Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3274 |
| ensemblid | ENSG00000113749.8 |
| hgncid | 5183 |
| symbol | HRH2 |
| name | histamine receptor H2 |
| refseq_nuc | NM_001367711.1 |
| refseq_prot | NP_001354640.1 |
| ensembl_nuc | ENST00000636584.2 |
| ensembl_prot | ENSP00000489742.1 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 175658071 |
| end | 175710756 |
| strand | + |
| ver | v1.2 |
| region | chr5:175658071-175710756 |
| region5000 | chr5:175653071-175715756 |
| regionname0 | HRH2_chr5_175658071_175710756 |
| regionname5000 | HRH2_chr5_175653071_175715756 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 422 | 259 | 94 | 40 | 94 | 8 | 21 | 67 | HRH2_chr5_175653071_175715756 | HRH2 | MAPNG others(417): Show |
chr5 | 175653071 | 175715756 |
| a0002 | 0/0 | 422 | 4 | 0 | 0 | 3 | 0 | 1 | 3 | HRH2_chr5_175653071_175715756 | HRH2 | MAPNG others(417): Show |
chr5 | 175653071 | 175715756 |
| a0003 | 0/0 | 422 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | MAPNG others(417): Show |
chr5 | 175653071 | 175715756 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1266 | 236 | 83 | 37 | 89 | 7 | 18 | HRH2_chr5_175653071_175715756 | HRH2 | ATGGC others(1261): Show |
chr5 | 175653071 | 175715756 | ||
| a0001c0002 | 0/0 | 1266 | 11 | 0 | 3 | 4 | 1 | 3 | HRH2_chr5_175653071_175715756 | HRH2 | ATGGC others(1261): Show |
chr5 | 175653071 | 175715756 | ||
| a0001c0003 | 0/0 | 1266 | 10 | 10 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | ATGGC others(1261): Show |
chr5 | 175653071 | 175715756 | ||
| a0001c0006 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | ATGGC others(1261): Show |
chr5 | 175653071 | 175715756 | ||
| a0001c0007 | 0/0 | 1266 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | ATGGC others(1261): Show |
chr5 | 175653071 | 175715756 | ||
| a0002c0004 | 0/0 | 1266 | 4 | 0 | 0 | 3 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | ATGGC others(1261): Show |
chr5 | 175653071 | 175715756 | ||
| a0003c0005 | 0/0 | 1266 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | ATGGC others(1261): Show |
chr5 | 175653071 | 175715756 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4664 | 123 | 24 | 27 | 51 | 7 | 12 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4659): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0002 | 0/0 | 4664 | 12 | 5 | 2 | 4 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4659): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0003 | 0/0 | 4668 | 15 | 6 | 0 | 7 | 0 | 2 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4663): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0004 | 0/0 | 4668 | 10 | 6 | 0 | 3 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4663): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0005 | 0/0 | 4669 | 8 | 4 | 0 | 4 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4664): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0006 | 0/0 | 4650 | 6 | 6 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4645): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0007 | 0/0 | 4664 | 5 | 0 | 0 | 5 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4659): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0008 | 0/0 | 4654 | 4 | 4 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4649): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0009 | 0/0 | 4667 | 3 | 2 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4662): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0011 | 0/0 | 4667 | 2 | 0 | 0 | 2 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4662): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0012 | 0/0 | 4650 | 3 | 2 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4645): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0013 | 0/0 | 4664 | 3 | 0 | 0 | 3 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4659): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0014 | 0/0 | 4664 | 3 | 0 | 0 | 3 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4659): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0015 | 0/0 | 4653 | 2 | 2 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4648): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0016 | 0/0 | 4668 | 2 | 2 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4663): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0019 | 0/0 | 4654 | 2 | 2 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4649): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0020 | 0/0 | 4668 | 2 | 0 | 0 | 2 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4663): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0021 | 0/0 | 4664 | 2 | 0 | 0 | 0 | 0 | 2 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4659): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0022 | 0/0 | 4664 | 2 | 0 | 2 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4659): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0023 | 0/0 | 4650 | 2 | 0 | 2 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4645): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0024 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4662): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0025 | 0/0 | 4655 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4650): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0030 | 0/0 | 4669 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4664): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0031 | 0/0 | 4655 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4650): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0032 | 0/0 | 4655 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4650): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0033 | 0/0 | 4654 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4649): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0034 | 0/0 | 4668 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4663): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0035 | 0/0 | 4668 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4663): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0036 | 0/0 | 4654 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4649): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0037 | 0/0 | 4654 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4649): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0038 | 0/0 | 4667 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4662): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0039 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4662): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0040 | 0/0 | 4653 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4648): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0041 | 0/0 | 4664 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4659): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0042 | 0/0 | 4664 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4659): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0043 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4645): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0044 | 0/0 | 4681 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4676): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0045 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4645): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0046 | 0/0 | 4650 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4645): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0047 | 0/0 | 4664 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4659): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0048 | 0/0 | 4664 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4659): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0049 | 0/0 | 4664 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4659): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0050 | 0/0 | 4664 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4659): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0051 | 0/0 | 4664 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4659): Show |
chr5 | 175653071 | 175715756 |
| a0001c0001t0052 | 0/0 | 4664 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4659): Show |
chr5 | 175653071 | 175715756 |
| a0001c0002t0001 | 0/0 | 4664 | 7 | 0 | 0 | 4 | 1 | 2 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4659): Show |
chr5 | 175653071 | 175715756 |
| a0001c0002t0002 | 0/0 | 4664 | 4 | 0 | 3 | 0 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4659): Show |
chr5 | 175653071 | 175715756 |
| a0001c0003t0010 | 0/0 | 4669 | 3 | 3 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4664): Show |
chr5 | 175653071 | 175715756 |
| a0001c0003t0017 | 0/0 | 4654 | 2 | 2 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4649): Show |
chr5 | 175653071 | 175715756 |
| a0001c0003t0018 | 0/0 | 4653 | 2 | 2 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4648): Show |
chr5 | 175653071 | 175715756 |
| a0001c0003t0026 | 0/0 | 4654 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4649): Show |
chr5 | 175653071 | 175715756 |
| a0001c0003t0027 | 0/0 | 4668 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4663): Show |
chr5 | 175653071 | 175715756 |
| a0001c0003t0028 | 0/0 | 4654 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4649): Show |
chr5 | 175653071 | 175715756 |
| a0001c0006t0029 | 0/0 | 4669 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4664): Show |
chr5 | 175653071 | 175715756 |
| a0001c0007t0001 | 0/0 | 4664 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4659): Show |
chr5 | 175653071 | 175715756 |
| a0002c0004t0001 | 0/0 | 4664 | 3 | 0 | 0 | 2 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4659): Show |
chr5 | 175653071 | 175715756 |
| a0002c0004t0011 | 0/0 | 4667 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4662): Show |
chr5 | 175653071 | 175715756 |
| a0003c0005t0001 | 0/0 | 4664 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | GCATC others(4659): Show |
chr5 | 175653071 | 175715756 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0005 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0017 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0021 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0005g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0007g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0007g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0007g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0008g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0008g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0009g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0009g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0011g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0011g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0012g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0012g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0012g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0013g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0013g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0013g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0014g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0014g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0014g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0015g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0016g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0016g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0019g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0019g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0020g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0021g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0021g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0022g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0022g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0023g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0024g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0025g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0030g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0031g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0032g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0033g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0034g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0035g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0036g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0037g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0038g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0039g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0040g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0041g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0042g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0043g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0044g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0045g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0046g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0047g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0048g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0049g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0050g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0051g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0001t0052g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0003t0010g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0003t0017g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0003t0017g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0003t0018g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0003t0018g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0003t0026g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0003t0027g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0003t0028g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0006t0029g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0001c0007t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0002c0004t0001g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0002c0004t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0002c0004t0011g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| a0003c0005t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0001 | t0050 | g0171 | EAS | CHS | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0192 | EAS | CHS | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0038 | EAS | CHS | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG00642 | hp2 | a0001 | c0001 | t0022 | g0125 | AMR | PUR | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01069 | hp2 | a0001 | c0001 | t0052 | g0022 | AMR | PUR | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01081 | hp2 | a0001 | c0001 | t0022 | g0145 | AMR | PUR | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0082 | AMR | PUR | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01109 | hp2 | a0001 | c0001 | t0009 | g0094 | AMR | PUR | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01243 | hp2 | a0001 | c0001 | t0012 | g0131 | AMR | PUR | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01255 | hp2 | a0001 | c0001 | t0048 | g0180 | AMR | CLM | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01256 | hp2 | a0001 | c0001 | t0023 | g0019 | AMR | CLM | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01258 | hp2 | a0001 | c0001 | t0023 | g0019 | AMR | CLM | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0165 | AMR | CLM | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0108 | EUR | IBS | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | IBS | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0216 | AFR | ACB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01884 | hp2 | a0001 | c0001 | t0012 | g0200 | AFR | ACB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01891 | hp2 | a0001 | c0001 | t0016 | g0085 | AFR | ACB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02015 | hp1 | a0001 | c0001 | t0047 | g0204 | EAS | KHV | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | KHV | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02055 | hp2 | a0001 | c0001 | t0035 | g0059 | AFR | ACB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | KHV | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02083 | hp1 | a0001 | c0007 | t0001 | g0006 | EAS | KHV | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02132 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | KHV | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02145 | hp1 | a0001 | c0003 | t0017 | g0090 | AFR | ACB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02145 | hp2 | a0001 | c0001 | t0004 | g0188 | AFR | ACB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CDX | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CDX | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0202 | AFR | ACB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | ACB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | ACB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02300 | hp1 | a0001 | c0002 | t0002 | g0083 | AMR | PEL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02451 | hp1 | a0001 | c0003 | t0010 | g0004 | AFR | ACB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0129 | AFR | ACB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02523 | hp1 | a0003 | c0005 | t0001 | g0006 | EAS | KHV | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02572 | hp1 | a0001 | c0003 | t0028 | g0071 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02572 | hp2 | a0001 | c0001 | t0031 | g0032 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0099 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02615 | hp2 | a0001 | c0003 | t0018 | g0181 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02622 | hp2 | a0001 | c0003 | t0018 | g0201 