Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10021 |
| ensemblid | ENSG00000138622.4 |
| hgncid | 16882 |
| symbol | HCN4 |
| name | hyperpolarization activated cyclic nucleotide gated potassium channel 4 |
| refseq_nuc | NM_005477.3 |
| refseq_prot | NP_005468.1 |
| ensembl_nuc | ENST00000261917.4 |
| ensembl_prot | ENSP00000261917.3 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 73319859 |
| end | 73368958 |
| strand | - |
| ver | v1.2 |
| region | chr15:73319859-73368958 |
| region5000 | chr15:73314859-73373958 |
| regionname0 | HCN4_chr15_73319859_73368958 |
| regionname5000 | HCN4_chr15_73314859_73373958 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1203 | 329 | 88 | 64 | 125 | 11 | 39 | 85 | HCN4_chr15_73314859_73373958 | HCN4 | MDKLP others(1198): Show |
chr15 | 73314859 | 73373958 |
| a0002 | 0/0 | 1203 | 5 | 0 | 3 | 0 | 0 | 2 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | MDKLP others(1198): Show |
chr15 | 73314859 | 73373958 |
| a0003 | 0/0 | 1203 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | MDKLP others(1198): Show |
chr15 | 73314859 | 73373958 |
| a0004 | 0/0 | 1203 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | MDKLP others(1198): Show |
chr15 | 73314859 | 73373958 |
| a0005 | 0/0 | 1203 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | MDKLP others(1198): Show |
chr15 | 73314859 | 73373958 |
| a0006 | 0/0 | 1203 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | MDKLP others(1198): Show |
chr15 | 73314859 | 73373958 |
| a0007 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | MDKLP others(1198): Show |
chr15 | 73314859 | 73373958 |
| a0008 | 0/0 | 1203 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | MDKLP others(1198): Show |
chr15 | 73314859 | 73373958 |
| a0009 | 0/0 | 1203 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | MDKLP others(1198): Show |
chr15 | 73314859 | 73373958 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3609 | 219 | 44 | 39 | 99 | 8 | 29 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0001c0002 | 1/0 | 3609 | 48 | 19 | 4 | 19 | 1 | 4 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0001c0003 | 0/0 | 3609 | 22 | 8 | 6 | 0 | 2 | 6 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0001c0004 | 0/0 | 3609 | 10 | 0 | 5 | 5 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0001c0005 | 0/1 | 3609 | 8 | 0 | 7 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0001c0006 | 0/0 | 3609 | 7 | 6 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0001c0007 | 0/0 | 3609 | 6 | 6 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0001c0009 | 0/0 | 3609 | 2 | 1 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0001c0013 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0001c0014 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0001c0016 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0001c0017 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0001c0020 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0001c0022 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0001c0023 | 0/0 | 3609 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0002c0008 | 0/0 | 3609 | 5 | 0 | 3 | 0 | 0 | 2 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0003c0012 | 0/0 | 3609 | 2 | 0 | 1 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0004c0010 | 0/0 | 3609 | 2 | 0 | 1 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0005c0011 | 0/0 | 3609 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0006c0019 | 0/0 | 3609 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0007c0018 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0008c0015 | 0/0 | 3609 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 | ||
| a0009c0021 | 0/0 | 3609 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | ATGGA others(3604): Show |
chr15 | 73314859 | 73373958 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6922 | 70 | 6 | 15 | 34 | 2 | 13 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0002 | 0/0 | 6919 | 82 | 3 | 10 | 53 | 4 | 12 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6914): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0003 | 0/0 | 6922 | 6 | 5 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0004 | 0/0 | 6922 | 23 | 17 | 5 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0005 | 0/0 | 6922 | 3 | 1 | 2 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0006 | 0/0 | 6922 | 9 | 6 | 0 | 3 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0007 | 0/0 | 6922 | 6 | 3 | 0 | 3 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0011 | 0/0 | 6919 | 3 | 0 | 3 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6914): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0012 | 0/0 | 6919 | 2 | 0 | 2 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6914): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0013 | 0/0 | 6912 | 2 | 0 | 0 | 0 | 2 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6907): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0015 | 0/0 | 6919 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6914): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0016 | 0/0 | 6919 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6914): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0017 | 0/0 | 6922 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0018 | 0/0 | 6922 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0019 | 0/0 | 6919 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6914): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0021 | 0/0 | 6922 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0022 | 0/0 | 6922 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0023 | 0/0 | 6922 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0026 | 0/0 | 6919 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6914): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0027 | 0/0 | 6919 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6914): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0028 | 0/0 | 6919 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6914): Show |
chr15 | 73314859 | 73373958 |
| a0001c0001t0029 | 0/0 | 6919 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6914): Show |
chr15 | 73314859 | 73373958 |
| a0001c0002t0003 | 1/0 | 6922 | 40 | 16 | 4 | 17 | 0 | 2 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0002t0008 | 0/0 | 6922 | 3 | 0 | 0 | 0 | 1 | 2 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0002t0010 | 0/0 | 6922 | 3 | 3 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0002t0024 | 0/0 | 6922 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0002t0025 | 0/0 | 6922 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0003t0001 | 0/0 | 6922 | 18 | 8 | 4 | 0 | 1 | 5 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0003t0009 | 0/0 | 6922 | 3 | 0 | 2 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0003t0020 | 0/0 | 6922 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0004t0001 | 0/0 | 6922 | 10 | 0 | 5 | 5 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0005t0005 | 0/1 | 6922 | 8 | 0 | 7 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0006t0003 | 0/0 | 6922 | 7 | 6 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0007t0003 | 0/0 | 6922 | 6 | 6 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0009t0014 | 0/0 | 6922 | 2 | 1 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0013t0001 | 0/0 | 6922 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0014t0003 | 0/0 | 6922 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0016t0001 | 0/0 | 6922 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0017t0004 | 0/0 | 6922 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0020t0007 | 0/0 | 6922 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0001c0022t0002 | 0/0 | 6919 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6914): Show |
chr15 | 73314859 | 73373958 |
| a0001c0023t0001 | 0/0 | 6922 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0002c0008t0002 | 0/0 | 6919 | 5 | 0 | 3 | 0 | 0 | 2 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6914): Show |
chr15 | 73314859 | 73373958 |
| a0003c0012t0001 | 0/0 | 6922 | 2 | 0 | 1 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0004c0010t0003 | 0/0 | 6922 | 2 | 0 | 1 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0005c0011t0004 | 0/0 | 6922 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0006c0019t0001 | 0/0 | 6922 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0007c0018t0003 | 0/0 | 6922 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0008c0015t0007 | 0/0 | 6922 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| a0009c0021t0006 | 0/0 | 6922 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | GCTGG others(6917): Show |
chr15 | 73314859 | 73373958 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0002 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0023 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0004g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0005g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0006g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0006g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0006g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0007g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0007g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0007g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0007g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0007g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0011g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0012g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0012g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0013g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0015g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0015g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0016g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0017g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0018g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0019g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0021g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0022g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0023g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0026g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0027g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0028g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0001t0029g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0001 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0003g0284 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0008g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0008g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0008g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0010g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0010g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0024g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0002t0025g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0003t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0003t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0003t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0003t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0003t0009g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0003t0009g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0003t0009g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0003t0020g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0004t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0004t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0004t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0004t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0004t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0005t0005g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0005t0005g0120 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0005t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0005t0005g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0005t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0005t0005g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0006t0003g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0006t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0006t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0006t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0006t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0006t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0007t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0007t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0007t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0007t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0009t0014g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0009t0014g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0013t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0014t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0016t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0017t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0020t0007g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0022t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0001c0023t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0002c0008t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0002c0008t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0002c0008t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0002c0008t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0003c0012t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0003c0012t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0004c0010t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0004c0010t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0005c0011t0004g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0005c0011t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0006c0019t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0007c0018t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0008c0015t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| a0009c0021t0006g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0023 | EUR | GBR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0235 | EUR | GBR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0256 | EUR | FIN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00280 | hp2 | a0001 | c0003 | t0009 | g0238 | EUR | FIN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00438 | hp1 | a0001 | c0002 | t0003 | g0217 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00558 | hp1 | a0001 | c0002 | t0003 | g0212 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00558 | hp2 | a0001 | c0001 | t0029 | g0155 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00609 | hp2 | a0001 | c0002 | t0003 | g0117 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00621 | hp1 | a0001 | c0002 | t0003 | g0193 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00639 | hp1 | a0001 | c0002 | t0003 | g0052 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00733 | hp1 | a0001 | c0004 | t0001 | g0028 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00733 | hp2 | a0001 | c0003 | t0009 | g0239 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0237 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00735 | hp2 | a0001 | c0004 | t0001 | g0028 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0019 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0226 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0019 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01069 | hp2 | a0001 | c0001 | t0011 | g0004 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01070 | hp1 | a0002 | c0008 | t0002 | g0048 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0053 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01074 | hp2 | a0001 | c0005 | t0005 | g0290 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01081 | hp2 | a0002 | c0008 | t0002 | g0046 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0261 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0229 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0037 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0037 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01169 | hp2 | a0001 | c0023 | t0001 | g0296 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01175 | hp1 | a0001 | c0005 | t0005 | g0125 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0248 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01192 | hp1 | a0001 | c0001 | t0011 | g0004 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01192 | hp2 | a0001 | c0001 | t0016 | g0040 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01243 | hp1 | a0001 | c0001 | t0017 | g0043 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01243 | hp2 | a0001 | c0002 | t0003 | g0094 | AMR | PUR | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01255 | hp1 | a0001 | c0009 | t0014 | g0264 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01257 | hp2 | a0003 | c0012 | t0001 | g0152 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0024 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01346 | hp1 | a0001 | c0006 | t0003 | g0056 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01346 | hp2 | a0002 | c0008 | t0002 | g0047 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01358 | hp2 | a0001 | c0003 | t0009 | g0096 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01361 | hp1 | a0001 | c0005 | t0005 | g0005 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01433 | hp1 | a0004 | c0010 | t0003 | g0272 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0024 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01496 | hp2 | a0001 | c0002 | t0003 | g0129 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0166 | EUR | IBS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01516 | hp1 | a0001 | c0001 | t0013 | g0006 | EUR | IBS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01516 | hp2 | a0001 | c0002 | t0008 | g0154 | EUR | IBS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0165 | EUR | IBS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01517 | hp2 | a0001 | c0001 | t0013 | g0006 | EUR | IBS | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01884 | hp2 | a0001 | c0002 | t0003 | g0036 