Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51564 |
| ensemblid | ENSG00000061273.18 |
| hgncid | 14067 |
| symbol | HDAC7 |
| name | histone deacetylase 7 |
| refseq_nuc | NM_015401.5 |
| refseq_prot | NP_056216.2 |
| ensembl_nuc | ENST00000080059.12 |
| ensembl_prot | ENSP00000080059.7 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 47782722 |
| end | 47819903 |
| strand | - |
| ver | v1.2 |
| region | chr12:47782722-47819903 |
| region5000 | chr12:47777722-47824903 |
| regionname0 | HDAC7_chr12_47782722_47819903 |
| regionname5000 | HDAC7_chr12_47777722_47824903 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 991 | 364 | 89 | 75 | 137 | 17 | 44 | 101 | HDAC7_chr12_47777722_47824903 | HDAC7 | MHSPG others(986): Show |
chr12 | 47777722 | 47824903 |
| a0002 | 0/0 | 991 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | MHSPG others(986): Show |
chr12 | 47777722 | 47824903 |
| a0003 | 0/0 | 991 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | MHSPG others(986): Show |
chr12 | 47777722 | 47824903 |
| a0004 | 0/0 | 991 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | MHSPG others(986): Show |
chr12 | 47777722 | 47824903 |
| a0005 | 0/0 | 991 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | MHSPG others(986): Show |
chr12 | 47777722 | 47824903 |
| a0006 | 0/0 | 991 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | MHSPG others(986): Show |
chr12 | 47777722 | 47824903 |
| a0007 | 0/0 | 991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | MHSPG others(986): Show |
chr12 | 47777722 | 47824903 |
| a0008 | 0/0 | 991 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | MHSPG others(986): Show |
chr12 | 47777722 | 47824903 |
| a0009 | 0/0 | 991 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | MHSPG others(986): Show |
chr12 | 47777722 | 47824903 |
| a0010 | 0/0 | 991 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | MHSPG others(986): Show |
chr12 | 47777722 | 47824903 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2973 | 283 | 59 | 53 | 124 | 11 | 34 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0001c0002 | 0/0 | 2973 | 29 | 13 | 9 | 1 | 2 | 4 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0001c0003 | 0/0 | 2973 | 13 | 11 | 2 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0001c0004 | 0/0 | 2973 | 11 | 1 | 6 | 0 | 1 | 3 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0001c0005 | 0/0 | 2973 | 8 | 0 | 0 | 8 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0001c0007 | 0/0 | 2973 | 4 | 1 | 2 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0001c0008 | 0/0 | 2973 | 3 | 0 | 1 | 0 | 2 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0001c0009 | 0/0 | 2973 | 2 | 2 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0001c0011 | 0/0 | 2973 | 2 | 0 | 0 | 2 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0001c0012 | 0/0 | 2973 | 2 | 0 | 0 | 0 | 0 | 2 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0001c0016 | 0/0 | 2973 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0001c0018 | 0/0 | 2973 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0001c0019 | 0/0 | 2973 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0001c0020 | 0/0 | 2973 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0001c0021 | 0/0 | 2973 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0001c0024 | 0/0 | 2973 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0001c0025 | 0/0 | 2973 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0002c0006 | 0/0 | 2973 | 4 | 3 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0002c0013 | 0/0 | 2973 | 2 | 2 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0003c0014 | 0/0 | 2973 | 2 | 1 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0004c0010 | 0/0 | 2973 | 2 | 2 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0005c0015 | 0/0 | 2973 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0006c0026 | 0/0 | 2973 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0007c0017 | 0/0 | 2973 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0008c0023 | 0/0 | 2973 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0009c0027 | 0/0 | 2973 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 | ||
| a0010c0022 | 0/0 | 2973 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | ATGCA others(2968): Show |
chr12 | 47777722 | 47824903 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4213 | 104 | 22 | 25 | 42 | 0 | 15 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0001t0002 | 0/0 | 4213 | 53 | 0 | 1 | 40 | 5 | 7 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0001t0003 | 0/0 | 4211 | 36 | 15 | 3 | 17 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4206): Show |
chr12 | 47777722 | 47824903 |
| a0001c0001t0004 | 1/1 | 4213 | 46 | 11 | 13 | 12 | 2 | 6 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0001t0005 | 0/0 | 4211 | 25 | 3 | 4 | 12 | 1 | 5 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4206): Show |
chr12 | 47777722 | 47824903 |
| a0001c0001t0007 | 0/0 | 4211 | 8 | 1 | 6 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4206): Show |
chr12 | 47777722 | 47824903 |
| a0001c0001t0008 | 0/0 | 4213 | 2 | 2 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0001t0009 | 0/0 | 4213 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0001t0011 | 0/0 | 4213 | 3 | 2 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0001t0012 | 0/0 | 4213 | 2 | 2 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0001t0014 | 0/0 | 4213 | 2 | 0 | 0 | 0 | 1 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0001t0015 | 0/0 | 4213 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0002t0001 | 0/0 | 4213 | 6 | 4 | 0 | 1 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0002t0002 | 0/0 | 4213 | 2 | 1 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0002t0003 | 0/0 | 4211 | 8 | 5 | 2 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4206): Show |
chr12 | 47777722 | 47824903 |
| a0001c0002t0004 | 0/0 | 4213 | 5 | 0 | 4 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0002t0005 | 0/0 | 4211 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4206): Show |
chr12 | 47777722 | 47824903 |
| a0001c0002t0008 | 0/0 | 4213 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0002t0010 | 0/0 | 4211 | 3 | 1 | 1 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4206): Show |
chr12 | 47777722 | 47824903 |
| a0001c0002t0012 | 0/0 | 4213 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0002t0013 | 0/0 | 4213 | 2 | 0 | 1 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0003t0001 | 0/0 | 4213 | 6 | 4 | 2 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0003t0003 | 0/0 | 4211 | 2 | 2 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4206): Show |
chr12 | 47777722 | 47824903 |
| a0001c0003t0008 | 0/0 | 4213 | 2 | 2 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0003t0009 | 0/0 | 4213 | 3 | 3 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0004t0006 | 0/0 | 4201 | 11 | 1 | 6 | 0 | 1 | 3 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4196): Show |
chr12 | 47777722 | 47824903 |
| a0001c0005t0001 | 0/0 | 4213 | 8 | 0 | 0 | 8 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0007t0006 | 0/0 | 4201 | 4 | 1 | 2 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4196): Show |
chr12 | 47777722 | 47824903 |
| a0001c0008t0006 | 0/0 | 4201 | 3 | 0 | 1 | 0 | 2 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4196): Show |
chr12 | 47777722 | 47824903 |
| a0001c0009t0003 | 0/0 | 4211 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4206): Show |
chr12 | 47777722 | 47824903 |
| a0001c0009t0009 | 0/0 | 4213 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0011t0001 | 0/0 | 4213 | 2 | 0 | 0 | 2 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0012t0001 | 0/0 | 4213 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0012t0005 | 0/0 | 4211 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4206): Show |
chr12 | 47777722 | 47824903 |
| a0001c0016t0003 | 0/0 | 4211 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4206): Show |
chr12 | 47777722 | 47824903 |
| a0001c0018t0002 | 0/0 | 4213 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0019t0001 | 0/0 | 4213 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0020t0005 | 0/0 | 4211 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4206): Show |
chr12 | 47777722 | 47824903 |
| a0001c0021t0001 | 0/0 | 4213 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0001c0024t0006 | 0/0 | 4201 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4196): Show |
chr12 | 47777722 | 47824903 |
| a0001c0025t0004 | 0/0 | 4213 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0002c0006t0001 | 0/0 | 4213 | 2 | 2 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0002c0006t0003 | 0/0 | 4211 | 2 | 1 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4206): Show |
chr12 | 47777722 | 47824903 |
| a0002c0013t0001 | 0/0 | 4213 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0002c0013t0002 | 0/0 | 4213 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0003c0014t0003 | 0/0 | 4211 | 2 | 1 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4206): Show |
chr12 | 47777722 | 47824903 |
| a0004c0010t0001 | 0/0 | 4213 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0004c0010t0016 | 0/0 | 4213 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0005c0015t0003 | 0/0 | 4211 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4206): Show |
chr12 | 47777722 | 47824903 |
| a0006c0026t0001 | 0/0 | 4213 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0007c0017t0003 | 0/0 | 4211 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4206): Show |
chr12 | 47777722 | 47824903 |
| a0008c0023t0001 | 0/0 | 4213 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0009c0027t0002 | 0/0 | 4213 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| a0010c0022t0004 | 0/0 | 4213 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | CTTCC others(4208): Show |