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0189 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0079 | SAS | PJL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0186 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02717 | hp2 | a0001 | c0003 | t0027 | g0105 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0198 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02809 | hp1 | a0001 | c0001 | t0019 | g0093 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02809 | hp2 | a0001 | c0001 | t0024 | g0214 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02818 | hp1 | a0001 | c0001 | t0038 | g0095 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0043 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02886 | hp1 | a0001 | c0003 | t0017 | g0168 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0040 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0084 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0067 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02896 | hp2 | a0001 | c0003 | t0010 | g0004 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02897 | hp2 | a0001 | c0001 | t0040 | g0068 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0215 | AFR | ESN | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02922 | hp2 | a0001 | c0001 | t0015 | g0033 | AFR | ESN | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0102 | AFR | ESN | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0092 | AFR | ESN | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ESN | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0100 | AFR | ESN | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03098 | hp1 | a0001 | c0001 | t0008 | g0044 | AFR | MSL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03130 | hp1 | a0001 | c0001 | t0037 | g0032 | AFR | ESN | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | ESN | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | ESN | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03139 | hp2 | a0001 | c0001 | t0034 | g0096 | AFR | ESN | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03209 | hp1 | a0001 | c0001 | t0045 | g0120 | AFR | MSL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03209 | hp2 | a0001 | c0006 | t0029 | g0073 | AFR | MSL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0042 | AFR | MSL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03453 | hp1 | a0001 | c0001 | t0016 | g0193 | AFR | MSL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03453 | hp2 | a0001 | c0003 | t0010 | g0004 | AFR | MSL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0133 | AFR | MSL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03516 | hp1 | a0001 | c0001 | t0015 | g0033 | AFR | ESN | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03516 | hp2 | a0001 | c0003 | t0026 | g0199 | AFR | ESN | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03540 | hp1 | a0001 | c0001 | t0025 | g0194 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03579 | hp1 | a0001 | c0001 | t0051 | g0109 | AFR | MSL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0078 | SAS | PJL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | STU | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0081 | SAS | PJL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03927 | hp1 | a0002 | c0004 | t0001 | g0011 | SAS | BEB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03927 | hp2 | a0001 | c0001 | t0021 | g0022 | SAS | BEB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0066 | SAS | BEB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0072 | SAS | BEB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | BEB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG04184 | hp2 | a0001 | c0001 | t0021 | g0016 | SAS | BEB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0057 | SAS | STU | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | STU | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18522 | hp1 | a0001 | c0001 | t0036 | g0169 | AFR | YRI | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18747 | hp2 | a0001 | c0001 | t0041 | g0047 | EAS | CHB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | YRI | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0101 | AFR | YRI | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18939 | hp2 | a0001 | c0001 | t0020 | g0024 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18940 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18943 | hp1 | a0002 | c0004 | t0001 | g0137 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18943 | hp2 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18949 | hp2 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18951 | hp1 | a0001 | c0001 | t0007 | g0164 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18960 | hp1 | a0001 | c0001 | t0039 | g0166 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18964 | hp1 | a0001 | c0001 | t0014 | g0128 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18964 | hp2 | a0002 | c0004 | t0011 | g0175 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18966 | hp2 | a0001 | c0001 | t0014 | g0025 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18972 | hp2 | a0001 | c0001 | t0011 | g0112 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18979 | hp1 | a0001 | c0001 | t0013 | g0025 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18980 | hp1 | a0001 | c0001 | t0020 | g0024 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0212 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19004 | hp1 | a0001 | c0001 | t0007 | g0056 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19005 | hp2 | a0002 | c0004 | t0001 | g0011 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19011 | hp2 | a0001 | c0001 | t0049 | g0153 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | LWK | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19043 | hp1 | a0001 | c0001 | t0046 | g0063 | AFR | LWK | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19043 | hp2 | a0001 | c0001 | t0019 | g0130 | AFR | LWK | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19056 | hp2 | a0001 | c0001 | t0014 | g0213 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19060 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19062 | hp1 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19067 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19070 | hp2 | a0001 | c0001 | t0013 | g0001 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19079 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19088 | hp1 | a0001 | c0001 | t0013 | g0031 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19240 | hp1 | a0001 | c0001 | t0033 | g0190 | AFR | YRI | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA19240 | hp2 | a0001 | c0001 | t0043 | g0091 | AFR | YRI | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0195 | AFR | ASW | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ASW | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | TSI | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0127 | EUR | TSI | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02486 | hp1 | a0001 | c0001 | t0030 | g0077 | AFR | ACB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02486 | hp2 | a0001 | c0001 | t0044 | g0119 | AFR | ACB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | ACB | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03471 | hp1 | a0001 | c0001 | t0032 | g0187 | AFR | MSL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG03471 | hp2 | a0001 | c0001 | t0012 | g0103 | AFR | MSL | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0139 | AFR | USA | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | USA | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | USA | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA20300 | hp2 | a0001 | c0001 | t0042 | g0126 | AFR | USA | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | LWK | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0017 | REF | REF | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0021 | REF | REF | HRH2_chr5_175653071_175715756 | HRH2 | chr5 | 175653071 | 175715756 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:175707802 | C | T | 1 | a0003 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.1100C>T | p.Thr367Met | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 1710/4664 | 1100/1269 | 367/422 | chr5 | 175707802 | |||
| chr5:175707910 | A | T | 1 | a0002 | 4 | HG03927.hp1 NA18943.hp1 NA18964.hp2 others(1): Show |
missense_variant | MODERATE | c.1208A>T | p.Glu403Val | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 1818/4664 | 1208/1269 | 403/422 | chr5 | 175707910 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:175683278 | C | T | 1 | a0001c0003 | 10 | HG02145.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
synonymous_variant | LOW | c.45C>T | p.Thr15Thr | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/3 | 655/4664 | 45/1269 | 15/422 | chr5 | 175683278 | |||
| chr5:175683587 | C | T | 1 | a0001c0007 | 1 | HG02083.hp1 | synonymous_variant | LOW | c.354C>T | p.Cys118Cys | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/3 | 964/4664 | 354/1269 | 118/422 | chr5 | 175683587 | |||
| chr5:175683608 | G | T | 1 | a0001c0006 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.375G>T | p.Arg125Arg | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/3 | 985/4664 | 375/1269 | 125/422 | chr5 | 175683608 | |||
| chr5:175683776 | G | A | 1 | a0001c0002 | 11 | HG01106.hp1 HG01361.hp2 HG02300.hp1 others(8): Show |
synonymous_variant | LOW | c.543G>A | p.Val181Val | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/3 | 1153/4664 | 543/1269 | 181/422 | chr5 | 175683776 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:175682729 | C | G | 1 | a0001c0001t0052 | 1 | HG01069.hp2 | 5_prime_UTR_variant | MODIFIER | c.-505C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/3 | 505 | chr5 | 175682729 | ||||||
| chr5:175682807 | G | A | 3 | a0001c0001t0009 a0001c0001t0015 a0001c0001t0024 |
6 | HG01109.hp2 HG02809.hp2 HG02922.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-427G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/3 | 427 | chr5 | 175682807 | ||||||
| chr5:175682885 | C | T | 1 | a0001c0001t0051 | 1 | HG03579.hp1 | 5_prime_UTR_variant | MODIFIER | c.-349C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/3 | 349 | chr5 | 175682885 | ||||||
| chr5:175682969 | G | A | 8 | a0001c0001t0016 a0001c0001t0025 a0001c0003t0010 others(5): Show |
13 | HG01891.hp2 HG02145.hp1 HG02451.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-265G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/3 | 265 | chr5 | 175682969 | ||||||
| chr5:175683091 | C | CAAA | 9 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0015 others(6): Show |
14 | HG01109.hp2 HG02615.hp2 HG02622.hp2 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-124_-122dupAAA | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/3 | 121 | INFO_REALIGN_3_PRIME | chr5 | 175683091 | |||||
| chr5:175683091 | C | CAAAA | 15 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0008 others(12): Show |
45 | HG00438.hp2 HG00558.hp2 HG01891.hp2 others(42): Show |
5_prime_UTR_variant | MODIFIER | c.-125_-122dupAAAA | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/3 | 121 | INFO_REALIGN_3_PRIME | chr5 | 175683091 | |||||
| chr5:175683091 | C | CAAAAA | 7 | a0001c0001t0005 a0001c0001t0025 a0001c0001t0030 others(4): Show |
16 | HG02257.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-126_-122dupAAAAA | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/3 | 121 | INFO_REALIGN_3_PRIME | chr5 | 175683091 | |||||
| chr5:175683143 | G | A | 1 | a0001c0001t0033 | 1 | NA19240.hp1 | 5_prime_UTR_variant | MODIFIER | c.-91G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/3 | 91 | chr5 | 175683143 | ||||||
| chr5:175708072 | G | A | 1 | a0001c0001t0041 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*101G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 101 | chr5 | 175708072 | ||||||
| chr5:175708131 | C | T | 1 | a0001c0003t0028 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*160C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 160 | chr5 | 175708131 | ||||||
| chr5:175708190 | C | T | 7 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0032 others(4): Show |
17 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*219C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 219 | chr5 | 175708190 | ||||||
| chr5:175708191 | G | A | 2 | a0001c0001t0034 a0001c0006t0029 |
2 | HG03139.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*220G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 220 | chr5 | 175708191 | ||||||
| chr5:175708258 | G | A | 1 | a0001c0001t0042 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*287G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 287 | chr5 | 175708258 | ||||||
| chr5:175708298 | G | T | 1 | a0001c0001t0050 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*327G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 327 | chr5 | 175708298 | ||||||
| chr5:175708313 | G | A | 10 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0016 others(7): Show |
34 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*342G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 342 | chr5 | 175708313 | ||||||
| chr5:175708363 | C | T | 1 | a0001c0001t0035 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*392C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 392 | chr5 | 175708363 | ||||||
| chr5:175708396 | G | GAAAGGAA others(10): Show |
1 | a0001c0001t0044 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*427_*443dupAAGGAA others(11): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 444 | INFO_REALIGN_3_PRIME | chr5 | 175708396 | |||||
| chr5:175708517 | A | T | 7 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0032 others(4): Show |
17 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*546A>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 546 | chr5 | 175708517 | ||||||
| chr5:175708862 | A | G | 2 | a0001c0001t0033 a0001c0001t0043 |
2 | NA19240.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*891A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 891 | chr5 | 175708862 | ||||||
| chr5:175708903 | T | G | 29 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(26): Show |
69 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*932T>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 932 | chr5 | 175708903 | ||||||
| chr5:175709140 | G | T | 2 | a0001c0001t0014 a0001c0001t0020 |
5 | NA18939.hp2 NA18964.hp1 NA18966.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1169G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 1169 | chr5 | 175709140 | ||||||
| chr5:175709235 | G | A | 1 | a0001c0001t0015 | 2 | HG02922.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1264G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 1264 | chr5 | 175709235 | ||||||
| chr5:175709428 | G | A | 1 | a0001c0001t0032 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1457G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 1457 | chr5 | 175709428 | ||||||
| chr5:175709448 | C | T | 2 | a0001c0001t0007 a0001c0001t0039 |
6 | HG02132.hp1 NA18949.hp2 NA18951.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1477C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 1477 | chr5 | 175709448 | ||||||
| chr5:175709487 | T | C | 2 | a0001c0001t0025 a0001c0001t0045 |
2 | HG03209.hp1 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1516T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 1516 | chr5 | 175709487 | ||||||
| chr5:175709488 | C | G | 4 | a0001c0001t0031 a0001c0001t0037 a0001c0001t0046 others(1): Show |
4 | HG02572.hp2 HG03130.hp1 HG03516.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1517C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 1517 | chr5 | 175709488 | ||||||
| chr5:175709501 | TCTGCAGC others(7): Show |
T | 20 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0012 others(17): Show |
35 | HG01243.hp2 HG01256.hp2 HG01258.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1549_*1562delAGCT others(10): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 1549 | INFO_REALIGN_3_PRIME | chr5 | 175709501 | |||||
| chr5:175709613 | C | A | 1 | a0001c0001t0047 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1642C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 1642 | chr5 | 175709613 | ||||||
| chr5:175709626 | G | A | 1 | a0001c0001t0036 | 1 | NA18522.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1655G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 1655 | chr5 | 175709626 | ||||||
| chr5:175709764 | A | C | 1 | a0001c0001t0013 | 3 | NA18979.hp1 NA19070.hp2 NA19088.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1793A>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 1793 | chr5 | 175709764 | ||||||
| chr5:175709779 | T | C | 13 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0016 others(10): Show |
39 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1808T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 1808 | chr5 | 175709779 | ||||||
| chr5:175709889 | C | G | 1 | a0001c0001t0022 | 2 | HG00642.hp2 HG01081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1918C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 1918 | chr5 | 175709889 | ||||||
| chr5:175709965 | T | C | 1 | a0001c0003t0028 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1994T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 1994 | chr5 | 175709965 | ||||||
| chr5:175710104 | C | T | 1 | a0001c0001t0021 | 2 | HG03927.hp2 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2133C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 2133 | chr5 | 175710104 | ||||||
| chr5:175710214 | C | T | 2 | a0001c0001t0030 a0001c0001t0051 |
2 | HG02486.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2243C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 2243 | chr5 | 175710214 | ||||||