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0236 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01891 | hp2 | a0001 | c0001 | t0021 | g0242 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01934 | hp2 | a0001 | c0001 | t0012 | g0041 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01943 | hp2 | a0001 | c0004 | t0001 | g0160 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01952 | hp1 | a0001 | c0005 | t0005 | g0232 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01981 | hp1 | a0001 | c0001 | t0012 | g0042 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01981 | hp2 | a0006 | c0019 | t0001 | g0100 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01993 | hp1 | a0001 | c0004 | t0001 | g0253 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01993 | hp2 | a0001 | c0005 | t0005 | g0005 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02004 | hp1 | a0001 | c0001 | t0011 | g0004 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02055 | hp1 | a0001 | c0002 | t0003 | g0265 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0285 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02071 | hp1 | a0001 | c0004 | t0001 | g0142 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02080 | hp2 | a0001 | c0002 | t0003 | g0199 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02083 | hp2 | a0001 | c0004 | t0001 | g0293 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02129 | hp1 | a0001 | c0002 | t0024 | g0107 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02135 | hp1 | a0001 | c0004 | t0001 | g0157 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02135 | hp2 | a0001 | c0001 | t0015 | g0095 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02145 | hp1 | a0001 | c0006 | t0003 | g0059 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02145 | hp2 | a0001 | c0007 | t0003 | g0017 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02155 | hp1 | a0001 | c0002 | t0003 | g0159 | EAS | CDX | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02155 | hp2 | a0001 | c0002 | t0025 | g0140 | EAS | CDX | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | CDX | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | CDX | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0121 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02257 | hp2 | a0001 | c0002 | t0003 | g0001 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02258 | hp2 | a0007 | c0018 | t0003 | g0291 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02280 | hp1 | a0001 | c0001 | t0004 | g0270 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02293 | hp1 | a0001 | c0005 | t0005 | g0005 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02293 | hp2 | a0001 | c0004 | t0001 | g0099 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PEL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02451 | hp1 | a0001 | c0009 | t0014 | g0263 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0068 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02572 | hp1 | a0001 | c0013 | t0001 | g0221 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02572 | hp2 | a0001 | c0007 | t0003 | g0015 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0271 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0064 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02622 | hp1 | a0001 | c0006 | t0003 | g0008 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0076 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02630 | hp1 | a0001 | c0001 | t0023 | g0067 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0287 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02683 | hp1 | a0001 | c0003 | t0020 | g0230 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0231 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0262 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0054 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02735 | hp1 | a0004 | c0010 | t0003 | g0153 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0119 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0267 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02818 | hp2 | a0001 | c0002 | t0010 | g0292 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02886 | hp1 | a0001 | c0002 | t0003 | g0081 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02896 | hp1 | a0001 | c0002 | t0003 | g0083 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02922 | hp1 | a0001 | c0007 | t0003 | g0015 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02965 | hp1 | a0001 | c0002 | t0003 | g0163 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0036 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0241 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0283 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02976 | hp2 | a0001 | c0002 | t0003 | g0001 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0188 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03041 | hp1 | a0001 | c0002 | t0003 | g0269 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0286 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03098 | hp2 | a0001 | c0006 | t0003 | g0057 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0065 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0254 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0001 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03195 | hp1 | a0001 | c0002 | t0003 | g0164 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03195 | hp2 | a0001 | c0002 | t0003 | g0268 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03209 | hp1 | a0001 | c0002 | t0003 | g0001 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0289 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03225 | hp1 | a0001 | c0007 | t0003 | g0078 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03225 | hp2 | a0001 | c0003 | t0001 | g0051 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0086 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0266 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0227 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0258 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03486 | hp2 | a0001 | c0002 | t0003 | g0127 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03491 | hp2 | a0002 | c0008 | t0002 | g0007 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03492 | hp1 | a0001 | c0001 | t0026 | g0190 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03492 | hp2 | a0002 | c0008 | t0002 | g0007 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03516 | hp1 | a0001 | c0017 | t0004 | g0176 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03516 | hp2 | a0008 | c0015 | t0007 | g0250 | AFR | ESN | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03540 | hp1 | a0001 | c0014 | t0003 | g0082 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0124 | AFR | GWD | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0161 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | STU | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0114 | SAS | STU | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0074 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0228 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03710 | hp2 | a0001 | c0002 | t0003 | g0098 | SAS | PJL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0022 | SAS | BEB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03834 | hp2 | a0001 | c0001 | t0022 | g0089 | SAS | BEB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | BEB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0247 | SAS | BEB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03942 | hp2 | a0001 | c0002 | t0008 | g0146 | SAS | BEB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | STU | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG04115 | hp2 | a0001 | c0002 | t0003 | g0138 | SAS | STU | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | BEB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG04204 | hp1 | a0001 | c0003 | t0001 | g0245 | SAS | STU | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG04228 | hp1 | a0001 | c0002 | t0008 | g0115 | SAS | STU | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | STU | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0061 | AFR | YRI | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0260 | AFR | YRI | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | CHB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | CHB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | YRI | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18906 | hp2 | a0001 | c0007 | t0003 | g0017 | AFR | YRI | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18939 | hp2 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18944 | hp1 | a0001 | c0001 | t0028 | g0280 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18954 | hp2 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18961 | hp2 | a0001 | c0002 | t0003 | g0103 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18967 | hp2 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18990 | hp1 | a0001 | c0002 | t0003 | g0087 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18991 | hp1 | a0009 | c0021 | t0006 | g0294 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18998 | hp1 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19000 | hp1 | a0001 | c0002 | t0003 | g0014 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19003 | hp1 | a0001 | c0002 | t0003 | g0101 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19003 | hp2 | a0001 | c0001 | t0007 | g0198 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19005 | hp2 | a0001 | c0001 | t0015 | g0204 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19007 | hp2 | a0001 | c0001 | t0006 | g0071 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19009 | hp1 | a0001 | c0004 | t0001 | g0090 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19012 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19012 | hp2 | a0001 | c0001 | t0019 | g0045 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0240 | AFR | LWK | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19030 | hp2 | a0001 | c0006 | t0003 | g0008 | AFR | LWK | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | LWK | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | LWK | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19062 | hp1 | a0001 | c0001 | t0027 | g0278 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19065 | hp2 | a0001 | c0001 | t0007 | g0186 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19068 | hp1 | a0001 | c0020 | t0007 | g0208 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19068 | hp2 | a0001 | c0001 | t0006 | g0072 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19074 | hp1 | a0001 | c0001 | t0007 | g0203 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19074 | hp2 | a0001 | c0016 | t0001 | g0145 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19077 | hp1 | a0001 | c0004 | t0001 | g0170 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19083 | hp2 | a0001 | c0001 | t0006 | g0070 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19088 | hp2 | a0001 | c0002 | t0003 | g0172 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19240 | hp1 | a0001 | c0002 | t0010 | g0013 | AFR | YRI | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA19240 | hp2 | a0001 | c0002 | t0003 | g0001 | AFR | YRI | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | ASW | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ASW | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA20805 | hp2 | a0003 | c0012 | t0001 | g0151 | EUR | TSI | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | GIH | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | GIH | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG01123 | hp2 | a0001 | c0005 | t0005 | g0234 | AMR | CLM | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02109 | hp1 | a0001 | c0002 | t0003 | g0162 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02109 | hp2 | a0001 | c0002 | t0010 | g0013 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0259 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02486 | hp2 | a0001 | c0022 | t0002 | g0295 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0069 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0288 | AFR | ACB | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03471 | hp1 | a0001 | c0001 | t0018 | g0044 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG03471 | hp2 | a0001 | c0007 | t0003 | g0156 | AFR | MSL | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG06807 | hp1 | a0005 | c0011 | t0004 | g0073 | AFR | USA | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| HG06807 | hp2 | a0001 | c0006 | t0003 | g0058 | AFR | USA | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA18955 | hp2 | a0001 | c0002 | t0003 | g0091 | EAS | JPT | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0050 | AFR | USA | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA20300 | hp2 | a0001 | c0006 | t0003 | g0060 | AFR | USA | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA21309 | hp1 | a0005 | c0011 | t0004 | g0084 | AFR | LWK | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | LWK | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| homoSapiens | chm13v2 | a0001 | c0005 | t0005 | g0120 | REF | REF | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0003 | g0284 | REF | REF | HCN4_chr15_73314859_73373958 | HCN4 | chr15 | 73314859 | 73373958 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:73322756 | T | C | 2 | a0004 a0007 |
3 | HG01433.hp1 HG02258.hp2 HG02735.hp1 |
missense_variant | MODERATE | c.3337A>G | p.Met1113Val | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 4025/6922 | 3337/3612 | 1113/1203 | chr15 | 73322756 | |||
| chr15:73322788 | C | T | 1 | a0006 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.3305G>A | p.Arg1102His | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3993/6922 | 3305/3612 | 1102/1203 | chr15 | 73322788 | |||
| chr15:73323262 | G | A | 1 | a0005 | 2 | HG06807.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.2831C>T | p.Ala944Val | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3519/6922 | 2831/3612 | 944/1203 | chr15 | 73323262 | |||
| chr15:73323293 | G | A | 1 | a0007 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.2800C>T | p.Arg934Cys | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3488/6922 | 2800/3612 | 934/1203 | chr15 | 73323293 | |||
| chr15:73323436 | G | A | 1 | a0008 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.2657C>T | p.Ala886Val | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3345/6922 | 2657/3612 | 886/1203 | chr15 | 73323436 | |||
| chr15:73323445 | G | C | 1 | a0003 | 2 | HG01257.hp2 NA20805.hp2 |
missense_variant | MODERATE | c.2648C>G | p.Pro883Arg | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3336/6922 | 2648/3612 | 883/1203 | chr15 | 73323445 | |||
| chr15:73367687 | G | A | 1 | a0009 | 1 | NA18991.hp1 | missense_variant | MODERATE | c.584C>T | p.Ala195Val | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 1272/6922 | 584/3612 | 195/1203 | chr15 | 73367687 | |||
| chr15:73368164 | C | T | 1 | a0002 | 5 | HG01070.hp1 HG01081.hp2 HG01346.hp2 others(2): Show |
missense_variant | MODERATE | c.107G>A | p.Gly36Glu | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 795/6922 | 107/3612 | 36/1203 | chr15 | 73368164 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:73322493 | T | C | 18 | a0001c0001 a0001c0003 a0001c0004 others(15): Show |
285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
synonymous_variant | LOW | c.3600A>G | p.Pro1200Pro | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 4288/6922 | 3600/3612 | 1200/1203 | chr15 | 73322493 | |||
| chr15:73322805 | G | A | 1 | a0001c0017 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.3288C>T | p.Asp1096Asp | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3976/6922 | 3288/3612 | 1096/1203 | chr15 | 73322805 | |||
| chr15:73323060 | A | C | 1 | a0001c0009 | 2 | HG01255.hp1 HG02451.hp1 |
synonymous_variant | LOW | c.3033T>G | p.Ser1011Ser | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3721/6922 | 3033/3612 | 1011/1203 | chr15 | 73323060 | |||
| chr15:73323114 | C | T | 2 | a0001c0007 a0001c0016 |
7 | HG02145.hp2 HG02572.hp2 HG02922.hp1 others(4): Show |
synonymous_variant | LOW | c.2979G>A | p.Thr993Thr | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3667/6922 | 2979/3612 | 993/1203 | chr15 | 73323114 | |||
| chr15:73323420 | C | T | 1 | a0001c0009 | 2 | HG01255.hp1 HG02451.hp1 |
synonymous_variant | LOW | c.2673G>A | p.Ser891Ser | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3361/6922 | 2673/3612 | 891/1203 | chr15 | 73323420 | |||
| chr15:73323492 | G | T | 1 | a0008c0015 | 1 | HG03516.hp2 | synonymous_variant | LOW | c.2601C>A | p.Ala867Ala | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3289/6922 | 2601/3612 | 867/1203 | chr15 | 73323492 | |||
| chr15:73323537 | C | T | 1 | a0001c0005 | 7 | HG01074.hp2 HG01123.hp2 HG01175.hp1 others(4): Show |
synonymous_variant | LOW | c.2556G>A | p.Pro852Pro | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 3244/6922 | 2556/3612 | 852/1203 | chr15 | 73323537 | |||
| chr15:73325094 | G | A | 2 | a0001c0004 a0006c0019 |
11 | HG00733.hp1 HG00735.hp2 HG01943.hp2 others(8): Show |
synonymous_variant | LOW | c.1839C>T | p.Phe613Phe | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/8 | 2527/6922 | 1839/3612 | 613/1203 | chr15 | 73325094 | |||
| chr15:73325118 | C | T | 1 | a0001c0014 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.1815G>A | p.Thr605Thr | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/8 | 2503/6922 | 1815/3612 | 605/1203 | chr15 | 73325118 | |||
| chr15:73325352 | G | T | 1 | a0001c0006 | 7 | HG01346.hp1 HG02145.hp1 HG02622.hp1 others(4): Show |
synonymous_variant | LOW | c.1683C>A | p.Gly561Gly | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 5/8 | 2371/6922 | 1683/3612 | 561/1203 | chr15 | 73325352 | |||
| chr15:73325382 | G | T | 1 | a0001c0013 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.1653C>A | p.Ile551Ile | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 5/8 | 2341/6922 | 1653/3612 | 551/1203 | chr15 | 73325382 | |||
| chr15:73329600 | G | A | 1 | a0001c0020 | 1 | NA19068.hp1 | synonymous_variant | LOW | c.1563C>T | p.Asp521Asp | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/8 | 2251/6922 | 1563/3612 | 521/1203 | chr15 | 73329600 | |||