chr12 | 47777722 | 47824903 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0252 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0255 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0005g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0007g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0007g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0007g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0007g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0007g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0008g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0008g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0009g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0011g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0011g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0011g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0012g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0012g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0014g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0014g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0001t0015g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0004g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0004g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0004g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0005g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0010g0025 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0010g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0012g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0013g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0002t0013g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0003t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0003t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0003t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0003t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0003t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0003t0008g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0003t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0003t0009g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0003t0009g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0003t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0004t0006g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0004t0006g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0004t0006g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0004t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0004t0006g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0004t0006g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0004t0006g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0004t0006g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0004t0006g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0005t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0005t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0005t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0005t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0005t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0005t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0007t0006g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0007t0006g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0007t0006g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0007t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0008t0006g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0008t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0009t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0009t0009g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0011t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0011t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0012t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0012t0005g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0016t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0018t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0019t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0020t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0021t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0024t0006g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0001c0025t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0002c0006t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0002c0006t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0002c0006t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0002c0006t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0002c0013t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0002c0013t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0003c0014t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0003c0014t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0004c0010t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0004c0010t0016g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0005c0015t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0006c0026t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0007c0017t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0008c0023t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0009c0027t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| a0010c0022t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0078 | EUR | GBR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00099 | hp2 | a0005 | c0015 | t0003 | g0162 | EUR | GBR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00140 | hp1 | a0001 | c0007 | t0006 | g0054 | EUR | GBR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00140 | hp2 | a0001 | c0002 | t0013 | g0134 | EUR | GBR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0065 | EUR | FIN | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00280 | hp2 | a0001 | c0001 | t0014 | g0161 | EUR | FIN | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0105 | EUR | FIN | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00323 | hp2 | a0001 | c0004 | t0006 | g0052 | EUR | FIN | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | CHS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | CHS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | CHS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00544 | hp2 | a0001 | c0005 | t0001 | g0177 | EAS | CHS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | CHS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | CHS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | CHS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | CHS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | CHS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | CHS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00639 | hp2 | a0001 | c0001 | t0007 | g0057 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00642 | hp2 | a0003 | c0014 | t0003 | g0208 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | CHS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | CHS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00733 | hp2 | a0001 | c0001 | t0007 | g0009 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0009 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00738 | hp2 | a0001 | c0001 | t0004 | g0175 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00741 | hp1 | a0001 | c0002 | t0003 | g0220 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG00741 | hp2 | a0001 | c0007 | t0006 | g0235 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01069 | hp2 | a0001 | c0008 | t0006 | g0044 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01070 | hp1 | a0001 | c0004 | t0006 | g0011 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01070 | hp2 | a0001 | c0001 | t0007 | g0008 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01071 | hp2 | a0001 | c0004 | t0006 | g0011 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01074 | hp1 | a0001 | c0002 | t0004 | g0225 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0251 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0035 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01081 | hp2 | a0001 | c0002 | t0005 | g0221 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01099 | hp1 | a0001 | c0001 | t0004 | g0187 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0035 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01106 | hp1 | a0001 | c0002 | t0013 | g0047 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0159 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0172 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01167 | hp1 | a0001 | c0001 | t0011 | g0265 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0029 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01168 | hp2 | a0002 | c0006 | t0003 | g0259 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0029 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01175 | hp1 | a0001 | c0004 | t0006 | g0040 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0236 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0051 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0242 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01243 | hp1 | a0001 | c0004 | t0006 | g0058 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0046 | AMR | PUR | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01255 | hp2 | a0001 | c0002 | t0010 | g0256 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01256 | hp1 | a0001 | c0002 | t0004 | g0015 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0042 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0249 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01258 | hp2 | a0001 | c0002 | t0004 | g0015 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0119 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0155 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01346 | hp1 | a0001 | c0001 | t0005 | g0166 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0169 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0253 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0112 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01361 | hp1 | a0001 | c0004 | t0006 | g0156 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0107 