| chr5:175710227 | A | G | 1 | a0001c0001t0049 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2256A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 2256 | chr5 | 175710227 | ||||||
| chr5:175710312 | G | C | 1 | a0001c0001t0048 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2341G>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 2341 | chr5 | 175710312 | ||||||
| chr5:175710600 | G | T | 1 | a0001c0001t0038 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2629G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 3/3 | 2629 | chr5 | 175710600 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:175658295 | T | G | 6 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0035 others(3): Show |
7 | HG00558.hp2 HG00639.hp2 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.-526+140T>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175658295 | |||||||
| chr5:175658337 | G | T | 4 | a0001c0001t0006g0216 a0001c0001t0009g0215 a0001c0001t0015g0033 others(1): Show |
5 | HG01884.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-526+182G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175658337 | |||||||
| chr5:175658437 | C | T | 2 | a0001c0001t0031g0032 a0001c0001t0037g0032 |
2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-526+282C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175658437 | |||||||
| chr5:175658699 | T | TGCC | 16 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(13): Show |
19 | HG00408.hp2 HG00597.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.-526+548_-526+550d others(5): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 175658699 | ||||||
| chr5:175658713 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-526+558G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175658713 | |||||||
| chr5:175658713 | G | GGATGACC | 39 | a0001c0001t0001g0012 a0001c0001t0001g0041 a0001c0001t0001g0045 others(36): Show |
44 | HG00438.hp1 HG02055.hp1 HG02055.hp2 others(41): Show |
intron_variant | MODIFIER | c.-526+567_-526+573d others(9): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 175658713 | ||||||
| chr5:175658728 | G | A | 1 | a0001c0001t0004g0040 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-526+573G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175658728 | |||||||
| chr5:175659454 | T | A | 56 | a0001c0001t0001g0012 a0001c0001t0001g0041 a0001c0001t0001g0045 others(53): Show |
61 | HG00408.hp2 HG00438.hp1 HG01081.hp1 others(58): Show |
intron_variant | MODIFIER | c.-526+1299T>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175659454 | |||||||
| chr5:175659718 | C | A | 1 | a0001c0001t0001g0089 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-526+1563C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175659718 | |||||||
| chr5:175659907 | A | G | 1 | a0001c0001t0005g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-526+1752A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175659907 | |||||||
| chr5:175659915 | A | G | 1 | a0001c0003t0018g0201 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-526+1760A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175659915 | |||||||
| chr5:175659953 | C | A | 12 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(9): Show |
12 | HG00408.hp2 HG01081.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.-526+1798C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175659953 | |||||||
| chr5:175660108 | G | A | 38 | a0001c0001t0001g0012 a0001c0001t0001g0041 a0001c0001t0001g0045 others(35): Show |
43 | HG00438.hp1 HG02055.hp1 HG02055.hp2 others(40): Show |
intron_variant | MODIFIER | c.-526+1953G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175660108 | |||||||
| chr5:175660239 | G | A | 13 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(10): Show |
13 | HG00408.hp2 HG01081.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.-526+2084G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175660239 | |||||||
| chr5:175660289 | T | A | 7 | a0001c0001t0003g0014 a0001c0001t0005g0092 a0001c0001t0009g0094 others(4): Show |
8 | HG01109.hp2 HG02145.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-526+2134T>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175660289 | |||||||
| chr5:175660365 | C | A | 38 | a0001c0001t0001g0012 a0001c0001t0001g0041 a0001c0001t0001g0045 others(35): Show |
43 | HG00438.hp1 HG02055.hp1 HG02055.hp2 others(40): Show |
intron_variant | MODIFIER | c.-526+2210C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175660365 | |||||||
| chr5:175660367 | A | T | 1 | a0001c0001t0012g0200 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-526+2212A>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175660367 | |||||||
| chr5:175660534 | T | C | 7 | a0001c0001t0001g0098 a0001c0001t0002g0097 a0001c0001t0003g0100 others(4): Show |
7 | HG02559.hp2 HG02615.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-526+2379T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175660534 | |||||||
| chr5:175660723 | G | A | 7 | a0001c0001t0003g0014 a0001c0001t0005g0092 a0001c0001t0009g0094 others(4): Show |
8 | HG01109.hp2 HG02145.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-526+2568G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175660723 | |||||||
| chr5:175661264 | GTTGCCAG others(19): Show |
G | 1 | a0001c0003t0026g0199 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-526+3120_-526+314 others(30): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 175661264 | ||||||
| chr5:175661275 | A | C | 86 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0041 others(83): Show |
94 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.-526+3120A>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175661275 | |||||||
| chr5:175661325 | G | T | 5 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0002g0087 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.-526+3170G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175661325 | |||||||
| chr5:175661401 | A | G | 12 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(9): Show |
12 | HG00408.hp2 HG01081.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.-526+3246A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175661401 | |||||||
| chr5:175661432 | T | G | 17 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0016 others(14): Show |
19 | HG00558.hp2 HG00639.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.-526+3277T>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175661432 | |||||||
| chr5:175661650 | A | G | 87 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0041 others(84): Show |
95 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.-526+3495A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175661650 | |||||||
| chr5:175661784 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-526+3629G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175661784 | |||||||
| chr5:175661807 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-526+3652G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175661807 | |||||||
| chr5:175661894 | C | T | 6 | a0001c0001t0001g0098 a0001c0001t0002g0097 a0001c0001t0003g0100 others(3): Show |
6 | HG02559.hp2 HG02615.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-526+3739C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175661894 | |||||||
| chr5:175661973 | G | C | 25 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(22): Show |
26 | HG00408.hp2 HG01081.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.-526+3818G>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175661973 | |||||||
| chr5:175662022 | A | AAAAT | 62 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0041 others(59): Show |
69 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.-526+3891_-526+389 others(8): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 175662022 | ||||||
| chr5:175662078 | G | A | 11 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(8): Show |
12 | HG01109.hp2 HG02145.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.-526+3923G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175662078 | |||||||
| chr5:175662090 | G | A | 1 | a0001c0001t0005g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-526+3935G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175662090 | |||||||
| chr5:175662118 | G | A | 4 | a0001c0001t0004g0186 a0001c0001t0004g0188 a0001c0001t0008g0189 others(1): Show |
4 | HG02145.hp2 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-526+3963G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175662118 | |||||||
| chr5:175662400 | C | A | 1 | a0001c0001t0033g0190 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-526+4245C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175662400 | |||||||
| chr5:175662404 | A | G | 24 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(21): Show |
25 | HG00408.hp2 HG01081.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-526+4249A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175662404 | |||||||
| chr5:175662584 | C | G | 1 | a0001c0001t0003g0072 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-526+4429C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175662584 | |||||||
| chr5:175662656 | C | G | 14 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0004g0186 others(11): Show |
15 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-526+4501C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175662656 | |||||||
| chr5:175663118 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-526+4963C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175663118 | |||||||
| chr5:175663298 | C | T | 83 | a0001c0001t0001g0012 a0001c0001t0001g0041 a0001c0001t0001g0045 others(80): Show |
90 | HG00408.hp2 HG00438.hp1 HG01081.hp1 others(87): Show |
intron_variant | MODIFIER | c.-526+5143C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175663298 | |||||||
| chr5:175663367 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-526+5212C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175663367 | |||||||
| chr5:175663384 | G | A | 2 | a0001c0001t0005g0113 a0001c0001t0011g0112 |
2 | NA18972.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-526+5229G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175663384 | |||||||
| chr5:175663516 | A | G | 42 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0041 others(39): Show |
48 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-526+5361A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175663516 | |||||||
| chr5:175663525 | G | T | 2 | a0001c0001t0001g0179 a0001c0001t0048g0180 |
2 | HG01255.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-526+5370G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175663525 | |||||||
| chr5:175663917 | A | G | 4 | a0001c0001t0004g0186 a0001c0001t0004g0188 a0001c0001t0008g0189 others(1): Show |
4 | HG02145.hp2 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-526+5762A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175663917 | |||||||
| chr5:175663948 | C | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0176 a0001c0001t0001g0177 others(16): Show |
27 | HG00408.hp1 HG01192.hp2 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.-526+5793C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175663948 | |||||||
| chr5:175664109 | G | A | 48 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0041 others(45): Show |
54 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.-526+5954G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175664109 | |||||||
| chr5:175664440 | G | A | 11 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0002g0097 others(8): Show |
12 | HG01884.hp1 HG01891.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-526+6285G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175664440 | |||||||
| chr5:175664528 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-526+6373G>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175664528 | |||||||
| chr5:175664540 | G | A | 4 | a0001c0001t0004g0186 a0001c0001t0004g0188 a0001c0001t0008g0189 others(1): Show |
4 | HG02145.hp2 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-526+6385G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175664540 | |||||||
| chr5:175664616 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-526+6461G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175664616 | |||||||
| chr5:175664633 | T | C | 3 | a0001c0001t0006g0042 a0001c0001t0008g0043 a0001c0001t0008g0044 |
3 | HG02818.hp2 HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-526+6478T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175664633 | |||||||
| chr5:175664659 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-526+6504T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175664659 | |||||||
| chr5:175664670 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-526+6515T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175664670 | |||||||
| chr5:175664683 | G | A | 1 | a0001c0001t0005g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-526+6528G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175664683 | |||||||
| chr5:175664695 | C | T | 13 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(10): Show |
13 | HG00408.hp2 HG01081.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.-526+6540C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175664695 | |||||||
| chr5:175664720 | G | A | 7 | a0001c0001t0001g0098 a0001c0001t0002g0097 a0001c0001t0003g0100 others(4): Show |
7 | HG02559.hp2 HG02615.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.-526+6565G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175664720 | |||||||
| chr5:175664739 | G | A | 87 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0041 others(84): Show |
95 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.-526+6584G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175664739 | |||||||
| chr5:175664800 | C | G | 1 | a0001c0001t0001g0182 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-526+6645C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175664800 | |||||||
| chr5:175664901 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-526+6746G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175664901 | |||||||
| chr5:175664975 | C | T | 1 | a0001c0001t0005g0113 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-526+6820C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175664975 | |||||||
| chr5:175665068 | G | C | 110 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(107): Show |
120 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.-526+6913G>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175665068 | |||||||
| chr5:175665096 | G | A | 1 | a0001c0001t0005g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-526+6941G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175665096 | |||||||
| chr5:175665242 | G | C | 1 | a0001c0001t0001g0076 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-526+7087G>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175665242 | |||||||
| chr5:175665243 | G | T | 48 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0041 others(45): Show |
54 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.-526+7088G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175665243 | |||||||
| chr5:175665253 | C | T | 4 | a0001c0001t0004g0186 a0001c0001t0004g0188 a0001c0001t0008g0189 others(1): Show |
4 | HG02145.hp2 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-526+7098C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175665253 | |||||||
| chr5:175665352 | G | A | 10 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0003g0014 others(7): Show |
11 | HG01109.hp2 HG02145.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.-526+7197G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175665352 | |||||||
| chr5:175665542 | G | A | 4 | a0001c0001t0004g0186 a0001c0001t0004g0188 a0001c0001t0008g0189 others(1): Show |
4 | HG02145.hp2 HG02630.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.-526+7387G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175665542 | |||||||
| chr5:175665590 | C | T | 1 | a0001c0001t0005g0084 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-526+7435C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175665590 | |||||||
| chr5:175665591 | G | A | 7 | a0001c0001t0003g0014 a0001c0001t0005g0092 a0001c0001t0009g0094 others(4): Show |
8 | HG01109.hp2 HG02145.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-526+7436G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175665591 | |||||||
| chr5:175665741 | T | G | 5 | a0001c0001t0001g0116 a0001c0001t0004g0186 a0001c0001t0004g0188 others(2): Show |
5 | HG02145.hp2 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-526+7586T>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175665741 | |||||||
| chr5:175665776 | A | G | 3 | a0001c0001t0001g0076 a0001c0002t0002g0082 a0001c0002t0002g0083 |
3 | HG01106.hp1 HG01433.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-526+7621A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175665776 | |||||||
| chr5:175665839 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-526+7684G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175665839 | |||||||
| chr5:175665906 | A | G | 5 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0004g0040 others(2): Show |
5 | HG02257.hp2 HG02886.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-526+7751A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175665906 | |||||||
| chr5:175665915 | A | AG | 5 | a0001c0001t0001g0116 a0001c0001t0004g0186 a0001c0001t0004g0188 others(2): Show |
5 | HG02145.hp2 HG02630.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-526+7761dupG | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 175665915 | ||||||
| chr5:175666095 | A | C | 1 | a0001c0001t0004g0192 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-526+7940A>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175666095 | |||||||