| chr15:73329605 | G | A | 1 | a0001c0003 | 22 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(19): Show |
synonymous_variant | LOW | c.1558C>T | p.Leu520Leu | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/8 | 2246/6922 | 1558/3612 | 520/1203 | chr15 | 73329605 | |||
| chr15:73367743 | G | A | 1 | a0001c0022 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.528C>T | p.Ser176Ser | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 1216/6922 | 528/3612 | 176/1203 | chr15 | 73367743 | |||
| chr15:73368235 | G | C | 1 | a0001c0023 | 1 | HG01169.hp2 | synonymous_variant | LOW | c.36C>G | p.Leu12Leu | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 724/6922 | 36/3612 | 12/1203 | chr15 | 73368235 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:73319864 | G | C | 1 | a0001c0001t0028 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2617C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 2617 | chr15 | 73319864 | ||||||
| chr15:73320036 | G | A | 3 | a0001c0001t0004 a0001c0017t0004 a0005c0011t0004 |
26 | HG00738.hp2 HG01109.hp1 HG01167.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2445C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 2445 | chr15 | 73320036 | ||||||
| chr15:73320060 | G | C | 1 | a0001c0001t0021 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2421C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 2421 | chr15 | 73320060 | ||||||
| chr15:73320088 | G | C | 2 | a0001c0001t0005 a0001c0005t0005 |
10 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2393C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 2393 | chr15 | 73320088 | ||||||
| chr15:73320127 | T | C | 1 | a0001c0001t0022 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2354A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 2354 | chr15 | 73320127 | ||||||
| chr15:73320230 | A | G | 1 | a0001c0001t0027 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2251T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 2251 | chr15 | 73320230 | ||||||
| chr15:73320380 | C | T | 1 | a0001c0001t0026 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2101G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 2101 | chr15 | 73320380 | ||||||
| chr15:73320492 | C | T | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(26): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*1989G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 1989 | chr15 | 73320492 | ||||||
| chr15:73320822 | T | C | 5 | a0001c0001t0006 a0001c0001t0017 a0001c0001t0018 others(2): Show |
13 | HG01243.hp1 HG02451.hp2 HG02559.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1659A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 1659 | chr15 | 73320822 | ||||||
| chr15:73320999 | T | C | 1 | a0001c0001t0011 | 3 | HG01069.hp2 HG01192.hp1 HG02004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1482A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 1482 | chr15 | 73320999 | ||||||
| chr15:73321284 | A | G | 1 | a0001c0003t0009 | 3 | HG00280.hp2 HG00733.hp2 HG01358.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1197T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 1197 | chr15 | 73321284 | ||||||
| chr15:73321309 | T | C | 1 | a0001c0001t0029 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1172A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 1172 | chr15 | 73321309 | ||||||
| chr15:73321341 | C | T | 1 | a0001c0002t0008 | 3 | HG01516.hp2 HG03942.hp2 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1140G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 1140 | chr15 | 73321341 | ||||||
| chr15:73321545 | C | T | 1 | a0001c0009t0014 | 2 | HG01255.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*936G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 936 | chr15 | 73321545 | ||||||
| chr15:73321639 | T | C | 1 | a0001c0009t0014 | 2 | HG01255.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*842A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 842 | chr15 | 73321639 | ||||||
| chr15:73321773 | T | C | 34 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(31): Show |
259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*708A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 708 | chr15 | 73321773 | ||||||
| chr15:73321778 | CA | C | 12 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0012 others(9): Show |
101 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*702delT | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 702 | chr15 | 73321778 | ||||||
| chr15:73321816 | T | C | 1 | a0001c0002t0010 | 3 | HG02109.hp2 HG02818.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*665A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 665 | chr15 | 73321816 | ||||||
| chr15:73321839 | C | T | 1 | a0001c0003t0020 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*642G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 642 | chr15 | 73321839 | ||||||
| chr15:73321876 | T | C | 1 | a0001c0009t0014 | 2 | HG01255.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*605A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 605 | chr15 | 73321876 | ||||||
| chr15:73322014 | G | A | 1 | a0001c0002t0024 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*467C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 467 | chr15 | 73322014 | ||||||
| chr15:73322022 | C | A | 1 | a0001c0002t0025 | 1 | HG02155.hp2 | 3_prime_UTR_variant | MODIFIER | c.*459G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 459 | chr15 | 73322022 | ||||||
| chr15:73322067 | G | T | 12 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0012 others(9): Show |
101 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*414C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 414 | chr15 | 73322067 | ||||||
| chr15:73322361 | GGT | G | 12 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0012 others(9): Show |
101 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*118_*119delAC | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 8/8 | 118 | chr15 | 73322361 | ||||||
| chr15:73368304 | G | A | 2 | a0001c0001t0017 a0001c0001t0018 |
2 | HG01243.hp1 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-34C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 34 | chr15 | 73368304 | ||||||
| chr15:73368459 | C | T | 2 | a0001c0001t0017 a0001c0001t0018 |
2 | HG01243.hp1 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-189G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 189 | chr15 | 73368459 | ||||||
| chr15:73368537 | TCCCTCTG others(3): Show |
T | 1 | a0001c0001t0013 | 2 | HG01516.hp1 HG01517.hp2 |
5_prime_UTR_variant | MODIFIER | c.-277_-268delCGCCAG others(4): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 268 | chr15 | 73368537 | ||||||
| chr15:73368611 | G | T | 1 | a0001c0001t0019 | 1 | NA19012.hp2 | 5_prime_UTR_variant | MODIFIER | c.-341C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 341 | chr15 | 73368611 | ||||||
| chr15:73368677 | G | A | 1 | a0001c0001t0018 | 1 | HG03471.hp1 | 5_prime_UTR_variant | MODIFIER | c.-407C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 407 | chr15 | 73368677 | ||||||
| chr15:73368768 | G | T | 2 | a0001c0001t0017 a0001c0001t0018 |
2 | HG01243.hp1 HG03471.hp1 |
5_prime_UTR_variant | MODIFIER | c.-498C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 498 | chr15 | 73368768 | ||||||
| chr15:73368852 | A | G | 1 | a0001c0001t0012 | 2 | HG01934.hp2 HG01981.hp1 |
5_prime_UTR_variant | MODIFIER | c.-582T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 582 | chr15 | 73368852 | ||||||
| chr15:73368855 | G | T | 1 | a0001c0001t0016 | 1 | HG01192.hp2 | 5_prime_UTR_variant | MODIFIER | c.-585C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/8 | 585 | chr15 | 73368855 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:73324004 | T | C | 1 | a0001c0001t0021g0242 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2144-55A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 7/7 | chr15 | 73324004 | |||||||
| chr15:73324055 | C | A | 1 | a0001c0001t0001g0202 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2143+34G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 7/7 | chr15 | 73324055 | |||||||
| chr15:73324294 | T | C | 215 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(212): Show |
251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.1979-41A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/7 | chr15 | 73324294 | |||||||
| chr15:73324403 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(78): Show |
93 | HG00423.hp2 HG00673.hp2 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.1979-150G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/7 | chr15 | 73324403 | |||||||
| chr15:73324460 | G | A | 1 | a0001c0001t0004g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1979-207C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/7 | chr15 | 73324460 | |||||||
| chr15:73324605 | G | A | 1 | a0001c0001t0003g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1978+350C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/7 | chr15 | 73324605 | |||||||
| chr15:73324694 | A | G | 289 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(286): Show |
333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.1978+261T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/7 | chr15 | 73324694 | |||||||
| chr15:73324695 | A | T | 9 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0007g0186 others(6): Show |
9 | HG02135.hp2 HG02622.hp2 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.1978+260T>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/7 | chr15 | 73324695 | |||||||
| chr15:73324703 | G | A | 57 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0022 others(54): Show |
76 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.1978+252C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/7 | chr15 | 73324703 | |||||||
| chr15:73324728 | C | A | 1 | a0001c0001t0007g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1978+227G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/7 | chr15 | 73324728 | |||||||
| chr15:73324909 | C | T | 1 | a0001c0001t0022g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1978+46G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 6/7 | chr15 | 73324909 | |||||||
| chr15:73325278 | C | T | 4 | a0001c0007t0003g0015 a0001c0007t0003g0017 a0001c0007t0003g0078 others(1): Show |
6 | HG02145.hp2 HG02572.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1737+20G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 5/7 | chr15 | 73325278 | |||||||
| chr15:73325458 | AAGGGGGC others(17): Show |
A | 1 | a0001c0002t0003g0163 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1591-38_1591-15del others(24): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73325458 | |||||||
| chr15:73325463 | G | T | 2 | a0003c0012t0001g0151 a0003c0012t0001g0152 |
2 | HG01257.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.1591-19C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73325463 | |||||||
| chr15:73325529 | C | T | 1 | a0001c0001t0006g0072 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1591-85G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73325529 | |||||||
| chr15:73325681 | G | A | 3 | a0001c0001t0004g0077 a0001c0001t0004g0258 a0001c0002t0003g0127 |
3 | HG02809.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1591-237C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73325681 | |||||||
| chr15:73325714 | G | A | 1 | a0001c0002t0003g0091 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1591-270C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73325714 | |||||||
| chr15:73325790 | T | C | 1 | a0001c0013t0001g0221 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1591-346A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73325790 | |||||||
| chr15:73325897 | C | T | 125 | a0001c0001t0001g0062 a0001c0001t0001g0130 a0001c0001t0001g0222 others(122): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1591-453G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73325897 | |||||||
| chr15:73325950 | G | A | 1 | a0001c0001t0004g0241 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1591-506C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73325950 | |||||||
| chr15:73325968 | C | T | 126 | a0001c0001t0001g0062 a0001c0001t0001g0130 a0001c0001t0001g0222 others(123): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1591-524G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73325968 | |||||||
| chr15:73325983 | G | A | 5 | a0001c0003t0001g0009 a0001c0003t0001g0050 a0001c0003t0001g0051 others(2): Show |
6 | HG02559.hp1 HG03225.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.1591-539C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73325983 | |||||||
| chr15:73326141 | C | T | 1 | a0001c0001t0003g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1591-697G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326141 | |||||||
| chr15:73326227 | C | T | 1 | a0001c0001t0003g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1591-783G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326227 | |||||||
| chr15:73326280 | C | T | 1 | a0001c0004t0001g0160 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1591-836G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326280 | |||||||
| chr15:73326353 | G | A | 2 | a0001c0002t0003g0001 a0001c0002t0003g0163 |
6 | HG02257.hp2 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1591-909C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326353 | |||||||
| chr15:73326402 | C | T | 1 | a0001c0005t0005g0232 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1591-958G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326402 | |||||||
| chr15:73326468 | A | G | 247 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(244): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.1591-1024T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326468 | |||||||
| chr15:73326717 | C | T | 2 | a0001c0001t0002g0027 a0001c0001t0002g0181 |
3 | HG02056.hp1 NA18612.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1591-1273G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326717 | |||||||
| chr15:73326744 | G | A | 5 | a0001c0001t0001g0062 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
5 | HG02258.hp1 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1591-1300C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326744 | |||||||
| chr15:73326769 | T | TTTTA | 5 | a0001c0001t0004g0257 a0001c0001t0004g0260 a0001c0001t0004g0266 others(2): Show |
5 | HG02055.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1591-1329_1591-132 others(8): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326769 | |||||||
| chr15:73326785 | A | T | 1 | a0001c0001t0001g0102 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1591-1341T>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326785 | |||||||
| chr15:73326789 | A | T | 45 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0092 others(42): Show |
52 | HG00673.hp2 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.1591-1345T>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326789 | |||||||
| chr15:73326790 | T | A | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG01261.hp1 HG01952.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.1591-1346A>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326790 | |||||||
| chr15:73326792 | T | A | 1 | a0008c0015t0007g0250 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1591-1348A>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326792 | |||||||
| chr15:73326793 | A | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(69): Show |
81 | HG00544.hp1 HG00673.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.1591-1349T>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326793 | |||||||
| chr15:73326797 | T | A | 35 | a0001c0001t0003g0116 a0001c0001t0004g0037 a0001c0001t0004g0049 others(32): Show |
36 | HG00738.hp2 HG01109.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.1591-1353A>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326797 | |||||||
| chr15:73326879 | T | TG | 10 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0007g0186 others(7): Show |
10 | HG02135.hp2 HG02622.hp2 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.1591-1436dupC | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326879 | |||||||
| chr15:73326918 | C | T | 1 | a0001c0001t0007g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1591-1474G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326918 | |||||||
| chr15:73326984 | G | C | 1 | a0001c0001t0001g0148 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1591-1540C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73326984 | |||||||
| chr15:73327094 | C | T | 1 | a0005c0011t0004g0073 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1591-1650G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327094 | |||||||
| chr15:73327108 | C | CT | 11 | a0001c0001t0002g0200 a0001c0001t0003g0075 a0001c0001t0003g0076 others(8): Show |
11 | HG02135.hp2 HG02622.hp2 HG03130.hp2 others(8): Show |
intron_variant | MODIFIER | c.1591-1665dupA | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327108 | |||||||
| chr15:73327108 | CT | C | 8 | a0001c0001t0001g0106 a0001c0001t0001g0185 a0001c0001t0001g0202 others(5): Show |
8 | HG01070.hp2 HG01515.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1591-1665delA | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327108 | |||||||
| chr15:73327358 | G | A | 129 | a0001c0001t0001g0062 a0001c0001t0001g0104 a0001c0001t0001g0222 others(126): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1591-1914C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327358 | |||||||
| chr15:73327391 | G | A | 25 | a0001c0001t0004g0037 a0001c0001t0004g0049 a0001c0001t0004g0077 others(22): Show |
26 | HG00738.hp2 HG01109.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.1591-1947C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327391 | |||||||
| chr15:73327415 | A | G | 2 | a0001c0009t0014g0263 a0001c0009t0014g0264 |
2 | HG01255.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1591-1971T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327415 | |||||||
| chr15:73327463 | G | A | 2 | a0001c0009t0014g0263 a0001c0009t0014g0264 |
