Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51458 |
| ensemblid | ENSG00000140519.14 |
| hgncid | 18140 |
| symbol | RHCG |
| name | Rh family C glycoprotein |
| refseq_nuc | NM_016321.3 |
| refseq_prot | NP_057405.1 |
| ensembl_nuc | ENST00000268122.9 |
| ensembl_prot | ENSP00000268122.4 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 89471407 |
| end | 89496583 |
| strand | - |
| ver | v1.2 |
| region | chr15:89471407-89496583 |
| region5000 | chr15:89466407-89501583 |
| regionname0 | RHCG_chr15_89471407_89496583 |
| regionname5000 | RHCG_chr15_89466407_89501583 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 479 | 323 | 89 | 62 | 132 | 9 | 29 | 93 | RHCG_chr15_89466407_89501583 | RHCG | MAWNT others(474): Show |
chr15 | 89466407 | 89501583 |
| a0002 | 0/0 | 479 | 20 | 2 | 8 | 4 | 2 | 4 | 3 | RHCG_chr15_89466407_89501583 | RHCG | MAWNT others(474): Show |
chr15 | 89466407 | 89501583 |
| a0003 | 0/0 | 479 | 7 | 0 | 4 | 2 | 1 | 0 | 2 | RHCG_chr15_89466407_89501583 | RHCG | MAWNT others(474): Show |
chr15 | 89466407 | 89501583 |
| a0004 | 0/0 | 479 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | RHCG_chr15_89466407_89501583 | RHCG | MAWNT others(474): Show |
chr15 | 89466407 | 89501583 |
| a0005 | 0/0 | 479 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | MAWNT others(474): Show |
chr15 | 89466407 | 89501583 |
| a0006 | 0/0 | 479 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | MAWNT others(474): Show |
chr15 | 89466407 | 89501583 |
| a0007 | 0/0 | 479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | MAWNT others(474): Show |
chr15 | 89466407 | 89501583 |
| a0008 | 0/0 | 479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | MAWNT others(474): Show |
chr15 | 89466407 | 89501583 |
| a0009 | 0/0 | 479 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | MAWNT others(474): Show |
chr15 | 89466407 | 89501583 |
| a0010 | 0/0 | 479 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RHCG_chr15_89466407_89501583 | RHCG | MAWNT others(474): Show |
chr15 | 89466407 | 89501583 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1437 | 318 | 85 | 61 | 132 | 9 | 29 | RHCG_chr15_89466407_89501583 | RHCG | ATGGC others(1432): Show |
chr15 | 89466407 | 89501583 | ||
| a0001c0005 | 0/0 | 1437 | 2 | 1 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | ATGGC others(1432): Show |
chr15 | 89466407 | 89501583 | ||
| a0001c0007 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | ATGGC others(1432): Show |
chr15 | 89466407 | 89501583 | ||
| a0001c0009 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | ATGGC others(1432): Show |
chr15 | 89466407 | 89501583 | ||
| a0001c0012 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | ATGGC others(1432): Show |
chr15 | 89466407 | 89501583 | ||
| a0002c0002 | 0/0 | 1437 | 20 | 2 | 8 | 4 | 2 | 4 | RHCG_chr15_89466407_89501583 | RHCG | ATGGC others(1432): Show |
chr15 | 89466407 | 89501583 | ||
| a0003c0003 | 0/0 | 1437 | 7 | 0 | 4 | 2 | 1 | 0 | RHCG_chr15_89466407_89501583 | RHCG | ATGGC others(1432): Show |
chr15 | 89466407 | 89501583 | ||
| a0004c0004 | 0/0 | 1437 | 4 | 0 | 0 | 4 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | ATGGC others(1432): Show |
chr15 | 89466407 | 89501583 | ||
| a0005c0008 | 0/0 | 1437 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | ATGGC others(1432): Show |
chr15 | 89466407 | 89501583 | ||
| a0006c0013 | 0/0 | 1437 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | ATGGC others(1432): Show |
chr15 | 89466407 | 89501583 | ||
| a0007c0006 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | ATGGC others(1432): Show |
chr15 | 89466407 | 89501583 | ||
| a0008c0010 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | ATGGC others(1432): Show |
chr15 | 89466407 | 89501583 | ||
| a0009c0011 | 0/0 | 1437 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | ATGGC others(1432): Show |
chr15 | 89466407 | 89501583 | ||
| a0010c0014 | 0/0 | 1437 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | ATGGC others(1432): Show |
chr15 | 89466407 | 89501583 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1952 | 150 | 15 | 29 | 81 | 6 | 18 | RHCG_chr15_89466407_89501583 | RHCG | GAACC others(1947): Show |
chr15 | 89466407 | 89501583 |
| a0001c0001t0002 | 0/1 | 1952 | 84 | 54 | 14 | 11 | 2 | 2 | RHCG_chr15_89466407_89501583 | RHCG | GAACC others(1947): Show |
chr15 | 89466407 | 89501583 |
| a0001c0001t0003 | 0/0 | 1952 | 84 | 16 | 18 | 40 | 1 | 9 | RHCG_chr15_89466407_89501583 | RHCG | GAACC others(1947): Show |
chr15 | 89466407 | 89501583 |
| a0001c0005t0001 | 0/0 | 1952 | 2 | 1 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | GAACC others(1947): Show |
chr15 | 89466407 | 89501583 |
| a0001c0007t0002 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | GAACC others(1947): Show |
chr15 | 89466407 | 89501583 |
| a0001c0009t0003 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | GAACC others(1947): Show |
chr15 | 89466407 | 89501583 |
| a0001c0012t0003 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | GAACC others(1947): Show |
chr15 | 89466407 | 89501583 |
| a0002c0002t0002 | 0/0 | 1952 | 19 | 2 | 8 | 3 | 2 | 4 | RHCG_chr15_89466407_89501583 | RHCG | GAACC others(1947): Show |
chr15 | 89466407 | 89501583 |
| a0002c0002t0005 | 0/0 | 1952 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | GAACC others(1947): Show |
chr15 | 89466407 | 89501583 |
| a0003c0003t0004 | 0/0 | 1952 | 7 | 0 | 4 | 2 | 1 | 0 | RHCG_chr15_89466407_89501583 | RHCG | GAACC others(1947): Show |
chr15 | 89466407 | 89501583 |
| a0004c0004t0001 | 0/0 | 1952 | 4 | 0 | 0 | 4 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | GAACC others(1947): Show |
chr15 | 89466407 | 89501583 |
| a0005c0008t0001 | 0/0 | 1952 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | GAACC others(1947): Show |
chr15 | 89466407 | 89501583 |
| a0006c0013t0001 | 0/0 | 1952 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | GAACC others(1947): Show |
chr15 | 89466407 | 89501583 |
| a0007c0006t0002 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | GAACC others(1947): Show |
chr15 | 89466407 | 89501583 |
| a0008c0010t0002 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | GAACC others(1947): Show |
chr15 | 89466407 | 89501583 |
| a0009c0011t0003 | 0/0 | 1952 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | GAACC others(1947): Show |
chr15 | 89466407 | 89501583 |
| a0010c0014t0005 | 0/0 | 1952 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | GAACC others(1947): Show |
chr15 | 89466407 | 89501583 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 29 | 2 | 3 | 19 | 2 | 3 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0006 | 1/0 | 6 | 0 | 3 | 2 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0018 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0002 | 0/0 | 19 | 0 | 2 | 14 | 0 | 3 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0003 | 0/0 | 12 | 0 | 3 | 9 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0007 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0013 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0005t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0007t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0009t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0001c0012t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0002c0002t0002g0004 | 0/0 | 7 | 0 | 4 | 2 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0002c0002t0002g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0002c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0002c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0002c0002t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0003c0003t0004g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0003c0003t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0003c0003t0004g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0003c0003t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0003c0003t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0003c0003t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0004c0004t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0004c0004t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0005c0008t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0006c0013t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0007c0006t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0008c0010t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0009c0011t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| a0010c0014t0005g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0018 | EUR | GBR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0213 | EUR | GBR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | GBR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | GBR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0100 | EUR | FIN | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0202 | EUR | FIN | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00323 | hp2 | a0003 | c0003 | t0004 | g0224 | EUR | FIN | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | CHS | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | CHS | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00639 | hp2 | a0005 | c0008 | t0001 | g0159 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00733 | hp1 | a0006 | c0013 | t0001 | g0172 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0136 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0038 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0038 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0066 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0108 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0107 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0103 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0030 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01346 | hp1 | a0001 | c0005 | t0001 | g0029 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0036 | EUR | IBS | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0084 | EUR | IBS | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | ACB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | ACB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01934 | hp2 | a0003 | c0003 | t0004 | g0226 | AMR | PEL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01943 | hp1 | a0003 | c0003 | t0004 | g0047 | AMR | PEL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | PEL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | ACB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | ACB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | KHV | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | KHV | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | KHV | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | ACB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | ACB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02148 | hp2 | a0003 | c0003 | t0004 | g0047 | AMR | PEL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CDX | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | CDX | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0112 | AMR | PEL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02293 | hp2 | a0003 | c0003 | t0004 | g0225 | AMR | PEL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | KHV | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | KHV | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02622 | hp1 | a0001 | c0012 | t0003 | g0065 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0216 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02647 | hp2 | a0007 | c0006 | t0002 | g0217 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0069 | SAS | PJL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0195 | SAS | PJL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0183 | SAS | PJL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02886 | hp1 | a0001 | c0005 | t0001 | g0029 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02886 | hp2 | a0008 | c0010 | t0002 | g0188 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | ESN | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0219 | AFR | ESN | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | ESN | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | ESN | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | ESN | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0101 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | MSL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | MSL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | ESN | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0094 | AFR | ESN | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | MSL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | MSL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0205 | AFR | MSL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | MSL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | MSL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | MSL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03490 | hp2 | a0002 | c0002 | t0002 | g0072 | SAS | PJL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | ESN | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03540 | hp2 | a0001 | c0009 | t0003 | g0089 | AFR | GWD | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03579 | hp1 | a0001 | c0007 | t0002 | g0098 | AFR | MSL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | MSL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0004 | SAS | PJL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0131 | SAS | PJL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0030 | SAS | STU | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0137 | SAS | BEB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0190 | SAS | BEB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | STU | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0049 | AFR | YRI | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | YRI | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | CHB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | YRI | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | YRI | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18957 | hp1 | a0003 | c0003 | t0004 | g0223 