| chr5:175666372 | T | C | 116 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(113): Show |
130 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-526+8217T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175666372 | |||||||
| chr5:175666404 | C | G | 10 | a0001c0001t0002g0106 a0001c0001t0003g0014 a0001c0001t0005g0092 others(7): Show |
11 | HG01109.hp2 HG02622.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.-526+8249C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175666404 | |||||||
| chr5:175666461 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-526+8306C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175666461 | |||||||
| chr5:175666468 | T | C | 21 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0086 others(18): Show |
22 | HG01884.hp2 HG01891.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-526+8313T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175666468 | |||||||
| chr5:175666620 | A | G | 24 | a0001c0001t0001g0041 a0001c0001t0001g0069 a0001c0001t0001g0070 others(21): Show |
25 | HG02055.hp1 HG02055.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.-526+8465A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175666620 | |||||||
| chr5:175666925 | G | A | 2 | a0001c0001t0016g0085 a0001c0001t0016g0193 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-526+8770G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175666925 | |||||||
| chr5:175667017 | C | CATATAT | 7 | a0001c0001t0001g0062 a0001c0001t0005g0084 a0001c0001t0009g0094 others(4): Show |
8 | HG01109.hp2 HG02145.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-526+8871_-526+887 others(10): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 175667017 | ||||||
| chr5:175667017 | C | CATATATA others(3): Show |
1 | a0001c0001t0016g0193 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-526+8867_-526+887 others(14): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 175667017 | ||||||
| chr5:175667017 | C | CATATATA others(5): Show |
1 | a0001c0001t0016g0085 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-526+8865_-526+887 others(16): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 175667017 | ||||||
| chr5:175667017 | C | CATATATA others(15): Show |
1 | a0001c0001t0030g0077 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-526+8876_-526+887 others(26): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 175667017 | ||||||
| chr5:175667027 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0134 others(1): Show |
7 | HG01069.hp1 HG01070.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.-526+8872T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175667027 | |||||||
| chr5:175667075 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-526+8920A>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175667075 | |||||||
| chr5:175667166 | G | A | 1 | a0001c0001t0012g0200 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-526+9011G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175667166 | |||||||
| chr5:175667186 | G | A | 2 | a0001c0001t0016g0085 a0001c0001t0016g0193 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-526+9031G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175667186 | |||||||
| chr5:175667250 | T | C | 1 | a0001c0001t0003g0136 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-526+9095T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175667250 | |||||||
| chr5:175667401 | A | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0028 others(110): Show |
130 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.-526+9246A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175667401 | |||||||
| chr5:175667451 | C | G | 28 | a0001c0001t0003g0002 a0001c0001t0003g0066 a0001c0001t0003g0072 others(25): Show |
31 | HG00558.hp2 HG01243.hp2 HG02015.hp2 others(28): Show |
intron_variant | MODIFIER | c.-526+9296C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175667451 | |||||||
| chr5:175667809 | G | A | 2 | a0001c0001t0001g0138 a0002c0004t0001g0137 |
2 | NA18943.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-526+9654G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175667809 | |||||||
| chr5:175667956 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-526+9801G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175667956 | |||||||
| chr5:175668279 | G | C | 1 | a0001c0001t0006g0099 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-526+10124G>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175668279 | |||||||
| chr5:175668314 | C | T | 6 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0007g0056 others(3): Show |
7 | NA18940.hp1 NA18969.hp1 NA18979.hp2 others(4): Show |
intron_variant | MODIFIER | c.-526+10159C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175668314 | |||||||
| chr5:175668368 | A | G | 5 | a0001c0001t0002g0106 a0001c0001t0003g0014 a0001c0001t0005g0092 others(2): Show |
6 | HG02622.hp1 HG02970.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-526+10213A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175668368 | |||||||
| chr5:175668393 | TGTTGCTC others(5): Show |
T | 1 | a0001c0001t0005g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-526+10241_-526+10 others(18): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 175668393 | ||||||
| chr5:175668720 | C | A | 29 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0028 others(26): Show |
38 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.-526+10565C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175668720 | |||||||
| chr5:175669352 | ATTTC | A | 2 | a0001c0001t0001g0036 a0001c0001t0023g0019 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-526+11209_-526+11 others(10): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 175669352 | ||||||
| chr5:175669364 | CT | C | 90 | a0001c0001t0001g0041 a0001c0001t0001g0054 a0001c0001t0001g0055 others(87): Show |
99 | HG00558.hp1 HG00558.hp2 HG01106.hp1 others(96): Show |
intron_variant | MODIFIER | c.-526+11226delT | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 175669364 | ||||||
| chr5:175669369 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-526+11214T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175669369 | |||||||
| chr5:175669373 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-526+11218T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175669373 | |||||||
| chr5:175669433 | G | A | 1 | a0001c0001t0019g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-526+11278G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175669433 | |||||||
| chr5:175669564 | A | G | 1 | a0001c0001t0015g0033 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-526+11409A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175669564 | |||||||
| chr5:175669624 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0134 others(1): Show |
7 | HG01069.hp1 HG01070.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.-526+11469G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175669624 | |||||||
| chr5:175669653 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-526+11498G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175669653 | |||||||
| chr5:175669892 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-526+11737A>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175669892 | |||||||
| chr5:175670040 | G | A | 9 | a0001c0001t0016g0085 a0001c0001t0016g0193 a0001c0001t0025g0194 others(6): Show |
11 | HG01891.hp2 HG02451.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-526+11885G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175670040 | |||||||
| chr5:175670187 | A | T | 1 | a0001c0001t0001g0160 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-526+12032A>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175670187 | |||||||
| chr5:175670274 | A | AT | 10 | a0001c0001t0002g0097 a0001c0001t0003g0060 a0001c0001t0003g0100 others(7): Show |
10 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-526+12129dupT | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 175670274 | ||||||
| chr5:175670274 | A | ATT | 6 | a0001c0003t0010g0004 a0001c0003t0017g0168 a0001c0003t0018g0181 others(3): Show |
8 | HG02451.hp1 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-526+12128_-526+12 others(8): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr5 | 175670274 | ||||||
| chr5:175670417 | G | A | 1 | a0002c0004t0001g0137 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-526+12262G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175670417 | |||||||
| chr5:175670589 | C | T | 1 | a0001c0001t0019g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-525-12120C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175670589 | |||||||
| chr5:175670746 | A | G | 1 | a0001c0001t0019g0130 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-525-11963A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175670746 | |||||||
| chr5:175670784 | G | T | 28 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0001t0002g0097 others(25): Show |
32 | HG01109.hp2 HG01891.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.-525-11925G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175670784 | |||||||
| chr5:175670932 | A | G | 7 | a0001c0003t0010g0004 a0001c0003t0017g0168 a0001c0003t0018g0181 others(4): Show |
9 | HG02451.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-525-11777A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175670932 | |||||||
| chr5:175671082 | T | C | 12 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0001t0003g0013 others(9): Show |
14 | HG01109.hp2 HG02486.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.-525-11627T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175671082 | |||||||
| chr5:175671235 | G | A | 7 | a0001c0003t0010g0004 a0001c0003t0017g0168 a0001c0003t0018g0181 others(4): Show |
9 | HG02451.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-525-11474G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175671235 | |||||||
| chr5:175671644 | A | T | 7 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0001t0001g0124 others(4): Show |
8 | HG01243.hp2 HG02647.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-525-11065A>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175671644 | |||||||
| chr5:175671795 | C | T | 1 | a0001c0001t0014g0213 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-525-10914C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175671795 | |||||||
| chr5:175671932 | G | A | 7 | a0001c0001t0009g0094 a0001c0001t0009g0133 a0001c0001t0009g0215 others(4): Show |
8 | HG01109.hp2 HG02486.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-525-10777G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175671932 | |||||||
| chr5:175672059 | A | T | 14 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0001t0001g0124 others(11): Show |
16 | HG01109.hp2 HG01243.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-525-10650A>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175672059 | |||||||
| chr5:175672419 | G | A | 5 | a0001c0001t0002g0097 a0001c0001t0003g0060 a0001c0001t0003g0100 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-525-10290G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175672419 | |||||||
| chr5:175672496 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-525-10213T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175672496 | |||||||
| chr5:175672608 | G | A | 1 | a0001c0003t0027g0105 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-525-10101G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175672608 | |||||||
| chr5:175672668 | T | C | 2 | a0001c0001t0001g0062 a0001c0001t0005g0084 |
2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-525-10041T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175672668 | |||||||
| chr5:175672760 | T | C | 1 | a0001c0001t0025g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-525-9949T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175672760 | |||||||
| chr5:175672799 | G | A | 7 | a0001c0001t0002g0097 a0001c0001t0003g0060 a0001c0001t0003g0100 others(4): Show |
7 | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-525-9910G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175672799 | |||||||
| chr5:175672875 | T | C | 14 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0001t0001g0124 others(11): Show |
16 | HG01109.hp2 HG01243.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-525-9834T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175672875 | |||||||
| chr5:175672898 | C | T | 1 | a0001c0001t0002g0159 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-525-9811C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175672898 | |||||||
| chr5:175672990 | G | A | 11 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0015 others(8): Show |
15 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.-525-9719G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175672990 | |||||||
| chr5:175673263 | G | A | 12 | a0001c0001t0001g0076 a0001c0001t0003g0066 a0001c0002t0001g0026 others(9): Show |
13 | HG01106.hp1 HG01361.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.-525-9446G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175673263 | |||||||
| chr5:175673323 | G | A | 17 | a0001c0001t0002g0097 a0001c0001t0003g0060 a0001c0001t0003g0100 others(14): Show |
19 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-525-9386G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175673323 | |||||||
| chr5:175673515 | G | C | 17 | a0001c0001t0002g0097 a0001c0001t0003g0060 a0001c0001t0003g0100 others(14): Show |
19 | HG01891.hp2 HG02055.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-525-9194G>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175673515 | |||||||
| chr5:175673704 | T | G | 1 | a0001c0001t0001g0080 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-525-9005T>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175673704 | |||||||
| chr5:175673709 | G | T | 2 | a0001c0001t0001g0124 a0001c0001t0012g0131 |
2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-525-9000G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175673709 | |||||||
| chr5:175673718 | T | G | 15 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0001t0001g0124 others(12): Show |
17 | HG01109.hp2 HG01243.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.-525-8991T>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175673718 | |||||||
| chr5:175673746 | C | T | 1 | a0001c0001t0039g0166 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-525-8963C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175673746 | |||||||
| chr5:175673774 | G | A | 3 | a0001c0001t0004g0195 a0001c0001t0008g0043 a0001c0001t0008g0044 |
3 | HG02818.hp2 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-525-8935G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175673774 | |||||||
| chr5:175673829 | C | T | 4 | a0001c0001t0003g0014 a0001c0001t0005g0092 a0001c0001t0006g0101 others(1): Show |
5 | HG02970.hp1 HG02970.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-525-8880C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175673829 | |||||||
| chr5:175673839 | G | C | 19 | a0001c0001t0002g0097 a0001c0001t0003g0060 a0001c0001t0003g0100 others(16): Show |
21 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.-525-8870G>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175673839 | |||||||
| chr5:175673929 | T | G | 2 | a0001c0001t0001g0124 a0001c0001t0012g0131 |
2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-525-8780T>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175673929 | |||||||
| chr5:175674217 | G | A | 5 | a0001c0001t0002g0097 a0001c0001t0003g0060 a0001c0001t0003g0100 others(2): Show |
5 | HG02055.hp2 HG02258.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-525-8492G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175674217 | |||||||
| chr5:175674227 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-525-8482G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175674227 | |||||||
| chr5:175674413 | T | C | 1 | a0001c0001t0001g0008 | 3 | HG01256.hp1 HG01258.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.-525-8296T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175674413 | |||||||
| chr5:175674715 | C | T | 11 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0001t0003g0013 others(8): Show |
13 | HG01109.hp2 HG02647.hp1 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.-525-7994C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175674715 | |||||||
| chr5:175674846 | C | T | 1 | a0001c0001t0001g0123 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-525-7863C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175674846 | |||||||
| chr5:175675152 | A | C | 3 | a0001c0001t0001g0211 a0001c0001t0007g0164 a0001c0001t0042g0126 |
3 | HG00733.hp2 NA18951.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-525-7557A>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175675152 | |||||||
| chr5:175675205 | C | G | 11 | a0001c0001t0001g0076 a0001c0002t0001g0026 a0001c0002t0001g0052 others(8): Show |
12 | HG01106.hp1 HG01361.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.-525-7504C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175675205 | |||||||
| chr5:175675582 | G | T | 3 | a0001c0001t0001g0138 a0002c0004t0001g0011 a0002c0004t0001g0137 |
4 | HG03927.hp1 NA18943.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.-525-7127G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175675582 | |||||||
| chr5:175675635 | G | A | 1 | a0001c0001t0002g0106 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-525-7074G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175675635 | |||||||
| chr5:175675709 | A | C | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | HG01358.hp2 HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-525-7000A>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175675709 | |||||||