2 | HG01255.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1591-2019C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327463 | |||||||
| chr15:73327631 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1590+1942C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327631 | |||||||
| chr15:73327656 | T | C | 245 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(242): Show |
282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.1590+1917A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327656 | |||||||
| chr15:73327830 | T | C | 1 | a0001c0001t0006g0070 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1590+1743A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327830 | |||||||
| chr15:73327849 | C | T | 2 | a0001c0009t0014g0263 a0001c0009t0014g0264 |
2 | HG01255.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1590+1724G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327849 | |||||||
| chr15:73327969 | C | T | 129 | a0001c0001t0001g0062 a0001c0001t0001g0104 a0001c0001t0001g0222 others(126): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1590+1604G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73327969 | |||||||
| chr15:73328057 | G | A | 3 | a0001c0006t0003g0008 a0001c0006t0003g0058 a0001c0006t0003g0060 |
4 | HG02622.hp1 HG06807.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1590+1516C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328057 | |||||||
| chr15:73328108 | C | T | 131 | a0001c0001t0001g0062 a0001c0001t0001g0104 a0001c0001t0001g0222 others(128): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1590+1465G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328108 | |||||||
| chr15:73328119 | C | T | 129 | a0001c0001t0001g0062 a0001c0001t0001g0104 a0001c0001t0001g0222 others(126): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1590+1454G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328119 | |||||||
| chr15:73328184 | C | T | 131 | a0001c0001t0001g0062 a0001c0001t0001g0104 a0001c0001t0001g0222 others(128): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1590+1389G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328184 | |||||||
| chr15:73328188 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1590+1385G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328188 | |||||||
| chr15:73328231 | G | A | 82 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(79): Show |
94 | HG00423.hp2 HG00673.hp2 HG00733.hp1 others(91): Show |
intron_variant | MODIFIER | c.1590+1342C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328231 | |||||||
| chr15:73328437 | C | G | 7 | a0001c0001t0007g0186 a0001c0001t0007g0198 a0001c0001t0007g0203 others(4): Show |
7 | HG02135.hp2 HG03130.hp2 NA19003.hp2 others(4): Show |
intron_variant | MODIFIER | c.1590+1136G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328437 | |||||||
| chr15:73328495 | C | T | 30 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0110 others(27): Show |
33 | HG00423.hp2 HG00733.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1590+1078G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328495 | |||||||
| chr15:73328694 | G | A | 1 | a0001c0001t0002g0256 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1590+879C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328694 | |||||||
| chr15:73328791 | G | C | 1 | a0001c0001t0002g0033 | 2 | NA18952.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.1590+782C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328791 | |||||||
| chr15:73328858 | C | T | 218 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(215): Show |
254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1590+715G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73328858 | |||||||
| chr15:73329090 | G | A | 24 | a0001c0001t0004g0037 a0001c0001t0004g0049 a0001c0001t0004g0077 others(21): Show |
25 | HG00738.hp2 HG01109.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1590+483C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73329090 | |||||||
| chr15:73329094 | C | T | 104 | a0001c0001t0001g0062 a0001c0001t0001g0104 a0001c0001t0001g0222 others(101): Show |
127 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1590+479G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73329094 | |||||||
| chr15:73329176 | T | G | 2 | a0001c0009t0014g0263 a0001c0009t0014g0264 |
2 | HG01255.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1590+397A>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73329176 | |||||||
| chr15:73329191 | G | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(78): Show |
93 | HG00423.hp2 HG00673.hp2 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.1590+382C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73329191 | |||||||
| chr15:73329208 | C | T | 1 | a0001c0001t0002g0256 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1590+365G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73329208 | |||||||
| chr15:73329270 | C | T | 1 | a0001c0001t0004g0287 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1590+303G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73329270 | |||||||
| chr15:73329513 | G | A | 1 | a0001c0001t0006g0071 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1590+60C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 4/7 | chr15 | 73329513 | |||||||
| chr15:73329818 | A | G | 1 | a0001c0023t0001g0296 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1372-27T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73329818 | |||||||
| chr15:73329940 | T | G | 1 | a0001c0001t0007g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1372-149A>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73329940 | |||||||
| chr15:73330103 | G | A | 80 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(77): Show |
92 | HG00423.hp2 HG00673.hp2 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.1372-312C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73330103 | |||||||
| chr15:73330113 | A | G | 5 | a0001c0001t0001g0062 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
5 | HG02258.hp1 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1372-322T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73330113 | |||||||
| chr15:73330180 | C | G | 1 | a0001c0002t0003g0103 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1372-389G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73330180 | |||||||
| chr15:73330183 | A | C | 1 | a0001c0002t0003g0103 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1372-392T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73330183 | |||||||
| chr15:73330184 | T | A | 1 | a0001c0002t0003g0103 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1372-393A>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73330184 | |||||||
| chr15:73330852 | C | T | 50 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(47): Show |
59 | HG00673.hp2 HG00738.hp1 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.1372-1061G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73330852 | |||||||
| chr15:73330970 | C | G | 3 | a0001c0001t0001g0182 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG01934.hp1 HG01943.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1371+1161G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73330970 | |||||||
| chr15:73331076 | A | C | 289 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(286): Show |
333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.1371+1055T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331076 | |||||||
| chr15:73331121 | A | C | 50 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(47): Show |
59 | HG00673.hp2 HG00738.hp1 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.1371+1010T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331121 | |||||||
| chr15:73331163 | T | G | 1 | a0001c0001t0002g0228 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1371+968A>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331163 | |||||||
| chr15:73331196 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(78): Show |
93 | HG00423.hp2 HG00673.hp2 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.1371+935G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331196 | |||||||
| chr15:73331348 | C | G | 222 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(219): Show |
258 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.1371+783G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331348 | |||||||
| chr15:73331350 | A | G | 255 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(252): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1371+781T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331350 | |||||||
| chr15:73331441 | G | A | 80 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(77): Show |
92 | HG00423.hp2 HG00673.hp2 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.1371+690C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331441 | |||||||
| chr15:73331577 | C | A | 1 | a0004c0010t0003g0272 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1371+554G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331577 | |||||||
| chr15:73331596 | G | A | 131 | a0001c0001t0001g0062 a0001c0001t0001g0104 a0001c0001t0001g0222 others(128): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1371+535C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331596 | |||||||
| chr15:73331749 | G | C | 129 | a0001c0001t0001g0062 a0001c0001t0001g0104 a0001c0001t0001g0222 others(126): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1371+382C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331749 | |||||||
| chr15:73331980 | G | A | 2 | a0001c0001t0004g0257 a0001c0001t0004g0260 |
2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1371+151C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73331980 | |||||||
| chr15:73332067 | C | T | 1 | a0001c0001t0007g0254 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1371+64G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 3/7 | chr15 | 73332067 | |||||||
| chr15:73332395 | G | C | 7 | a0001c0002t0003g0081 a0001c0002t0003g0083 a0001c0002t0003g0094 others(4): Show |
8 | HG01243.hp2 HG01496.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1210-103C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73332395 | |||||||
| chr15:73332508 | C | A | 50 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(47): Show |
59 | HG00673.hp2 HG00738.hp1 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.1210-216G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73332508 | |||||||
| chr15:73332549 | T | A | 1 | a0001c0001t0007g0124 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1210-257A>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73332549 | |||||||
| chr15:73332559 | G | T | 1 | a0001c0001t0002g0196 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1210-267C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73332559 | |||||||
| chr15:73333006 | T | C | 1 | a0001c0009t0014g0264 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1210-714A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73333006 | |||||||
| chr15:73333178 | C | T | 129 | a0001c0001t0001g0062 a0001c0001t0001g0104 a0001c0001t0001g0222 others(126): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1210-886G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73333178 | |||||||
| chr15:73333227 | A | C | 1 | a0001c0001t0007g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1210-935T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73333227 | |||||||
| chr15:73333311 | T | G | 10 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0007g0186 others(7): Show |
10 | HG02135.hp2 HG02622.hp2 HG03130.hp2 others(7): Show |
intron_variant | MODIFIER | c.1210-1019A>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73333311 | |||||||
| chr15:73333321 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1210-1029C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73333321 | |||||||
| chr15:73333554 | G | A | 131 | a0001c0001t0001g0062 a0001c0001t0001g0104 a0001c0001t0001g0222 others(128): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1210-1262C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73333554 | |||||||
| chr15:73333565 | C | A | 5 | a0001c0002t0003g0127 a0001c0007t0003g0015 a0001c0007t0003g0017 others(2): Show |
7 | HG02145.hp2 HG02572.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1210-1273G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73333565 | |||||||
| chr15:73333882 | G | A | 130 | a0001c0001t0001g0062 a0001c0001t0001g0104 a0001c0001t0001g0222 others(127): Show |
154 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1210-1590C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73333882 | |||||||
| chr15:73334098 | C | T | 78 | a0001c0001t0001g0104 a0001c0001t0002g0002 a0001c0001t0002g0010 others(75): Show |
99 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.1210-1806G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334098 | |||||||
| chr15:73334104 | C | T | 1 | a0001c0001t0017g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1210-1812G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334104 | |||||||
| chr15:73334113 | T | C | 26 | a0001c0001t0004g0037 a0001c0001t0004g0049 a0001c0001t0004g0077 others(23): Show |
27 | HG00738.hp2 HG01109.hp1 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.1210-1821A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334113 | |||||||
| chr15:73334629 | G | A | 76 | a0001c0001t0001g0104 a0001c0001t0002g0002 a0001c0001t0002g0010 others(73): Show |
97 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.1210-2337C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334629 | |||||||
| chr15:73334652 | G | A | 5 | a0001c0001t0001g0062 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
5 | HG02258.hp1 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1210-2360C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334652 | |||||||
| chr15:73334652 | G | C | 1 | a0001c0001t0001g0085 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1210-2360C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334652 | |||||||
| chr15:73334693 | C | T | 29 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0110 others(26): Show |
32 | HG00423.hp2 HG00733.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1210-2401G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334693 | |||||||
| chr15:73334723 | CCT | C | 28 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0110 others(25): Show |
31 | HG00423.hp2 HG00733.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1210-2433_1210-243 others(6): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334723 | |||||||
| chr15:73334781 | C | A | 129 | a0001c0001t0001g0062 a0001c0001t0001g0104 a0001c0001t0001g0222 others(126): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1210-2489G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334781 | |||||||
| chr15:73334782 | G | A | 28 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0110 others(25): Show |
31 | HG00423.hp2 HG00733.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.1210-2490C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334782 | |||||||
| chr15:73334862 | T | C | 224 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(221): Show |
260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.1210-2570A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334862 | |||||||
| chr15:73334921 | C | T | 1 | a0001c0003t0001g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1210-2629G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73334921 | |||||||
| chr15:73335129 | A | G | 4 | a0001c0001t0004g0086 a0001c0001t0004g0226 a0001c0001t0004g0248 others(1): Show |
4 | HG00738.hp2 HG01175.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1210-2837T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335129 | |||||||
| chr15:73335146 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1210-2854G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335146 | |||||||
| chr15:73335190 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1210-2898A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335190 | |||||||
| chr15:73335260 | G | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0139 a0001c0001t0001g0143 |
4 | HG02083.hp1 HG02132.hp2 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.1210-2968C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335260 | |||||||
| chr15:73335382 | A | G | 53 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(50): Show |
62 | HG00673.hp2 HG00738.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.1210-3090T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335382 | |||||||
| chr15:73335421 | C | T | 1 | a0001c0001t0006g0065 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1210-3129G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335421 | |||||||
| chr15:73335429 | A | C | 97 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(94): Show |
107 | HG00673.hp2 HG00738.hp1 HG00741.hp1 others(104): Show |
intron_variant | MODIFIER | c.1210-3137T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335429 | |||||||
| chr15:73335530 | C | G | 235 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(232): Show |
272 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.1210-3238G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335530 | |||||||
| chr15:73335745 | T | C | 140 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0080 others(137): Show |
164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1210-3453A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335745 | |||||||
| chr15:73335781 | A | G | 1 | a0001c0001t0002g0179 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1210-3489T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335781 | |||||||
| chr15:73335827 | T | C | 140 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0038 others(137): Show |
167 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.1210-3535A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335827 | |||||||
| chr15:73335830 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1210-3538G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335830 | |||||||
| chr15:73335873 | C | A | 161 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0020 others(158): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.1210-3581G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335873 | |||||||
