1 | a0001 | c0001 | t0006 | g0103 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0139 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03225 | hp1 | a0001 | c0004 | t0002 | g0042 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0119 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | STU | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0045 | SAS | BEB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | BEB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | BEB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0034 | SAS | STU | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG04115 | hp2 | a0001 | c0001 | t0007 | g0082 | SAS | STU | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | BEB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | BEB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | STU | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0034 | SAS | STU | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | STU | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | CHB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | YRI | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18941 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18949 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18953 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18968 | hp2 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18971 | hp2 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18981 | hp1 | a0004 | c0007 | t0002 | g0102 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18986 | hp2 | a0002 | c0003 | t0001 | g0063 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18991 | hp1 | a0001 | c0001 | t0010 | g0138 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18992 | hp1 | a0002 | c0003 | t0001 | g0072 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18995 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18997 | hp2 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | LWK | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19043 | hp1 | a0001 | c0004 | t0002 | g0042 | AFR | LWK | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | LWK | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19055 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19055 | hp2 | a0005 | c0006 | t0002 | g0098 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19063 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19067 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19078 | hp2 | a0006 | c0008 | t0002 | g0052 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19079 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19079 | hp2 | a0002 | c0003 | t0001 | g0049 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19081 | hp1 | a0002 | c0003 | t0001 | g0007 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | YRI | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ASW | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ASW | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0075 | EUR | TSI | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | TSI | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | TSI | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0064 | AFR | ACB | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | USA | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | USA | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | USA | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | USA | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | LWK | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | LWK | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0006 | REF | REF | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0062 | REF | REF | SHF_chr15_45162214_45192966 | SHF | chr15 | 45162214 | 45192966 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:45167951 | A | C | 1 | a0004 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.1463T>G | p.Leu488Arg | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 1478/2215 | 1463/1467 | 488/488 | chr15 | 45167951 | |||
| chr15:45168132 | TCCTGGGA others(6): Show |
T | 1 | a0005 | 1 | NA19055.hp2 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.1281-12_1281delTCC others(10): Show |
p.Ser428fs | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 1296/2215 | 1281/1467 | 427/488 | chr15 | 45168132 | |||
| chr15:45172312 | A | G | 1 | a0003 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.995T>C | p.Phe332Ser | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 5/7 | 1010/2215 | 995/1467 | 332/488 | chr15 | 45172312 | |||
| chr15:45175342 | C | G | 5 | a0001 a0003 a0004 others(2): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
missense_variant | MODERATE | c.724G>C | p.Ala242Pro | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/7 | 739/2215 | 724/1467 | 242/488 | chr15 | 45175342 | |||
| chr15:45175419 | C | G | 1 | a0006 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.647G>C | p.Arg216Pro | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/7 | 662/2215 | 647/1467 | 216/488 | chr15 | 45175419 | |||
| chr15:45175420 | G | C | 1 | a0006 | 1 | NA19078.hp2 | missense_variant | MODERATE | c.646C>G | p.Arg216Gly | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/7 | 661/2215 | 646/1467 | 216/488 | chr15 | 45175420 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:45175343 | G | A | 1 | a0002c0003 | 14 | NA18941.hp1 NA18949.hp1 NA18953.hp1 others(11): Show |
synonymous_variant | LOW | c.723C>T | p.Thr241Thr | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/7 | 738/2215 | 723/1467 | 241/488 | chr15 | 45175343 | |||
| chr15:45178271 | A | G | 1 | a0001c0004 | 2 | HG03225.hp1 NA19043.hp1 |
synonymous_variant | LOW | c.534T>C | p.Asp178Asp | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/7 | 549/2215 | 534/1467 | 178/488 | chr15 | 45178271 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:45167360 | G | A | 1 | a0001c0001t0007 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*587C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 587 | chr15 | 45167360 | ||||||
| chr15:45167366 | G | A | 10 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(7): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*581C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 581 | chr15 | 45167366 | ||||||
| chr15:45167439 | C | G | 1 | a0001c0001t0007 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*508G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 508 | chr15 | 45167439 | ||||||
| chr15:45167534 | G | A | 1 | a0001c0001t0008 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*413C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 413 | chr15 | 45167534 | ||||||