| chr5:175675777 | C | T | 1 | a0001c0002t0002g0083 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-525-6932C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175675777 | |||||||
| chr5:175675893 | A | G | 2 | a0001c0001t0001g0124 a0001c0001t0012g0131 |
2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-525-6816A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175675893 | |||||||
| chr5:175675923 | A | T | 2 | a0001c0001t0001g0124 a0001c0001t0012g0131 |
2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-525-6786A>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175675923 | |||||||
| chr5:175675975 | A | G | 2 | a0001c0001t0001g0124 a0001c0001t0012g0131 |
2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-525-6734A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175675975 | |||||||
| chr5:175676217 | A | C | 6 | a0001c0001t0004g0037 a0001c0001t0004g0038 a0001c0001t0005g0058 others(3): Show |
6 | HG00558.hp2 HG02015.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.-525-6492A>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175676217 | |||||||
| chr5:175676234 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0012g0131 |
2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-525-6475C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175676234 | |||||||
| chr5:175676262 | T | C | 1 | a0001c0001t0019g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-525-6447T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175676262 | |||||||
| chr5:175676321 | G | A | 1 | a0001c0001t0012g0200 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-525-6388G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175676321 | |||||||
| chr5:175676333 | A | G | 66 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0001t0001g0124 others(63): Show |
73 | HG00558.hp2 HG01109.hp2 HG01243.hp2 others(70): Show |
intron_variant | MODIFIER | c.-525-6376A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175676333 | |||||||
| chr5:175676515 | G | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0001t0005g0084 |
3 | HG02647.hp2 HG02895.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-525-6194G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175676515 | |||||||
| chr5:175676666 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-525-6043G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175676666 | |||||||
| chr5:175676700 | G | C | 2 | a0001c0001t0001g0124 a0001c0001t0012g0131 |
2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-525-6009G>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175676700 | |||||||
| chr5:175677100 | T | A | 2 | a0001c0001t0001g0124 a0001c0001t0012g0131 |
2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-525-5609T>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175677100 | |||||||
| chr5:175677106 | C | T | 1 | a0001c0001t0019g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-525-5603C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175677106 | |||||||
| chr5:175677111 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-525-5598C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175677111 | |||||||
| chr5:175677131 | C | A | 2 | a0001c0001t0001g0124 a0001c0001t0012g0131 |
2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-525-5578C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175677131 | |||||||
| chr5:175677158 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0012g0131 |
2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-525-5551C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175677158 | |||||||
| chr5:175677261 | C | G | 1 | a0001c0001t0012g0200 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-525-5448C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175677261 | |||||||
| chr5:175677325 | T | C | 2 | a0001c0001t0033g0190 a0001c0001t0034g0096 |
2 | HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-525-5384T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175677325 | |||||||
| chr5:175677382 | G | T | 11 | a0001c0001t0001g0076 a0001c0002t0001g0026 a0001c0002t0001g0052 others(8): Show |
12 | HG01106.hp1 HG01361.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.-525-5327G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175677382 | |||||||
| chr5:175677507 | G | A | 61 | a0001c0001t0001g0041 a0001c0001t0001g0062 a0001c0001t0001g0088 others(58): Show |
67 | HG00558.hp2 HG01109.hp2 HG01243.hp2 others(64): Show |
intron_variant | MODIFIER | c.-525-5202G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175677507 | |||||||
| chr5:175677677 | G | T | 1 | a0001c0001t0001g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-525-5032G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175677677 | |||||||
| chr5:175677885 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-525-4824A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175677885 | |||||||
| chr5:175677889 | C | T | 2 | a0001c0001t0002g0023 a0001c0001t0002g0172 |
3 | NA18993.hp1 NA19062.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-525-4820C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175677889 | |||||||
| chr5:175677961 | C | T | 1 | a0001c0001t0039g0166 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-525-4748C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175677961 | |||||||
| chr5:175677962 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-525-4747G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175677962 | |||||||
| chr5:175678064 | T | C | 64 | a0001c0001t0001g0041 a0001c0001t0001g0062 a0001c0001t0001g0088 others(61): Show |
71 | HG00558.hp2 HG01109.hp2 HG01243.hp2 others(68): Show |
intron_variant | MODIFIER | c.-525-4645T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175678064 | |||||||
| chr5:175678067 | T | C | 5 | a0001c0001t0009g0094 a0001c0001t0009g0133 a0001c0001t0009g0215 others(2): Show |
6 | HG01109.hp2 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-525-4642T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175678067 | |||||||
| chr5:175678275 | T | C | 1 | a0001c0001t0025g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-525-4434T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175678275 | |||||||
| chr5:175678601 | T | C | 15 | a0001c0001t0003g0060 a0001c0001t0003g0100 a0001c0001t0004g0061 others(12): Show |
17 | HG02055.hp2 HG02145.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.-525-4108T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175678601 | |||||||
| chr5:175678638 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-525-4071C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175678638 | |||||||
| chr5:175678850 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-525-3859C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175678850 | |||||||
| chr5:175679107 | C | G | 1 | a0001c0001t0025g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-525-3602C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175679107 | |||||||
| chr5:175679276 | C | T | 30 | a0001c0001t0003g0002 a0001c0001t0003g0014 a0001c0001t0003g0066 others(27): Show |
34 | HG00438.hp2 HG00558.hp2 HG02015.hp2 others(31): Show |
intron_variant | MODIFIER | c.-525-3433C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175679276 | |||||||
| chr5:175679293 | A | T | 32 | a0001c0001t0003g0002 a0001c0001t0003g0014 a0001c0001t0003g0072 others(29): Show |
36 | HG00438.hp2 HG00558.hp2 HG02015.hp2 others(33): Show |
intron_variant | MODIFIER | c.-525-3416A>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175679293 | |||||||
| chr5:175679581 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-525-3128G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175679581 | |||||||
| chr5:175679929 | C | A | 19 | a0001c0001t0003g0060 a0001c0001t0003g0100 a0001c0001t0004g0061 others(16): Show |
21 | HG01891.hp2 HG02055.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.-525-2780C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175679929 | |||||||
| chr5:175680019 | G | A | 1 | a0001c0001t0004g0188 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-525-2690G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175680019 | |||||||
| chr5:175680083 | G | T | 1 | a0001c0001t0034g0096 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-525-2626G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175680083 | |||||||
| chr5:175680196 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-525-2513C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175680196 | |||||||
| chr5:175680339 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-525-2370C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175680339 | |||||||
| chr5:175680456 | T | C | 2 | a0001c0001t0001g0124 a0001c0001t0012g0131 |
2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-525-2253T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175680456 | |||||||
| chr5:175680460 | T | C | 73 | a0001c0001t0001g0041 a0001c0001t0001g0062 a0001c0001t0001g0088 others(70): Show |
81 | HG00438.hp2 HG00558.hp2 HG01109.hp2 others(78): Show |
intron_variant | MODIFIER | c.-525-2249T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175680460 | |||||||
| chr5:175680486 | C | T | 2 | a0001c0001t0022g0125 a0001c0001t0023g0019 |
3 | HG00642.hp2 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-525-2223C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175680486 | |||||||
| chr5:175680777 | G | T | 1 | a0001c0002t0002g0081 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-525-1932G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175680777 | |||||||
| chr5:175680790 | G | T | 1 | a0001c0001t0001g0035 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-525-1919G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175680790 | |||||||
| chr5:175680950 | G | A | 5 | a0001c0001t0009g0094 a0001c0001t0009g0133 a0001c0001t0009g0215 others(2): Show |
6 | HG01109.hp2 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.-525-1759G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175680950 | |||||||
| chr5:175681723 | G | A | 2 | a0001c0001t0031g0032 a0001c0001t0037g0032 |
2 | HG02572.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-525-986G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175681723 | |||||||
| chr5:175682216 | G | A | 45 | a0001c0001t0001g0041 a0001c0001t0001g0062 a0001c0001t0001g0088 others(42): Show |
50 | HG00438.hp2 HG00558.hp2 HG02015.hp2 others(47): Show |
intron_variant | MODIFIER | c.-525-493G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175682216 | |||||||
| chr5:175682256 | A | G | 1 | a0001c0001t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-525-453A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175682256 | |||||||
| chr5:175682642 | A | G | 52 | a0001c0001t0001g0041 a0001c0001t0001g0062 a0001c0001t0001g0088 others(49): Show |
58 | HG00438.hp2 HG00558.hp2 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.-525-67A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 1/2 | chr5 | 175682642 | |||||||
| chr5:175684423 | C | T | 1 | a0001c0001t0006g0099 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1076+114C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175684423 | |||||||
| chr5:175684809 | G | C | 2 | a0001c0001t0003g0136 a0001c0001t0007g0009 |
4 | HG02132.hp1 NA18949.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+500G>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175684809 | |||||||
| chr5:175684813 | G | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
7 | HG01256.hp1 HG01258.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.1076+504G>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175684813 | |||||||
| chr5:175684861 | C | T | 2 | a0001c0001t0006g0101 a0001c0001t0006g0102 |
2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1076+552C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175684861 | |||||||
| chr5:175684970 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1076+661C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175684970 | |||||||
| chr5:175685009 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1076+700G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175685009 | |||||||
| chr5:175685074 | C | A | 1 | a0001c0001t0004g0188 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1076+765C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175685074 | |||||||
| chr5:175685118 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1076+809G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175685118 | |||||||
| chr5:175685320 | G | T | 66 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0001t0001g0124 others(63): Show |
73 | HG00438.hp2 HG00558.hp2 HG01109.hp2 others(70): Show |
intron_variant | MODIFIER | c.1076+1011G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175685320 | |||||||
| chr5:175685325 | A | G | 66 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0001t0001g0124 others(63): Show |
73 | HG00438.hp2 HG00558.hp2 HG01109.hp2 others(70): Show |
intron_variant | MODIFIER | c.1076+1016A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175685325 | |||||||
| chr5:175685327 | A | G | 66 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0001t0001g0124 others(63): Show |
73 | HG00438.hp2 HG00558.hp2 HG01109.hp2 others(70): Show |
intron_variant | MODIFIER | c.1076+1018A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175685327 | |||||||
| chr5:175685742 | A | G | 5 | a0001c0001t0009g0094 a0001c0001t0009g0133 a0001c0001t0009g0215 others(2): Show |
6 | HG01109.hp2 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1076+1433A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175685742 | |||||||
| chr5:175685766 | T | C | 2 | a0001c0001t0001g0124 a0001c0001t0012g0131 |
2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1076+1457T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175685766 | |||||||
| chr5:175685796 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1076+1487C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175685796 | |||||||
| chr5:175685965 | C | T | 1 | a0001c0001t0025g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1076+1656C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175685965 | |||||||
| chr5:175685967 | C | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0191 a0001c0001t0001g0205 others(1): Show |
5 | HG00597.hp2 HG02293.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.1076+1658C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175685967 | |||||||
| chr5:175686021 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1076+1712A>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175686021 | |||||||
| chr5:175686035 | G | T | 64 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0001t0001g0124 others(61): Show |
70 | HG00438.hp2 HG00558.hp2 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.1076+1726G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175686035 | |||||||
| chr5:175686510 | G | C | 3 | a0001c0001t0004g0040 a0001c0001t0004g0186 a0001c0001t0004g0198 |
3 | HG02717.hp1 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1076+2201G>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175686510 | |||||||
| chr5:175686514 | A | C | 1 | a0001c0001t0006g0216 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1076+2205A>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175686514 | |||||||
| chr5:175686536 | C | T | 9 | a0001c0001t0003g0002 a0001c0001t0003g0066 a0001c0001t0003g0072 others(6): Show |
12 | HG02155.hp1 HG02165.hp1 HG03942.hp1 others(9): Show |
intron_variant | MODIFIER | c.1076+2227C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175686536 | |||||||
| chr5:175686652 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1076+2343C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175686652 | |||||||
| chr5:175686895 | A | C | 5 | a0001c0001t0009g0133 a0001c0001t0009g0215 a0001c0001t0015g0033 others(2): Show |
6 | HG02717.hp2 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1076+2586A>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175686895 | |||||||
| chr5:175686912 | C | G | 1 | a0001c0001t0003g0013 | 2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1076+2603C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175686912 | |||||||
| chr5:175686977 | A | G | 28 | a0001c0001t0001g0088 a0001c0001t0001g0124 a0001c0001t0003g0013 others(25): Show |
30 | HG01243.hp2 HG01891.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.1076+2668A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175686977 | |||||||
| chr5:175687038 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0042g0126 |
2 | HG00733.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1076+2729G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175687038 | |||||||
| chr5:175687196 | C | T | 1 | a0001c0001t0009g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1076+2887C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175687196 | |||||||
| chr5:175687250 | G | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | NA18971.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1076+2941G>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175687250 | |||||||
| chr5:175687273 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | NA19030.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1076+2964G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175687273 | |||||||
| chr5:175687532 | A | G | 1 | a0001c0001t0002g0159 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1076+3223A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175687532 | |||||||
| chr5:175687917 | T | G | 1 | a0001c0001t0009g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1076+3608T>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175687917 | |||||||