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18962 | hp1 | a0003 | c0003 | t0004 | g0228 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18971 | hp2 | a0004 | c0004 | t0001 | g0034 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19009 | hp1 | a0002 | c0002 | t0005 | g0102 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | LWK | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0091 | AFR | LWK | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19068 | hp1 | a0004 | c0004 | t0001 | g0034 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19079 | hp1 | a0004 | c0004 | t0001 | g0042 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19084 | hp1 | a0004 | c0004 | t0001 | g0042 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | YRI | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | YRI | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ASW | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ASW | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0109 | EUR | TSI | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA20905 | hp2 | a0010 | c0014 | t0005 | g0227 | SAS | GIH | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | CLM | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ACB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | ACB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | MSL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG06807 | hp1 | a0009 | c0011 | t0003 | g0064 | AFR | USA | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0135 | AFR | USA | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | USA | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | USA | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0118 | AFR | LWK | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0211 | REF | REF | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0006 | REF | REF | RHCG_chr15_89466407_89501583 | RHCG | chr15 | 89466407 | 89501583 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:89477160 | C | T | 1 | a0008 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.1159G>A | p.Ala387Thr | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 8/11 | 1198/1952 | 1159/1440 | 387/479 | chr15 | 89477160 | |||
| chr15:89477569 | C | T | 1 | a0009 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1060G>A | p.Val354Met | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 7/11 | 1099/1952 | 1060/1440 | 354/479 | chr15 | 89477569 | |||
| chr15:89477575 | C | T | 1 | a0004 | 4 | NA18971.hp2 NA19068.hp1 NA19079.hp1 others(1): Show |
missense_variant | MODERATE | c.1054G>A | p.Gly352Ser | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 7/11 | 1093/1952 | 1054/1440 | 352/479 | chr15 | 89477575 | |||
| chr15:89477899 | C | T | 1 | a0005 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.913G>A | p.Gly305Ser | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 6/11 | 952/1952 | 913/1440 | 305/479 | chr15 | 89477899 | |||
| chr15:89480327 | G | A | 2 | a0002 a0010 |
21 | HG00099.hp2 HG00280.hp1 HG01070.hp2 others(18): Show |
missense_variant | MODERATE | c.604C>T | p.Arg202Cys | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 4/11 | 643/1952 | 604/1440 | 202/479 | chr15 | 89480327 | |||
| chr15:89480385 | C | T | 1 | a0007 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.546G>A | p.Met182Ile | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 4/11 | 585/1952 | 546/1440 | 182/479 | chr15 | 89480385 | |||
| chr15:89483135 | G | A | 1 | a0006 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.454C>T | p.Leu152Phe | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/11 | 493/1952 | 454/1440 | 152/479 | chr15 | 89483135 | |||
| chr15:89496412 | T | C | 2 | a0003 a0010 |
8 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(5): Show |
missense_variant | MODERATE | c.133A>G | p.Thr45Ala | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/11 | 172/1952 | 133/1440 | 45/479 | chr15 | 89496412 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:89477597 | A | G | 1 | a0001c0009 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.1032T>C | p.His344His | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 7/11 | 1071/1952 | 1032/1440 | 344/479 | chr15 | 89477597 | |||
| chr15:89477606 | G | A | 1 | a0001c0005 | 2 | HG01346.hp1 HG02886.hp1 |
synonymous_variant | LOW | c.1023C>T | p.Asn341Asn | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 7/11 | 1062/1952 | 1023/1440 | 341/479 | chr15 | 89477606 | |||
| chr15:89479475 | C | T | 1 | a0001c0007 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.684G>A | p.Leu228Leu | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 5/11 | 723/1952 | 684/1440 | 228/479 | chr15 | 89479475 | |||
| chr15:89483103 | G | A | 2 | a0001c0012 a0009c0011 |
2 | HG02622.hp1 HG06807.hp1 |
synonymous_variant | LOW | c.486C>T | p.Phe162Phe | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/11 | 525/1952 | 486/1440 | 162/479 | chr15 | 89483103 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:89471517 | G | A | 1 | a0003c0003t0004 | 7 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*363C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 11/11 | 1218 | chr15 | 89471517 | ||||||
| chr15:89471714 | T | G | 12 | a0001c0001t0002 a0001c0001t0003 a0001c0007t0002 others(9): Show |
201 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(198): Show |
3_prime_UTR_variant | MODIFIER | c.*166A>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 11/11 | 1021 | chr15 | 89471714 | ||||||
| chr15:89471719 | C | T | 2 | a0002c0002t0005 a0010c0014t0005 |
2 | NA19009.hp1 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*161G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 11/11 | 1016 | chr15 | 89471719 | ||||||
| chr15:89471802 | A | G | 5 | a0001c0001t0003 a0001c0009t0003 a0001c0012t0003 others(2): Show |
94 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*78T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 11/11 | 933 | chr15 | 89471802 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:89471949 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.*25-94T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 10/10 | chr15 | 89471949 | |||||||
| chr15:89471965 | C | A | 1 | a0001c0001t0002g0021 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.*25-110G>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 10/10 | chr15 | 89471965 | |||||||
| chr15:89472248 | A | G | 37 | a0001c0001t0001g0148 a0001c0001t0003g0002 a0001c0001t0003g0003 others(34): Show |
77 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.*25-393T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 10/10 | chr15 | 89472248 | |||||||
| chr15:89472602 | A | C | 6 | a0003c0003t0004g0047 a0003c0003t0004g0223 a0003c0003t0004g0224 others(3): Show |
7 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.*24+109T>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 10/10 | chr15 | 89472602 | |||||||
| chr15:89472873 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1312-10C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89472873 | |||||||
| chr15:89473033 | C | A | 1 | a0001c0001t0003g0082 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1312-170G>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89473033 | |||||||
| chr15:89473081 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1312-218C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89473081 | |||||||
| chr15:89473179 | C | T | 7 | a0001c0001t0003g0063 a0001c0001t0003g0066 a0001c0001t0003g0093 others(4): Show |
7 | HG01106.hp1 HG01884.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1312-316G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89473179 | |||||||
| chr15:89473250 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1312-387G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89473250 | |||||||
| chr15:89473260 | T | C | 101 | a0001c0001t0001g0177 a0001c0001t0002g0010 a0001c0001t0002g0011 others(98): Show |
165 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.1312-397A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89473260 | |||||||
| chr15:89473444 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1312-581T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89473444 | |||||||
| chr15:89473480 | G | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0147 a0001c0001t0001g0160 |
6 | NA18612.hp2 NA18961.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1312-617C>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89473480 | |||||||
| chr15:89473521 | G | T | 2 | a0001c0001t0002g0048 a0001c0001t0002g0049 |
2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1312-658C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89473521 | |||||||
| chr15:89473683 | G | T | 1 | a0001c0001t0001g0204 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1312-820C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89473683 | |||||||
| chr15:89473908 | T | C | 1 | a0001c0001t0002g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1312-1045A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89473908 | |||||||
| chr15:89473923 | C | T | 1 | a0001c0001t0002g0021 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1312-1060G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89473923 | |||||||
| chr15:89473940 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1312-1077C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89473940 | |||||||
| chr15:89474104 | C | T | 7 | a0001c0001t0003g0063 a0001c0001t0003g0066 a0001c0001t0003g0093 others(4): Show |
7 | HG01106.hp1 HG01884.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1312-1241G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474104 | |||||||
| chr15:89474139 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1312-1276G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474139 | |||||||
| chr15:89474141 | T | C | 2 | a0001c0001t0002g0048 a0001c0001t0003g0083 |
2 | HG02922.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1312-1278A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474141 | |||||||
| chr15:89474144 | A | G | 4 | a0001c0001t0002g0035 a0001c0001t0002g0086 a0001c0001t0002g0157 others(1): Show |
5 | HG02145.hp1 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1312-1281T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474144 | |||||||
| chr15:89474169 | G | T | 2 | a0001c0001t0002g0096 a0001c0001t0002g0097 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1312-1306C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474169 | |||||||
| chr15:89474263 | C | T | 24 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0019 others(21): Show |
32 | HG01106.hp1 HG01496.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1312-1400G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474263 | |||||||
| chr15:89474483 | T | A | 1 | a0001c0001t0002g0022 | 2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1312-1620A>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474483 | |||||||
| chr15:89474493 | A | G | 7 | a0001c0001t0002g0022 a0003c0003t0004g0047 a0003c0003t0004g0223 others(4): Show |
9 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1312-1630T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474493 | |||||||
| chr15:89474643 | A | G | 4 | a0001c0001t0003g0025 a0001c0001t0003g0110 a0001c0001t0003g0111 others(1): Show |
5 | HG02055.hp2 HG02486.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1312-1780T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474643 | |||||||
| chr15:89474676 | G | A | 2 | a0001c0001t0002g0205 a0001c0001t0002g0208 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1312-1813C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474676 | |||||||
| chr15:89474735 | T | C | 1 | a0001c0001t0002g0021 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1312-1872A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474735 | |||||||
| chr15:89474756 | T | G | 34 | a0001c0001t0001g0148 a0001c0001t0003g0002 a0001c0001t0003g0003 others(31): Show |
72 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1312-1893A>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474756 | |||||||
| chr15:89474760 | T | TCCTG | 24 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0019 others(21): Show |
32 | HG01106.hp1 HG01496.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1312-1901_1312-189 others(8): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474760 | |||||||
| chr15:89474784 | G | T | 1 | a0001c0001t0002g0216 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1312-1921C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474784 | |||||||
| chr15:89474788 | TCCTTCCT others(9): Show |
T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0163 a0001c0001t0001g0194 |
3 | HG03688.hp2 HG03834.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1312-1941_1312-192 others(20): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474788 | |||||||
| chr15:89474796 | TCCTGCCT others(45): Show |
T | 26 | a0001c0001t0002g0017 a0001c0001t0002g0026 a0001c0001t0002g0043 others(23): Show |
38 | HG00280.hp1 HG00438.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1311+1907_1312-193 others(56): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474796 | |||||||
| chr15:89474828 | T | TCCTGCCT others(205): Show |
1 | a0001c0001t0002g0022 | 2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1311+1926_1311+192 others(216): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474828 | |||||||
| chr15:89474828 | TCCTGCCT others(13): Show |
T | 1 | a0001c0001t0002g0193 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1311+1907_1311+192 others(24): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474828 | |||||||
| chr15:89474832 | G | T | 15 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0019 others(12): Show |
23 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1311+1923C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474832 | |||||||
| chr15:89474840 | T | G | 15 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0019 others(12): Show |
23 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1311+1915A>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474840 | |||||||