| chr15:45167587 | C | A | 1 | a0001c0001t0009 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*360G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 360 | chr15 | 45167587 | ||||||
| chr15:45167675 | C | T | 1 | a0001c0001t0006 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*272G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 272 | chr15 | 45167675 | ||||||
| chr15:45167773 | C | G | 1 | a0001c0001t0003 | 60 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*174G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 174 | chr15 | 45167773 | ||||||
| chr15:45167774 | C | A | 1 | a0001c0001t0010 | 1 | NA18991.hp1 | 3_prime_UTR_variant | MODIFIER | c.*173G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 173 | chr15 | 45167774 | ||||||
| chr15:45167792 | T | C | 1 | a0001c0001t0004 | 4 | HG01167.hp1 HG01169.hp1 HG02280.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*155A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 7/7 | 155 | chr15 | 45167792 | ||||||
| chr15:45187965 | C | A | 1 | a0001c0001t0005 | 2 | HG00642.hp2 HG01358.hp1 |
5_prime_UTR_variant | MODIFIER | c.-14G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/7 | 14 | chr15 | 45187965 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:45168224 | A | G | 73 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0041 others(70): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1281-91T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45168224 | |||||||
| chr15:45168386 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1281-253C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45168386 | |||||||
| chr15:45168404 | C | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0030 others(43): Show |
120 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.1281-271G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45168404 | |||||||
| chr15:45168435 | T | G | 1 | a0001c0001t0001g0087 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1281-302A>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45168435 | |||||||
| chr15:45168480 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1281-347C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45168480 | |||||||
| chr15:45168527 | C | T | 7 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0070 others(4): Show |
8 | HG01243.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1281-394G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45168527 | |||||||
| chr15:45168530 | G | A | 8 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0065 others(5): Show |
11 | HG00642.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1281-397C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45168530 | |||||||
| chr15:45169180 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1281-1047G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45169180 | |||||||
| chr15:45169203 | A | G | 24 | a0001c0001t0001g0041 a0001c0001t0001g0116 a0001c0001t0001g0117 others(21): Show |
52 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(49): Show |
intron_variant | MODIFIER | c.1281-1070T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45169203 | |||||||
| chr15:45169559 | C | T | 7 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0070 others(4): Show |
8 | HG01243.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1281-1426G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45169559 | |||||||
| chr15:45169856 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1281-1723C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45169856 | |||||||
| chr15:45169893 | C | G | 1 | a0001c0001t0003g0136 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1281-1760G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45169893 | |||||||
| chr15:45170241 | C | T | 8 | a0001c0001t0002g0010 a0001c0001t0002g0014 a0001c0001t0002g0073 others(5): Show |
17 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1280+1642G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170241 | |||||||
| chr15:45170383 | C | T | 1 | a0001c0001t0001g0011 | 5 | HG01496.hp2 HG01884.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1280+1500G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170383 | |||||||
| chr15:45170486 | G | A | 1 | a0001c0001t0002g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1280+1397C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170486 | |||||||
| chr15:45170538 | C | T | 4 | a0001c0001t0002g0008 a0001c0001t0002g0123 a0001c0001t0004g0018 others(1): Show |
15 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1280+1345G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170538 | |||||||
| chr15:45170645 | C | CT | 4 | a0001c0001t0001g0116 a0001c0001t0001g0147 a0001c0001t0002g0021 others(1): Show |
6 | HG00741.hp2 HG01081.hp1 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.1280+1237dupA | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170645 | |||||||
| chr15:45170645 | CT | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(69): Show |
195 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(192): Show |
intron_variant | MODIFIER | c.1280+1237delA | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170645 | |||||||
| chr15:45170645 | CTT | C | 8 | a0001c0001t0001g0067 a0001c0001t0001g0081 a0001c0001t0001g0088 others(5): Show |
11 | HG02451.hp1 HG02896.hp1 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.1280+1236_1280+123 others(6): Show |
SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170645 | |||||||
| chr15:45170649 | T | C | 36 | a0001c0001t0001g0050 a0001c0001t0001g0108 a0001c0001t0002g0003 others(33): Show |
107 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.1280+1234A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170649 | |||||||
| chr15:45170650 | T | C | 1 | a0001c0001t0002g0097 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1280+1233A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170650 | |||||||
| chr15:45170653 | T | C | 1 | a0001c0001t0002g0092 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1280+1230A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170653 | |||||||
| chr15:45170747 | G | A | 3 | a0001c0001t0002g0008 a0001c0001t0004g0018 a0001c0001t0004g0078 |
14 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1280+1136C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170747 | |||||||
| chr15:45170758 | TTTCCTGC others(14): Show |
T | 1 | a0006c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1280+1104_1280+112 others(25): Show |
SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170758 | |||||||