| chr15:73335883 | A | G | 2 | a0001c0001t0001g0213 a0001c0001t0001g0215 |
2 | HG01261.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1210-3591T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73335883 | |||||||
| chr15:73336068 | G | C | 1 | a0001c0001t0002g0194 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1210-3776C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336068 | |||||||
| chr15:73336159 | G | C | 1 | a0001c0001t0004g0259 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1210-3867C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336159 | |||||||
| chr15:73336205 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1210-3913G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336205 | |||||||
| chr15:73336373 | T | C | 126 | a0001c0001t0001g0062 a0001c0001t0001g0102 a0001c0001t0001g0137 others(123): Show |
150 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.1210-4081A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336373 | |||||||
| chr15:73336506 | T | A | 16 | a0001c0001t0004g0241 a0001c0001t0004g0285 a0001c0001t0004g0286 others(13): Show |
16 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.1210-4214A>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336506 | |||||||
| chr15:73336534 | A | G | 4 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0039 others(1): Show |
7 | NA18939.hp1 NA18942.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.1210-4242T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336534 | |||||||
| chr15:73336591 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1210-4299C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336591 | |||||||
| chr15:73336736 | C | T | 7 | a0001c0003t0001g0074 a0001c0003t0001g0229 a0001c0003t0001g0231 others(4): Show |
7 | HG00280.hp2 HG00733.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.1210-4444G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336736 | |||||||
| chr15:73336788 | G | A | 2 | a0001c0001t0002g0173 a0001c0022t0002g0295 |
2 | HG01358.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1210-4496C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336788 | |||||||
| chr15:73336799 | C | A | 2 | a0001c0001t0002g0034 a0001c0001t0002g0249 |
3 | NA18939.hp1 NA18942.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1210-4507G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336799 | |||||||
| chr15:73336844 | C | A | 1 | a0001c0001t0003g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1210-4552G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336844 | |||||||
| chr15:73336937 | C | T | 1 | a0001c0001t0002g0281 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1210-4645G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336937 | |||||||
| chr15:73336992 | G | A | 1 | a0001c0002t0003g0083 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1210-4700C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73336992 | |||||||
| chr15:73337029 | C | T | 28 | a0001c0001t0002g0224 a0001c0001t0002g0225 a0001c0001t0003g0055 others(25): Show |
31 | HG01243.hp1 HG01516.hp1 HG01517.hp2 others(28): Show |
intron_variant | MODIFIER | c.1210-4737G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73337029 | |||||||
| chr15:73337400 | A | G | 49 | a0001c0001t0001g0018 a0001c0001t0001g0021 a0001c0001t0001g0038 others(46): Show |
55 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.1210-5108T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73337400 | |||||||
| chr15:73337405 | A | G | 123 | a0001c0001t0001g0021 a0001c0001t0001g0062 a0001c0001t0001g0093 others(120): Show |
144 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.1210-5113T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73337405 | |||||||
| chr15:73337741 | C | G | 1 | a0001c0001t0001g0277 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1210-5449G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73337741 | |||||||
| chr15:73337881 | A | G | 1 | a0001c0001t0002g0187 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1209+5504T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73337881 | |||||||
| chr15:73338007 | G | A | 2 | a0001c0001t0002g0031 a0001c0001t0002g0134 |
3 | NA18957.hp2 NA18979.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1209+5378C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338007 | |||||||
| chr15:73338067 | TA | T | 47 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0085 others(44): Show |
52 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1209+5317delT | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338067 | |||||||
| chr15:73338125 | G | T | 1 | a0001c0001t0001g0018 | 2 | HG02040.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1209+5260C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338125 | |||||||
| chr15:73338138 | G | A | 1 | a0001c0001t0018g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1209+5247C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338138 | |||||||
| chr15:73338345 | G | A | 98 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0085 others(95): Show |
105 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.1209+5040C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338345 | |||||||
| chr15:73338352 | G | A | 9 | a0001c0001t0003g0054 a0001c0001t0003g0055 a0001c0001t0004g0049 others(6): Show |
10 | HG01346.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.1209+5033C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338352 | |||||||
| chr15:73338462 | C | T | 2 | a0001c0001t0003g0054 a0001c0001t0022g0089 |
2 | HG02717.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1209+4923G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338462 | |||||||
| chr15:73338602 | A | C | 1 | a0001c0002t0008g0146 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1209+4783T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338602 | |||||||
| chr15:73338614 | A | G | 1 | a0002c0008t0002g0007 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1209+4771T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338614 | |||||||
| chr15:73338870 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1209+4515G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338870 | |||||||
| chr15:73338934 | A | T | 4 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0246 others(1): Show |
4 | HG02280.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1209+4451T>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338934 | |||||||
| chr15:73338947 | G | A | 14 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0246 others(11): Show |
14 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.1209+4438C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73338947 | |||||||
| chr15:73339024 | C | A | 1 | a0001c0001t0004g0248 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1209+4361G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339024 | |||||||
| chr15:73339045 | C | T | 2 | a0001c0001t0004g0241 a0001c0001t0005g0240 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1209+4340G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339045 | |||||||
| chr15:73339216 | A | G | 48 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0085 others(45): Show |
53 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.1209+4169T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339216 | |||||||
| chr15:73339237 | G | A | 74 | a0001c0001t0001g0093 a0001c0001t0001g0137 a0001c0001t0001g0182 others(71): Show |
92 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1209+4148C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339237 | |||||||
| chr15:73339257 | G | A | 1 | a0001c0001t0001g0018 | 2 | HG02040.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1209+4128C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339257 | |||||||
| chr15:73339360 | G | A | 13 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0246 others(10): Show |
13 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1209+4025C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339360 | |||||||
| chr15:73339379 | C | T | 1 | a0001c0001t0004g0226 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1209+4006G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339379 | |||||||
| chr15:73339381 | G | C | 1 | a0001c0001t0004g0226 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1209+4004C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339381 | |||||||
| chr15:73339393 | A | G | 1 | a0001c0003t0001g0024 | 2 | HG01261.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1209+3992T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339393 | |||||||
| chr15:73339489 | G | A | 75 | a0001c0001t0001g0093 a0001c0001t0001g0137 a0001c0001t0001g0182 others(72): Show |
93 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1209+3896C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339489 | |||||||
| chr15:73339507 | G | A | 1 | a0005c0011t0004g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1209+3878C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339507 | |||||||
| chr15:73339801 | C | T | 62 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0085 others(59): Show |
67 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1209+3584G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339801 | |||||||
| chr15:73339850 | G | T | 13 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0246 others(10): Show |
13 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1209+3535C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73339850 | |||||||
| chr15:73340035 | G | A | 74 | a0001c0001t0001g0093 a0001c0001t0001g0137 a0001c0001t0001g0182 others(71): Show |
92 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1209+3350C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73340035 | |||||||
| chr15:73340528 | C | T | 61 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0085 others(58): Show |
66 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1209+2857G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73340528 | |||||||
| chr15:73340571 | G | A | 47 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0085 others(44): Show |
52 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1209+2814C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73340571 | |||||||
| chr15:73340704 | C | T | 1 | a0001c0001t0021g0242 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1209+2681G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73340704 | |||||||
| chr15:73340742 | G | A | 1 | a0001c0001t0005g0019 | 2 | HG00738.hp1 HG00741.hp1 |
intron_variant | MODIFIER | c.1209+2643C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73340742 | |||||||
| chr15:73341054 | G | A | 1 | a0001c0001t0007g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1209+2331C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341054 | |||||||
| chr15:73341069 | G | GGGGTGTG others(29): Show |
1 | a0001c0001t0021g0242 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1209+2315_1209+231 others(40): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | |||||||
| chr15:73341069 | G | GGGTGTGT others(32): Show |
1 | a0001c0001t0003g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1209+2315_1209+231 others(43): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | |||||||
| chr15:73341069 | G | GGT | 20 | a0001c0001t0001g0206 a0001c0001t0001g0222 a0001c0001t0001g0223 others(17): Show |
21 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.1209+2314_1209+231 others(6): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | |||||||
| chr15:73341069 | G | GGTGT | 10 | a0001c0001t0002g0210 a0001c0001t0004g0049 a0001c0001t0007g0186 others(7): Show |
11 | HG01346.hp1 HG02165.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1209+2312_1209+231 others(8): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | |||||||
| chr15:73341069 | G | GGTGTGT | 10 | a0001c0001t0001g0202 a0001c0001t0001g0207 a0001c0001t0001g0209 others(7): Show |
10 | HG00738.hp2 HG02145.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1209+2310_1209+231 others(10): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | |||||||
| chr15:73341069 | G | GGTGTGTG others(1): Show |
10 | a0001c0001t0004g0257 a0001c0001t0004g0259 a0001c0001t0004g0260 others(7): Show |
10 | HG01255.hp1 HG02055.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1209+2308_1209+231 others(12): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | |||||||
| chr15:73341069 | G | GGTGTGTG others(3): Show |
12 | a0001c0001t0001g0139 a0001c0001t0001g0144 a0001c0001t0001g0277 others(9): Show |
14 | HG00558.hp2 HG01884.hp2 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.1209+2306_1209+231 others(14): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | |||||||
| chr15:73341069 | G | GGTGTGTG others(5): Show |
19 | a0001c0001t0001g0085 a0001c0001t0001g0143 a0001c0001t0001g0147 others(16): Show |
21 | HG00621.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.1209+2304_1209+231 others(16): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | |||||||
| chr15:73341069 | G | GGTGTGTG others(7): Show |
16 | a0001c0001t0001g0021 a0001c0001t0001g0141 a0001c0001t0001g0148 others(13): Show |
17 | HG00423.hp2 HG01109.hp1 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.1209+2302_1209+231 others(18): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | |||||||
| chr15:73341069 | G | GGTGTGTG others(9): Show |
6 | a0001c0001t0001g0062 a0001c0001t0001g0255 a0001c0001t0002g0066 others(3): Show |
6 | HG01109.hp2 HG02258.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1209+2300_1209+231 others(20): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | |||||||
| chr15:73341069 | G | GGTGTGTG others(11): Show |
1 | a0001c0001t0028g0280 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1209+2298_1209+231 others(22): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | |||||||
| chr15:73341069 | G | GGTGTGTG others(13): Show |
1 | a0001c0001t0001g0038 | 2 | NA18993.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1209+2296_1209+231 others(24): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | |||||||
| chr15:73341069 | GGT | G | 93 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(90): Show |
110 | HG00438.hp1 HG00544.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.1209+2314_1209+231 others(6): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | |||||||
| chr15:73341069 | GGTGT | G | 76 | a0001c0001t0001g0093 a0001c0001t0001g0137 a0001c0001t0001g0182 others(73): Show |
94 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.1209+2312_1209+231 others(8): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | |||||||
| chr15:73341069 | GGTGTGTG others(3): Show |
G | 1 | a0001c0001t0013g0006 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1209+2306_1209+231 others(14): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341069 | |||||||
| chr15:73341265 | C | T | 1 | a0001c0001t0003g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1209+2120G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341265 | |||||||
| chr15:73341266 | G | A | 1 | a0001c0003t0001g0024 | 2 | HG01261.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1209+2119C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341266 | |||||||
| chr15:73341322 | A | G | 1 | a0001c0002t0025g0140 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1209+2063T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341322 | |||||||
| chr15:73341328 | G | GA | 15 | a0001c0001t0001g0062 a0001c0001t0002g0066 a0001c0001t0006g0063 others(12): Show |
16 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1209+2056dupT | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341328 | |||||||
| chr15:73341331 | G | A | 13 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0246 others(10): Show |
13 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1209+2054C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341331 | |||||||
| chr15:73341343 | C | T | 14 | a0001c0001t0001g0147 a0001c0001t0001g0222 a0001c0001t0001g0223 others(11): Show |
14 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.1209+2042G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341343 | |||||||
| chr15:73341394 | G | A | 13 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0246 others(10): Show |
13 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1209+1991C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341394 | |||||||
| chr15:73341430 | C | T | 1 | a0001c0004t0001g0099 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1209+1955G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341430 | |||||||
| chr15:73341587 | T | C | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0004t0001g0253 |
3 | HG01934.hp1 HG01993.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1209+1798A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341587 | |||||||
| chr15:73341806 | C | T | 5 | a0001c0001t0004g0285 a0001c0001t0004g0286 a0001c0001t0004g0287 others(2): Show |
5 | HG02055.hp2 HG02559.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1209+1579G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341806 | |||||||
| chr15:73341847 | G | A | 1 | a0001c0001t0004g0226 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1209+1538C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341847 | |||||||
| chr15:73341894 | C | G | 1 | a0001c0001t0021g0242 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1209+1491G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341894 | |||||||
| chr15:73341965 | G | T | 1 | a0001c0001t0002g0029 | 2 | NA18948.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.1209+1420C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73341965 | |||||||
| chr15:73342012 | G | A | 1 | a0001c0001t0002g0169 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1209+1373C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73342012 | |||||||
| chr15:73342024 | TCCATGGA others(12): Show |
T | 1 | a0001c0001t0002g0035 | 2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1209+1342_1209+136 others(23): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73342024 | |||||||
| chr15:73342241 | G | A | 13 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0246 others(10): Show |
13 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1209+1144C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73342241 | |||||||