| chr15:89474848 | G | T | 24 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0019 others(21): Show |
32 | HG01106.hp1 HG01496.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1311+1907C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474848 | |||||||
| chr15:89474848 | GCCTGCCT others(9): Show |
G | 2 | a0001c0001t0002g0212 a0001c0001t0002g0220 |
2 | HG00642.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1311+1891_1311+190 others(20): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474848 | |||||||
| chr15:89474852 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1311+1903C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474852 | |||||||
| chr15:89474856 | G | T | 18 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0019 others(15): Show |
27 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.1311+1899C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474856 | |||||||
| chr15:89474864 | T | G | 2 | a0001c0001t0002g0022 a0001c0001t0002g0187 |
3 | HG02965.hp2 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1311+1891A>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474864 | |||||||
| chr15:89474868 | G | T | 1 | a0001c0001t0002g0097 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1311+1887C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474868 | |||||||
| chr15:89474872 | G | T | 7 | a0001c0001t0003g0063 a0001c0001t0003g0066 a0001c0001t0003g0093 others(4): Show |
7 | HG01106.hp1 HG01884.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1311+1883C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474872 | |||||||
| chr15:89474876 | T | G | 2 | a0001c0001t0002g0097 a0002c0002t0002g0101 |
2 | HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1311+1879A>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474876 | |||||||
| chr15:89474884 | G | T | 1 | a0001c0001t0002g0097 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1311+1871C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474884 | |||||||
| chr15:89474884 | GCCTGCCT others(21): Show |
G | 1 | a0002c0002t0002g0101 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1311+1843_1311+187 others(32): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474884 | |||||||
| chr15:89474892 | T | G | 16 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0019 others(13): Show |
24 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.1311+1863A>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474892 | |||||||
| chr15:89474892 | TCCTTCCT others(9): Show |
T | 1 | a0001c0001t0001g0162 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1311+1847_1311+186 others(20): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474892 | |||||||
| chr15:89474896 | TCCTTCCT others(81): Show |
T | 7 | a0001c0001t0003g0063 a0001c0001t0003g0066 a0001c0001t0003g0093 others(4): Show |
7 | HG01106.hp1 HG01884.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1311+1771_1311+185 others(92): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474896 | |||||||
| chr15:89474900 | T | G | 1 | a0001c0001t0002g0096 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1311+1855A>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474900 | |||||||
| chr15:89474900 | TCCTGCCT others(77): Show |
T | 15 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0019 others(12): Show |
23 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1311+1771_1311+185 others(88): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474900 | |||||||
| chr15:89474908 | G | T | 1 | a0001c0001t0002g0096 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1311+1847C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474908 | |||||||
| chr15:89474920 | G | T | 1 | a0001c0001t0002g0097 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1311+1835C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474920 | |||||||
| chr15:89474924 | G | T | 1 | a0002c0002t0002g0101 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1311+1831C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474924 | |||||||
| chr15:89474926 | C | A | 1 | a0002c0002t0002g0101 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1311+1829G>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474926 | |||||||
| chr15:89474928 | G | T | 2 | a0001c0001t0002g0096 a0002c0002t0002g0101 |
2 | HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1311+1827C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474928 | |||||||
| chr15:89474930 | C | A | 1 | a0002c0002t0002g0101 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1311+1825G>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474930 | |||||||
| chr15:89474940 | T | G | 1 | a0002c0002t0002g0101 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1311+1815A>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474940 | |||||||
| chr15:89474940 | T | TCCTGCCT others(17): Show |
1 | a0001c0001t0001g0175 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1311+1791_1311+181 others(28): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474940 | |||||||
| chr15:89474942 | CTGCCTTC others(5): Show |
C | 1 | a0001c0001t0002g0096 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1311+1801_1311+181 others(16): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474942 | |||||||
| chr15:89474950 | A | C | 1 | a0001c0001t0002g0097 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1311+1805T>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474950 | |||||||
| chr15:89474954 | A | C | 1 | a0001c0001t0002g0097 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1311+1801T>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474954 | |||||||
| chr15:89474960 | G | T | 1 | a0001c0001t0002g0096 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1311+1795C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474960 | |||||||
| chr15:89474966 | CTGCCTTC others(5): Show |
C | 1 | a0001c0001t0002g0097 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1311+1777_1311+178 others(16): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474966 | |||||||
| chr15:89474978 | A | C | 1 | a0002c0002t0002g0101 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1311+1777T>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474978 | |||||||
| chr15:89474984 | G | T | 3 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0002c0002t0002g0101 |
3 | HG02896.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1311+1771C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474984 | |||||||
| chr15:89474989 | C | A | 15 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0019 others(12): Show |
23 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.1311+1766G>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474989 | |||||||
| chr15:89474991 | T | C | 16 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0019 others(13): Show |
24 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(21): Show |
intron_variant | MODIFIER | c.1311+1764A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474991 | |||||||
| chr15:89474996 | T | G | 9 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0003g0063 others(6): Show |
9 | HG01106.hp1 HG01884.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1311+1759A>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89474996 | |||||||
| chr15:89475009 | C | A | 9 | a0001c0001t0002g0096 a0001c0001t0002g0097 a0001c0001t0003g0063 others(6): Show |
9 | HG01106.hp1 HG01884.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1311+1746G>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475009 | |||||||
| chr15:89475016 | T | TCCTTCCT others(9): Show |
2 | a0001c0001t0002g0205 a0001c0001t0002g0208 |
2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1311+1723_1311+173 others(20): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475016 | |||||||
| chr15:89475016 | TCCTTCCT others(9): Show |
T | 1 | a0001c0001t0002g0206 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1311+1723_1311+173 others(20): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475016 | |||||||
| chr15:89475032 | G | GCCTT | 24 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0019 others(21): Show |
32 | HG01106.hp1 HG01496.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1311+1719_1311+172 others(8): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475032 | |||||||
| chr15:89475036 | TCCTTCCT others(33): Show |
T | 1 | a0001c0001t0003g0153 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1311+1679_1311+171 others(44): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475036 | |||||||
| chr15:89475048 | G | A | 9 | a0001c0001t0002g0018 a0001c0001t0002g0143 a0001c0001t0002g0192 others(6): Show |
11 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.1311+1707C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475048 | |||||||
| chr15:89475078 | CTTCCTGC others(17): Show |
C | 31 | a0001c0001t0001g0162 a0001c0001t0003g0002 a0001c0001t0003g0003 others(28): Show |
68 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.1311+1653_1311+167 others(28): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475078 | |||||||
| chr15:89475084 | G | T | 1 | a0001c0001t0003g0153 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1311+1671C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475084 | |||||||
| chr15:89475098 | A | C | 1 | a0001c0001t0003g0153 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1311+1657T>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475098 | |||||||
| chr15:89475100 | T | G | 1 | a0001c0001t0003g0153 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1311+1655A>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475100 | |||||||
| chr15:89475102 | A | C | 1 | a0001c0001t0003g0153 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1311+1653T>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475102 | |||||||
| chr15:89475130 | C | T | 1 | a0001c0001t0002g0021 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1311+1625G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475130 | |||||||
| chr15:89475156 | T | TCCTTCCT others(9): Show |
4 | a0001c0001t0001g0036 a0001c0001t0001g0166 a0001c0001t0001g0176 others(1): Show |
5 | HG00140.hp2 HG00733.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.1311+1583_1311+159 others(20): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475156 | |||||||
| chr15:89475184 | G | A | 7 | a0001c0001t0002g0134 a0001c0001t0002g0205 a0001c0001t0002g0206 others(4): Show |
7 | HG02615.hp2 HG02630.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1311+1571C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475184 | |||||||
| chr15:89475188 | GCCTTCCT others(9): Show |
G | 1 | a0001c0001t0003g0076 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1311+1551_1311+156 others(20): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475188 | |||||||
| chr15:89475190 | CTTCCTTC others(5): Show |
C | 33 | a0001c0001t0002g0021 a0001c0001t0003g0002 a0001c0001t0003g0003 others(30): Show |
72 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1311+1553_1311+156 others(16): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475190 | |||||||
| chr15:89475329 | C | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0181 |
2 | HG02080.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.1311+1426G>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475329 | |||||||
| chr15:89475403 | C | T | 4 | a0001c0001t0003g0025 a0001c0001t0003g0110 a0001c0001t0003g0111 others(1): Show |
5 | HG02055.hp2 HG02486.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1311+1352G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475403 | |||||||
| chr15:89475720 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1311+1035G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475720 | |||||||
| chr15:89475756 | C | G | 3 | a0001c0001t0001g0009 a0001c0001t0001g0147 a0001c0001t0001g0160 |
6 | NA18612.hp2 NA18961.hp1 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.1311+999G>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475756 | |||||||
| chr15:89475839 | G | A | 6 | a0003c0003t0004g0047 a0003c0003t0004g0223 a0003c0003t0004g0224 others(3): Show |
7 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1311+916C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475839 | |||||||
| chr15:89475875 | A | C | 1 | a0001c0001t0002g0022 | 2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1311+880T>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475875 | |||||||
| chr15:89475924 | C | T | 1 | a0001c0001t0002g0022 | 2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1311+831G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475924 | |||||||
| chr15:89475989 | T | TTC | 37 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0019 others(34): Show |
49 | HG00323.hp2 HG01106.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.1311+764_1311+765d others(4): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89475989 | |||||||
| chr15:89476006 | G | GCT | 3 | a0001c0001t0003g0063 a0001c0001t0003g0093 a0001c0001t0003g0094 |
3 | HG01884.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1311+747_1311+748d others(4): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89476006 | |||||||
| chr15:89476010 | TCG | T | 11 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0020 others(8): Show |
18 | HG01496.hp2 HG02257.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.1311+743_1311+744d others(4): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89476010 | |||||||
| chr15:89476012 | G | GCT | 8 | a0001c0001t0001g0008 a0001c0001t0001g0092 a0001c0001t0003g0002 others(5): Show |
13 | HG00423.hp1 HG01257.hp1 HG01258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1311+741_1311+742d others(4): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89476012 | |||||||
| chr15:89476012 | G | T | 15 | a0001c0001t0002g0019 a0001c0001t0002g0022 a0001c0001t0002g0050 others(12): Show |
17 | HG00099.hp2 HG01106.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.1311+743C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89476012 | |||||||
| chr15:89476081 | G | C | 3 | a0001c0001t0003g0024 a0001c0001t0003g0091 a0001c0001t0003g0214 |
4 | HG01109.hp2 HG02922.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1311+674C>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89476081 | |||||||