| chr15:45170843 | G | T | 1 | a0006c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1280+1040C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170843 | |||||||
| chr15:45170863 | G | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0023 others(50): Show |
131 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.1280+1020C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170863 | |||||||
| chr15:45170903 | C | T | 3 | a0001c0001t0002g0051 a0001c0001t0002g0101 a0006c0008t0002g0052 |
3 | NA18993.hp1 NA19066.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1280+980G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170903 | |||||||
| chr15:45170996 | A | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0055 |
3 | HG01109.hp1 HG02055.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1280+887T>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45170996 | |||||||
| chr15:45171082 | A | G | 1 | a0006c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1280+801T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45171082 | |||||||
| chr15:45171083 | T | A | 1 | a0006c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1280+800A>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45171083 | |||||||
| chr15:45171084 | G | T | 1 | a0006c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1280+799C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45171084 | |||||||
| chr15:45171117 | A | T | 1 | a0006c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1280+766T>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45171117 | |||||||
| chr15:45171122 | G | C | 1 | a0001c0001t0002g0094 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1280+761C>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45171122 | |||||||
| chr15:45171298 | C | T | 1 | a0001c0001t0002g0043 | 2 | HG00099.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.1280+585G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45171298 | |||||||
| chr15:45171357 | A | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0065 others(1): Show |
7 | HG00642.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.1280+526T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45171357 | |||||||
| chr15:45171426 | C | G | 24 | a0001c0001t0001g0041 a0001c0001t0001g0116 a0001c0001t0001g0117 others(21): Show |
52 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(49): Show |
intron_variant | MODIFIER | c.1280+457G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45171426 | |||||||
| chr15:45171438 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1280+445G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45171438 | |||||||
| chr15:45171692 | A | G | 3 | a0001c0001t0002g0008 a0001c0001t0004g0018 a0001c0001t0004g0078 |
14 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1280+191T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 6/6 | chr15 | 45171692 | |||||||
| chr15:45172378 | T | C | 1 | a0001c0001t0001g0030 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.989-60A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172378 | |||||||
| chr15:45172467 | G | C | 1 | a0001c0001t0002g0095 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.989-149C>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172467 | |||||||
| chr15:45172570 | A | G | 127 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0019 others(124): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.989-252T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172570 | |||||||
| chr15:45172804 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.989-486C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172804 | |||||||
| chr15:45172836 | G | C | 60 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(57): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.989-518C>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172836 | |||||||
| chr15:45172845 | C | T | 8 | a0001c0001t0002g0010 a0001c0001t0002g0014 a0001c0001t0002g0073 others(5): Show |
17 | HG00735.hp2 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.989-527G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172845 | |||||||
| chr15:45172918 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.989-600C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172918 | |||||||
| chr15:45172959 | G | C | 1 | a0001c0001t0003g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.988+617C>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172959 | |||||||
| chr15:45172960 | T | C | 1 | a0001c0001t0003g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.988+616A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172960 | |||||||
| chr15:45172962 | G | T | 1 | a0001c0001t0003g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.988+614C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172962 | |||||||
| chr15:45172980 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.988+596G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172980 | |||||||
| chr15:45172995 | G | A | 8 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0065 others(5): Show |
11 | HG00642.hp1 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.988+581C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172995 | |||||||
| chr15:45172995 | G | T | 1 | a0006c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.988+581C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45172995 | |||||||
| chr15:45173053 | G | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0025 others(117): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.988+523C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45173053 | |||||||
| chr15:45173085 | T | A | 1 | a0001c0001t0003g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.988+491A>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45173085 | |||||||
| chr15:45173134 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0068 |
2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.988+442C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45173134 | |||||||
| chr15:45173335 | T | A | 1 | a0006c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.988+241A>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45173335 | |||||||
| chr15:45173388 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.988+188G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45173388 | |||||||
| chr15:45173453 | C | G | 1 | a0001c0001t0003g0134 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.988+123G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45173453 | |||||||
| chr15:45173457 | A | C | 1 | a0002c0002t0001g0061 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.988+119T>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45173457 | |||||||