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01433 | hp1 | a0001 | c0001 | t0007 | g0053 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01433 | hp2 | a0001 | c0021 | t0001 | g0152 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01496 | hp1 | a0001 | c0001 | t0007 | g0008 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01515 | hp1 | a0001 | c0008 | t0006 | g0010 | EUR | IBS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01515 | hp2 | a0001 | c0001 | t0007 | g0049 | EUR | IBS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01516 | hp1 | a0001 | c0002 | t0010 | g0025 | EUR | IBS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0013 | EUR | IBS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0013 | EUR | IBS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01517 | hp2 | a0001 | c0008 | t0006 | g0010 | EUR | IBS | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01884 | hp1 | a0001 | c0003 | t0008 | g0198 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0140 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0262 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0222 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0207 | AMR | PEL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01978 | hp1 | a0001 | c0024 | t0006 | g0043 | AMR | PEL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PEL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02004 | hp2 | a0006 | c0026 | t0001 | g0267 | AMR | PEL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | KHV | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | KHV | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | KHV | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | KHV | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | KHV | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | CDX | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | CDX | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0205 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PEL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02300 | hp1 | a0001 | c0004 | t0006 | g0189 | AMR | PEL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02451 | hp1 | a0001 | c0003 | t0001 | g0160 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0327 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | KHV | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02572 | hp1 | a0002 | c0013 | t0002 | g0304 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0325 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0204 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02615 | hp1 | a0001 | c0003 | t0009 | g0147 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02615 | hp2 | a0001 | c0004 | t0006 | g0041 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0336 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02647 | hp1 | a0001 | c0003 | t0009 | g0151 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0211 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02698 | hp1 | a0001 | c0004 | t0006 | g0131 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0254 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0270 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02723 | hp1 | a0004 | c0010 | t0016 | g0319 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0136 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02735 | hp1 | a0001 | c0012 | t0001 | g0180 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02735 | hp2 | a0001 | c0002 | t0004 | g0028 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0158 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0274 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02886 | hp2 | a0001 | c0003 | t0008 | g0197 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0215 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02896 | hp1 | a0002 | c0006 | t0003 | g0315 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02896 | hp2 | a0001 | c0002 | t0003 | g0016 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02897 | hp1 | a0001 | c0002 | t0003 | g0016 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0212 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02922 | hp1 | a0001 | c0001 | t0012 | g0213 | AFR | ESN | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02922 | hp2 | a0002 | c0006 | t0001 | g0317 | AFR | ESN | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02970 | hp1 | a0001 | c0016 | t0003 | g0223 | AFR | ESN | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02970 | hp2 | a0001 | c0001 | t0011 | g0164 | AFR | ESN | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02976 | hp1 | a0001 | c0001 | t0012 | g0059 | AFR | ESN | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03017 | hp1 | a0001 | c0004 | t0006 | g0007 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0167 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03098 | hp1 | a0002 | c0013 | t0001 | g0303 | AFR | MSL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | MSL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03139 | hp1 | a0001 | c0003 | t0003 | g0146 | AFR | ESN | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | ESN | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | MSL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0135 | AFR | MSL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03225 | hp1 | a0001 | c0001 | t0008 | g0148 | AFR | MSL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03225 | hp2 | a0001 | c0002 | t0003 | g0273 | AFR | MSL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03239 | hp2 | a0007 | c0017 | t0003 | g0133 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0216 | AFR | MSL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0243 | AFR | MSL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03486 | hp1 | a0001 | c0001 | t0011 | g0194 | AFR | MSL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0023 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03490 | hp2 | a0001 | c0001 | t0005 | g0308 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0019 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0307 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03492 | hp1 | a0001 | c0001 | t0005 | g0023 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0019 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | ESN | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03516 | hp2 | a0001 | c0003 | t0001 | g0305 | AFR | ESN | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03540 | hp2 | a0001 | c0003 | t0009 | g0150 | AFR | GWD | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0276 | AFR | MSL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0026 | AFR | MSL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0048 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | STU | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | STU | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03704 | hp1 | a0001 | c0025 | t0004 | g0071 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0045 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0250 | SAS | BEB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03834 | hp2 | a0001 | c0004 | t0006 | g0007 | SAS | BEB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03927 | hp1 | a0001 | c0012 | t0005 | g0139 | SAS | BEB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03942 | hp1 | a0001 | c0002 | t0003 | g0226 | SAS | BEB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | BEB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | STU | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0099 | SAS | STU | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG04184 | hp1 | a0001 | c0001 | t0014 | g0231 | SAS | BEB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | BEB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG04199 | hp1 | a0008 | c0023 | t0001 | g0174 | SAS | STU | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | STU | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | STU | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG04228 | hp2 | a0001 | c0001 | t0005 | g0219 | SAS | STU | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18522 | hp1 | a0001 | c0003 | t0003 | g0326 | AFR | YRI | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0330 | AFR | YRI | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | CHB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | YRI | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18906 | hp2 | a0001 | c0009 | t0003 | g0320 | AFR | YRI | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18941 | hp1 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18948 | hp1 | a0001 | c0001 | t0015 | g0234 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0279 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18950 | hp2 | a0001 | c0001 | t0005 | g0240 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18953 | hp1 | a0001 | c0001 | t0005 | g0323 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0334 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18954 | hp2 | a0001 | c0011 | t0001 | g0092 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18956 | hp1 | a0001 | c0005 | t0001 | g0021 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18956 | hp2 | a0001 | c0001 | t0005 | g0199 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18959 | hp1 | a0001 | c0018 | t0002 | g0120 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18959 | hp2 | a0001 | c0001 | t0005 | g0322 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0238 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18961 | hp2 | a0001 | c0005 | t0001 | g0020 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18966 | hp2 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0333 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18975 | hp1 | a0009 | c0027 | t0002 | g0335 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18975 | hp2 | a0001 | c0005 | t0001 | g0157 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0073 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0313 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18985 | hp1 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18993 | hp1 | a0001 | c0005 | t0001 | g0021 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0229 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19009 | hp1 | a0001 | c0001 | t0005 | g0294 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19030 | hp1 | a0001 | c0002 | t0003 | g0275 | AFR | LWK | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | LWK | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19043 | hp1 | a0001 | c0002 | t0012 | g0318 | AFR | LWK | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | LWK | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0312 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19062 | hp2 | a0001 | c0005 | t0001 | g0191 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19064 | hp1 | a0001 | c0005 | t0001 | g0020 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19067 | hp2 | a0001 | c0005 | t0001 | g0190 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0331 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19079 | hp1 | a0001 | c0001 | t0005 | g0239 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19081 | hp2 | a0001 | c0011 | t0001 | g0117 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19083 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19083 | hp2 | a0001 | c0020 | t0005 | g0200 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0332 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19240 | hp1 | a0002 | c0006 | t0001 | g0316 | AFR | YRI | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA19240 | hp2 | a0001 | c0002 | t0008 | g0195 | AFR | YRI | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA20129 | hp1 | a0001 | c0003 | t0001 | g0210 | AFR | ASW | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0193 | AFR | ASW | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0245 | EUR | TSI | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0141 | EUR | TSI | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0056 | EUR | TSI | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0115 | EUR | TSI | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | GIH | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0069 | SAS | GIH | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01123 | hp1 | a0001 | c0007 | t0006 | g0070 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG01123 | hp2 | a0001 | c0002 | t0004 | g0028 | AMR | CLM | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0171 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0055 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02486 | hp2 | a0003 | c0014 | t0003 | g0186 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02559 | hp1 | a0001 | c0019 | t0001 | g0302 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0224 | AFR | ACB | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | MSL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG03471 | hp2 | a0004 | c0010 | t0001 | g0314 | AFR | MSL | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG06807 | hp1 | a0001 | c0009 | t0009 | g0321 | AFR | USA | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| HG06807 | hp2 | a0001 | c0002 | t0002 | g0062 | AFR | USA | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA20300 | hp1 | a0010 | c0022 | t0004 | g0244 | AFR | USA | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA20300 | hp2 | a0001 | c0002 | t0010 | g0025 | AFR | USA | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA21309 | hp1 | a0001 | c0001 | t0008 | g0260 | AFR | LWK | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| NA21309 | hp2 | a0001 | c0007 | t0006 | g0306 | AFR | LWK | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0255 | REF | REF | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0252 | REF | REF | HDAC7_chr12_47777722_47824903 | HDAC7 | chr12 | 47777722 | 47824903 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:47784187 | G | T | 1 | a0007 | 1 | HG03239.hp2 | missense_variant | MODERATE | c.2822C>A | p.Ala941Asp | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 25/26 | 2940/4213 | 2822/2976 | 941/991 | chr12 | 47784187 | |||
| chr12:47791666 | G | A | 1 | a0002 | 6 | HG01168.hp2 HG02572.hp1 HG02896.hp1 others(3): Show |
missense_variant | MODERATE | c.1853C>T | p.Ser618Leu | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 15/26 | 1971/4213 | 1853/2976 | 618/991 | chr12 | 47791666 | |||
| chr12:47793546 | G | A | 1 | a0003 | 2 | HG00642.hp2 HG02486.hp2 |
missense_variant | MODERATE | c.1501C>T | p.Arg501Trp | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/26 | 1619/4213 | 1501/2976 | 501/991 | chr12 | 47793546 | |||
| chr12:47795598 | G | T | 1 | a0004 | 2 | HG02723.hp1 HG03471.hp2 |
missense_variant | MODERATE | c.1076C>A | p.Pro359Gln | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 10/26 | 1194/4213 | 1076/2976 | 359/991 | chr12 | 47795598 | |||
| chr12:47795733 | C | A | 1 | a0010 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.941G>T | p.Gly314Val | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 10/26 | 1059/4213 | 941/2976 | 314/991 | chr12 | 47795733 | |||
| chr12:47795970 | G | A | 1 | a0008 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.842C>T | p.Pro281Leu | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 9/26 | 960/4213 | 842/2976 | 281/991 | chr12 | 47795970 | |||
| chr12:47797464 | C | T | 1 | a0005 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.497G>A | p.Arg166His | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 6/26 | 615/4213 | 497/2976 | 166/991 | chr12 | 47797464 | |||
| chr12:47798916 | G | A | 1 | a0006 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.127C>T | p.Arg43Trp | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 3/26 | 245/4213 | 127/2976 | 43/991 | chr12 | 47798916 | |||
| chr12:47798954 | G | A | 1 | a0009 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.89C>T | p.Ala30Val | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 3/26 | 207/4213 | 89/2976 | 30/991 | chr12 | 47798954 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:47783880 | C | T | 1 | a0001c0019 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.2937G>A | p.Ser979Ser | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 26/26 | 3055/4213 | 2937/2976 | 979/991 | chr12 | 47783880 | |||
| chr12:47784123 | C | T | 4 | a0001c0004 a0001c0007 a0001c0008 others(1): Show |
19 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(16): Show |
synonymous_variant | LOW | c.2886G>A | p.Val962Val | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 25/26 | 3004/4213 | 2886/2976 | 962/991 | chr12 | 47784123 | |||
| chr12:47784189 | C | T | 1 | a0001c0018 | 1 | NA18959.hp1 | synonymous_variant | LOW | c.2820G>A | p.Leu940Leu | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 25/26 | 2938/4213 | 2820/2976 | 940/991 | chr12 | 47784189 | |||
| chr12:47788063 | C | T | 1 | a0001c0016 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.2337G>A | p.Gly779Gly | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 20/26 | 2455/4213 | 2337/2976 | 779/991 | chr12 | 47788063 | |||
| chr12:47788066 | C | T | 1 | a0001c0008 | 3 | HG01069.hp2 HG01515.hp1 HG01517.hp2 |
synonymous_variant | LOW | c.2334G>A | p.Pro778Pro | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 20/26 | 2452/4213 | 2334/2976 | 778/991 | chr12 | 47788066 | |||
| chr12:47791635 | G | A | 1 | a0001c0020 | 1 | NA19083.hp2 | synonymous_variant | LOW | c.1884C>T | p.Tyr628Tyr | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 15/26 | 2002/4213 | 1884/2976 | 628/991 | chr12 | 47791635 | |||
| chr12:47791644 | C | T | 1 | a0001c0012 | 2 | HG02735.hp1 HG03927.hp1 |
synonymous_variant | LOW | c.1875G>A | p.Val625Val | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 15/26 | 1993/4213 | 1875/2976 | 625/991 | chr12 | 47791644 | |||
| chr12:47793427 | G | A | 2 | a0001c0003 a0001c0009 |
15 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(12): Show |
synonymous_variant | LOW | c.1620C>T | p.Ser540Ser | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/26 | 1738/4213 | 1620/2976 | 540/991 | chr12 | 47793427 | |||
| chr12:47794835 | A | G | 1 | a0001c0011 | 2 | NA18954.hp2 NA19081.hp2 |
synonymous_variant | LOW | c.1383T>C | p.Asp461Asp | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 12/26 | 1501/4213 | 1383/2976 | 461/991 | chr12 | 47794835 | |||
| chr12:47795265 | G | A | 1 | a0001c0021 | 1 | HG01433.hp2 | synonymous_variant | LOW | c.1203C>T | p.Pro401Pro | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 11/26 | 1321/4213 | 1203/2976 | 401/991 | chr12 | 47795265 | |||
| chr12:47795966 | G | A | 1 | a0001c0005 | 8 | HG00544.hp2 NA18956.hp1 NA18961.hp2 others(5): Show |
synonymous_variant | LOW | c.846C>T | p.Phe282Phe | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 9/26 | 964/4213 | 846/2976 | 282/991 | chr12 | 47795966 | |||
| chr12:47796261 | C | T | 11 | a0001c0002 a0001c0004 a0001c0008 others(8): Show |
55 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(52): Show |
synonymous_variant | LOW | c.741G>A | p.Gly247Gly | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 8/26 | 859/4213 | 741/2976 | 247/991 | chr12 | 47796261 | |||
| chr12:47797021 | G | A | 1 | a0001c0024 | 1 | HG01978.hp1 | synonymous_variant | LOW | c.699C>T | p.Leu233Leu | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 7/26 | 817/4213 | 699/2976 | 233/991 | chr12 | 47797021 | |||
| chr12:47797117 | G | A | 1 | a0001c0024 | 1 | HG01978.hp1 | synonymous_variant | LOW | c.603C>T | p.Arg201Arg | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 7/26 | 721/4213 | 603/2976 | 201/991 | chr12 | 47797117 | |||
| chr12:47798119 | G | C | 1 | a0001c0025 | 1 | HG03704.hp1 | synonymous_variant | LOW | c.450C>G | p.Gly150Gly | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/26 | 568/4213 | 450/2976 | 150/991 | chr12 | 47798119 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:47782841 | ACT | A | 10 | a0001c0001t0003 a0001c0001t0007 a0001c0002t0003 others(7): Show |