| chr15:89476106 | G | T | 22 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0019 others(19): Show |
30 | HG01106.hp1 HG01496.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1311+649C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89476106 | |||||||
| chr15:89476213 | C | G | 1 | a0001c0001t0002g0022 | 2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1311+542G>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89476213 | |||||||
| chr15:89476244 | A | G | 1 | a0001c0001t0002g0115 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1311+511T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89476244 | |||||||
| chr15:89476356 | C | T | 3 | a0001c0001t0002g0022 a0001c0001t0002g0096 a0001c0001t0002g0097 |
4 | HG02896.hp2 HG02897.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1311+399G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89476356 | |||||||
| chr15:89476384 | C | T | 1 | a0001c0001t0002g0197 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1311+371G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89476384 | |||||||
| chr15:89476526 | G | C | 2 | a0001c0001t0002g0096 a0001c0001t0002g0097 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1311+229C>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89476526 | |||||||
| chr15:89476611 | T | G | 4 | a0001c0001t0003g0025 a0001c0001t0003g0110 a0001c0001t0003g0111 others(1): Show |
5 | HG02055.hp2 HG02486.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1311+144A>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 9/10 | chr15 | 89476611 | |||||||
| chr15:89476957 | C | T | 25 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0019 others(22): Show |
34 | HG01106.hp1 HG01496.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.1237+125G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 8/10 | chr15 | 89476957 | |||||||
| chr15:89477007 | G | A | 22 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0019 others(19): Show |
30 | HG01106.hp1 HG01496.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1237+75C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 8/10 | chr15 | 89477007 | |||||||
| chr15:89477048 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0160 |
5 | NA18612.hp2 NA18974.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1237+34T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 8/10 | chr15 | 89477048 | |||||||
| chr15:89477271 | C | T | 7 | a0001c0001t0003g0063 a0001c0001t0003g0066 a0001c0001t0003g0093 others(4): Show |
7 | HG01106.hp1 HG01884.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1113-65G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 7/10 | chr15 | 89477271 | |||||||
| chr15:89477330 | C | T | 2 | a0001c0001t0002g0011 a0001c0001t0002g0061 |
4 | HG02257.hp1 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1113-124G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 7/10 | chr15 | 89477330 | |||||||
| chr15:89477400 | T | A | 2 | a0001c0001t0002g0096 a0001c0001t0002g0097 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1112+117A>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 7/10 | chr15 | 89477400 | |||||||
| chr15:89477684 | C | T | 2 | a0001c0001t0002g0096 a0001c0001t0002g0097 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.976-31G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 6/10 | chr15 | 89477684 | |||||||
| chr15:89477685 | G | A | 15 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0019 others(12): Show |
23 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.976-32C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 6/10 | chr15 | 89477685 | |||||||
| chr15:89478129 | G | A | 6 | a0003c0003t0004g0047 a0003c0003t0004g0223 a0003c0003t0004g0224 others(3): Show |
7 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.838-155C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 5/10 | chr15 | 89478129 | |||||||
| chr15:89478316 | C | T | 31 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0019 others(28): Show |
42 | HG00323.hp2 HG01106.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.838-342G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 5/10 | chr15 | 89478316 | |||||||
| chr15:89478350 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.838-376G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 5/10 | chr15 | 89478350 | |||||||
| chr15:89478417 | G | A | 24 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0019 others(21): Show |
32 | HG01106.hp1 HG01496.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.838-443C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 5/10 | chr15 | 89478417 | |||||||
| chr15:89478440 | C | T | 8 | a0001c0001t0002g0021 a0001c0007t0002g0098 a0003c0003t0004g0047 others(5): Show |
10 | HG00323.hp2 HG01243.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.838-466G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 5/10 | chr15 | 89478440 | |||||||
| chr15:89478813 | C | G | 71 | a0001c0001t0001g0095 a0001c0001t0001g0148 a0001c0001t0002g0010 others(68): Show |
121 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.837+509G>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 5/10 | chr15 | 89478813 | |||||||
| chr15:89479101 | A | AAAAAACA others(42): Show |
14 | a0001c0001t0002g0011 a0001c0001t0002g0019 a0001c0001t0002g0020 others(11): Show |
19 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.837+220_837+221ins others(49): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 5/10 | chr15 | 89479101 | |||||||
| chr15:89479102 | AAAAACAA others(3): Show |
A | 1 | a0001c0001t0002g0209 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.837+210_837+219del others(10): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 5/10 | chr15 | 89479102 | |||||||
| chr15:89479113 | A | AAAACAAA others(42): Show |
1 | a0001c0001t0002g0010 | 4 | HG02723.hp2 HG03130.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+208_837+209ins others(49): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 5/10 | chr15 | 89479113 | |||||||
| chr15:89479122 | C | CAAAACAA others(43): Show |
7 | a0001c0001t0003g0063 a0001c0001t0003g0066 a0001c0001t0003g0093 others(4): Show |
7 | HG01106.hp1 HG01884.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.837+199_837+200ins others(50): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 5/10 | chr15 | 89479122 | |||||||
| chr15:89479123 | A | AAAAAAAA others(41): Show |
1 | a0001c0001t0002g0021 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.837+198_837+199ins others(48): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 5/10 | chr15 | 89479123 | |||||||
| chr15:89479123 | A | AAAAAAAA others(40): Show |
12 | a0001c0001t0002g0022 a0001c0001t0003g0025 a0001c0001t0003g0110 others(9): Show |
15 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.837+198_837+199ins others(47): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 5/10 | chr15 | 89479123 | |||||||
| chr15:89479127 | A | C | 1 | a0001c0001t0002g0117 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.837+195T>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 5/10 | chr15 | 89479127 | |||||||
| chr15:89479131 | A | G | 16 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 others(13): Show |
16 | HG02055.hp1 HG02145.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.837+191T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 5/10 | chr15 | 89479131 | |||||||
| chr15:89479178 | T | C | 1 | a0001c0001t0002g0021 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.837+144A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 5/10 | chr15 | 89479178 | |||||||
| chr15:89479207 | A | G | 47 | a0001c0001t0001g0095 a0001c0001t0001g0148 a0001c0001t0002g0021 others(44): Show |
88 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.837+115T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 5/10 | chr15 | 89479207 | |||||||
| chr15:89479271 | C | G | 1 | a0001c0001t0001g0152 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.837+51G>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 5/10 | chr15 | 89479271 | |||||||
| chr15:89479501 | G | C | 1 | a0001c0001t0002g0022 | 2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.671-13C>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 4/10 | chr15 | 89479501 | |||||||
| chr15:89479511 | A | G | 1 | a0001c0001t0002g0062 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.671-23T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 4/10 | chr15 | 89479511 | |||||||
| chr15:89479567 | T | C | 3 | a0001c0001t0001g0130 a0001c0001t0001g0156 a0001c0001t0001g0167 |
3 | HG00639.hp1 HG01070.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.671-79A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 4/10 | chr15 | 89479567 | |||||||
| chr15:89479598 | G | A | 22 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0019 others(19): Show |
30 | HG01106.hp1 HG01496.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.671-110C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 4/10 | chr15 | 89479598 | |||||||
| chr15:89479606 | C | T | 45 | a0001c0001t0001g0095 a0001c0001t0002g0021 a0001c0001t0002g0022 others(42): Show |
86 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.671-118G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 4/10 | chr15 | 89479606 | |||||||
| chr15:89479643 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.671-155C>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 4/10 | chr15 | 89479643 | |||||||
| chr15:89479752 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.671-264C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 4/10 | chr15 | 89479752 | |||||||
| chr15:89479821 | G | A | 99 | a0001c0001t0001g0095 a0001c0001t0001g0148 a0001c0001t0002g0011 others(96): Show |
158 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.671-333C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 4/10 | chr15 | 89479821 | |||||||
| chr15:89479853 | T | A | 6 | a0003c0003t0004g0047 a0003c0003t0004g0223 a0003c0003t0004g0224 others(3): Show |
7 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.671-365A>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 4/10 | chr15 | 89479853 | |||||||
| chr15:89480030 | T | C | 1 | a0001c0001t0003g0081 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.670+231A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 4/10 | chr15 | 89480030 | |||||||
| chr15:89480114 | C | A | 1 | a0001c0001t0001g0168 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.670+147G>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 4/10 | chr15 | 89480114 | |||||||
| chr15:89480148 | GATCATGG others(12): Show |
G | 3 | a0001c0001t0002g0055 a0001c0001t0002g0117 a0001c0001t0002g0189 |
3 | HG02572.hp1 HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.670+94_670+112delG others(18): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 4/10 | chr15 | 89480148 | |||||||
| chr15:89480176 | G | GGCCTTCA others(12): Show |
1 | a0001c0001t0002g0192 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.670+66_670+84dupAG others(17): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 4/10 | chr15 | 89480176 | |||||||
| chr15:89480513 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0146 |
3 | NA18946.hp1 NA18957.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.523-105G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89480513 | |||||||
| chr15:89481153 | A | G | 3 | a0001c0001t0002g0048 a0001c0001t0002g0049 a0001c0001t0002g0050 |
3 | HG02630.hp2 HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.523-745T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89481153 | |||||||
| chr15:89481190 | C | T | 1 | a0001c0001t0002g0115 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.523-782G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89481190 | |||||||
| chr15:89481251 | A | C | 7 | a0001c0001t0003g0063 a0001c0001t0003g0066 a0001c0001t0003g0093 others(4): Show |
7 | HG01106.hp1 HG01884.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.523-843T>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89481251 | |||||||
| chr15:89481324 | C | T | 33 | a0001c0001t0001g0095 a0001c0001t0003g0002 a0001c0001t0003g0003 others(30): Show |
70 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.523-916G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89481324 | |||||||
| chr15:89481451 | G | GA | 5 | a0001c0001t0002g0057 a0001c0001t0003g0025 a0001c0001t0003g0110 others(2): Show |
6 | HG02055.hp2 HG02145.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.523-1044dupT | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89481451 | |||||||
| chr15:89481527 | A | G | 7 | a0001c0001t0002g0022 a0003c0003t0004g0047 a0003c0003t0004g0223 others(4): Show |
9 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.523-1119T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89481527 | |||||||
| chr15:89481625 | T | C | 21 | a0001c0001t0002g0011 a0001c0001t0002g0019 a0001c0001t0002g0020 others(18): Show |
26 | HG01106.hp1 HG01496.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.523-1217A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89481625 | |||||||
| chr15:89481676 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.523-1268C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89481676 | |||||||
| chr15:89481790 | T | G | 1 | a0001c0001t0003g0091 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.522+1277A>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89481790 | |||||||
| chr15:89481795 | T | G | 2 | a0001c0001t0001g0077 a0001c0001t0001g0169 |
2 | HG01934.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.522+1272A>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89481795 | |||||||
| chr15:89481799 | G | T | 3 | a0001c0001t0001g0184 a0001c0001t0003g0190 a0001c0001t0003g0195 |
3 | HG02056.hp2 HG02738.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.522+1268C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89481799 | |||||||
| chr15:89481996 | T | A | 1 | a0001c0001t0001g0170 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.522+1071A>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89481996 | |||||||
| chr15:89482093 | T | C | 12 | a0001c0001t0002g0022 a0001c0001t0003g0025 a0001c0001t0003g0110 others(9): Show |