| chr15:45173538 | G | T | 1 | a0006c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.988+38C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 4/6 | chr15 | 45173538 | |||||||
| chr15:45173794 | C | A | 1 | a0006c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.848-78G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45173794 | |||||||
| chr15:45173832 | GGGCAGA | G | 4 | a0001c0001t0002g0009 a0001c0001t0002g0120 a0001c0001t0002g0126 others(1): Show |
11 | HG00099.hp2 HG00140.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.848-122_848-117del others(6): Show |
SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45173832 | |||||||
| chr15:45173897 | C | T | 3 | a0001c0001t0002g0008 a0001c0001t0004g0018 a0001c0001t0004g0078 |
14 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.848-181G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45173897 | |||||||
| chr15:45173996 | T | G | 1 | a0006c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.848-280A>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45173996 | |||||||
| chr15:45174211 | T | C | 23 | a0001c0001t0001g0041 a0001c0001t0001g0116 a0001c0001t0001g0117 others(20): Show |
51 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(48): Show |
intron_variant | MODIFIER | c.848-495A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174211 | |||||||
| chr15:45174234 | A | G | 23 | a0001c0001t0001g0041 a0001c0001t0001g0116 a0001c0001t0001g0117 others(20): Show |
51 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(48): Show |
intron_variant | MODIFIER | c.848-518T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174234 | |||||||
| chr15:45174273 | C | T | 1 | a0006c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.848-557G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174273 | |||||||
| chr15:45174274 | T | C | 1 | a0006c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.848-558A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174274 | |||||||
| chr15:45174278 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0149 |
2 | HG02572.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.848-562C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174278 | |||||||
| chr15:45174281 | T | G | 1 | a0006c0008t0002g0052 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.848-565A>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174281 | |||||||
| chr15:45174463 | C | A | 3 | a0001c0001t0002g0008 a0001c0001t0004g0018 a0001c0001t0004g0078 |
14 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.848-747G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174463 | |||||||
| chr15:45174532 | A | T | 1 | a0001c0001t0003g0140 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.847+687T>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174532 | |||||||
| chr15:45174646 | C | T | 1 | a0001c0001t0002g0104 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.847+573G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174646 | |||||||
| chr15:45174750 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0068 |
2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.847+469T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174750 | |||||||
| chr15:45174894 | A | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0019 others(97): Show |
252 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(249): Show |
intron_variant | MODIFIER | c.847+325T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45174894 | |||||||
| chr15:45175075 | C | G | 1 | a0001c0001t0003g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.847+144G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 3/6 | chr15 | 45175075 | |||||||
| chr15:45175543 | G | C | 1 | a0001c0001t0002g0074 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.641-118C>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175543 | |||||||
| chr15:45175600 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.641-175G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175600 | |||||||
| chr15:45175611 | A | G | 9 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0057 others(6): Show |
12 | HG01243.hp1 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.641-186T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175611 | |||||||
| chr15:45175819 | CT | C | 5 | a0001c0001t0001g0085 a0001c0001t0001g0113 a0001c0001t0001g0121 others(2): Show |
6 | HG02109.hp1 HG03195.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.641-395delA | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175819 | |||||||
| chr15:45175819 | CTT | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0022 others(115): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.641-396_641-395del others(2): Show |
SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175819 | |||||||
| chr15:45175819 | CTTT | C | 5 | a0001c0001t0001g0025 a0001c0001t0002g0008 a0001c0001t0002g0044 others(2): Show |
18 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.641-397_641-395del others(3): Show |
SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175819 | |||||||
| chr15:45175826 | T | C | 45 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0070 others(42): Show |
118 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.641-401A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175826 | |||||||
| chr15:45175827 | T | C | 1 | a0001c0001t0001g0025 | 2 | HG01243.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.641-402A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175827 | |||||||
| chr15:45175841 | C | T | 21 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0021 others(18): Show |
48 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(45): Show |
intron_variant | MODIFIER | c.641-416G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175841 | |||||||
| chr15:45175905 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.641-480C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175905 | |||||||
| chr15:45175936 | A | G | 1 | a0001c0001t0007g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.641-511T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175936 | |||||||
| chr15:45175967 | C | T | 1 | a0001c0001t0003g0136 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.641-542G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45175967 | |||||||
| chr15:45176336 | T | C | 1 | a0001c0001t0007g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.641-911A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45176336 | |||||||
| chr15:45176428 | T | C | 73 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0041 others(70): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.641-1003A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45176428 | |||||||