62 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*998_*999delAG | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 26/26 | 998 | chr12 | 47782841 | ||||||
| chr12:47782841 | ACTCACAC others(5): Show |
A | 4 | a0001c0004t0006 a0001c0007t0006 a0001c0008t0006 others(1): Show |
19 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*988_*999delCGTGTG others(6): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 26/26 | 988 | chr12 | 47782841 | ||||||
| chr12:47782872 | TCA | T | 5 | a0001c0001t0005 a0001c0002t0005 a0001c0002t0010 others(2): Show |
31 | HG01081.hp1 HG01081.hp2 HG01099.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*967_*968delTG | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 26/26 | 967 | chr12 | 47782872 | ||||||
| chr12:47783009 | C | T | 49 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(46): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
3_prime_UTR_variant | MODIFIER | c.*832G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 26/26 | 832 | chr12 | 47783009 | ||||||
| chr12:47783110 | C | T | 1 | a0001c0001t0014 | 2 | HG00280.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*731G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 26/26 | 731 | chr12 | 47783110 | ||||||
| chr12:47783117 | T | G | 46 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(43): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
3_prime_UTR_variant | MODIFIER | c.*724A>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 26/26 | 724 | chr12 | 47783117 | ||||||
| chr12:47783231 | G | T | 1 | a0001c0001t0011 | 3 | HG01167.hp1 HG02970.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*610C>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 26/26 | 610 | chr12 | 47783231 | ||||||
| chr12:47783260 | C | T | 1 | a0001c0002t0010 | 3 | HG01255.hp2 HG01516.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*581G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 26/26 | 581 | chr12 | 47783260 | ||||||
| chr12:47783263 | C | T | 1 | a0001c0002t0013 | 2 | HG00140.hp2 HG01106.hp1 |
3_prime_UTR_variant | MODIFIER | c.*578G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 26/26 | 578 | chr12 | 47783263 | ||||||
| chr12:47783290 | A | G | 46 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(43): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
3_prime_UTR_variant | MODIFIER | c.*551T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 26/26 | 551 | chr12 | 47783290 | ||||||
| chr12:47783387 | C | G | 5 | a0001c0001t0002 a0001c0002t0002 a0001c0018t0002 others(2): Show |
58 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*454G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 26/26 | 454 | chr12 | 47783387 | ||||||
| chr12:47783441 | C | T | 3 | a0001c0001t0008 a0001c0002t0008 a0001c0003t0008 |
5 | HG01884.hp1 HG02886.hp2 HG03225.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*400G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 26/26 | 400 | chr12 | 47783441 | ||||||
| chr12:47783445 | G | T | 1 | a0001c0001t0015 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*396C>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 26/26 | 396 | chr12 | 47783445 | ||||||
| chr12:47783455 | A | G | 46 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(43): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
3_prime_UTR_variant | MODIFIER | c.*386T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 26/26 | 386 | chr12 | 47783455 | ||||||
| chr12:47783516 | G | A | 1 | a0001c0001t0007 | 8 | HG00639.hp2 HG00733.hp2 HG00735.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*325C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 26/26 | 325 | chr12 | 47783516 | ||||||
| chr12:47783642 | G | A | 2 | a0001c0001t0012 a0001c0002t0012 |
3 | HG02922.hp1 HG02976.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*199C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 26/26 | 199 | chr12 | 47783642 | ||||||
| chr12:47783673 | G | A | 1 | a0004c0010t0016 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*168C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 26/26 | 168 | chr12 | 47783673 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:47784074 | A | G | 7 | a0001c0001t0001g0014 a0001c0001t0001g0143 a0001c0001t0001g0145 others(4): Show |
8 | HG01168.hp1 HG01169.hp2 HG01255.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.2930+5T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 25/25 | chr12 | 47784074 | |||||||
| chr12:47784260 | C | T | 1 | a0001c0001t0003g0270 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2792-43G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 24/25 | chr12 | 47784260 | |||||||
| chr12:47784344 | A | G | 288 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(285): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.2792-127T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 24/25 | chr12 | 47784344 | |||||||
| chr12:47784411 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(238): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.2792-194T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 24/25 | chr12 | 47784411 | |||||||
| chr12:47784429 | G | A | 16 | a0001c0004t0006g0007 a0001c0004t0006g0011 a0001c0004t0006g0040 others(13): Show |
19 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.2792-212C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 24/25 | chr12 | 47784429 | |||||||
| chr12:47784479 | G | T | 1 | a0001c0003t0001g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2792-262C>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 24/25 | chr12 | 47784479 | |||||||
| chr12:47784682 | T | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(281): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.2792-465A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 24/25 | chr12 | 47784682 | |||||||
| chr12:47784703 | C | T | 4 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0001t0003g0193 others(1): Show |
4 | HG02257.hp1 HG02486.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.2792-486G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 24/25 | chr12 | 47784703 | |||||||
| chr12:47784730 | A | G | 97 | a0001c0001t0001g0039 a0001c0001t0001g0066 a0001c0001t0001g0103 others(94): Show |
108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.2792-513T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 24/25 | chr12 | 47784730 | |||||||
| chr12:47784821 | T | C | 80 | a0001c0001t0001g0039 a0001c0001t0001g0066 a0001c0001t0001g0103 others(77): Show |
88 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.2791+566A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 24/25 | chr12 | 47784821 | |||||||
| chr12:47784856 | C | G | 1 | a0001c0003t0001g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2791+531G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 24/25 | chr12 | 47784856 | |||||||
| chr12:47784989 | T | A | 2 | a0001c0001t0001g0102 a0001c0002t0001g0277 |
2 | NA18961.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2791+398A>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 24/25 | chr12 | 47784989 | |||||||
| chr12:47784990 | A | G | 2 | a0001c0001t0001g0102 a0001c0002t0001g0277 |
2 | NA18961.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2791+397T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 24/25 | chr12 | 47784990 | |||||||
| chr12:47784991 | T | C | 2 | a0001c0001t0001g0102 a0001c0002t0001g0277 |
2 | NA18961.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.2791+396A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 24/25 | chr12 | 47784991 | |||||||
| chr12:47785001 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(65): Show |
81 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.2791+386G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 24/25 | chr12 | 47785001 | |||||||
| chr12:47785126 | C | A | 282 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(279): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.2791+261G>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 24/25 | chr12 | 47785126 | |||||||
| chr12:47785194 | G | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
151 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.2791+193C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 24/25 | chr12 | 47785194 | |||||||
| chr12:47785214 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
151 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.2791+173G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 24/25 | chr12 | 47785214 | |||||||
| chr12:47785261 | C | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(277): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.2791+126G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 24/25 | chr12 | 47785261 | |||||||
| chr12:47785265 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
151 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(148): Show |
intron_variant | MODIFIER | c.2791+122G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 24/25 | chr12 | 47785265 | |||||||
| chr12:47785320 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2791+67G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 24/25 | chr12 | 47785320 | |||||||
| chr12:47785564 | C | T | 16 | a0001c0004t0006g0007 a0001c0004t0006g0011 a0001c0004t0006g0040 others(13): Show |
19 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.2707-93G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 23/25 | chr12 | 47785564 | |||||||
| chr12:47785619 | C | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(128): Show |
153 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.2706+133G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 23/25 | chr12 | 47785619 | |||||||
| chr12:47785680 | C | T | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(125): Show |
150 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(147): Show |
intron_variant | MODIFIER | c.2706+72G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 23/25 | chr12 | 47785680 | |||||||
| chr12:47785695 | T | G | 16 | a0001c0004t0006g0007 a0001c0004t0006g0011 a0001c0004t0006g0040 others(13): Show |