| chr5:175687920 | C | A | 1 | a0001c0001t0009g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1076+3611C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175687920 | |||||||
| chr5:175688092 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1076+3783C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175688092 | |||||||
| chr5:175688099 | T | G | 1 | a0001c0002t0002g0165 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1076+3790T>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175688099 | |||||||
| chr5:175688168 | G | A | 1 | a0001c0001t0003g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1076+3859G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175688168 | |||||||
| chr5:175688169 | C | A | 5 | a0001c0001t0001g0144 a0001c0001t0001g0179 a0001c0001t0002g0146 others(2): Show |
5 | HG01081.hp2 HG01255.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1076+3860C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175688169 | |||||||
| chr5:175688229 | A | T | 64 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0001t0001g0124 others(61): Show |
70 | HG00438.hp2 HG00558.hp2 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.1076+3920A>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175688229 | |||||||
| chr5:175688293 | G | A | 1 | a0001c0003t0028g0071 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1076+3984G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175688293 | |||||||
| chr5:175688336 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1076+4027G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175688336 | |||||||
| chr5:175688658 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1076+4349C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175688658 | |||||||
| chr5:175688706 | T | C | 65 | a0001c0001t0001g0041 a0001c0001t0001g0062 a0001c0001t0001g0088 others(62): Show |
71 | HG00438.hp2 HG00558.hp2 HG01109.hp2 others(68): Show |
intron_variant | MODIFIER | c.1076+4397T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175688706 | |||||||
| chr5:175688830 | CTG | C | 2 | a0001c0001t0003g0013 a0001c0001t0036g0169 |
3 | HG02647.hp1 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1076+4525_1076+452 others(6): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 175688830 | ||||||
| chr5:175688854 | G | T | 1 | a0001c0002t0001g0079 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1076+4545G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175688854 | |||||||
| chr5:175688874 | C | T | 6 | a0001c0001t0004g0195 a0001c0001t0008g0043 a0001c0001t0008g0044 others(3): Show |
7 | HG02572.hp2 HG02818.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1076+4565C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175688874 | |||||||
| chr5:175688969 | G | A | 7 | a0001c0002t0001g0078 a0001c0002t0001g0079 a0001c0002t0001g0127 others(4): Show |
7 | HG01106.hp1 HG01361.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.1076+4660G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175688969 | |||||||
| chr5:175688993 | C | A | 4 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0001t0005g0084 others(1): Show |
4 | HG02647.hp2 HG02809.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+4684C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175688993 | |||||||
| chr5:175689079 | A | G | 2 | a0001c0001t0003g0013 a0001c0001t0036g0169 |
3 | HG02647.hp1 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1076+4770A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175689079 | |||||||
| chr5:175689080 | A | G | 3 | a0001c0001t0001g0138 a0002c0004t0001g0011 a0002c0004t0001g0137 |
4 | HG03927.hp1 NA18943.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076+4771A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175689080 | |||||||
| chr5:175689336 | GACTT | G | 2 | a0001c0001t0003g0013 a0001c0001t0036g0169 |
3 | HG02647.hp1 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1076+5033_1076+503 others(8): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 175689336 | ||||||
| chr5:175689360 | C | T | 2 | a0001c0001t0003g0013 a0001c0001t0036g0169 |
3 | HG02647.hp1 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1076+5051C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175689360 | |||||||
| chr5:175689405 | C | A | 2 | a0001c0001t0003g0013 a0001c0001t0036g0169 |
3 | HG02647.hp1 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1076+5096C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175689405 | |||||||
| chr5:175689434 | G | T | 1 | a0001c0001t0004g0198 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1076+5125G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175689434 | |||||||
| chr5:175689671 | C | T | 1 | a0001c0002t0002g0165 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1076+5362C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175689671 | |||||||
| chr5:175689766 | G | GAACC | 2 | a0001c0001t0003g0013 a0001c0001t0036g0169 |
3 | HG02647.hp1 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1076+5457_1076+545 others(8): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175689766 | |||||||
| chr5:175689918 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1076+5609G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175689918 | |||||||
| chr5:175690251 | A | G | 2 | a0001c0001t0003g0013 a0001c0001t0036g0169 |
3 | HG02647.hp1 HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1076+5942A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175690251 | |||||||
| chr5:175690320 | A | C | 64 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0001t0001g0124 others(61): Show |
70 | HG00438.hp2 HG00558.hp2 HG01109.hp2 others(67): Show |
intron_variant | MODIFIER | c.1076+6011A>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175690320 | |||||||
| chr5:175690514 | A | G | 1 | a0001c0001t0051g0109 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1076+6205A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175690514 | |||||||
| chr5:175690538 | TCTGC | T | 18 | a0001c0001t0001g0124 a0001c0001t0003g0013 a0001c0001t0005g0139 others(15): Show |
19 | HG01243.hp2 HG01891.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1076+6248_1076+625 others(8): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 175690538 | ||||||
| chr5:175690628 | C | T | 56 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0001t0001g0124 others(53): Show |
62 | HG00438.hp2 HG00558.hp2 HG01109.hp2 others(59): Show |
intron_variant | MODIFIER | c.1076+6319C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175690628 | |||||||
| chr5:175690694 | C | T | 2 | a0001c0001t0004g0192 a0001c0001t0005g0058 |
2 | HG00438.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.1076+6385C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175690694 | |||||||
| chr5:175690735 | C | A | 1 | a0001c0001t0001g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1076+6426C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175690735 | |||||||
| chr5:175690787 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1076+6478C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175690787 | |||||||
| chr5:175690883 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1076+6574C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175690883 | |||||||
| chr5:175690986 | C | T | 2 | a0001c0001t0016g0085 a0001c0001t0016g0193 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1076+6677C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175690986 | |||||||
| chr5:175691055 | G | A | 1 | a0001c0001t0003g0110 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1076+6746G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175691055 | |||||||
| chr5:175691107 | G | T | 16 | a0001c0001t0001g0124 a0001c0001t0005g0139 a0001c0001t0005g0202 others(13): Show |
16 | HG01243.hp2 HG01891.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1076+6798G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175691107 | |||||||
| chr5:175691147 | T | A | 1 | a0001c0001t0014g0213 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1076+6838T>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175691147 | |||||||
| chr5:175691148 | C | A | 1 | a0001c0001t0014g0213 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1076+6839C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175691148 | |||||||
| chr5:175691154 | AGCGGCCA others(1): Show |
A | 19 | a0001c0001t0001g0124 a0001c0001t0002g0087 a0001c0001t0003g0013 others(16): Show |
20 | HG01243.hp2 HG01891.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1076+6858_1076+686 others(12): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 175691154 | ||||||
| chr5:175691168 | C | G | 1 | a0001c0001t0005g0212 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1076+6859C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175691168 | |||||||
| chr5:175691180 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | NA18971.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1076+6871C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175691180 | |||||||
| chr5:175691248 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1076+6939C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175691248 | |||||||
| chr5:175691345 | A | G | 1 | a0001c0001t0022g0125 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1076+7036A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175691345 | |||||||
| chr5:175691525 | C | T | 1 | a0001c0002t0002g0165 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1076+7216C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175691525 | |||||||
| chr5:175691630 | A | C | 1 | a0001c0001t0002g0172 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1076+7321A>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175691630 | |||||||
| chr5:175691798 | A | G | 65 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0001t0001g0124 others(62): Show |
71 | HG00438.hp2 HG00558.hp2 HG01109.hp2 others(68): Show |
intron_variant | MODIFIER | c.1076+7489A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175691798 | |||||||
| chr5:175691916 | G | A | 19 | a0001c0001t0001g0124 a0001c0001t0003g0013 a0001c0001t0005g0139 others(16): Show |
20 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1076+7607G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175691916 | |||||||
| chr5:175691946 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1076+7637C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175691946 | |||||||
| chr5:175692089 | G | A | 61 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0001t0001g0124 others(58): Show |
67 | HG00438.hp2 HG00558.hp2 HG01109.hp2 others(64): Show |
intron_variant | MODIFIER | c.1076+7780G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175692089 | |||||||
| chr5:175692306 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1076+7997G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175692306 | |||||||
| chr5:175692430 | C | A | 1 | a0001c0001t0009g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1076+8121C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175692430 | |||||||
| chr5:175692613 | C | T | 14 | a0001c0001t0001g0124 a0001c0001t0005g0139 a0001c0001t0005g0202 others(11): Show |
14 | HG01243.hp2 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1076+8304C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175692613 | |||||||
| chr5:175692699 | G | A | 18 | a0001c0001t0001g0124 a0001c0001t0005g0139 a0001c0001t0005g0202 others(15): Show |
18 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1076+8390G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175692699 | |||||||
| chr5:175692761 | C | T | 1 | a0001c0001t0003g0174 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1076+8452C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175692761 | |||||||
| chr5:175692915 | G | A | 1 | a0001c0001t0001g0008 | 3 | HG01256.hp1 HG01258.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1076+8606G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175692915 | |||||||
| chr5:175692988 | A | G | 4 | a0001c0001t0003g0060 a0001c0001t0003g0100 a0001c0001t0004g0061 others(1): Show |
4 | HG02055.hp2 HG02258.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076+8679A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175692988 | |||||||
| chr5:175693091 | G | A | 6 | a0001c0003t0017g0090 a0001c0003t0017g0168 a0001c0003t0018g0181 others(3): Show |
6 | HG02145.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1076+8782G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175693091 | |||||||
| chr5:175693178 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1076+8869G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175693178 | |||||||
| chr5:175693363 | G | A | 5 | a0001c0001t0004g0186 a0001c0001t0009g0133 a0001c0001t0009g0215 others(2): Show |
5 | HG02717.hp1 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1076+9054G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175693363 | |||||||
| chr5:175693459 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1076+9150C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175693459 | |||||||
| chr5:175693473 | C | T | 40 | a0001c0001t0001g0041 a0001c0001t0001g0062 a0001c0001t0001g0088 others(37): Show |
41 | HG01106.hp1 HG01109.hp2 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.1076+9164C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175693473 | |||||||
| chr5:175693474 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1076+9165G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175693474 | |||||||
| chr5:175693552 | A | C | 47 | a0001c0001t0001g0124 a0001c0001t0003g0002 a0001c0001t0003g0014 others(44): Show |
52 | HG00438.hp2 HG00558.hp2 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.1076+9243A>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175693552 | |||||||
| chr5:175693570 | C | T | 1 | a0001c0001t0009g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1076+9261C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175693570 | |||||||
| chr5:175693616 | G | A | 1 | a0001c0001t0038g0095 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1076+9307G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175693616 | |||||||
| chr5:175693721 | C | G | 6 | a0001c0001t0004g0186 a0001c0001t0009g0133 a0001c0001t0009g0215 others(3): Show |
6 | HG02717.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1076+9412C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175693721 | |||||||
| chr5:175693842 | A | G | 1 | a0001c0001t0001g0020 | 2 | HG01192.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1076+9533A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175693842 | |||||||
| chr5:175693895 | A | G | 93 | a0001c0001t0001g0041 a0001c0001t0001g0062 a0001c0001t0001g0069 others(90): Show |
102 | HG00438.hp2 HG00558.hp2 HG01106.hp1 others(99): Show |
intron_variant | MODIFIER | c.1076+9586A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175693895 | |||||||
| chr5:175693903 | C | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1076+9594C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175693903 | |||||||
| chr5:175693940 | T | C | 1 | a0001c0001t0009g0133 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1076+9631T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175693940 | |||||||
| chr5:175694057 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1076+9748G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175694057 | |||||||
| chr5:175694074 | G | T | 15 | a0001c0001t0004g0186 a0001c0001t0009g0133 a0001c0001t0009g0215 others(12): Show |
15 | HG01891.hp2 HG02145.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.1076+9765G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175694074 | |||||||
| chr5:175694100 | A | C | 1 | a0001c0001t0046g0063 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1076+9791A>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175694100 | |||||||
| chr5:175694307 | G | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1076+9998G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175694307 | |||||||
| chr5:175694338 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0134 a0001c0001t0001g0135 |
5 | HG01069.hp1 HG01070.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1076+10029C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175694338 | |||||||
| chr5:175694475 | A | G | 1 | a0001c0001t0036g0169 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1076+10166A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175694475 | |||||||
| chr5:175694597 | G | A | 11 | a0001c0001t0001g0041 a0001c0001t0001g0118 a0001c0001t0003g0060 others(8): Show |
11 | HG01106.hp1 HG01361.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1076+10288G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175694597 | |||||||
| chr5:175694716 | C | A | 1 | a0001c0001t0036g0169 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1076+10407C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175694716 | |||||||
| chr5:175694729 | C | T | 2 | a0001c0001t0004g0040 a0001c0001t0004g0198 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1076+10420C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175694729 | |||||||
| chr5:175694739 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1076+10430G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175694739 | |||||||
| chr5:175694911 | C | T | 1 | a0001c0001t0009g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1076+10602C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175694911 | |||||||
| chr5:175695053 | C | T | 13 | a0001c0001t0001g0041 a0001c0001t0003g0060 a0001c0001t0003g0100 others(10): Show |
13 | HG01106.hp1 HG01361.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1076+10744C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175695053 | |||||||
| chr5:175695079 | G | A | 2 | a0001c0001t0002g0097 a0001c0001t0043g0091 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1076+10770G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175695079 | |||||||