| chr15:45176551 | T | C | 1 | a0001c0001t0003g0141 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.641-1126A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45176551 | |||||||
| chr15:45176656 | C | T | 1 | a0001c0001t0001g0011 | 5 | HG01496.hp2 HG01884.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.641-1231G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45176656 | |||||||
| chr15:45176713 | T | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.641-1288A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45176713 | |||||||
| chr15:45176751 | A | G | 9 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0057 others(6): Show |
12 | HG01243.hp1 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.641-1326T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45176751 | |||||||
| chr15:45176839 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.640+1326A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45176839 | |||||||
| chr15:45177111 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.640+1054C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177111 | |||||||
| chr15:45177253 | G | T | 1 | a0001c0001t0001g0150 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.640+912C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177253 | |||||||
| chr15:45177288 | C | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0146 |
4 | HG03209.hp1 HG03579.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.640+877G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177288 | |||||||
| chr15:45177413 | C | CT | 6 | a0001c0001t0003g0046 a0001c0001t0003g0132 a0001c0001t0003g0136 others(3): Show |
7 | HG00423.hp2 HG02132.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.640+751dupA | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177413 | |||||||
| chr15:45177435 | A | G | 1 | a0001c0001t0002g0124 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.640+730T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177435 | |||||||
| chr15:45177496 | C | G | 37 | a0001c0001t0001g0108 a0001c0001t0002g0003 a0001c0001t0002g0005 others(34): Show |
107 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.640+669G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177496 | |||||||
| chr15:45177545 | C | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0026 others(29): Show |
74 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.640+620G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177545 | |||||||
| chr15:45177650 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.640+515G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177650 | |||||||
| chr15:45177689 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.640+476G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177689 | |||||||
| chr15:45177836 | T | C | 1 | a0001c0001t0003g0114 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.640+329A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177836 | |||||||
| chr15:45177853 | C | T | 3 | a0001c0001t0002g0008 a0001c0001t0004g0018 a0001c0001t0004g0078 |
14 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.640+312G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177853 | |||||||
| chr15:45177874 | T | A | 1 | a0001c0001t0003g0115 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.640+291A>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45177874 | |||||||
| chr15:45178105 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.640+60G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 2/6 | chr15 | 45178105 | |||||||
| chr15:45178352 | C | A | 1 | a0001c0001t0001g0053 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.499-46G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178352 | |||||||
| chr15:45178511 | A | G | 1 | a0001c0001t0002g0122 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.499-205T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178511 | |||||||
| chr15:45178534 | C | CT | 59 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0022 others(56): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.499-229dupA | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178534 | |||||||
| chr15:45178534 | CT | C | 8 | a0001c0001t0002g0033 a0001c0001t0002g0096 a0001c0001t0002g0097 others(5): Show |
9 | HG01070.hp2 HG01168.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.499-229delA | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178534 | |||||||
| chr15:45178565 | C | T | 1 | a0001c0001t0003g0135 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.499-259G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178565 | |||||||
| chr15:45178575 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.499-269G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178575 | |||||||
| chr15:45178604 | G | A | 1 | a0002c0002t0001g0064 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.499-298C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178604 | |||||||
| chr15:45178684 | A | G | 5 | a0001c0001t0002g0012 a0001c0001t0002g0020 a0001c0001t0002g0033 others(2): Show |
12 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(9): Show |
intron_variant | MODIFIER | c.499-378T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178684 | |||||||
| chr15:45178723 | T | C | 6 | a0001c0001t0001g0057 a0001c0001t0001g0070 a0001c0001t0001g0148 others(3): Show |
6 | HG02145.hp1 HG02615.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.499-417A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178723 | |||||||
| chr15:45178725 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.499-419C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178725 | |||||||
| chr15:45178779 | C | T | 1 | a0001c0001t0002g0035 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.499-473G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178779 | |||||||
| chr15:45178813 | G | A | 3 | a0001c0001t0002g0008 a0001c0001t0004g0018 a0001c0001t0004g0078 |
14 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.499-507C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178813 | |||||||
| chr15:45178824 | C | T | 1 | a0002c0002t0001g0059 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.499-518G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178824 | |||||||
| chr15:45178825 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.499-519C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178825 | |||||||
| chr15:45178851 | C | G | 7 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0070 others(4): Show |
8 | HG01243.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.499-545G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178851 | |||||||