19 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.2706+57A>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 23/25 | chr12 | 47785695 | |||||||
| chr12:47785736 | G | T | 1 | a0001c0001t0015g0234 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2706+16C>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 23/25 | chr12 | 47785736 | |||||||
| chr12:47786113 | G | A | 8 | a0001c0001t0005g0035 a0001c0001t0005g0166 a0001c0001t0005g0294 others(5): Show |
10 | HG01081.hp1 HG01099.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.2573-228C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 22/25 | chr12 | 47786113 | |||||||
| chr12:47786239 | T | C | 288 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(285): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.2572+346A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 22/25 | chr12 | 47786239 | |||||||
| chr12:47786356 | T | C | 1 | a0001c0002t0001g0136 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2572+229A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 22/25 | chr12 | 47786356 | |||||||
| chr12:47786413 | C | T | 1 | a0001c0002t0003g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2572+172G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 22/25 | chr12 | 47786413 | |||||||
| chr12:47786538 | G | C | 3 | a0001c0001t0003g0205 a0003c0014t0003g0186 a0003c0014t0003g0208 |
3 | HG00642.hp2 HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2572+47C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 22/25 | chr12 | 47786538 | |||||||
| chr12:47786725 | C | T | 23 | a0001c0001t0005g0035 a0001c0001t0005g0073 a0001c0001t0005g0098 others(20): Show |
25 | HG01081.hp1 HG01081.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.2454-22G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 21/25 | chr12 | 47786725 | |||||||
| chr12:47786733 | G | A | 1 | a0001c0001t0004g0022 | 2 | HG02145.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2454-30C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 21/25 | chr12 | 47786733 | |||||||
| chr12:47786852 | C | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0266 |
2 | HG02055.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2454-149G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 21/25 | chr12 | 47786852 | |||||||
| chr12:47786880 | A | G | 2 | a0001c0002t0001g0211 a0002c0013t0001g0303 |
2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2454-177T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 21/25 | chr12 | 47786880 | |||||||
| chr12:47786890 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2454-187T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 21/25 | chr12 | 47786890 | |||||||
| chr12:47787059 | C | T | 1 | a0001c0001t0002g0182 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2454-356G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 21/25 | chr12 | 47787059 | |||||||
| chr12:47787078 | G | A | 2 | a0001c0001t0001g0209 a0001c0001t0003g0183 |
2 | HG02523.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2454-375C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 21/25 | chr12 | 47787078 | |||||||
| chr12:47787125 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2454-422C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 21/25 | chr12 | 47787125 | |||||||
| chr12:47787156 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2454-453G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 21/25 | chr12 | 47787156 | |||||||
| chr12:47787198 | G | C | 2 | a0001c0001t0001g0209 a0001c0001t0003g0183 |
2 | HG02523.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.2454-495C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 21/25 | chr12 | 47787198 | |||||||
| chr12:47787201 | C | T | 16 | a0001c0004t0006g0007 a0001c0004t0006g0011 a0001c0004t0006g0040 others(13): Show |
19 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.2454-498G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 21/25 | chr12 | 47787201 | |||||||
| chr12:47787245 | C | CCG | 284 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(281): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.2453+466_2453+467i others(4): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 21/25 | chr12 | 47787245 | |||||||
| chr12:47787361 | C | G | 2 | a0002c0006t0001g0316 a0002c0006t0001g0317 |
2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2453+351G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 21/25 | chr12 | 47787361 | |||||||
| chr12:47787477 | C | T | 25 | a0001c0001t0001g0149 a0001c0001t0008g0148 a0001c0001t0008g0260 others(22): Show |
28 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.2453+235G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 21/25 | chr12 | 47787477 | |||||||
| chr12:47787510 | C | T | 1 | a0001c0004t0006g0052 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2453+202G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 21/25 | chr12 | 47787510 | |||||||
| chr12:47787582 | C | T | 1 | a0001c0003t0001g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2453+130G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 21/25 | chr12 | 47787582 | |||||||
| chr12:47787591 | A | G | 66 | a0001c0001t0001g0039 a0001c0001t0001g0066 a0001c0001t0001g0103 others(63): Show |
74 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.2453+121T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 21/25 | chr12 | 47787591 | |||||||
| chr12:47787645 | C | G | 1 | a0001c0002t0001g0136 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2453+67G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 21/25 | chr12 | 47787645 | |||||||
| chr12:47787888 | C | T | 5 | a0001c0003t0009g0147 a0001c0003t0009g0150 a0001c0003t0009g0151 others(2): Show |
5 | HG02615.hp1 HG02647.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.2356-79G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 20/25 | chr12 | 47787888 | |||||||
| chr12:47787995 | T | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(276): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.2355+50A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 20/25 | chr12 | 47787995 | |||||||
| chr12:47788289 | G | T | 17 | a0001c0001t0004g0019 a0001c0003t0008g0198 a0001c0004t0006g0007 others(14): Show |
21 | HG00140.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.2236-125C>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 19/25 | chr12 | 47788289 | |||||||
| chr12:47788304 | C | T | 313 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(310): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(349): Show |
intron_variant | MODIFIER | c.2236-140G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 19/25 | chr12 | 47788304 | |||||||
| chr12:47788402 | G | A | 1 | a0001c0001t0012g0213 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2236-238C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 19/25 | chr12 | 47788402 | |||||||
| chr12:47788450 | A | C | 4 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0217 others(1): Show |
4 | HG01346.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.2236-286T>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 19/25 | chr12 | 47788450 | |||||||
| chr12:47788458 | A | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
137 | HG00140.hp2 HG00544.hp2 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.2236-294T>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 19/25 | chr12 | 47788458 | |||||||
| chr12:47788625 | C | T | 1 | a0001c0001t0002g0012 | 2 | HG02135.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.2236-461G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 19/25 | chr12 | 47788625 | |||||||
| chr12:47788670 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2236-506C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 19/25 | chr12 | 47788670 | |||||||
| chr12:47788723 | ACATAG | A | 19 | a0001c0001t0001g0096 a0001c0001t0002g0279 a0001c0001t0004g0027 others(16): Show |
20 | HG00408.hp2 HG01099.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.2235+533_2235+537d others(7): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 19/25 | chr12 | 47788723 | |||||||
| chr12:47788795 | G | A | 46 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0013 others(43): Show |
51 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.2235+466C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 19/25 | chr12 | 47788795 | |||||||
| chr12:47789230 | G | A | 3 | a0001c0001t0003g0217 a0001c0001t0012g0059 a0001c0001t0012g0213 |
3 | HG02922.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2235+31C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 19/25 | chr12 | 47789230 | |||||||
| chr12:47789418 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2148-70C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 18/25 | chr12 | 47789418 | |||||||
| chr12:47789674 | G | A | 2 | a0001c0001t0001g0248 a0001c0001t0001g0296 |
2 | HG02056.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2092-96C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 17/25 | chr12 | 47789674 | |||||||
| chr12:47790122 | C | A | 2 | a0001c0001t0004g0107 a0001c0001t0004g0119 |
2 | HG01261.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1984-202G>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 16/25 | chr12 | 47790122 | |||||||
| chr12:47790212 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1984-292C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 16/25 | chr12 | 47790212 | |||||||
| chr12:47790500 | A | C | 2 | a0001c0001t0005g0212 a0001c0001t0005g0215 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1984-580T>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 16/25 | chr12 | 47790500 | |||||||
| chr12:47790723 | C | T | 1 | a0001c0001t0004g0263 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1983+536G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 16/25 | chr12 | 47790723 | |||||||
| chr12:47790769 | C | T | 1 | a0001c0012t0001g0180 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1983+490G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 16/25 | chr12 | 47790769 | |||||||
| chr12:47790772 | G | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0017 others(67): Show |