| chr15:73342255 | G | A | 1 | a0001c0001t0003g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1209+1130C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73342255 | |||||||
| chr15:73342392 | C | T | 2 | a0001c0001t0004g0257 a0001c0001t0004g0260 |
2 | HG02976.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1209+993G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73342392 | |||||||
| chr15:73342400 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1209+985C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73342400 | |||||||
| chr15:73342420 | G | A | 2 | a0001c0001t0004g0241 a0001c0001t0005g0240 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1209+965C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73342420 | |||||||
| chr15:73342771 | C | T | 2 | a0001c0003t0001g0050 a0001c0003t0001g0051 |
2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1209+614G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73342771 | |||||||
| chr15:73342829 | C | A | 2 | a0001c0001t0004g0241 a0001c0001t0005g0240 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1209+556G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73342829 | |||||||
| chr15:73343011 | A | G | 4 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0039 others(1): Show |
7 | NA18939.hp1 NA18942.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.1209+374T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73343011 | |||||||
| chr15:73343020 | T | C | 48 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0085 others(45): Show |
54 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1209+365A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73343020 | |||||||
| chr15:73343174 | T | C | 1 | a0001c0003t0009g0238 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1209+211A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73343174 | |||||||
| chr15:73343262 | T | C | 4 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0246 others(1): Show |
4 | HG02280.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1209+123A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73343262 | |||||||
| chr15:73343307 | T | C | 1 | a0001c0004t0001g0160 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1209+78A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73343307 | |||||||
| chr15:73343321 | C | A | 1 | a0001c0001t0002g0174 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1209+64G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 2/7 | chr15 | 73343321 | |||||||
| chr15:73343900 | A | G | 2 | a0001c0003t0001g0050 a0001c0003t0001g0051 |
2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.786-92T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73343900 | |||||||
| chr15:73344260 | T | C | 1 | a0007c0018t0003g0291 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.786-452A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73344260 | |||||||
| chr15:73344311 | G | A | 1 | a0001c0023t0001g0296 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.786-503C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73344311 | |||||||
| chr15:73344732 | G | C | 1 | a0001c0001t0001g0085 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.786-924C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73344732 | |||||||
| chr15:73344792 | G | A | 47 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0085 others(44): Show |
52 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.786-984C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73344792 | |||||||
| chr15:73344810 | A | C | 47 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0085 others(44): Show |
52 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.786-1002T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73344810 | |||||||
| chr15:73345103 | G | A | 1 | a0001c0001t0017g0043 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.786-1295C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345103 | |||||||
| chr15:73345299 | C | A | 1 | a0001c0007t0003g0078 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.786-1491G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345299 | |||||||
| chr15:73345315 | A | T | 1 | a0001c0001t0004g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.786-1507T>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345315 | |||||||
| chr15:73345431 | C | T | 12 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0233 others(9): Show |
14 | HG01074.hp2 HG01123.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.786-1623G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345431 | |||||||
| chr15:73345487 | C | A | 1 | a0001c0001t0002g0175 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.786-1679G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345487 | |||||||
| chr15:73345559 | C | G | 1 | a0001c0001t0003g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.786-1751G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345559 | |||||||
| chr15:73345666 | C | T | 27 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0139 others(24): Show |
30 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.786-1858G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345666 | |||||||
| chr15:73345870 | C | T | 1 | a0001c0001t0013g0006 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.786-2062G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345870 | |||||||
| chr15:73345881 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.786-2073G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345881 | |||||||
| chr15:73345882 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.786-2074C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345882 | |||||||
| chr15:73345903 | C | T | 1 | a0002c0008t0002g0047 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.786-2095G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73345903 | |||||||
| chr15:73346116 | G | T | 1 | a0001c0001t0002g0228 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.786-2308C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73346116 | |||||||
| chr15:73346321 | A | G | 2 | a0001c0001t0001g0184 a0001c0001t0001g0185 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.786-2513T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73346321 | |||||||
| chr15:73346390 | G | A | 2 | a0001c0001t0004g0241 a0001c0001t0005g0240 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.786-2582C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73346390 | |||||||
| chr15:73346410 | G | T | 3 | a0001c0001t0002g0118 a0001c0002t0003g0117 a0001c0002t0003g0217 |
3 | HG00438.hp1 HG00544.hp1 HG00609.hp2 |
intron_variant | MODIFIER | c.786-2602C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73346410 | |||||||
| chr15:73346642 | C | T | 7 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0004g0077 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.786-2834G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73346642 | |||||||
| chr15:73346785 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0135 |
2 | NA18942.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.786-2977C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73346785 | |||||||
| chr15:73346961 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.786-3153C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73346961 | |||||||
| chr15:73347010 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.786-3202G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73347010 | |||||||
| chr15:73347057 | A | C | 1 | a0001c0001t0002g0224 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.786-3249T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73347057 | |||||||
| chr15:73347066 | G | C | 2 | a0001c0001t0004g0241 a0001c0001t0005g0240 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.786-3258C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73347066 | |||||||
| chr15:73347150 | C | G | 2 | a0001c0001t0004g0241 a0001c0001t0005g0240 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.786-3342G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73347150 | |||||||
| chr15:73347563 | C | T | 1 | a0001c0001t0013g0006 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.786-3755G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73347563 | |||||||
| chr15:73347805 | C | T | 1 | a0001c0003t0001g0061 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.786-3997G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73347805 | |||||||
| chr15:73347849 | C | T | 3 | a0001c0003t0001g0229 a0001c0003t0001g0231 a0001c0003t0020g0230 |
3 | HG01167.hp1 HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.786-4041G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73347849 | |||||||
| chr15:73347885 | C | T | 3 | a0001c0004t0001g0099 a0001c0004t0001g0160 a0006c0019t0001g0100 |
3 | HG01943.hp2 HG01981.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.786-4077G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73347885 | |||||||
| chr15:73347984 | G | A | 8 | a0001c0001t0006g0068 a0001c0001t0006g0070 a0001c0001t0006g0071 others(5): Show |
9 | HG02451.hp2 HG02559.hp1 NA18522.hp1 others(6): Show |
intron_variant | MODIFIER | c.786-4176C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73347984 | |||||||
| chr15:73348030 | G | T | 5 | a0001c0001t0003g0116 a0001c0002t0008g0115 a0001c0002t0008g0146 others(2): Show |
5 | HG01516.hp2 HG03942.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.786-4222C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73348030 | |||||||
| chr15:73348389 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.786-4581G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73348389 | |||||||
| chr15:73348542 | T | C | 1 | a0007c0018t0003g0291 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.786-4734A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73348542 | |||||||
| chr15:73348626 | C | T | 1 | a0001c0001t0003g0055 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.786-4818G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73348626 | |||||||
| chr15:73348963 | G | A | 2 | a0001c0001t0003g0243 a0001c0001t0021g0242 |
2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.786-5155C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73348963 | |||||||
| chr15:73349143 | G | A | 11 | a0001c0001t0003g0054 a0001c0001t0003g0055 a0001c0001t0004g0049 others(8): Show |
12 | HG01346.hp1 HG02145.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.786-5335C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73349143 | |||||||
| chr15:73349345 | T | C | 7 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0004g0077 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.786-5537A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73349345 | |||||||
| chr15:73349360 | C | A | 1 | a0001c0001t0007g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.786-5552G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73349360 | |||||||
| chr15:73349551 | T | C | 53 | a0001c0001t0001g0137 a0001c0001t0001g0182 a0001c0001t0002g0002 others(50): Show |
70 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.786-5743A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73349551 | |||||||
| chr15:73349724 | G | A | 1 | a0001c0001t0001g0020 | 2 | HG01081.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.786-5916C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73349724 | |||||||
| chr15:73350112 | G | A | 1 | a0001c0003t0001g0237 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.786-6304C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73350112 | |||||||
| chr15:73350225 | T | C | 1 | a0001c0001t0018g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.786-6417A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73350225 | |||||||
| chr15:73350256 | C | T | 1 | a0002c0008t0002g0046 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.786-6448G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73350256 | |||||||
| chr15:73350414 | A | G | 1 | a0001c0001t0021g0242 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.786-6606T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73350414 | |||||||
| chr15:73350516 | G | A | 1 | a0001c0001t0002g0210 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.786-6708C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73350516 | |||||||
| chr15:73350782 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.786-6974G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73350782 | |||||||
| chr15:73350853 | A | C | 1 | a0001c0001t0001g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.786-7045T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73350853 | |||||||
| chr15:73350888 | C | G | 1 | a0001c0001t0002g0180 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.786-7080G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73350888 | |||||||
| chr15:73350949 | C | T | 1 | a0001c0002t0003g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.786-7141G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73350949 | |||||||
| chr15:73351222 | G | A | 1 | a0004c0010t0003g0153 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.786-7414C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73351222 | |||||||
| chr15:73351222 | G | C | 2 | a0001c0001t0004g0241 a0001c0001t0005g0240 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.786-7414C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73351222 | |||||||
| chr15:73351223 | G | A | 2 | a0001c0001t0004g0241 a0001c0001t0005g0240 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.786-7415C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73351223 | |||||||
| chr15:73351270 | G | A | 1 | a0001c0001t0004g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.786-7462C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73351270 | |||||||
| chr15:73351506 | T | G | 9 | a0001c0003t0001g0074 a0001c0003t0001g0229 a0001c0003t0001g0231 others(6): Show |
9 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.786-7698A>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73351506 | |||||||
| chr15:73351706 | C | T | 15 | a0001c0001t0001g0062 a0001c0001t0002g0066 a0001c0001t0006g0063 others(12): Show |
16 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.786-7898G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73351706 | |||||||
| chr15:73351959 | C | T | 1 | a0001c0002t0003g0199 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.786-8151G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73351959 | |||||||
| chr15:73352055 | C | T | 47 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0085 others(44): Show |
52 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.786-8247G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73352055 | |||||||
| chr15:73352170 | T | C | 2 | a0001c0002t0003g0268 a0001c0002t0003g0269 |
2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.786-8362A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73352170 | |||||||
| chr15:73352237 | ATGCCATG others(17): Show |
A | 7 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0004g0077 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.786-8453_786-8430d others(26): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73352237 | |||||||
| chr15:73352632 | C | T | 1 | a0001c0002t0003g0036 | 2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.786-8824G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73352632 | |||||||
| chr15:73352641 | C | T | 2 | a0001c0001t0004g0241 a0001c0001t0005g0240 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.786-8833G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73352641 | |||||||
| chr15:73352655 | C | A | 1 | a0001c0001t0002g0195 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.786-8847G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73352655 | |||||||
| chr15:73352729 | G | A | 1 | a0001c0002t0003g0138 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.786-8921C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73352729 | |||||||
| chr15:73352996 | G | GGATGGAC others(1): Show |
37 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0085 others(34): Show |
42 | HG00558.hp2 HG00621.hp2 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.786-9196_786-9189d others(10): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73352996 | |||||||
| chr15:73353004 | A | AGATG | 33 | a0001c0001t0001g0062 a0001c0001t0001g0097 a0001c0001t0001g0182 others(30): Show |
37 | HG00438.hp2 HG00733.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.786-9200_786-9197d others(6): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353004 | |||||||
| chr15:73353004 | A | AGATGGAC others(5): Show |
3 | a0001c0001t0004g0257 a0001c0001t0004g0258 a0001c0001t0004g0259 |
3 | HG02486.hp1 HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.786-9197_786-9196i others(14): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353004 | |||||||
| chr15:73353004 | A | AGATGGAT others(1): Show |
3 | a0001c0001t0006g0070 a0001c0001t0006g0071 a0009c0021t0006g0294 |
3 | NA18991.hp1 NA19007.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.786-9204_786-9197d others(10): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353004 | |||||||
| chr15:73353004 | AGATG | A | 22 | a0001c0001t0001g0080 a0001c0001t0002g0079 a0001c0001t0002g0228 others(19): Show |
23 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(20): Show |
intron_variant | MODIFIER | c.786-9200_786-9197d others(6): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353004 | |||||||
| chr15:73353004 | AGATGGAT others(5): Show |
A | 1 | a0001c0002t0003g0083 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.786-9208_786-9197d others(14): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353004 | |||||||
| chr15:73353004 | AGATGGAT others(9): Show |
A | 3 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0007g0198 |
3 | NA18979.hp1 NA18990.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.786-9212_786-9197d others(18): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353004 | |||||||
| chr15:73353008 | G | GGACA | 6 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0158 others(3): Show |
6 | HG00423.hp2 HG01109.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.786-9201_786-9200i others(6): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353008 | |||||||
| chr15:73353011 | T | C | 1 | a0001c0001t0004g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.786-9203A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353011 | |||||||