| chr15:45178948 | C | G | 1 | a0001c0001t0003g0134 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.499-642G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45178948 | |||||||
| chr15:45179039 | T | C | 7 | a0001c0001t0001g0025 a0001c0001t0001g0057 a0001c0001t0001g0070 others(4): Show |
8 | HG01243.hp1 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.499-733A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45179039 | |||||||
| chr15:45179285 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.499-979A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45179285 | |||||||
| chr15:45179291 | C | T | 21 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0021 others(18): Show |
48 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(45): Show |
intron_variant | MODIFIER | c.499-985G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45179291 | |||||||
| chr15:45179444 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.499-1138A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45179444 | |||||||
| chr15:45179487 | TG | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0017 others(140): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.499-1182delC | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45179487 | |||||||
| chr15:45179724 | G | C | 1 | a0001c0001t0003g0143 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.499-1418C>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45179724 | |||||||
| chr15:45179851 | G | A | 3 | a0001c0001t0003g0039 a0001c0001t0003g0114 a0001c0001t0003g0115 |
4 | HG02451.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.499-1545C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45179851 | |||||||
| chr15:45180077 | G | A | 2 | a0001c0001t0002g0104 a0001c0001t0002g0110 |
2 | HG02683.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.499-1771C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45180077 | |||||||
| chr15:45180252 | C | A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0109 |
8 | HG01074.hp2 HG01257.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.499-1946G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45180252 | |||||||
| chr15:45180373 | G | A | 1 | a0001c0001t0002g0105 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.499-2067C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45180373 | |||||||
| chr15:45180512 | A | G | 36 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0041 others(33): Show |
67 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(64): Show |
intron_variant | MODIFIER | c.499-2206T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45180512 | |||||||
| chr15:45180683 | T | C | 15 | a0001c0001t0001g0108 a0001c0001t0002g0003 a0001c0001t0002g0015 others(12): Show |
46 | HG00438.hp2 HG00544.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.499-2377A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45180683 | |||||||
| chr15:45180845 | T | C | 9 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0057 others(6): Show |
12 | HG01243.hp1 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.499-2539A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45180845 | |||||||
| chr15:45180947 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0065 others(1): Show |
7 | HG00642.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.499-2641C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45180947 | |||||||
| chr15:45181021 | C | A | 1 | a0001c0001t0001g0070 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.499-2715G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181021 | |||||||
| chr15:45181030 | C | G | 1 | a0001c0001t0003g0134 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.499-2724G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181030 | |||||||
| chr15:45181111 | G | A | 1 | a0001c0001t0001g0032 | 2 | NA18995.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.499-2805C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181111 | |||||||
| chr15:45181145 | G | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0022 others(128): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.499-2839C>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181145 | |||||||
| chr15:45181153 | C | T | 1 | a0002c0002t0001g0058 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.499-2847G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181153 | |||||||
| chr15:45181308 | C | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0068 |
2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.499-3002G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181308 | |||||||
| chr15:45181412 | C | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0029 others(19): Show |
61 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.499-3106G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181412 | |||||||
| chr15:45181482 | G | A | 1 | a0001c0001t0002g0105 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.499-3176C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181482 | |||||||
| chr15:45181553 | T | G | 1 | a0001c0001t0002g0106 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.499-3247A>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181553 | |||||||
| chr15:45181636 | C | A | 1 | a0001c0001t0007g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.499-3330G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181636 | |||||||
| chr15:45181744 | T | C | 3 | a0001c0001t0001g0148 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | HG02615.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.499-3438A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181744 | |||||||
| chr15:45181768 | A | G | 1 | a0001c0001t0003g0133 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.499-3462T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181768 | |||||||
| chr15:45181782 | G | C | 1 | a0001c0001t0003g0144 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.499-3476C>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181782 | |||||||
| chr15:45181840 | A | G | 2 | a0001c0001t0001g0054 a0001c0001t0001g0068 |
2 | HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.499-3534T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181840 | |||||||
| chr15:45181858 | A | G | 1 | a0001c0001t0001g0023 | 2 | HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.499-3552T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181858 | |||||||
| chr15:45181877 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.499-3571C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181877 | |||||||