15 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(12): Show |
intron_variant | MODIFIER | c.522+974A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89482093 | |||||||
| chr15:89482116 | T | C | 1 | a0001c0001t0002g0021 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.522+951A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89482116 | |||||||
| chr15:89482123 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | NA18953.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.522+944C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89482123 | |||||||
| chr15:89482216 | C | A | 6 | a0003c0003t0004g0047 a0003c0003t0004g0223 a0003c0003t0004g0224 others(3): Show |
7 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.522+851G>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89482216 | |||||||
| chr15:89482276 | A | G | 34 | a0001c0001t0002g0011 a0001c0001t0002g0019 a0001c0001t0002g0020 others(31): Show |
43 | HG00323.hp2 HG01106.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.522+791T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89482276 | |||||||
| chr15:89482410 | C | T | 2 | a0001c0001t0002g0011 a0001c0001t0002g0061 |
4 | HG02257.hp1 HG02559.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.522+657G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89482410 | |||||||
| chr15:89482562 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.522+505C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89482562 | |||||||
| chr15:89482650 | G | A | 1 | a0001c0001t0002g0209 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.522+417C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89482650 | |||||||
| chr15:89482660 | T | C | 7 | a0001c0001t0002g0022 a0003c0003t0004g0047 a0003c0003t0004g0223 others(4): Show |
9 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.522+407A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89482660 | |||||||
| chr15:89482858 | T | C | 6 | a0001c0001t0002g0022 a0003c0003t0004g0047 a0003c0003t0004g0223 others(3): Show |
8 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.522+209A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89482858 | |||||||
| chr15:89482948 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.522+119G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89482948 | |||||||
| chr15:89482958 | G | A | 2 | a0001c0001t0002g0048 a0001c0001t0002g0049 |
2 | HG02922.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.522+109C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89482958 | |||||||
| chr15:89483007 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.522+60T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 3/10 | chr15 | 89483007 | |||||||
| chr15:89483254 | T | C | 66 | a0001c0001t0001g0095 a0001c0001t0002g0011 a0001c0001t0002g0019 others(63): Show |
111 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.372-37A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89483254 | |||||||
| chr15:89483288 | G | C | 1 | a0001c0007t0002g0098 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.372-71C>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89483288 | |||||||
| chr15:89483329 | T | C | 67 | a0001c0001t0001g0095 a0001c0001t0002g0011 a0001c0001t0002g0019 others(64): Show |
113 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.372-112A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89483329 | |||||||
| chr15:89483461 | C | T | 58 | a0001c0001t0001g0095 a0001c0001t0002g0011 a0001c0001t0002g0019 others(55): Show |
101 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.372-244G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89483461 | |||||||
| chr15:89483525 | T | C | 67 | a0001c0001t0001g0095 a0001c0001t0002g0011 a0001c0001t0002g0019 others(64): Show |
113 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.372-308A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89483525 | |||||||
| chr15:89483555 | G | A | 2 | a0001c0001t0002g0212 a0001c0001t0002g0220 |
2 | HG00642.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.372-338C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89483555 | |||||||
| chr15:89483703 | T | C | 11 | a0001c0001t0003g0025 a0001c0001t0003g0110 a0001c0001t0003g0111 others(8): Show |
13 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.372-486A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89483703 | |||||||
| chr15:89483825 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.372-608C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89483825 | |||||||
| chr15:89483991 | C | T | 1 | a0001c0001t0002g0157 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.372-774G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89483991 | |||||||
| chr15:89483996 | T | G | 2 | a0002c0002t0002g0103 a0002c0002t0002g0108 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.372-779A>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89483996 | |||||||
| chr15:89484065 | G | A | 31 | a0001c0001t0001g0116 a0001c0001t0001g0196 a0001c0001t0002g0011 others(28): Show |
45 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.372-848C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89484065 | |||||||
| chr15:89484104 | T | G | 1 | a0001c0001t0001g0150 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.372-887A>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89484104 | |||||||
| chr15:89484175 | A | G | 1 | a0001c0007t0002g0098 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.372-958T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89484175 | |||||||
| chr15:89484199 | G | C | 1 | a0001c0001t0002g0203 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.372-982C>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89484199 | |||||||
| chr15:89484237 | C | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0181 |
2 | HG02080.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.372-1020G>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89484237 | |||||||
| chr15:89484274 | A | G | 1 | a0001c0001t0003g0195 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.372-1057T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89484274 | |||||||
| chr15:89484465 | T | C | 1 | a0001c0001t0002g0021 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.372-1248A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89484465 | |||||||
| chr15:89484490 | G | A | 11 | a0001c0001t0003g0025 a0001c0001t0003g0110 a0001c0001t0003g0111 others(8): Show |
13 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.372-1273C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89484490 | |||||||
| chr15:89484775 | G | T | 1 | a0001c0007t0002g0098 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.372-1558C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89484775 | |||||||
| chr15:89484779 | C | CA | 27 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0149 others(24): Show |
31 | HG00673.hp1 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.372-1563dupT | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89484779 | |||||||
| chr15:89484779 | CA | C | 35 | a0001c0001t0001g0138 a0001c0001t0001g0146 a0001c0001t0001g0155 others(32): Show |
42 | HG00323.hp1 HG00423.hp1 HG01070.hp1 others(39): Show |
intron_variant | MODIFIER | c.372-1563delT | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89484779 | |||||||
| chr15:89484779 | CAA | C | 52 | a0001c0001t0001g0095 a0001c0001t0001g0196 a0001c0001t0002g0017 others(49): Show |
101 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.372-1564_372-1563d others(4): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89484779 | |||||||
| chr15:89484779 | CAAA | C | 8 | a0001c0001t0003g0090 a0001c0009t0003g0089 a0002c0002t0002g0101 others(5): Show |
9 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.372-1565_372-1563d others(5): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89484779 | |||||||
| chr15:89484859 | C | T | 6 | a0003c0003t0004g0047 a0003c0003t0004g0223 a0003c0003t0004g0224 others(3): Show |
7 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.372-1642G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89484859 | |||||||
| chr15:89484915 | A | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0179 |
3 | HG01981.hp1 NA19065.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.372-1698T>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89484915 | |||||||
| chr15:89485040 | C | G | 15 | a0001c0001t0002g0011 a0001c0001t0002g0019 a0001c0001t0002g0020 others(12): Show |
20 | HG01496.hp2 HG02257.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.371+1759G>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89485040 | |||||||
| chr15:89485204 | TA | T | 34 | a0001c0001t0001g0114 a0001c0001t0002g0011 a0001c0001t0002g0019 others(31): Show |
42 | HG00323.hp2 HG01106.hp1 HG01496.hp2 others(39): Show |
intron_variant | MODIFIER | c.371+1594delT | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89485204 | |||||||
| chr15:89485310 | G | A | 1 | a0004c0004t0001g0042 | 2 | NA19079.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.371+1489C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89485310 | |||||||
| chr15:89485325 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.371+1474G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89485325 | |||||||
| chr15:89485341 | T | C | 62 | a0001c0001t0001g0095 a0001c0001t0001g0177 a0001c0001t0001g0196 others(59): Show |
111 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.371+1458A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89485341 | |||||||
| chr15:89485423 | A | G | 1 | a0001c0001t0002g0022 | 2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.371+1376T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89485423 | |||||||
| chr15:89485522 | A | T | 11 | a0001c0001t0003g0025 a0001c0001t0003g0110 a0001c0001t0003g0111 others(8): Show |
13 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.371+1277T>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89485522 | |||||||
| chr15:89485570 | G | A | 1 | a0008c0010t0002g0188 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.371+1229C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89485570 | |||||||
| chr15:89485655 | AT | A | 21 | a0001c0001t0002g0011 a0001c0001t0002g0019 a0001c0001t0002g0020 others(18): Show |
26 | HG01106.hp1 HG01496.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.371+1143delA | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89485655 | |||||||
| chr15:89485692 | A | AT | 6 | a0001c0001t0003g0063 a0001c0001t0003g0066 a0001c0001t0003g0093 others(3): Show |
6 | HG01106.hp1 HG01884.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.371+1106dupA | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89485692 | |||||||
| chr15:89485767 | C | A | 1 | a0001c0001t0001g0151 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.371+1032G>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89485767 | |||||||
| chr15:89485847 | T | C | 1 | a0001c0001t0002g0021 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.371+952A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89485847 | |||||||
| chr15:89485880 | T | C | 2 | a0001c0001t0002g0192 a0001c0001t0002g0193 |
2 | HG01109.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.371+919A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89485880 | |||||||
| chr15:89485969 | T | C | 1 | a0001c0001t0002g0022 | 2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.371+830A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89485969 | |||||||
| chr15:89485978 | T | G | 1 | a0001c0001t0002g0022 | 2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.371+821A>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89485978 | |||||||
| chr15:89486024 | A | T | 6 | a0001c0001t0001g0028 a0001c0001t0001g0138 a0001c0001t0001g0154 others(3): Show |
8 | HG01346.hp1 HG02258.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.371+775T>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486024 | |||||||
| chr15:89486098 | T | C | 1 | a0001c0001t0002g0022 | 2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.371+701A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486098 | |||||||
| chr15:89486103 | A | G | 6 | a0001c0001t0003g0063 a0001c0001t0003g0066 a0001c0001t0003g0093 others(3): Show |
6 | HG01106.hp1 HG01884.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.371+696T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486103 | |||||||
| chr15:89486143 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.371+656G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486143 | |||||||
| chr15:89486238 | G | T | 1 | a0001c0001t0003g0182 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.371+561C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486238 | |||||||
| chr15:89486342 | G | C | 1 | a0001c0001t0002g0021 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.371+457C>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486342 | |||||||
| chr15:89486350 | A | G | 1 | a0001c0007t0002g0098 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.371+449T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486350 | |||||||
| chr15:89486564 | C | CAGAGAG | 3 | a0001c0001t0002g0216 a0003c0003t0004g0047 a0003c0003t0004g0228 |
4 | HG01943.hp1 HG02148.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.371+229_371+234dup others(6): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486564 | |||||||
| chr15:89486564 | C | CAGAGAGA others(3): Show |
2 | a0001c0001t0002g0215 a0003c0003t0004g0224 |
2 | HG00323.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.371+225_371+234dup others(10): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486564 | |||||||
| chr15:89486564 | C | CAGAGAGA others(5): Show |
1 | a0003c0003t0004g0223 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.371+223_371+234dup others(12): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486564 | |||||||
| chr15:89486564 | CAG | C | 12 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0067 others(9): Show |
15 | HG00140.hp2 HG00733.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.371+233_371+234del others(2): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486564 | |||||||