| chr15:73353012 | G | A | 1 | a0001c0001t0004g0270 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.786-9204C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353012 | |||||||
| chr15:73353015 | T | C | 1 | a0001c0001t0002g0220 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.786-9207A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353015 | |||||||
| chr15:73353026 | A | G | 2 | a0001c0001t0012g0041 a0001c0001t0012g0042 |
2 | HG01934.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.786-9218T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353026 | |||||||
| chr15:73353043 | T | C | 3 | a0001c0003t0001g0009 a0001c0003t0001g0061 a0001c0003t0001g0069 |
4 | HG02559.hp1 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.786-9235A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353043 | |||||||
| chr15:73353047 | T | C | 1 | a0004c0010t0003g0153 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.786-9239A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353047 | |||||||
| chr15:73353047 | TGGAC | T | 3 | a0001c0003t0001g0009 a0001c0003t0001g0061 a0001c0003t0001g0069 |
4 | HG02559.hp1 NA18522.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.786-9243_786-9240d others(6): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353047 | |||||||
| chr15:73353059 | C | T | 1 | a0001c0001t0003g0243 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.786-9251G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353059 | |||||||
| chr15:73353062 | G | A | 15 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0246 others(12): Show |
15 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.786-9254C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353062 | |||||||
| chr15:73353478 | C | T | 289 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(286): Show |
333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.786-9670G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353478 | |||||||
| chr15:73353519 | G | A | 4 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0246 others(1): Show |
4 | HG02280.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.786-9711C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353519 | |||||||
| chr15:73353897 | C | T | 4 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0246 others(1): Show |
4 | HG02280.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.786-10089G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353897 | |||||||
| chr15:73353901 | A | G | 4 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0246 others(1): Show |
4 | HG02280.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.786-10093T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353901 | |||||||
| chr15:73353936 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.786-10128G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73353936 | |||||||
| chr15:73354005 | C | T | 2 | a0001c0003t0009g0238 a0001c0003t0009g0239 |
2 | HG00280.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.786-10197G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354005 | |||||||
| chr15:73354079 | A | C | 1 | a0001c0001t0015g0095 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.786-10271T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354079 | |||||||
| chr15:73354083 | C | T | 9 | a0001c0003t0001g0074 a0001c0003t0001g0229 a0001c0003t0001g0231 others(6): Show |
9 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.786-10275G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354083 | |||||||
| chr15:73354146 | A | C | 33 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0246 others(30): Show |
34 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.786-10338T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354146 | |||||||
| chr15:73354175 | A | G | 7 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0004g0077 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.786-10367T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354175 | |||||||
| chr15:73354223 | A | G | 1 | a0007c0018t0003g0291 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.786-10415T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354223 | |||||||
| chr15:73354253 | G | A | 15 | a0001c0001t0001g0202 a0001c0001t0001g0206 a0001c0001t0001g0207 others(12): Show |
17 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.786-10445C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354253 | |||||||
| chr15:73354429 | C | T | 7 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0004g0077 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.786-10621G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354429 | |||||||
| chr15:73354444 | T | C | 4 | a0001c0006t0003g0008 a0001c0006t0003g0058 a0001c0006t0003g0059 others(1): Show |
5 | HG02145.hp1 HG02622.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.786-10636A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354444 | |||||||
| chr15:73354778 | C | CCAT | 7 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0004g0077 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.786-10973_786-1097 others(7): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354778 | |||||||
| chr15:73354787 | T | G | 2 | a0001c0001t0004g0241 a0001c0001t0005g0240 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.786-10979A>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73354787 | |||||||
| chr15:73355073 | A | T | 2 | a0001c0001t0004g0241 a0001c0001t0005g0240 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.786-11265T>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355073 | |||||||
| chr15:73355216 | C | T | 4 | a0001c0001t0001g0092 a0001c0001t0001g0112 a0001c0001t0001g0113 others(1): Show |
4 | HG01255.hp2 HG01358.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.786-11408G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355216 | |||||||
| chr15:73355242 | G | A | 2 | a0001c0001t0004g0241 a0001c0001t0005g0240 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.786-11434C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355242 | |||||||
| chr15:73355253 | G | A | 7 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0004g0077 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.786-11445C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355253 | |||||||
| chr15:73355326 | T | C | 1 | a0001c0003t0001g0069 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.786-11518A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355326 | |||||||
| chr15:73355328 | G | A | 5 | a0001c0001t0001g0038 a0001c0001t0001g0273 a0001c0001t0002g0279 others(2): Show |
6 | NA18944.hp1 NA18962.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.786-11520C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355328 | |||||||
| chr15:73355401 | T | TA | 13 | a0001c0001t0001g0233 a0001c0003t0001g0074 a0001c0003t0001g0229 others(10): Show |
15 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.786-11594dupT | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355401 | |||||||
| chr15:73355466 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.786-11658C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355466 | |||||||
| chr15:73355522 | C | T | 2 | a0001c0001t0004g0241 a0001c0001t0005g0240 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.786-11714G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355522 | |||||||
| chr15:73355540 | G | A | 1 | a0001c0001t0003g0055 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.786-11732C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355540 | |||||||
| chr15:73355734 | A | G | 2 | a0001c0001t0004g0241 a0001c0001t0005g0240 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.785+11752T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355734 | |||||||
| chr15:73355759 | G | GCA | 7 | a0001c0001t0001g0255 a0001c0001t0002g0026 a0001c0001t0002g0169 others(4): Show |
8 | HG01109.hp2 HG01433.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.785+11725_785+1172 others(6): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355759 | |||||||
| chr15:73355761 | A | G | 2 | a0001c0001t0002g0027 a0001c0001t0002g0181 |
3 | HG02056.hp1 NA18612.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.785+11725T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355761 | |||||||
| chr15:73355811 | T | C | 22 | a0001c0001t0001g0233 a0001c0001t0003g0075 a0001c0001t0003g0076 others(19): Show |
24 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.785+11675A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73355811 | |||||||
| chr15:73356189 | C | CT | 119 | a0001c0001t0001g0038 a0001c0001t0001g0062 a0001c0001t0001g0085 others(116): Show |
131 | HG00438.hp2 HG00558.hp1 HG00639.hp1 others(128): Show |
intron_variant | MODIFIER | c.785+11296dupA | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356189 | |||||||
| chr15:73356189 | C | CTT | 7 | a0001c0001t0001g0274 a0001c0001t0003g0243 a0001c0001t0004g0285 others(4): Show |
7 | HG01891.hp2 HG02055.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+11295_785+1129 others(6): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356189 | |||||||
| chr15:73356189 | CT | C | 21 | a0001c0001t0001g0215 a0001c0001t0001g0233 a0001c0001t0003g0075 others(18): Show |
23 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.785+11296delA | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356189 | |||||||
| chr15:73356217 | C | T | 1 | a0001c0002t0003g0094 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.785+11269G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356217 | |||||||
| chr15:73356232 | G | T | 4 | a0001c0001t0004g0285 a0001c0001t0004g0286 a0001c0001t0004g0287 others(1): Show |
4 | HG02055.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.785+11254C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356232 | |||||||
| chr15:73356241 | T | C | 2 | a0003c0012t0001g0151 a0003c0012t0001g0152 |
2 | HG01257.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.785+11245A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356241 | |||||||
| chr15:73356293 | C | T | 4 | a0001c0001t0001g0093 a0001c0001t0001g0213 a0001c0001t0001g0214 others(1): Show |
4 | HG01261.hp1 HG01952.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.785+11193G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356293 | |||||||
| chr15:73356320 | T | C | 2 | a0001c0001t0004g0241 a0001c0001t0005g0240 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.785+11166A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356320 | |||||||
| chr15:73356323 | G | A | 7 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0004g0077 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+11163C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356323 | |||||||
| chr15:73356374 | C | CT | 19 | a0001c0001t0001g0038 a0001c0001t0001g0092 a0001c0001t0001g0251 others(16): Show |
21 | HG01106.hp2 HG01123.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.785+11111dupA | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356374 | |||||||
| chr15:73356374 | CT | C | 20 | a0001c0001t0002g0177 a0001c0001t0002g0200 a0001c0001t0002g0211 others(17): Show |
21 | HG00558.hp2 HG00741.hp2 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.785+11111delA | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356374 | |||||||
| chr15:73356378 | T | C | 3 | a0001c0001t0003g0054 a0001c0001t0003g0055 a0001c0001t0004g0049 |
3 | HG02717.hp2 HG02896.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.785+11108A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356378 | |||||||
| chr15:73356379 | T | C | 7 | a0001c0006t0003g0008 a0001c0006t0003g0056 a0001c0006t0003g0057 others(4): Show |
8 | HG01346.hp1 HG02145.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.785+11107A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356379 | |||||||
| chr15:73356573 | T | C | 1 | a0001c0001t0007g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.785+10913A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356573 | |||||||
| chr15:73356633 | C | A | 1 | a0001c0001t0013g0006 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.785+10853G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356633 | |||||||
| chr15:73356648 | G | C | 16 | a0001c0001t0001g0038 a0001c0001t0001g0251 a0001c0001t0001g0252 others(13): Show |
17 | HG00280.hp1 HG01106.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.785+10838C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356648 | |||||||
| chr15:73356739 | C | T | 13 | a0001c0001t0001g0233 a0001c0003t0001g0074 a0001c0003t0001g0229 others(10): Show |
15 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.785+10747G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356739 | |||||||
| chr15:73356751 | A | G | 26 | a0001c0001t0001g0233 a0001c0001t0003g0075 a0001c0001t0003g0076 others(23): Show |
28 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.785+10735T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356751 | |||||||
| chr15:73356816 | A | C | 1 | a0001c0001t0002g0244 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.785+10670T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356816 | |||||||
| chr15:73356830 | A | G | 1 | a0001c0001t0021g0242 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.785+10656T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356830 | |||||||
| chr15:73356925 | G | A | 1 | a0001c0004t0001g0157 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.785+10561C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73356925 | |||||||
| chr15:73357004 | A | G | 1 | a0001c0001t0022g0089 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.785+10482T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357004 | |||||||
| chr15:73357020 | A | G | 38 | a0001c0001t0001g0038 a0001c0001t0001g0085 a0001c0001t0001g0251 others(35): Show |
41 | HG00280.hp1 HG01106.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.785+10466T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357020 | |||||||
| chr15:73357054 | G | A | 22 | a0001c0001t0001g0233 a0001c0001t0003g0075 a0001c0001t0003g0076 others(19): Show |
24 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.785+10432C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357054 | |||||||
| chr15:73357097 | A | G | 7 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0004g0077 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+10389T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357097 | |||||||
| chr15:73357252 | C | T | 38 | a0001c0001t0001g0038 a0001c0001t0001g0085 a0001c0001t0001g0251 others(35): Show |
41 | HG00280.hp1 HG01106.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.785+10234G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357252 | |||||||
| chr15:73357370 | G | A | 7 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0004g0077 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+10116C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357370 | |||||||
| chr15:73357425 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.785+10061C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357425 | |||||||
| chr15:73357627 | C | T | 1 | a0001c0002t0003g0087 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.785+9859G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357627 | |||||||
| chr15:73357632 | C | T | 1 | a0005c0011t0004g0084 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.785+9854G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357632 | |||||||
| chr15:73357698 | TGGAG | T | 4 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0246 others(1): Show |
4 | HG02280.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.785+9784_785+9787d others(6): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357698 | |||||||
| chr15:73357981 | G | C | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0004t0001g0253 |
3 | HG01934.hp1 HG01993.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.785+9505C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357981 | |||||||
| chr15:73357984 | T | G | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0004t0001g0253 |
3 | HG01934.hp1 HG01993.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.785+9502A>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73357984 | |||||||
| chr15:73358039 | G | A | 1 | a0001c0002t0003g0159 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.785+9447C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73358039 | |||||||
| chr15:73358065 | A | G | 22 | a0001c0001t0001g0233 a0001c0001t0003g0075 a0001c0001t0003g0076 others(19): Show |
24 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.785+9421T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73358065 | |||||||
| chr15:73358196 | C | T | 1 | a0001c0001t0002g0256 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.785+9290G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73358196 | |||||||
| chr15:73358206 | G | A | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0004t0001g0253 |
3 | HG01934.hp1 HG01993.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.785+9280C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73358206 | |||||||
| chr15:73358380 | T | G | 3 | a0001c0003t0001g0235 a0001c0003t0001g0236 a0001c0003t0001g0237 |
3 | HG00099.hp2 HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.785+9106A>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73358380 | |||||||
| chr15:73358483 | G | A | 48 | a0001c0001t0001g0182 a0001c0001t0001g0184 a0001c0001t0001g0185 others(45): Show |
65 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.785+9003C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73358483 | |||||||
| chr15:73358497 | T | C | 1 | a0001c0004t0001g0160 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.785+8989A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73358497 | |||||||
| chr15:73358542 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.785+8944C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73358542 | |||||||
| chr15:73358861 | T | C | 13 | a0001c0001t0001g0233 a0001c0003t0001g0074 a0001c0003t0001g0229 others(10): Show |
15 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.785+8625A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73358861 | |||||||
| chr15:73358915 | ACCT | A | 17 | a0001c0001t0001g0062 a0001c0001t0002g0066 a0001c0001t0006g0063 others(14): Show |