| chr15:45181889 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.499-3583C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181889 | |||||||
| chr15:45181911 | G | C | 20 | a0001c0001t0002g0006 a0001c0001t0002g0009 a0001c0001t0002g0021 others(17): Show |
47 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(44): Show |
intron_variant | MODIFIER | c.499-3605C>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181911 | |||||||
| chr15:45181953 | A | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0065 others(1): Show |
7 | HG00642.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.499-3647T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45181953 | |||||||
| chr15:45182111 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.499-3805G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45182111 | |||||||
| chr15:45182173 | A | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0019 others(74): Show |
201 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(198): Show |
intron_variant | MODIFIER | c.499-3867T>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45182173 | |||||||
| chr15:45182209 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0053 |
6 | HG02486.hp1 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.499-3903C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45182209 | |||||||
| chr15:45182252 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.499-3946C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45182252 | |||||||
| chr15:45182533 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0050 others(1): Show |
7 | HG02280.hp2 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.499-4227G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45182533 | |||||||
| chr15:45182739 | T | C | 14 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0065 others(11): Show |
17 | HG00642.hp1 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.499-4433A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45182739 | |||||||
| chr15:45182743 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.499-4437T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45182743 | |||||||
| chr15:45183037 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.498+4417A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183037 | |||||||
| chr15:45183157 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.498+4297C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183157 | |||||||
| chr15:45183305 | T | C | 25 | a0001c0001t0001g0041 a0001c0001t0001g0116 a0001c0001t0001g0117 others(22): Show |
53 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(50): Show |
intron_variant | MODIFIER | c.498+4149A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183305 | |||||||
| chr15:45183332 | CAT | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0022 others(93): Show |
256 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.498+4120_498+4121d others(4): Show |
SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183332 | |||||||
| chr15:45183416 | CA | C | 10 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0146 others(7): Show |
13 | HG01891.hp2 HG02145.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.498+4037delT | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183416 | |||||||
| chr15:45183504 | T | C | 1 | a0002c0002t0001g0069 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.498+3950A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183504 | |||||||
| chr15:45183528 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.498+3926C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183528 | |||||||
| chr15:45183536 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.498+3918C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183536 | |||||||
| chr15:45183543 | G | A | 10 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0146 others(7): Show |
13 | HG01891.hp2 HG02145.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.498+3911C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183543 | |||||||
| chr15:45183565 | A | G | 2 | a0001c0001t0004g0018 a0001c0001t0004g0078 |
4 | HG01167.hp1 HG01169.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+3889T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183565 | |||||||
| chr15:45183597 | T | G | 2 | a0001c0001t0001g0070 a0001c0001t0002g0071 |
2 | HG02451.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.498+3857A>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183597 | |||||||
| chr15:45183618 | G | C | 40 | a0001c0001t0001g0022 a0001c0001t0001g0029 a0001c0001t0001g0047 others(37): Show |
89 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.498+3836C>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183618 | |||||||
| chr15:45183618 | G | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0030 others(53): Show |
167 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.498+3836C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183618 | |||||||
| chr15:45183667 | C | G | 11 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0146 others(8): Show |
14 | HG01891.hp2 HG02145.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.498+3787G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183667 | |||||||
| chr15:45183882 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.498+3572G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45183882 | |||||||
| chr15:45184230 | T | A | 3 | a0001c0001t0002g0008 a0001c0001t0004g0018 a0001c0001t0004g0078 |
14 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.498+3224A>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45184230 | |||||||
| chr15:45184321 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0022 others(116): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.498+3133G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45184321 | |||||||
| chr15:45184463 | G | A | 11 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0146 others(8): Show |
14 | HG01891.hp2 HG02145.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.498+2991C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45184463 | |||||||
| chr15:45184539 | G | T | 1 | a0001c0001t0002g0083 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.498+2915C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45184539 | |||||||
| chr15:45184543 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0022 others(112): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.498+2911C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45184543 | |||||||
| chr15:45184754 | C | T | 7 | a0001c0001t0001g0029 a0001c0001t0001g0081 a0001c0001t0002g0008 others(4): Show |