81 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1983+487C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 16/25 | chr12 | 47790772 | |||||||
| chr12:47790796 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1983+463C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 16/25 | chr12 | 47790796 | |||||||
| chr12:47790828 | C | T | 15 | a0001c0001t0001g0285 a0001c0001t0004g0019 a0001c0001t0007g0049 others(12): Show |
18 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1983+431G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 16/25 | chr12 | 47790828 | |||||||
| chr12:47790939 | G | A | 28 | a0001c0001t0002g0261 a0001c0001t0002g0289 a0001c0001t0002g0293 others(25): Show |
31 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.1983+320C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 16/25 | chr12 | 47790939 | |||||||
| chr12:47790947 | G | T | 55 | a0001c0001t0001g0050 a0001c0001t0001g0142 a0001c0001t0001g0143 others(52): Show |
60 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.1983+312C>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 16/25 | chr12 | 47790947 | |||||||
| chr12:47790986 | G | C | 1 | a0001c0003t0001g0029 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1983+273C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 16/25 | chr12 | 47790986 | |||||||
| chr12:47791003 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1983+256A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 16/25 | chr12 | 47791003 | |||||||
| chr12:47791010 | A | G | 295 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(292): Show |
334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.1983+249T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 16/25 | chr12 | 47791010 | |||||||
| chr12:47791021 | A | G | 6 | a0001c0001t0001g0228 a0001c0001t0004g0026 a0001c0001t0004g0171 others(3): Show |
7 | HG01891.hp2 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1983+238T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 16/25 | chr12 | 47791021 | |||||||
| chr12:47791034 | G | GC | 62 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0103 others(59): Show |
71 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.1983+224_1983+225i others(3): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 16/25 | chr12 | 47791034 | |||||||
| chr12:47791332 | G | A | 3 | a0001c0001t0001g0287 a0001c0001t0002g0126 a0001c0001t0002g0128 |
3 | HG00423.hp1 HG00597.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.1934-24C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 15/25 | chr12 | 47791332 | |||||||
| chr12:47791382 | G | A | 19 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0007g0053 others(16): Show |
25 | HG00140.hp2 HG00323.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.1934-74C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 15/25 | chr12 | 47791382 | |||||||
| chr12:47791384 | G | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(266): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.1934-76C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 15/25 | chr12 | 47791384 | |||||||
| chr12:47791394 | G | A | 1 | a0001c0001t0002g0012 | 2 | HG02135.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1934-86C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 15/25 | chr12 | 47791394 | |||||||
| chr12:47791409 | G | T | 13 | a0001c0001t0001g0050 a0001c0001t0001g0102 a0001c0001t0001g0103 others(10): Show |
13 | HG00639.hp1 HG01099.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.1934-101C>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 15/25 | chr12 | 47791409 | |||||||
| chr12:47791570 | G | A | 1 | a0001c0002t0001g0136 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1933+16C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 15/25 | chr12 | 47791570 | |||||||
| chr12:47791573 | A | G | 48 | a0001c0001t0001g0014 a0001c0001t0001g0038 a0001c0001t0001g0102 others(45): Show |
54 | HG00099.hp1 HG00621.hp1 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.1933+13T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 15/25 | chr12 | 47791573 | |||||||
| chr12:47791743 | G | A | 1 | a0001c0003t0001g0276 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1813-37C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 14/25 | chr12 | 47791743 | |||||||
| chr12:47791850 | G | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0030 others(10): Show |
20 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.1812+21C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 14/25 | chr12 | 47791850 | |||||||
| chr12:47791859 | G | A | 2 | a0001c0001t0001g0299 a0001c0001t0001g0300 |
2 | NA18948.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1812+12C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 14/25 | chr12 | 47791859 | |||||||
| chr12:47792027 | G | A | 2 | a0001c0001t0005g0212 a0001c0001t0005g0215 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1679-23C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/25 | chr12 | 47792027 | |||||||
| chr12:47792047 | C | T | 1 | a0001c0002t0001g0224 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1679-43G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/25 | chr12 | 47792047 | |||||||
| chr12:47792048 | G | A | 1 | a0001c0001t0001g0309 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1679-44C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/25 | chr12 | 47792048 | |||||||
| chr12:47792115 | G | A | 4 | a0001c0001t0003g0111 a0001c0001t0004g0238 a0001c0001t0004g0272 others(1): Show |
5 | HG00408.hp1 HG01256.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1679-111C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/25 | chr12 | 47792115 | |||||||
| chr12:47792199 | G | A | 4 | a0001c0001t0002g0121 a0001c0001t0004g0027 a0001c0001t0004g0163 others(1): Show |
5 | HG02129.hp2 NA18940.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.1679-195C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/25 | chr12 | 47792199 | |||||||
| chr12:47792274 | G | A | 1 | a0001c0001t0005g0294 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1679-270C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/25 | chr12 | 47792274 | |||||||
| chr12:47792288 | C | T | 7 | a0001c0003t0001g0029 a0001c0003t0001g0160 a0001c0003t0001g0210 others(4): Show |
8 | HG01167.hp2 HG01169.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1679-284G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/25 | chr12 | 47792288 | |||||||
| chr12:47792295 | G | A | 2 | a0001c0001t0005g0212 a0001c0001t0005g0215 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1679-291C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/25 | chr12 | 47792295 | |||||||
| chr12:47792317 | C | T | 1 | a0001c0002t0010g0025 | 2 | HG01516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1679-313G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/25 | chr12 | 47792317 | |||||||
| chr12:47792328 | C | T | 2 | a0001c0001t0005g0212 a0001c0001t0005g0215 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1679-324G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/25 | chr12 | 47792328 | |||||||
| chr12:47792331 | C | G | 2 | a0001c0001t0005g0212 a0001c0001t0005g0215 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1679-327G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/25 | chr12 | 47792331 | |||||||
| chr12:47792388 | G | A | 8 | a0001c0001t0001g0137 a0001c0001t0001g0202 a0001c0001t0001g0203 others(5): Show |
9 | HG01167.hp1 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1679-384C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/25 | chr12 | 47792388 | |||||||
| chr12:47792400 | C | G | 1 | a0001c0001t0012g0213 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1679-396G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/25 | chr12 | 47792400 | |||||||
| chr12:47792494 | G | C | 1 | a0001c0024t0006g0043 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1679-490C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/25 | chr12 | 47792494 | |||||||
| chr12:47792780 | T | A | 38 | a0001c0001t0001g0017 a0001c0001t0001g0188 a0001c0001t0001g0228 others(35): Show |
44 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(41): Show |
intron_variant | MODIFIER | c.1678+589A>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/25 | chr12 | 47792780 | |||||||
| chr12:47792865 | A | G | 16 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0149 others(13): Show |
18 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.1678+504T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/25 | chr12 | 47792865 | |||||||
| chr12:47792906 | A | G | 1 | a0001c0001t0004g0249 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1678+463T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/25 | chr12 | 47792906 | |||||||
| chr12:47792955 | T | G | 94 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(91): Show |
106 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1678+414A>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/25 | chr12 | 47792955 | |||||||
| chr12:47792988 | T | C | 1 | a0001c0016t0003g0223 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1678+381A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/25 | chr12 | 47792988 | |||||||
| chr12:47793361 | G | A | 1 | a0001c0001t0003g0325 | 1 | HG02572.hp2 | splice_region_variant&intron_variant | LOW | c.1678+8C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 13/25 | chr12 | 47793361 | |||||||
| chr12:47793818 | C | T | 18 | a0001c0002t0001g0048 a0001c0002t0002g0045 a0001c0002t0004g0028 others(15): Show |
22 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.1459-230G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 12/25 | chr12 | 47793818 | |||||||
| chr12:47793931 | T | C | 1 | a0001c0002t0001g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1459-343A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 12/25 | chr12 | 47793931 | |||||||
| chr12:47794072 | G | A | 1 | a0001c0001t0004g0112 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1459-484C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 12/25 | chr12 | 47794072 | |||||||