| chr15:89486564 | CAGAG | C | 5 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0003g0063 others(2): Show |
6 | HG01884.hp1 HG02976.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.371+231_371+234del others(4): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486564 | |||||||
| chr15:89486564 | CAGAGAGA others(3): Show |
C | 1 | a0001c0001t0003g0219 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.371+225_371+234del others(10): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486564 | |||||||
| chr15:89486564 | CAGAGAGA others(7): Show |
C | 2 | a0001c0001t0002g0020 a0001c0001t0002g0052 |
3 | HG02976.hp2 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.371+221_371+234del others(14): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486564 | |||||||
| chr15:89486564 | CAGAGAGA others(9): Show |
C | 6 | a0001c0001t0002g0011 a0001c0001t0002g0027 a0001c0001t0002g0053 others(3): Show |
9 | HG01496.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.371+219_371+234del others(16): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486564 | |||||||
| chr15:89486583 | AGAGAGAG others(11): Show |
A | 2 | a0001c0001t0002g0019 a0001c0001t0002g0061 |
3 | HG02717.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.371+198_371+215del others(18): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486583 | |||||||
| chr15:89486585 | AGAGAGAG others(9): Show |
A | 1 | a0001c0001t0002g0051 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.371+198_371+213del others(16): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486585 | |||||||
| chr15:89486591 | A | T | 1 | a0001c0001t0001g0037 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.371+208T>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486591 | |||||||
| chr15:89486593 | A | AGT | 3 | a0001c0001t0001g0001 a0001c0001t0001g0114 a0001c0001t0003g0025 |
3 | HG02056.hp1 HG03139.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.371+205_371+206ins others(2): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486593 | |||||||
| chr15:89486593 | A | AGTGT | 3 | a0001c0001t0001g0012 a0001c0001t0002g0099 a0001c0012t0003g0065 |
3 | HG02622.hp1 HG03453.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.371+205_371+206ins others(4): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486593 | |||||||
| chr15:89486593 | A | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0184 a0001c0001t0003g0078 |
3 | HG02056.hp2 HG03927.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.371+206T>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486593 | |||||||
| chr15:89486595 | A | AGT | 15 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(12): Show |
22 | HG00733.hp1 HG01943.hp2 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.371+203_371+204ins others(2): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486595 | |||||||
| chr15:89486595 | A | AGTGT | 25 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(22): Show |
29 | HG00639.hp1 HG01069.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.371+203_371+204ins others(4): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486595 | |||||||
| chr15:89486595 | A | AGTGTGT | 14 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0016 others(11): Show |
16 | HG00642.hp1 HG00673.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.371+203_371+204ins others(6): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486595 | |||||||
| chr15:89486595 | A | AGTGTGTG others(1): Show |
7 | a0001c0001t0001g0005 a0001c0001t0001g0077 a0001c0001t0001g0121 others(4): Show |
9 | HG02300.hp1 HG02886.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.371+203_371+204ins others(8): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486595 | |||||||
| chr15:89486595 | A | AGTGTGTG others(3): Show |
2 | a0001c0001t0002g0010 a0001c0001t0002g0015 |
2 | HG02015.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.371+203_371+204ins others(10): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486595 | |||||||
| chr15:89486595 | A | AGTGTGTG others(5): Show |
2 | a0001c0001t0001g0008 a0001c0001t0002g0189 |
2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.371+203_371+204ins others(12): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486595 | |||||||
| chr15:89486595 | A | AGTGTGTG others(7): Show |
1 | a0001c0001t0001g0119 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.371+203_371+204ins others(14): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486595 | |||||||
| chr15:89486595 | A | AGTGTGTG others(9): Show |
1 | a0001c0001t0001g0001 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.371+203_371+204ins others(16): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486595 | |||||||
| chr15:89486595 | A | T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0033 others(13): Show |
18 | HG01106.hp1 HG01106.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.371+204T>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486595 | |||||||
| chr15:89486595 | AGAGAGTG others(1): Show |
A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0005 |
4 | HG01074.hp1 HG01175.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.371+196_371+203del others(8): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486595 | |||||||
| chr15:89486595 | AGAGAGTG others(3): Show |
A | 1 | a0001c0001t0001g0154 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.371+194_371+203del others(10): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486595 | |||||||
| chr15:89486595 | AGAGAGTG others(7): Show |
A | 1 | a0001c0001t0001g0005 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.371+190_371+203del others(14): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486595 | |||||||
| chr15:89486597 | A | AGT | 5 | a0001c0001t0001g0001 a0001c0001t0001g0124 a0001c0001t0001g0132 others(2): Show |
6 | HG01257.hp1 HG01258.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.371+201_371+202ins others(2): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486597 | |||||||
| chr15:89486597 | A | AGTGT | 6 | a0001c0001t0001g0001 a0001c0001t0001g0085 a0001c0001t0001g0168 others(3): Show |
6 | HG00423.hp1 HG02083.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.371+201_371+202ins others(4): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486597 | |||||||
| chr15:89486597 | A | AGTGTGAG others(11): Show |
1 | a0002c0002t0002g0004 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.371+201_371+202ins others(18): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486597 | |||||||
| chr15:89486597 | A | AGTGTGT | 10 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0068 others(7): Show |
16 | HG00621.hp2 HG01243.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.371+201_371+202ins others(6): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486597 | |||||||
| chr15:89486597 | A | AGTGTGTG others(1): Show |
8 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0070 others(5): Show |
8 | HG00597.hp2 HG02132.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.371+201_371+202ins others(8): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486597 | |||||||
| chr15:89486597 | A | AGTGTGTG others(3): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0120 |
3 | HG00423.hp2 HG01433.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.371+201_371+202ins others(10): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486597 | |||||||
| chr15:89486597 | A | AGTGTGTG others(5): Show |
2 | a0001c0001t0001g0127 a0001c0001t0002g0187 |
2 | HG02970.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.371+201_371+202ins others(12): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486597 | |||||||
| chr15:89486597 | A | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(70): Show |
107 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.371+202T>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486597 | |||||||
| chr15:89486597 | AGAGTGTG others(3): Show |
A | 1 | a0001c0001t0002g0022 | 2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.371+192_371+201del others(10): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486597 | |||||||
| chr15:89486599 | A | AGAGAGAG others(7): Show |
1 | a0001c0001t0002g0097 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.371+199_371+200ins others(14): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGAGAG others(9): Show |
1 | a0001c0001t0002g0096 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.371+199_371+200ins others(16): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGAGAG others(5): Show |
1 | a0001c0001t0002g0018 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.371+199_371+200ins others(12): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGAGAG others(11): Show |
1 | a0001c0001t0002g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.371+199_371+200ins others(18): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGAGAG others(11): Show |
1 | a0001c0001t0002g0045 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.371+199_371+200ins others(18): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGAGAG others(9): Show |
1 | a0001c0001t0003g0002 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.371+199_371+200ins others(16): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGAGAG others(13): Show |
1 | a0001c0001t0003g0107 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.371+199_371+200ins others(20): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGAGAG others(17): Show |
1 | a0001c0001t0003g0007 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.371+199_371+200ins others(24): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGAGAG others(5): Show |
1 | a0001c0001t0002g0220 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.371+199_371+200ins others(12): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGAGAG others(7): Show |
1 | a0002c0002t0002g0213 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.371+199_371+200ins others(14): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGAGTG others(7): Show |
1 | a0002c0002t0002g0105 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.371+199_371+200ins others(14): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGAGTG others(9): Show |
2 | a0001c0001t0003g0002 a0002c0002t0002g0072 |
2 | HG03490.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.371+199_371+200ins others(16): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGAGTG others(15): Show |
2 | a0001c0001t0002g0017 a0001c0001t0002g0043 |
2 | NA18946.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.371+199_371+200ins others(22): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGAGTG others(3): Show |
2 | a0001c0001t0001g0128 a0001c0001t0002g0018 |
2 | HG00099.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.371+199_371+200ins others(10): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGAGTG others(9): Show |
1 | a0001c0001t0002g0209 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.371+199_371+200ins others(16): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGTGAG others(5): Show |
3 | a0001c0001t0002g0045 a0001c0001t0002g0071 a0001c0001t0002g0222 |
3 | HG01358.hp1 HG01496.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.371+199_371+200ins others(12): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGTGAG others(7): Show |
1 | a0001c0001t0002g0203 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.371+199_371+200ins others(14): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGTGTG others(3): Show |
1 | a0001c0001t0003g0007 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.371+199_371+200ins others(10): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGTGTG others(5): Show |
1 | a0001c0001t0003g0002 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.371+199_371+200ins others(12): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGTGTG others(7): Show |
7 | a0001c0001t0003g0002 a0001c0001t0003g0023 a0001c0001t0003g0073 others(4): Show |
12 | HG00438.hp2 HG00597.hp1 NA18747.hp2 others(9): Show |
intron_variant | MODIFIER | c.371+199_371+200ins others(14): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGTGTG others(9): Show |
1 | a0001c0001t0003g0002 | 2 | NA18967.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.371+199_371+200ins others(16): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGTGTG others(11): Show |
1 | a0001c0001t0001g0196 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.371+199_371+200ins others(18): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGTGTG others(13): Show |
3 | a0001c0001t0002g0017 a0001c0001t0002g0197 a0002c0002t0002g0030 |
3 | HG02074.hp1 HG03688.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.371+199_371+200ins others(20): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGTGTG others(21): Show |
1 | a0001c0001t0002g0115 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.371+199_371+200ins others(28): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGTGTG others(3): Show |
3 | a0001c0001t0002g0018 a0001c0001t0002g0056 a0001c0001t0002g0143 |
3 | HG00738.hp2 HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.371+199_371+200ins others(10): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGAGTGTG others(9): Show |
1 | a0001c0001t0002g0218 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.371+199_371+200ins others(16): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGT | 3 | a0001c0001t0001g0198 a0001c0001t0002g0050 a0005c0008t0001g0159 |
3 | HG00408.hp1 HG00639.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.371+198_371+199dup others(2): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGTGT | 5 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0185 others(2): Show |
6 | HG02148.hp1 HG02572.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.371+196_371+199dup others(4): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGTGTGAG others(7): Show |
1 | a0001c0001t0003g0131 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.371+199_371+200ins others(14): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGTGTGAG others(1): Show |
7 | a0001c0001t0001g0028 a0001c0001t0002g0117 a0001c0001t0003g0003 others(4): Show |