| chr5:175695162 | G | A | 1 | a0001c0001t0009g0094 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1076+10853G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175695162 | |||||||
| chr5:175695168 | C | G | 1 | a0001c0001t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1076+10859C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175695168 | |||||||
| chr5:175695206 | C | T | 6 | a0001c0001t0004g0186 a0001c0001t0009g0133 a0001c0001t0009g0215 others(3): Show |
6 | HG02717.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1076+10897C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175695206 | |||||||
| chr5:175695224 | G | A | 2 | a0001c0001t0004g0040 a0001c0001t0004g0198 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1076+10915G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175695224 | |||||||
| chr5:175695444 | A | G | 54 | a0001c0001t0003g0002 a0001c0001t0003g0014 a0001c0001t0003g0066 others(51): Show |
59 | HG00438.hp2 HG00558.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.1076+11135A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175695444 | |||||||
| chr5:175695445 | G | C | 54 | a0001c0001t0003g0002 a0001c0001t0003g0014 a0001c0001t0003g0066 others(51): Show |
59 | HG00438.hp2 HG00558.hp2 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.1076+11136G>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175695445 | |||||||
| chr5:175695481 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1076+11172G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175695481 | |||||||
| chr5:175695555 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1076+11246C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175695555 | |||||||
| chr5:175695624 | A | G | 18 | a0001c0001t0005g0139 a0001c0001t0005g0202 a0001c0001t0006g0102 others(15): Show |
19 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1076+11315A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175695624 | |||||||
| chr5:175695703 | G | A | 1 | a0001c0001t0022g0125 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1076+11394G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175695703 | |||||||
| chr5:175695777 | C | T | 6 | a0001c0001t0004g0186 a0001c0001t0009g0133 a0001c0001t0009g0215 others(3): Show |
6 | HG02717.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1076+11468C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175695777 | |||||||
| chr5:175695989 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1076+11680C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175695989 | |||||||
| chr5:175696148 | G | A | 49 | a0001c0001t0001g0041 a0001c0001t0001g0203 a0001c0001t0002g0050 others(46): Show |
54 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.1077-11631G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175696148 | |||||||
| chr5:175696155 | T | C | 5 | a0001c0001t0004g0186 a0001c0001t0009g0133 a0001c0001t0009g0215 others(2): Show |
5 | HG02717.hp1 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077-11624T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175696155 | |||||||
| chr5:175696384 | G | A | 1 | a0001c0001t0023g0019 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1077-11395G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175696384 | |||||||
| chr5:175696393 | C | A | 2 | a0001c0001t0004g0040 a0001c0001t0004g0198 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1077-11386C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175696393 | |||||||
| chr5:175696397 | C | T | 42 | a0001c0001t0001g0041 a0001c0001t0001g0062 a0001c0001t0001g0114 others(39): Show |
48 | HG00438.hp2 HG00558.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.1077-11382C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175696397 | |||||||
| chr5:175696492 | TCA | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(222): Show |
261 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(258): Show |
intron_variant | MODIFIER | c.1077-11284_1077-11 others(8): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 175696492 | ||||||
| chr5:175696531 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1077-11248A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175696531 | |||||||
| chr5:175696582 | G | A | 1 | a0001c0001t0042g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1077-11197G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175696582 | |||||||
| chr5:175696811 | G | T | 1 | a0001c0001t0019g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1077-10968G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175696811 | |||||||
| chr5:175696827 | C | CT | 41 | a0001c0001t0001g0114 a0001c0001t0001g0122 a0001c0001t0001g0140 others(38): Show |
43 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.1077-10952_1077-10 others(7): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175696827 | |||||||
| chr5:175696829 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1077-10950C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175696829 | |||||||
| chr5:175697150 | C | T | 6 | a0001c0001t0012g0131 a0001c0001t0012g0200 a0001c0001t0019g0130 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1077-10629C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175697150 | |||||||
| chr5:175697182 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1077-10597G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175697182 | |||||||
| chr5:175697191 | C | T | 5 | a0001c0001t0001g0003 a0001c0001t0001g0107 a0001c0001t0001g0121 others(2): Show |
8 | HG00423.hp1 HG02080.hp1 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.1077-10588C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175697191 | |||||||
| chr5:175697224 | C | G | 5 | a0001c0001t0015g0033 a0001c0001t0031g0032 a0001c0001t0037g0032 others(2): Show |
6 | HG02572.hp2 HG02922.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1077-10555C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175697224 | |||||||
| chr5:175697234 | C | T | 8 | a0001c0001t0002g0039 a0001c0001t0002g0050 a0001c0001t0002g0154 others(5): Show |
8 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.1077-10545C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175697234 | |||||||
| chr5:175697260 | G | A | 1 | a0001c0001t0019g0093 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1077-10519G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175697260 | |||||||
| chr5:175697320 | G | A | 6 | a0001c0001t0001g0029 a0001c0001t0001g0147 a0001c0001t0001g0176 others(3): Show |
7 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077-10459G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175697320 | |||||||
| chr5:175697434 | G | T | 32 | a0001c0001t0001g0167 a0001c0001t0006g0042 a0001c0001t0006g0099 others(29): Show |
32 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1077-10345G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175697434 | |||||||
| chr5:175697462 | C | CA | 12 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0144 others(9): Show |
12 | HG01361.hp1 HG02145.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1077-10299dupA | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 175697462 | ||||||
| chr5:175697462 | C | CAAAAAAA | 21 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(18): Show |
22 | HG00438.hp1 HG01106.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.1077-10305_1077-10 others(13): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 175697462 | ||||||
| chr5:175697462 | CA | C | 22 | a0001c0001t0002g0039 a0001c0001t0002g0050 a0001c0001t0002g0154 others(19): Show |
22 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.1077-10299delA | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 175697462 | ||||||
| chr5:175697462 | CAA | C | 18 | a0001c0001t0006g0042 a0001c0001t0006g0099 a0001c0001t0006g0101 others(15): Show |
18 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1077-10300_1077-10 others(8): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 175697462 | ||||||
| chr5:175697469 | A | G | 1 | a0001c0001t0034g0096 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1077-10310A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175697469 | |||||||
| chr5:175697653 | A | G | 17 | a0001c0001t0006g0042 a0001c0001t0006g0099 a0001c0001t0006g0101 others(14): Show |
17 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1077-10126A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175697653 | |||||||
| chr5:175697659 | G | A | 44 | a0001c0001t0002g0023 a0001c0001t0002g0039 a0001c0001t0002g0050 others(41): Show |
46 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.1077-10120G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175697659 | |||||||
| chr5:175697679 | A | T | 2 | a0001c0001t0001g0179 a0001c0001t0048g0180 |
2 | HG01255.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1077-10100A>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175697679 | |||||||
| chr5:175697806 | A | G | 79 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(76): Show |
84 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.1077-9973A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175697806 | |||||||
| chr5:175697893 | T | C | 34 | a0001c0001t0006g0042 a0001c0001t0006g0099 a0001c0001t0006g0101 others(31): Show |
35 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1077-9886T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175697893 | |||||||
| chr5:175697978 | G | C | 17 | a0001c0001t0006g0042 a0001c0001t0006g0099 a0001c0001t0006g0101 others(14): Show |
17 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1077-9801G>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175697978 | |||||||
| chr5:175697991 | A | G | 4 | a0001c0001t0031g0032 a0001c0001t0037g0032 a0001c0001t0046g0063 others(1): Show |
4 | HG02572.hp2 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077-9788A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175697991 | |||||||
| chr5:175697992 | A | G | 34 | a0001c0001t0006g0042 a0001c0001t0006g0099 a0001c0001t0006g0101 others(31): Show |
35 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1077-9787A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175697992 | |||||||
| chr5:175698140 | C | T | 17 | a0001c0001t0006g0042 a0001c0001t0006g0099 a0001c0001t0006g0101 others(14): Show |
17 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1077-9639C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175698140 | |||||||
| chr5:175698280 | G | A | 2 | a0001c0001t0033g0190 a0001c0001t0043g0091 |
2 | NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1077-9499G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175698280 | |||||||
| chr5:175698293 | C | T | 34 | a0001c0001t0006g0042 a0001c0001t0006g0099 a0001c0001t0006g0101 others(31): Show |
35 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1077-9486C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175698293 | |||||||
| chr5:175698368 | G | A | 2 | a0001c0001t0033g0190 a0001c0001t0043g0091 |
2 | NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1077-9411G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175698368 | |||||||
| chr5:175698389 | G | A | 17 | a0001c0001t0006g0042 a0001c0001t0006g0099 a0001c0001t0006g0101 others(14): Show |
17 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1077-9390G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175698389 | |||||||
| chr5:175698484 | A | G | 4 | a0001c0001t0031g0032 a0001c0001t0037g0032 a0001c0001t0046g0063 others(1): Show |
4 | HG02572.hp2 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077-9295A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175698484 | |||||||
| chr5:175698551 | G | C | 17 | a0001c0001t0006g0042 a0001c0001t0006g0099 a0001c0001t0006g0101 others(14): Show |
17 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1077-9228G>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175698551 | |||||||
| chr5:175698574 | G | A | 1 | a0001c0002t0002g0165 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1077-9205G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175698574 | |||||||
| chr5:175698821 | C | T | 1 | a0001c0001t0012g0103 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1077-8958C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175698821 | |||||||
| chr5:175698862 | C | G | 2 | a0001c0001t0033g0190 a0001c0001t0043g0091 |
2 | NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1077-8917C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175698862 | |||||||
| chr5:175698998 | T | C | 75 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(72): Show |
77 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.1077-8781T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175698998 | |||||||
| chr5:175699021 | G | A | 1 | a0001c0001t0015g0033 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1077-8758G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175699021 | |||||||
| chr5:175699029 | T | G | 5 | a0001c0001t0019g0093 a0001c0001t0025g0194 a0001c0001t0030g0077 others(2): Show |
5 | HG02486.hp1 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077-8750T>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175699029 | |||||||
| chr5:175699105 | G | A | 1 | a0001c0001t0012g0103 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1077-8674G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175699105 | |||||||
| chr5:175699246 | C | G | 34 | a0001c0001t0006g0042 a0001c0001t0006g0099 a0001c0001t0006g0101 others(31): Show |
35 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1077-8533C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175699246 | |||||||
| chr5:175699385 | A | C | 1 | a0001c0001t0001g0138 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1077-8394A>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175699385 | |||||||
| chr5:175699400 | C | T | 12 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(9): Show |
12 | HG00438.hp1 HG01106.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.1077-8379C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175699400 | |||||||
| chr5:175699408 | C | A | 41 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(38): Show |
42 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(39): Show |
intron_variant | MODIFIER | c.1077-8371C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175699408 | |||||||
| chr5:175699540 | G | A | 1 | a0001c0001t0015g0033 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1077-8239G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175699540 | |||||||
| chr5:175699562 | G | GTTGTTTT others(5): Show |
1 | a0001c0001t0033g0190 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1077-8215_1077-820 others(16): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 175699562 | ||||||
| chr5:175699562 | G | GTTTTTTT others(5): Show |
30 | a0001c0001t0006g0042 a0001c0001t0006g0099 a0001c0001t0006g0101 others(27): Show |
31 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(28): Show |
intron_variant | MODIFIER | c.1077-8215_1077-821 others(16): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 175699562 | ||||||
| chr5:175699565 | G | T | 3 | a0001c0001t0012g0131 a0001c0001t0012g0200 a0001c0001t0019g0130 |
3 | HG01243.hp2 HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1077-8214G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175699565 | |||||||
| chr5:175699572 | T | TTTTTGTT others(9): Show |
3 | a0001c0001t0012g0131 a0001c0001t0012g0200 a0001c0001t0019g0130 |
3 | HG01243.hp2 HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1077-8204_1077-820 others(20): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 175699572 | ||||||
| chr5:175699660 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0207 |
3 | NA18977.hp1 NA18998.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1077-8119G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175699660 | |||||||
| chr5:175699698 | C | T | 34 | a0001c0001t0001g0107 a0001c0001t0006g0042 a0001c0001t0006g0099 others(31): Show |
35 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1077-8081C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175699698 | |||||||
| chr5:175699735 | G | A | 2 | a0001c0001t0033g0190 a0001c0001t0043g0091 |
2 | NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1077-8044G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175699735 | |||||||
| chr5:175699783 | C | A | 34 | a0001c0001t0006g0042 a0001c0001t0006g0099 a0001c0001t0006g0101 others(31): Show |
35 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1077-7996C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175699783 | |||||||
| chr5:175699819 | C | T | 17 | a0001c0001t0006g0042 a0001c0001t0006g0099 a0001c0001t0006g0101 others(14): Show |
17 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1077-7960C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175699819 | |||||||
| chr5:175699916 | A | G | 1 | a0001c0001t0015g0033 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1077-7863A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175699916 | |||||||
| chr5:175700110 | G | A | 4 | a0001c0001t0031g0032 a0001c0001t0037g0032 a0001c0001t0046g0063 others(1): Show |
4 | HG02572.hp2 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077-7669G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175700110 | |||||||
| chr5:175700128 | T | C | 78 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(75): Show |
81 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1077-7651T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175700128 | |||||||
| chr5:175700198 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1077-7581C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175700198 | |||||||
| chr5:175700277 | G | A | 28 | a0001c0001t0006g0042 a0001c0001t0006g0099 a0001c0001t0006g0101 others(25): Show |
29 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1077-7502G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175700277 | |||||||