18 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.785+8568_785+8570d others(5): Show |
HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73358915 | |||||||
| chr15:73359039 | T | G | 13 | a0001c0001t0001g0233 a0001c0003t0001g0074 a0001c0003t0001g0229 others(10): Show |
15 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.785+8447A>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73359039 | |||||||
| chr15:73359174 | C | T | 5 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0004g0077 others(2): Show |
5 | HG02622.hp2 HG02809.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.785+8312G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73359174 | |||||||
| chr15:73359220 | T | C | 1 | a0001c0001t0004g0283 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.785+8266A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73359220 | |||||||
| chr15:73359253 | G | A | 1 | a0001c0001t0004g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.785+8233C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73359253 | |||||||
| chr15:73359257 | C | T | 1 | a0001c0001t0002g0247 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.785+8229G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73359257 | |||||||
| chr15:73359259 | A | T | 2 | a0001c0001t0002g0165 a0001c0001t0002g0166 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.785+8227T>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73359259 | |||||||
| chr15:73359306 | G | C | 1 | a0001c0001t0002g0030 | 2 | HG00423.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.785+8180C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73359306 | |||||||
| chr15:73359615 | G | A | 2 | a0001c0001t0003g0243 a0001c0001t0021g0242 |
2 | HG01891.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.785+7871C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73359615 | |||||||
| chr15:73359697 | C | T | 1 | a0001c0004t0001g0293 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.785+7789G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73359697 | |||||||
| chr15:73359833 | A | G | 67 | a0001c0001t0001g0062 a0001c0001t0001g0202 a0001c0001t0001g0206 others(64): Show |
73 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.785+7653T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73359833 | |||||||
| chr15:73360061 | C | T | 1 | a0001c0001t0004g0086 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.785+7425G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73360061 | |||||||
| chr15:73360454 | C | G | 289 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(286): Show |
333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.785+7032G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73360454 | |||||||
| chr15:73360668 | G | A | 68 | a0001c0001t0001g0171 a0001c0001t0001g0182 a0001c0001t0001g0184 others(65): Show |
87 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.785+6818C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73360668 | |||||||
| chr15:73360802 | G | T | 4 | a0002c0008t0002g0007 a0002c0008t0002g0046 a0002c0008t0002g0047 others(1): Show |
5 | HG01070.hp1 HG01081.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.785+6684C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73360802 | |||||||
| chr15:73361114 | C | T | 1 | a0001c0001t0012g0041 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.785+6372G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361114 | |||||||
| chr15:73361144 | A | G | 115 | a0001c0001t0001g0038 a0001c0001t0001g0062 a0001c0001t0001g0085 others(112): Show |
124 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.785+6342T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361144 | |||||||
| chr15:73361161 | T | C | 76 | a0001c0001t0001g0062 a0001c0001t0001g0202 a0001c0001t0001g0206 others(73): Show |
82 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.785+6325A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361161 | |||||||
| chr15:73361199 | C | T | 15 | a0001c0001t0001g0062 a0001c0001t0002g0066 a0001c0001t0006g0063 others(12): Show |
16 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.785+6287G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361199 | |||||||
| chr15:73361525 | C | T | 1 | a0001c0003t0009g0238 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.785+5961G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361525 | |||||||
| chr15:73361599 | C | T | 3 | a0001c0002t0003g0081 a0001c0002t0003g0083 a0001c0014t0003g0082 |
3 | HG02886.hp1 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.785+5887G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361599 | |||||||
| chr15:73361630 | T | C | 50 | a0001c0001t0001g0062 a0001c0001t0001g0202 a0001c0001t0001g0206 others(47): Show |
54 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.785+5856A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361630 | |||||||
| chr15:73361749 | G | A | 1 | a0001c0002t0003g0212 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.785+5737C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361749 | |||||||
| chr15:73361782 | G | A | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG01261.hp1 HG01952.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.785+5704C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361782 | |||||||
| chr15:73361786 | C | T | 2 | a0001c0003t0001g0050 a0001c0003t0001g0051 |
2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.785+5700G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361786 | |||||||
| chr15:73361922 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0002g0031 |
3 | NA18957.hp1 NA18979.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.785+5564C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73361922 | |||||||
| chr15:73362135 | C | G | 1 | a0001c0001t0001g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.785+5351G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73362135 | |||||||
| chr15:73362501 | G | A | 13 | a0001c0001t0001g0233 a0001c0003t0001g0074 a0001c0003t0001g0229 others(10): Show |
15 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.785+4985C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73362501 | |||||||
| chr15:73362558 | G | A | 1 | a0001c0002t0003g0217 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.785+4928C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73362558 | |||||||
| chr15:73362689 | C | G | 4 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0246 others(1): Show |
4 | HG02280.hp2 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.785+4797G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73362689 | |||||||
| chr15:73362895 | C | A | 17 | a0001c0001t0001g0233 a0001c0001t0004g0285 a0001c0001t0004g0286 others(14): Show |
19 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.785+4591G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73362895 | |||||||
| chr15:73362942 | C | G | 1 | a0001c0001t0001g0080 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.785+4544G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73362942 | |||||||
| chr15:73363067 | C | T | 1 | a0001c0003t0001g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.785+4419G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363067 | |||||||
| chr15:73363210 | C | T | 1 | a0001c0001t0004g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.785+4276G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363210 | |||||||
| chr15:73363258 | C | T | 8 | a0001c0001t0003g0055 a0001c0001t0004g0049 a0001c0006t0003g0008 others(5): Show |
9 | HG01346.hp1 HG02145.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.785+4228G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363258 | |||||||
| chr15:73363367 | T | A | 2 | a0001c0001t0002g0218 a0001c0001t0002g0219 |
2 | HG00673.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.785+4119A>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363367 | |||||||
| chr15:73363556 | T | A | 15 | a0001c0001t0001g0062 a0001c0001t0002g0066 a0001c0001t0006g0063 others(12): Show |
16 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.785+3930A>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363556 | |||||||
| chr15:73363676 | G | A | 1 | a0001c0001t0003g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.785+3810C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363676 | |||||||
| chr15:73363822 | A | G | 1 | a0001c0023t0001g0296 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.785+3664T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363822 | |||||||
| chr15:73363920 | G | A | 11 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0246 others(8): Show |
13 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.785+3566C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363920 | |||||||
| chr15:73363921 | C | A | 1 | a0001c0001t0002g0220 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.785+3565G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363921 | |||||||
| chr15:73363966 | G | A | 11 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0246 others(8): Show |
13 | HG00738.hp2 HG01069.hp1 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.785+3520C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363966 | |||||||
| chr15:73363995 | G | A | 2 | a0001c0003t0009g0238 a0001c0003t0009g0239 |
2 | HG00280.hp2 HG00733.hp2 |
intron_variant | MODIFIER | c.785+3491C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73363995 | |||||||
| chr15:73364083 | C | T | 1 | a0001c0001t0003g0054 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.785+3403G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364083 | |||||||
| chr15:73364194 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.785+3292C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364194 | |||||||
| chr15:73364427 | G | T | 41 | a0001c0001t0001g0062 a0001c0001t0001g0233 a0001c0001t0002g0066 others(38): Show |
45 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.785+3059C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364427 | |||||||
| chr15:73364437 | A | G | 1 | a0001c0001t0007g0254 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.785+3049T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364437 | |||||||
| chr15:73364497 | G | T | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0004t0001g0253 |
3 | HG01934.hp1 HG01993.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.785+2989C>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364497 | |||||||
| chr15:73364680 | C | T | 7 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0004g0077 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+2806G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364680 | |||||||
| chr15:73364722 | C | T | 48 | a0001c0001t0001g0062 a0001c0001t0001g0233 a0001c0001t0002g0066 others(45): Show |
52 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.785+2764G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364722 | |||||||
| chr15:73364763 | A | C | 9 | a0001c0001t0003g0054 a0001c0001t0003g0055 a0001c0001t0004g0049 others(6): Show |
10 | HG01346.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.785+2723T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364763 | |||||||
| chr15:73364780 | T | A | 1 | a0008c0015t0007g0250 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.785+2706A>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364780 | |||||||
| chr15:73364853 | CA | C | 7 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0004g0077 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+2632delT | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364853 | |||||||
| chr15:73364855 | G | C | 7 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0004g0077 others(4): Show |
7 | HG01243.hp1 HG02622.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.785+2631C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364855 | |||||||
| chr15:73364926 | T | G | 43 | a0001c0001t0001g0062 a0001c0001t0001g0233 a0001c0001t0002g0066 others(40): Show |
47 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.785+2560A>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364926 | |||||||
| chr15:73364954 | G | A | 19 | a0001c0001t0001g0062 a0001c0001t0002g0066 a0001c0001t0003g0243 others(16): Show |
20 | HG01891.hp2 HG02258.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.785+2532C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364954 | |||||||
| chr15:73364974 | C | T | 1 | a0001c0001t0016g0040 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.785+2512G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364974 | |||||||
| chr15:73364980 | C | T | 2 | a0001c0001t0004g0285 a0001c0001t0004g0286 |
2 | HG02055.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.785+2506G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364980 | |||||||
| chr15:73364981 | G | A | 1 | a0001c0001t0004g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.785+2505C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73364981 | |||||||
| chr15:73365277 | A | T | 1 | a0001c0001t0002g0079 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.785+2209T>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73365277 | |||||||
| chr15:73365489 | A | C | 6 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0004g0077 others(3): Show |
6 | HG02258.hp2 HG02622.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.785+1997T>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73365489 | |||||||
| chr15:73365561 | T | C | 1 | a0001c0001t0002g0244 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.785+1925A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73365561 | |||||||
| chr15:73365593 | A | G | 1 | a0001c0003t0001g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.785+1893T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73365593 | |||||||
| chr15:73365679 | C | T | 1 | a0005c0011t0004g0073 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.785+1807G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73365679 | |||||||
| chr15:73365689 | T | C | 1 | a0001c0003t0001g0245 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.785+1797A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73365689 | |||||||
| chr15:73365809 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.785+1677C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73365809 | |||||||
| chr15:73365836 | A | G | 17 | a0001c0001t0001g0062 a0001c0001t0002g0066 a0001c0001t0006g0063 others(14): Show |
18 | HG02258.hp1 HG02451.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.785+1650T>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73365836 | |||||||
| chr15:73365841 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.785+1645C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73365841 | |||||||
| chr15:73366342 | G | A | 1 | a0001c0001t0018g0044 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.785+1144C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366342 | |||||||
| chr15:73366360 | T | C | 2 | a0001c0002t0010g0292 a0007c0018t0003g0291 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.785+1126A>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366360 | |||||||
| chr15:73366403 | G | A | 1 | a0001c0001t0004g0248 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.785+1083C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366403 | |||||||
| chr15:73366414 | G | C | 3 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0249 |
5 | NA18939.hp1 NA18942.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.785+1072C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366414 | |||||||
| chr15:73366422 | G | A | 1 | a0008c0015t0007g0250 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.785+1064C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366422 | |||||||
| chr15:73366465 | C | T | 9 | a0001c0001t0003g0054 a0001c0001t0003g0055 a0001c0001t0004g0049 others(6): Show |
10 | HG01346.hp1 HG02145.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.785+1021G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366465 | |||||||
| chr15:73366466 | C | G | 2 | a0001c0002t0003g0052 a0001c0002t0003g0053 |
2 | HG00639.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.785+1020G>C | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366466 | |||||||
| chr15:73366773 | G | A | 1 | a0001c0001t0002g0035 | 2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.785+713C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366773 | |||||||
| chr15:73366853 | A | T | 258 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(255): Show |
303 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.785+633T>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366853 | |||||||
| chr15:73366862 | G | A | 4 | a0001c0001t0004g0285 a0001c0001t0004g0286 a0001c0001t0004g0287 others(1): Show |
4 | HG02055.hp2 HG02559.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.785+624C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366862 | |||||||
| chr15:73366941 | G | C | 1 | a0001c0001t0006g0289 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.785+545C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366941 | |||||||
| chr15:73366999 | G | A | 1 | a0001c0005t0005g0290 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.785+487C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73366999 | |||||||
| chr15:73367002 | C | T | 2 | a0001c0003t0001g0050 a0001c0003t0001g0051 |
2 | HG03225.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.785+484G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73367002 | |||||||
| chr15:73367003 | G | A | 1 | a0001c0001t0002g0039 | 2 | NA18950.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.785+483C>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73367003 | |||||||
| chr15:73367141 | C | A | 2 | a0001c0002t0010g0292 a0007c0018t0003g0291 |
2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.785+345G>T | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73367141 | |||||||
| chr15:73367166 | G | C | 1 | a0001c0004t0001g0293 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.785+320C>G | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73367166 | |||||||
| chr15:73367457 | C | T | 1 | a0001c0001t0004g0049 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.785+29G>A | HCN4 | ENSG00000138622.4 | transcript | ENST00000261917.4 | protein_coding | 1/7 | chr15 | 73367457 |