7 | HG01358.hp2 HG01978.hp2 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.371+199_371+200ins others(8): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGTGTGAG others(3): Show |
6 | a0001c0001t0001g0028 a0001c0001t0001g0138 a0001c0001t0002g0062 others(3): Show |
7 | HG01099.hp1 HG01109.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.371+199_371+200ins others(10): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGTGTGAG others(5): Show |
5 | a0001c0001t0001g0095 a0001c0001t0003g0002 a0001c0001t0003g0003 others(2): Show |
7 | HG01070.hp2 HG01071.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.371+199_371+200ins others(12): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGTGTGAG others(7): Show |
11 | a0001c0001t0002g0043 a0001c0001t0002g0140 a0001c0001t0003g0002 others(8): Show |
16 | HG00438.hp1 HG01123.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.371+199_371+200ins others(14): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGTGTGAG others(9): Show |
9 | a0001c0001t0002g0026 a0001c0001t0003g0003 a0001c0001t0003g0014 others(6): Show |
14 | HG00621.hp1 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.371+199_371+200ins others(16): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGTGTGAG others(11): Show |
13 | a0001c0001t0002g0017 a0001c0001t0002g0191 a0001c0001t0002g0201 others(10): Show |
14 | HG00738.hp1 HG01074.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.371+199_371+200ins others(18): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGTGTGAG others(13): Show |
1 | a0001c0001t0003g0002 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.371+199_371+200ins others(20): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGTGTGAG others(15): Show |
2 | a0001c0001t0002g0109 a0001c0001t0003g0014 |
2 | HG02080.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.371+199_371+200ins others(22): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGTGTGT | 4 | a0001c0001t0001g0150 a0001c0001t0002g0015 a0001c0001t0002g0205 others(1): Show |
4 | HG00673.hp1 HG03098.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.371+194_371+199dup others(6): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGTGTGTG others(1): Show |
3 | a0001c0001t0001g0202 a0001c0001t0002g0010 a0001c0001t0002g0134 |
3 | HG00323.hp1 HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.371+192_371+199dup others(8): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | AGTGTGTG others(5): Show |
4 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0210 others(1): Show |
4 | HG02615.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.371+188_371+199dup others(12): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486599 | A | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(104): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.371+200T>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486599 | |||||||
| chr15:89486601 | T | A | 1 | a0001c0001t0002g0049 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.371+198A>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486601 | |||||||
| chr15:89486603 | T | A | 2 | a0001c0001t0001g0186 a0001c0001t0002g0049 |
2 | NA18522.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.371+196A>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486603 | |||||||
| chr15:89486638 | G | GTGTGTGT others(4): Show |
1 | a0001c0001t0001g0144 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.371+160_371+161ins others(11): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486638 | |||||||
| chr15:89486642 | G | A | 26 | a0001c0001t0001g0095 a0001c0001t0003g0002 a0001c0001t0003g0003 others(23): Show |
63 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.371+157C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486642 | |||||||
| chr15:89486642 | G | GTGTGTGT others(1): Show |
3 | a0001c0001t0003g0080 a0001c0001t0003g0081 a0001c0001t0003g0153 |
3 | HG00423.hp1 HG02083.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.371+156_371+157ins others(8): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 2/10 | chr15 | 89486642 | |||||||
| chr15:89487149 | T | G | 4 | a0001c0001t0003g0063 a0001c0001t0003g0093 a0001c0001t0003g0094 others(1): Show |
4 | HG01884.hp1 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.185-164A>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89487149 | |||||||
| chr15:89487159 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.185-174C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89487159 | |||||||
| chr15:89487175 | G | T | 1 | a0001c0001t0002g0099 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.185-190C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89487175 | |||||||
| chr15:89487247 | G | T | 1 | a0001c0001t0003g0075 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.185-262C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89487247 | |||||||
| chr15:89487265 | A | AT | 7 | a0003c0003t0004g0047 a0003c0003t0004g0223 a0003c0003t0004g0224 others(4): Show |
8 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.185-281dupA | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89487265 | |||||||
| chr15:89487500 | G | A | 74 | a0001c0001t0001g0095 a0001c0001t0001g0196 a0001c0001t0002g0017 others(71): Show |
127 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.185-515C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89487500 | |||||||
| chr15:89487601 | A | T | 2 | a0001c0001t0003g0078 a0001c0001t0003g0079 |
2 | NA19063.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.185-616T>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89487601 | |||||||
| chr15:89487612 | C | T | 1 | a0002c0002t0002g0137 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.185-627G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89487612 | |||||||
| chr15:89487708 | G | C | 1 | a0001c0001t0001g0144 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.185-723C>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89487708 | |||||||
| chr15:89487824 | T | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(193): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.185-839A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89487824 | |||||||
| chr15:89487865 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.185-880G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89487865 | |||||||
| chr15:89487925 | A | C | 3 | a0001c0001t0003g0063 a0001c0001t0003g0093 a0001c0001t0003g0094 |
3 | HG01884.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185-940T>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89487925 | |||||||
| chr15:89488138 | G | C | 11 | a0001c0001t0003g0025 a0001c0001t0003g0110 a0001c0001t0003g0111 others(8): Show |
13 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.185-1153C>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488138 | |||||||
| chr15:89488286 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0126 |
3 | NA18949.hp1 NA18998.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.185-1301T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488286 | |||||||
| chr15:89488289 | C | CTG | 79 | a0001c0001t0001g0028 a0001c0001t0001g0095 a0001c0001t0001g0138 others(76): Show |
134 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.185-1305_185-1304i others(4): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488289 | |||||||
| chr15:89488371 | G | A | 1 | a0001c0001t0003g0111 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.185-1386C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488371 | |||||||
| chr15:89488400 | A | T | 2 | a0001c0001t0002g0096 a0001c0001t0002g0097 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.185-1415T>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488400 | |||||||
| chr15:89488401 | T | A | 2 | a0001c0001t0002g0096 a0001c0001t0002g0097 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.185-1416A>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488401 | |||||||
| chr15:89488485 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.185-1500C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488485 | |||||||
| chr15:89488596 | A | G | 1 | a0001c0007t0002g0098 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.185-1611T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488596 | |||||||
| chr15:89488663 | A | G | 7 | a0003c0003t0004g0047 a0003c0003t0004g0223 a0003c0003t0004g0224 others(4): Show |
8 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.185-1678T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488663 | |||||||
| chr15:89488724 | T | A | 1 | a0001c0001t0001g0114 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.185-1739A>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488724 | |||||||
| chr15:89488773 | T | TG | 26 | a0001c0001t0001g0016 a0001c0001t0001g0039 a0001c0001t0001g0040 others(23): Show |
31 | HG00423.hp2 HG00597.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.185-1789dupC | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488773 | |||||||
| chr15:89488773 | TG | T | 76 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0077 others(73): Show |
135 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.185-1789delC | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488773 | |||||||
| chr15:89488775 | G | GC | 10 | a0001c0001t0003g0025 a0001c0001t0003g0111 a0001c0007t0002g0098 others(7): Show |
12 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.185-1791_185-1790i others(3): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488775 | |||||||
| chr15:89488777 | G | C | 68 | a0001c0001t0001g0028 a0001c0001t0001g0077 a0001c0001t0001g0095 others(65): Show |
120 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.185-1792C>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488777 | |||||||
| chr15:89488780 | G | C | 1 | a0001c0007t0002g0098 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.185-1795C>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488780 | |||||||
| chr15:89488780 | G | T | 7 | a0003c0003t0004g0047 a0003c0003t0004g0223 a0003c0003t0004g0224 others(4): Show |
8 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.185-1795C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488780 | |||||||
| chr15:89488787 | T | C | 3 | a0001c0001t0003g0025 a0001c0001t0003g0110 a0001c0001t0003g0111 |
4 | HG02055.hp2 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.185-1802A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488787 | |||||||
| chr15:89488841 | G | A | 1 | a0001c0001t0002g0021 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.185-1856C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488841 | |||||||
| chr15:89488857 | G | C | 1 | a0001c0001t0001g0184 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.185-1872C>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488857 | |||||||
| chr15:89488885 | A | G | 1 | a0001c0001t0002g0015 | 3 | HG02015.hp2 NA18962.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.185-1900T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488885 | |||||||
| chr15:89488944 | A | G | 1 | a0001c0001t0002g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.185-1959T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89488944 | |||||||
| chr15:89489057 | A | T | 5 | a0001c0001t0001g0077 a0001c0001t0003g0003 a0001c0001t0003g0075 others(2): Show |
16 | HG00621.hp1 HG01123.hp2 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.185-2072T>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89489057 | |||||||
| chr15:89489061 | G | A | 1 | a0001c0001t0002g0021 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.185-2076C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89489061 | |||||||
| chr15:89489245 | C | T | 1 | a0001c0001t0003g0074 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.185-2260G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89489245 | |||||||
| chr15:89489283 | A | AT | 7 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0144 others(4): Show |
7 | HG00544.hp2 HG00738.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.185-2299dupA | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89489283 | |||||||
| chr15:89489356 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.185-2371A>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89489356 | |||||||
| chr15:89489495 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.185-2510G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89489495 | |||||||
| chr15:89489559 | C | G | 53 | a0001c0001t0001g0028 a0001c0001t0001g0113 a0001c0001t0001g0114 others(50): Show |
65 | HG00408.hp2 HG00438.hp1 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.185-2574G>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89489559 | |||||||
| chr15:89489560 | C | T | 3 | a0001c0001t0003g0025 a0001c0001t0003g0110 a0001c0001t0003g0111 |
4 | HG02055.hp2 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.185-2575G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89489560 | |||||||
| chr15:89489561 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0185 a0001c0001t0001g0186 |
4 | HG02148.hp1 NA18967.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.185-2576C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89489561 | |||||||
| chr15:89489583 | C | T | 1 | a0001c0001t0003g0093 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.185-2598G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89489583 | |||||||
| chr15:89489590 | C | G | 3 | a0001c0001t0003g0025 a0001c0001t0003g0110 a0001c0001t0003g0111 |
4 | HG02055.hp2 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.185-2605G>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89489590 | |||||||
| chr15:89489670 | C | T | 19 | a0001c0001t0002g0011 a0001c0001t0002g0019 a0001c0001t0002g0020 others(16): Show |
24 | HG01106.hp1 HG01496.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.185-2685G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89489670 | |||||||
| chr15:89489772 | C | A | 19 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(16): Show |
23 | HG00323.hp2 HG00423.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.185-2787G>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89489772 | |||||||
| chr15:89489944 | T | C | 2 | a0001c0001t0002g0096 a0001c0001t0002g0097 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.185-2959A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89489944 | |||||||