19 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.498+2700G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45184754 | |||||||
| chr15:45184801 | T | C | 1 | a0001c0001t0002g0110 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.498+2653A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45184801 | |||||||
| chr15:45184814 | A | G | 47 | a0001c0001t0001g0041 a0001c0001t0001g0116 a0001c0001t0001g0117 others(44): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.498+2640T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45184814 | |||||||
| chr15:45184846 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.498+2608G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45184846 | |||||||
| chr15:45185126 | G | T | 1 | a0001c0001t0001g0111 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.498+2328C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45185126 | |||||||
| chr15:45185290 | T | C | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG02965.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.498+2164A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45185290 | |||||||
| chr15:45185293 | T | A | 1 | a0001c0001t0003g0145 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.498+2161A>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45185293 | |||||||
| chr15:45185330 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.498+2124G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45185330 | |||||||
| chr15:45185465 | T | C | 11 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0146 others(8): Show |
14 | HG01891.hp2 HG02145.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.498+1989A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45185465 | |||||||
| chr15:45185512 | C | T | 1 | a0001c0001t0003g0040 | 2 | HG02040.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.498+1942G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45185512 | |||||||
| chr15:45185752 | G | A | 1 | a0001c0001t0003g0016 | 4 | HG02630.hp2 HG02717.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+1702C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45185752 | |||||||
| chr15:45186076 | A | C | 1 | a0001c0001t0003g0079 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.498+1378T>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186076 | |||||||
| chr15:45186121 | C | T | 3 | a0001c0001t0003g0039 a0001c0001t0003g0114 a0001c0001t0003g0115 |
4 | HG02451.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+1333G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186121 | |||||||
| chr15:45186158 | G | A | 1 | a0001c0001t0003g0038 | 2 | HG02615.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.498+1296C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186158 | |||||||
| chr15:45186180 | C | A | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | HG02965.hp2 HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.498+1274G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186180 | |||||||
| chr15:45186184 | G | T | 1 | a0002c0003t0001g0072 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.498+1270C>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186184 | |||||||
| chr15:45186185 | A | G | 1 | a0002c0003t0001g0072 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.498+1269T>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186185 | |||||||
| chr15:45186187 | C | A | 1 | a0002c0003t0001g0072 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.498+1267G>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186187 | |||||||
| chr15:45186253 | G | A | 1 | a0002c0003t0001g0072 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.498+1201C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186253 | |||||||
| chr15:45186385 | T | C | 47 | a0001c0001t0001g0041 a0001c0001t0001g0116 a0001c0001t0001g0117 others(44): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.498+1069A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186385 | |||||||
| chr15:45186416 | C | T | 3 | a0001c0001t0002g0008 a0001c0001t0004g0018 a0001c0001t0004g0078 |
14 | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.498+1038G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186416 | |||||||
| chr15:45186451 | C | T | 1 | a0001c0001t0002g0077 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.498+1003G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186451 | |||||||
| chr15:45186463 | G | A | 10 | a0001c0001t0001g0022 a0001c0001t0001g0047 a0001c0001t0001g0146 others(7): Show |
13 | HG01891.hp2 HG02145.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.498+991C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186463 | |||||||
| chr15:45186523 | C | G | 1 | a0001c0001t0001g0076 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.498+931G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186523 | |||||||
| chr15:45186603 | A | C | 1 | a0001c0001t0002g0075 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.498+851T>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186603 | |||||||
| chr15:45186745 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.498+709A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186745 | |||||||
| chr15:45186970 | C | G | 1 | a0001c0001t0001g0050 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.498+484G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45186970 | |||||||
| chr15:45187134 | C | T | 2 | a0001c0001t0002g0073 a0001c0001t0002g0074 |
2 | HG01081.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.498+320G>A | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45187134 | |||||||
| chr15:45187153 | T | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0022 others(119): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.498+301A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45187153 | |||||||
| chr15:45187198 | G | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0131 a0001c0004t0002g0042 |
4 | HG00642.hp1 HG03225.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.498+256C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45187198 | |||||||
| chr15:45187200 | G | A | 1 | a0001c0001t0002g0155 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.498+254C>T | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45187200 | |||||||
| chr15:45187325 | T | C | 2 | a0001c0001t0001g0157 a0002c0002t0001g0156 |
2 | HG00558.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.498+129A>G | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45187325 | |||||||
| chr15:45187358 | C | G | 1 | a0002c0003t0001g0049 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.498+96G>C | SHF | ENSG00000138606.20 | transcript | ENST00000690270.1 | protein_coding | 1/6 | chr15 | 45187358 |