| chr5:175700390 | C | T | 1 | a0001c0001t0001g0010 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1077-7389C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175700390 | |||||||
| chr5:175700485 | G | C | 1 | a0001c0001t0001g0208 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1077-7294G>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175700485 | |||||||
| chr5:175700571 | G | A | 4 | a0001c0001t0031g0032 a0001c0001t0037g0032 a0001c0001t0046g0063 others(1): Show |
4 | HG02572.hp2 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077-7208G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175700571 | |||||||
| chr5:175700587 | A | G | 4 | a0001c0001t0031g0032 a0001c0001t0037g0032 a0001c0001t0046g0063 others(1): Show |
4 | HG02572.hp2 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077-7192A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175700587 | |||||||
| chr5:175700611 | T | A | 71 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(68): Show |
73 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1077-7168T>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175700611 | |||||||
| chr5:175700795 | A | G | 75 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(72): Show |
79 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.1077-6984A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175700795 | |||||||
| chr5:175700803 | G | A | 4 | a0001c0001t0031g0032 a0001c0001t0037g0032 a0001c0001t0046g0063 others(1): Show |
4 | HG02572.hp2 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077-6976G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175700803 | |||||||
| chr5:175700909 | A | T | 1 | a0001c0001t0003g0013 | 2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1077-6870A>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175700909 | |||||||
| chr5:175700933 | G | T | 2 | a0001c0001t0001g0062 a0001c0001t0005g0084 |
2 | HG02647.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1077-6846G>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175700933 | |||||||
| chr5:175701000 | A | C | 18 | a0001c0001t0006g0042 a0001c0001t0006g0099 a0001c0001t0006g0101 others(15): Show |
18 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1077-6779A>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175701000 | |||||||
| chr5:175701115 | G | A | 1 | a0001c0001t0005g0092 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1077-6664G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175701115 | |||||||
| chr5:175701157 | G | A | 2 | a0001c0001t0033g0190 a0001c0001t0043g0091 |
2 | NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1077-6622G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175701157 | |||||||
| chr5:175701241 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1077-6538C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175701241 | |||||||
| chr5:175701334 | C | A | 1 | a0001c0001t0004g0037 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1077-6445C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175701334 | |||||||
| chr5:175701414 | C | A | 34 | a0001c0001t0006g0042 a0001c0001t0006g0099 a0001c0001t0006g0101 others(31): Show |
35 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1077-6365C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175701414 | |||||||
| chr5:175701437 | T | C | 1 | a0001c0001t0003g0136 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1077-6342T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175701437 | |||||||
| chr5:175701468 | C | T | 1 | a0001c0001t0034g0096 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1077-6311C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175701468 | |||||||
| chr5:175701469 | G | A | 1 | a0001c0001t0003g0072 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1077-6310G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175701469 | |||||||
| chr5:175701478 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1077-6301C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175701478 | |||||||
| chr5:175701488 | C | G | 2 | a0001c0001t0033g0190 a0001c0001t0043g0091 |
2 | NA19240.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1077-6291C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175701488 | |||||||
| chr5:175701489 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1077-6290G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175701489 | |||||||
| chr5:175701696 | A | G | 7 | a0001c0001t0001g0122 a0001c0001t0003g0136 a0001c0001t0003g0173 others(4): Show |
9 | HG00544.hp2 HG02132.hp1 NA18949.hp2 others(6): Show |
intron_variant | MODIFIER | c.1077-6083A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175701696 | |||||||
| chr5:175701862 | C | G | 4 | a0001c0001t0031g0032 a0001c0001t0037g0032 a0001c0001t0046g0063 others(1): Show |
4 | HG02572.hp2 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077-5917C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175701862 | |||||||
| chr5:175701947 | A | G | 31 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(28): Show |
34 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1077-5832A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175701947 | |||||||
| chr5:175702088 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1077-5691G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175702088 | |||||||
| chr5:175702183 | T | A | 72 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(69): Show |
76 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1077-5596T>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175702183 | |||||||
| chr5:175702545 | C | CT | 70 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0020 others(67): Show |
77 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1077-5210dupT | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 175702545 | ||||||
| chr5:175702545 | C | CTT | 8 | a0001c0001t0002g0146 a0001c0001t0002g0172 a0001c0001t0012g0131 others(5): Show |
8 | HG01243.hp2 HG01361.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1077-5211_1077-521 others(6): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 175702545 | ||||||
| chr5:175702545 | CT | C | 9 | a0001c0001t0001g0176 a0001c0001t0002g0097 a0001c0001t0002g0106 others(6): Show |
9 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1077-5210delT | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 175702545 | ||||||
| chr5:175702591 | G | A | 31 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(28): Show |
34 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.1077-5188G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175702591 | |||||||
| chr5:175702621 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0023g0019 |
3 | HG01256.hp2 HG01258.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1077-5158G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175702621 | |||||||
| chr5:175702637 | C | T | 2 | a0001c0001t0001g0158 a0001c0003t0018g0181 |
2 | HG01358.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1077-5142C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175702637 | |||||||
| chr5:175702638 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1077-5141G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175702638 | |||||||
| chr5:175702646 | A | G | 72 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(69): Show |
76 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1077-5133A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175702646 | |||||||
| chr5:175702687 | G | A | 1 | a0001c0001t0023g0019 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1077-5092G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175702687 | |||||||
| chr5:175702701 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0044g0119 |
2 | HG02300.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1077-5078G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175702701 | |||||||
| chr5:175702712 | T | C | 72 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(69): Show |
76 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1077-5067T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175702712 | |||||||
| chr5:175702718 | A | AT | 18 | a0001c0001t0002g0097 a0001c0001t0002g0106 a0001c0001t0004g0057 others(15): Show |
18 | HG01243.hp2 HG01884.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1077-5055dupT | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr5 | 175702718 | ||||||
| chr5:175702724 | TC | T | 5 | a0001c0001t0001g0054 a0001c0001t0001g0064 a0001c0001t0008g0067 others(2): Show |
5 | HG01106.hp1 HG02300.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077-5054delC | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175702724 | |||||||
| chr5:175702725 | C | T | 65 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0065 others(62): Show |
69 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1077-5054C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175702725 | |||||||
| chr5:175702758 | T | C | 72 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(69): Show |
76 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1077-5021T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175702758 | |||||||
| chr5:175702809 | C | T | 4 | a0001c0001t0031g0032 a0001c0001t0037g0032 a0001c0001t0046g0063 others(1): Show |
4 | HG02572.hp2 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077-4970C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175702809 | |||||||
| chr5:175702819 | G | A | 4 | a0001c0001t0006g0129 a0001c0001t0008g0067 a0001c0001t0015g0033 others(1): Show |
5 | HG02451.hp2 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1077-4960G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175702819 | |||||||
| chr5:175702999 | C | T | 71 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(68): Show |
75 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.1077-4780C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175702999 | |||||||
| chr5:175703441 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1077-4338T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175703441 | |||||||
| chr5:175703488 | G | A | 1 | a0001c0001t0015g0033 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1077-4291G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175703488 | |||||||
| chr5:175703727 | C | T | 70 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(67): Show |
72 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1077-4052C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175703727 | |||||||
| chr5:175703852 | A | G | 10 | a0001c0001t0012g0103 a0001c0001t0012g0131 a0001c0001t0012g0200 others(7): Show |
10 | HG01243.hp2 HG01884.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1077-3927A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175703852 | |||||||
| chr5:175704042 | T | C | 3 | a0001c0001t0012g0131 a0001c0001t0012g0200 a0001c0001t0019g0130 |
3 | HG01243.hp2 HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1077-3737T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175704042 | |||||||
| chr5:175704094 | C | T | 70 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(67): Show |
72 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1077-3685C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175704094 | |||||||
| chr5:175704157 | G | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0196 |
2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1077-3622G>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175704157 | |||||||
| chr5:175704404 | C | A | 70 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(67): Show |
72 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1077-3375C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175704404 | |||||||
| chr5:175704409 | C | A | 36 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(33): Show |
37 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.1077-3370C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175704409 | |||||||
| chr5:175704584 | G | A | 1 | a0001c0001t0034g0096 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1077-3195G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175704584 | |||||||
| chr5:175704744 | A | G | 1 | a0001c0001t0038g0095 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1077-3035A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175704744 | |||||||
| chr5:175704767 | C | G | 1 | a0001c0001t0001g0151 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1077-3012C>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175704767 | |||||||
| chr5:175704871 | A | G | 1 | a0001c0001t0001g0049 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1077-2908A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175704871 | |||||||
| chr5:175704873 | G | A | 6 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(3): Show |
6 | HG00438.hp1 NA18969.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077-2906G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175704873 | |||||||
| chr5:175705492 | A | T | 68 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(65): Show |
70 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1077-2287A>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175705492 | |||||||
| chr5:175705493 | A | T | 63 | a0001c0001t0001g0045 a0001c0001t0001g0049 a0001c0001t0001g0054 others(60): Show |
65 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.1077-2286A>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175705493 | |||||||
| chr5:175705494 | A | T | 2 | a0001c0001t0025g0194 a0001c0001t0030g0077 |
2 | HG02486.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1077-2285A>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175705494 | |||||||
| chr5:175705574 | G | A | 2 | a0001c0001t0016g0085 a0001c0001t0016g0193 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077-2205G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175705574 | |||||||
| chr5:175705575 | C | A | 2 | a0001c0001t0016g0085 a0001c0001t0016g0193 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077-2204C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175705575 | |||||||
| chr5:175705946 | A | C | 4 | a0001c0001t0031g0032 a0001c0001t0037g0032 a0001c0001t0046g0063 others(1): Show |
4 | HG02572.hp2 HG03130.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1077-1833A>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175705946 | |||||||
| chr5:175705951 | T | C | 2 | a0001c0001t0016g0085 a0001c0001t0016g0193 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077-1828T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175705951 | |||||||
| chr5:175706088 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1077-1691C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175706088 | |||||||
| chr5:175706140 | T | C | 1 | a0001c0001t0009g0215 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1077-1639T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175706140 | |||||||
| chr5:175706252 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1077-1527A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175706252 | |||||||
| chr5:175706281 | CTTAATGC others(10): Show |
C | 1 | a0001c0001t0044g0119 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1077-1497_1077-148 others(21): Show |
HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175706281 | |||||||
| chr5:175706496 | G | A | 1 | a0001c0001t0003g0110 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1077-1283G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175706496 | |||||||
| chr5:175706740 | C | T | 17 | a0001c0001t0006g0042 a0001c0001t0006g0099 a0001c0001t0006g0101 others(14): Show |
17 | HG01884.hp1 HG02145.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.1077-1039C>T | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175706740 | |||||||
| chr5:175706741 | G | A | 1 | a0001c0003t0010g0004 | 3 | HG02451.hp1 HG02896.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1077-1038G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175706741 | |||||||
| chr5:175706746 | A | G | 2 | a0001c0001t0016g0085 a0001c0001t0016g0193 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1077-1033A>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175706746 | |||||||
| chr5:175706773 | T | G | 1 | a0001c0001t0012g0103 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1077-1006T>G | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175706773 | |||||||
| chr5:175706916 | G | A | 1 | a0001c0001t0003g0173 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1077-863G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175706916 | |||||||
| chr5:175707034 | C | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0163 a0001c0001t0001g0209 |
6 | NA18940.hp2 NA18953.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.1077-745C>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175707034 | |||||||
| chr5:175707097 | T | A | 32 | a0001c0001t0002g0023 a0001c0001t0002g0039 a0001c0001t0002g0050 others(29): Show |
33 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.1077-682T>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175707097 | |||||||
| chr5:175707097 | T | C | 9 | a0001c0001t0012g0103 a0001c0001t0012g0131 a0001c0001t0012g0200 others(6): Show |
9 | HG01243.hp2 HG01884.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1077-682T>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175707097 | |||||||
| chr5:175707323 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1077-456G>A | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175707323 | |||||||
| chr5:175707504 | G | C | 64 | a0001c0001t0002g0023 a0001c0001t0002g0039 a0001c0001t0002g0050 others(61): Show |
66 | HG00438.hp2 HG00558.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.1077-275G>C | HRH2 | ENSG00000113749.8 | transcript | ENST00000636584.2 | protein_coding | 2/2 | chr5 | 175707504 |