| chr15:89490025 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.185-3040T>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89490025 | |||||||
| chr15:89490127 | C | T | 1 | a0001c0001t0002g0021 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.185-3142G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89490127 | |||||||
| chr15:89490217 | C | A | 36 | a0001c0001t0001g0092 a0001c0001t0002g0011 a0001c0001t0002g0019 others(33): Show |
40 | HG01106.hp1 HG01884.hp1 HG02055.hp1 others(37): Show |
intron_variant | MODIFIER | c.185-3232G>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89490217 | |||||||
| chr15:89490232 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.185-3247A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89490232 | |||||||
| chr15:89490287 | C | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0003g0131 |
3 | HG03669.hp2 HG03710.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.185-3302G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89490287 | |||||||
| chr15:89490289 | A | G | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0003g0131 |
3 | HG03669.hp2 HG03710.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.185-3304T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89490289 | |||||||
| chr15:89490397 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.185-3412G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89490397 | |||||||
| chr15:89490450 | G | C | 2 | a0001c0001t0002g0218 a0007c0006t0002g0217 |
2 | HG01884.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.185-3465C>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89490450 | |||||||
| chr15:89490478 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.185-3493A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89490478 | |||||||
| chr15:89490692 | G | A | 1 | a0004c0004t0001g0042 | 2 | NA19079.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.185-3707C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89490692 | |||||||
| chr15:89490761 | C | T | 1 | a0001c0001t0003g0084 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.185-3776G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89490761 | |||||||
| chr15:89490774 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.185-3789T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89490774 | |||||||
| chr15:89490839 | G | C | 30 | a0001c0001t0002g0011 a0001c0001t0002g0019 a0001c0001t0002g0020 others(27): Show |
34 | HG01106.hp1 HG01884.hp1 HG02145.hp2 others(31): Show |
intron_variant | MODIFIER | c.185-3854C>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89490839 | |||||||
| chr15:89490862 | G | A | 1 | a0001c0001t0003g0190 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.185-3877C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89490862 | |||||||
| chr15:89491130 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.185-4145C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89491130 | |||||||
| chr15:89491374 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0003g0023 |
3 | NA18960.hp1 NA18961.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.185-4389G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89491374 | |||||||
| chr15:89491644 | T | C | 2 | a0001c0001t0002g0022 a0001c0001t0002g0062 |
3 | HG02965.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.185-4659A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89491644 | |||||||
| chr15:89491781 | T | TA | 30 | a0001c0001t0002g0011 a0001c0001t0002g0019 a0001c0001t0002g0020 others(27): Show |
35 | HG02055.hp2 HG02145.hp2 HG02257.hp1 others(32): Show |
intron_variant | MODIFIER | c.184+4579dupT | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89491781 | |||||||
| chr15:89491848 | C | CAGAACTT others(9): Show |
1 | a0002c0002t0002g0100 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.184+4497_184+4512d others(18): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89491848 | |||||||
| chr15:89491954 | C | T | 15 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(12): Show |
16 | HG02145.hp2 HG02257.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.184+4407G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89491954 | |||||||
| chr15:89491971 | G | T | 12 | a0001c0001t0002g0099 a0001c0001t0003g0025 a0001c0001t0003g0110 others(9): Show |
14 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.184+4390C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89491971 | |||||||
| chr15:89491998 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.184+4363C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89491998 | |||||||
| chr15:89492006 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.184+4355T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89492006 | |||||||
| chr15:89492019 | T | C | 1 | a0001c0007t0002g0098 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.184+4342A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89492019 | |||||||
| chr15:89492046 | A | C | 1 | a0001c0001t0002g0117 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.184+4315T>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89492046 | |||||||
| chr15:89492091 | C | T | 22 | a0001c0001t0001g0012 a0001c0001t0001g0070 a0001c0001t0001g0077 others(19): Show |
54 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.184+4270G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89492091 | |||||||
| chr15:89492149 | C | A | 7 | a0003c0003t0004g0047 a0003c0003t0004g0223 a0003c0003t0004g0224 others(4): Show |
8 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.184+4212G>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89492149 | |||||||
| chr15:89492149 | C | G | 2 | a0001c0001t0002g0099 a0001c0007t0002g0098 |
2 | HG03453.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.184+4212G>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89492149 | |||||||
| chr15:89492322 | G | A | 2 | a0001c0001t0002g0022 a0001c0001t0002g0062 |
3 | HG02965.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.184+4039C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89492322 | |||||||
| chr15:89492436 | CCTAA | C | 23 | a0001c0001t0002g0011 a0001c0001t0002g0019 a0001c0001t0002g0020 others(20): Show |
27 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.184+3921_184+3924d others(6): Show |
RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89492436 | |||||||
| chr15:89492482 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.184+3879G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89492482 | |||||||
| chr15:89492831 | T | G | 1 | a0001c0007t0002g0098 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.184+3530A>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89492831 | |||||||
| chr15:89492914 | G | C | 2 | a0001c0001t0002g0191 a0001c0001t0002g0201 |
2 | HG00738.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.184+3447C>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89492914 | |||||||
| chr15:89492920 | C | T | 9 | a0001c0001t0002g0099 a0001c0007t0002g0098 a0003c0003t0004g0047 others(6): Show |
10 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.184+3441G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89492920 | |||||||
| chr15:89493004 | C | G | 1 | a0001c0007t0002g0098 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.184+3357G>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89493004 | |||||||
| chr15:89493056 | G | C | 12 | a0001c0001t0002g0099 a0001c0001t0003g0025 a0001c0001t0003g0110 others(9): Show |
14 | HG00323.hp2 HG01934.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.184+3305C>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89493056 | |||||||
| chr15:89493173 | G | A | 2 | a0001c0001t0002g0192 a0001c0001t0002g0193 |
2 | HG01109.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.184+3188C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89493173 | |||||||
| chr15:89493181 | T | A | 1 | a0001c0001t0001g0194 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.184+3180A>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89493181 | |||||||
| chr15:89493264 | C | A | 56 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0070 others(53): Show |
108 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.184+3097G>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89493264 | |||||||
| chr15:89493354 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.184+3007G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89493354 | |||||||
| chr15:89493374 | C | T | 6 | a0001c0001t0003g0063 a0001c0001t0003g0066 a0001c0001t0003g0093 others(3): Show |
6 | HG01106.hp1 HG01884.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.184+2987G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89493374 | |||||||
| chr15:89493563 | C | G | 1 | a0001c0001t0003g0069 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.184+2798G>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89493563 | |||||||
| chr15:89493778 | C | G | 2 | a0001c0001t0002g0022 a0001c0001t0002g0062 |
3 | HG02965.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.184+2583G>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89493778 | |||||||
| chr15:89493783 | C | G | 2 | a0001c0001t0002g0022 a0001c0001t0002g0062 |
3 | HG02965.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.184+2578G>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89493783 | |||||||
| chr15:89493969 | C | G | 55 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0070 others(52): Show |
107 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.184+2392G>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89493969 | |||||||
| chr15:89494002 | T | G | 103 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0070 others(100): Show |
163 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.184+2359A>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89494002 | |||||||
| chr15:89494018 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.184+2343G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89494018 | |||||||
| chr15:89494050 | C | T | 3 | a0001c0001t0003g0025 a0001c0001t0003g0110 a0001c0001t0003g0111 |
4 | HG02055.hp2 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.184+2311G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89494050 | |||||||
| chr15:89494072 | CT | C | 11 | a0001c0001t0001g0104 a0001c0001t0002g0109 a0001c0001t0002g0117 others(8): Show |
17 | HG00280.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.184+2288delA | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89494072 | |||||||
| chr15:89494408 | C | G | 15 | a0001c0001t0002g0019 a0001c0001t0002g0051 a0001c0001t0002g0052 others(12): Show |
16 | HG02145.hp2 HG02257.hp2 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.184+1953G>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89494408 | |||||||
| chr15:89494513 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.184+1848C>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89494513 | |||||||
| chr15:89494636 | C | CT | 10 | a0001c0001t0001g0221 a0001c0001t0002g0022 a0001c0001t0002g0048 others(7): Show |
11 | HG01106.hp1 HG01884.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.184+1724dupA | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89494636 | |||||||
| chr15:89494636 | CT | C | 11 | a0001c0001t0001g0044 a0001c0001t0001g0198 a0001c0001t0001g0199 others(8): Show |
12 | HG00408.hp1 HG00642.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.184+1724delA | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89494636 | |||||||
| chr15:89494665 | T | C | 3 | a0001c0001t0003g0025 a0001c0001t0003g0110 a0001c0001t0003g0111 |
4 | HG02055.hp2 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.184+1696A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89494665 | |||||||
| chr15:89495065 | A | T | 1 | a0001c0001t0002g0021 | 2 | HG01243.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.184+1296T>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89495065 | |||||||
| chr15:89495066 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.184+1295A>G | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89495066 | |||||||
| chr15:89495162 | A | T | 222 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(219): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.184+1199T>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89495162 | |||||||
| chr15:89495172 | A | G | 17 | a0001c0001t0002g0011 a0001c0001t0002g0019 a0001c0001t0002g0020 others(14): Show |
21 | HG02145.hp2 HG02257.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.184+1189T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89495172 | |||||||
| chr15:89495181 | C | T | 5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
5 | HG00423.hp2 NA18953.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.184+1180G>A | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89495181 | |||||||
| chr15:89495365 | T | A | 17 | a0001c0001t0001g0046 a0001c0001t0002g0018 a0001c0001t0002g0205 others(14): Show |
20 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.184+996A>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89495365 | |||||||
| chr15:89495882 | G | A | 1 | a0002c0002t0002g0112 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.184+479C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89495882 | |||||||
| chr15:89495897 | G | A | 8 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(5): Show |
11 | HG00673.hp2 HG02080.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.184+464C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89495897 | |||||||
| chr15:89495929 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.184+432C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89495929 | |||||||
| chr15:89495974 | A | G | 95 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0067 others(92): Show |
154 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.184+387T>C | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89495974 | |||||||
| chr15:89496053 | G | A | 1 | a0001c0001t0002g0222 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.184+308C>T | RHCG | ENSG00000140519.14 | transcript | ENST00000268122.9 | protein_coding | 1/10 | chr15 | 89496053 |