| chr12:47794319 | C | T | 1 | a0001c0008t0006g0044 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1458+441G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 12/25 | chr12 | 47794319 | |||||||
| chr12:47794320 | G | A | 7 | a0001c0001t0001g0188 a0001c0001t0001g0328 a0001c0001t0004g0026 others(4): Show |
8 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1458+440C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 12/25 | chr12 | 47794320 | |||||||
| chr12:47794355 | T | C | 1 | a0001c0002t0001g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1458+405A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 12/25 | chr12 | 47794355 | |||||||
| chr12:47794442 | T | C | 1 | a0001c0001t0005g0332 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1458+318A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 12/25 | chr12 | 47794442 | |||||||
| chr12:47795115 | C | T | 36 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0030 others(33): Show |
46 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.1284+69G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 11/25 | chr12 | 47795115 | |||||||
| chr12:47795452 | G | C | 1 | a0001c0024t0006g0043 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1088-72C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 10/25 | chr12 | 47795452 | |||||||
| chr12:47795452 | G | T | 1 | a0001c0001t0001g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1088-72C>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 10/25 | chr12 | 47795452 | |||||||
| chr12:47795459 | C | G | 3 | a0001c0002t0003g0016 a0001c0002t0003g0158 a0001c0016t0003g0223 |
4 | HG02809.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1088-79G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 10/25 | chr12 | 47795459 | |||||||
| chr12:47795559 | C | T | 7 | a0001c0002t0001g0211 a0001c0002t0008g0195 a0001c0009t0003g0320 others(4): Show |
7 | HG02647.hp2 HG02896.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1087+28G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 10/25 | chr12 | 47795559 | |||||||
| chr12:47795829 | T | C | 2 | a0001c0001t0005g0322 a0001c0001t0005g0323 |
2 | NA18953.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.907-62A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 9/25 | chr12 | 47795829 | |||||||
| chr12:47796072 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.796-56G>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 8/25 | chr12 | 47796072 | |||||||
| chr12:47796381 | C | G | 1 | a0001c0003t0001g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.704-83G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 7/25 | chr12 | 47796381 | |||||||
| chr12:47796383 | G | A | 62 | a0001c0001t0001g0017 a0001c0001t0001g0142 a0001c0001t0001g0188 others(59): Show |
71 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.704-85C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 7/25 | chr12 | 47796383 | |||||||
| chr12:47796394 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.704-96G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 7/25 | chr12 | 47796394 | |||||||
| chr12:47796426 | C | CT | 12 | a0001c0001t0001g0149 a0001c0001t0001g0281 a0001c0001t0008g0148 others(9): Show |
13 | HG01167.hp2 HG01169.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.704-129dupA | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 7/25 | chr12 | 47796426 | |||||||
| chr12:47796426 | C | CTTTT | 46 | a0001c0001t0001g0142 a0001c0002t0001g0048 a0001c0002t0001g0136 others(43): Show |
53 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.704-132_704-129dup others(4): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 7/25 | chr12 | 47796426 | |||||||
| chr12:47796486 | C | T | 18 | a0001c0002t0002g0045 a0001c0002t0004g0028 a0001c0002t0010g0256 others(15): Show |
22 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.704-188G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 7/25 | chr12 | 47796486 | |||||||
| chr12:47796487 | G | A | 27 | a0001c0001t0001g0014 a0001c0001t0001g0149 a0001c0001t0001g0165 others(24): Show |
29 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.704-189C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 7/25 | chr12 | 47796487 | |||||||
| chr12:47796492 | C | T | 13 | a0001c0001t0001g0017 a0001c0001t0001g0188 a0001c0001t0001g0228 others(10): Show |
15 | HG00280.hp2 HG01109.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.704-194G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 7/25 | chr12 | 47796492 | |||||||
| chr12:47796638 | G | C | 1 | a0001c0001t0002g0182 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.704-340C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 7/25 | chr12 | 47796638 | |||||||
| chr12:47796895 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0129 a0001c0001t0001g0290 others(2): Show |
7 | NA18966.hp1 NA18969.hp2 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+122G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 7/25 | chr12 | 47796895 | |||||||
| chr12:47797202 | C | T | 29 | a0001c0001t0001g0014 a0001c0001t0001g0165 a0001c0001t0001g0168 others(26): Show |
33 | HG00741.hp1 HG01074.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.578-60G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 6/25 | chr12 | 47797202 | |||||||
| chr12:47797224 | A | G | 7 | a0001c0001t0001g0188 a0001c0001t0001g0328 a0001c0001t0004g0026 others(4): Show |
8 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.578-82T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 6/25 | chr12 | 47797224 | |||||||
| chr12:47797269 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.577+115G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 6/25 | chr12 | 47797269 | |||||||
| chr12:47797300 | G | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0165 a0001c0001t0001g0168 others(9): Show |
13 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.577+84C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 6/25 | chr12 | 47797300 | |||||||
| chr12:47797320 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0328 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.577+64G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 6/25 | chr12 | 47797320 | |||||||
| chr12:47797704 | G | T | 1 | a0001c0001t0003g0068 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.462-205C>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797704 | |||||||
| chr12:47797712 | G | A | 23 | a0001c0001t0001g0014 a0001c0001t0001g0165 a0001c0001t0001g0168 others(20): Show |
24 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.462-213C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797712 | |||||||
| chr12:47797855 | G | GGGGT | 4 | a0001c0001t0001g0118 a0001c0001t0002g0084 a0001c0001t0002g0085 others(1): Show |
4 | HG03942.hp2 HG04184.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.461+252_461+253ins others(4): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797855 | |||||||
| chr12:47797855 | G | GGT | 36 | a0001c0001t0001g0067 a0001c0001t0001g0096 a0001c0001t0001g0143 others(33): Show |
37 | HG00280.hp1 HG00408.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.461+251_461+252dup others(2): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797855 | |||||||
| chr12:47797855 | G | GGTGT | 16 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0257 others(13): Show |
20 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.461+249_461+252dup others(4): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797855 | |||||||
| chr12:47797855 | G | GGTGTGT | 46 | a0001c0001t0001g0001 a0001c0001t0001g0095 a0001c0001t0001g0124 others(43): Show |
52 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.461+247_461+252dup others(6): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797855 | |||||||
| chr12:47797855 | G | GGTGTGTG others(1): Show |
24 | a0001c0001t0001g0030 a0001c0001t0001g0123 a0001c0001t0001g0227 others(21): Show |
28 | HG01069.hp2 HG01070.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.461+245_461+252dup others(8): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797855 | |||||||
| chr12:47797855 | G | GGTGTGTG others(3): Show |
11 | a0001c0001t0001g0179 a0001c0001t0001g0284 a0001c0002t0004g0028 others(8): Show |
14 | HG00323.hp2 HG00544.hp2 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.461+243_461+252dup others(10): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797855 | |||||||
| chr12:47797855 | G | GGTGTGTG others(5): Show |
9 | a0001c0001t0002g0176 a0001c0002t0013g0134 a0001c0003t0009g0151 others(6): Show |
10 | HG00140.hp2 HG00621.hp1 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.461+241_461+252dup others(12): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797855 | |||||||
| chr12:47797855 | G | GGTGTGTG others(7): Show |
15 | a0001c0001t0001g0149 a0001c0001t0003g0205 a0001c0001t0005g0023 others(12): Show |
18 | HG00099.hp2 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.461+239_461+252dup others(14): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797855 | |||||||
| chr12:47797855 | G | GGTGTGTG others(9): Show |
1 | a0001c0002t0013g0047 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.461+237_461+252dup others(16): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797855 | |||||||
| chr12:47797855 | G | GTGTGTGT others(6): Show |
1 | a0001c0001t0001g0196 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.461+252_461+253ins others(13): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797855 | |||||||
| chr12:47797855 | G | T | 1 | a0001c0001t0002g0125 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.461+253C>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797855 | |||||||
| chr12:47797855 | GGT | G | 7 | a0001c0001t0001g0129 a0001c0001t0002g0090 a0001c0001t0003g0089 others(4): Show |
7 | HG00673.hp1 HG01099.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.461+251_461+252del others(2): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797855 | |||||||
| chr12:47797855 | GGTGT | G | 17 | a0001c0001t0001g0014 a0001c0001t0001g0165 a0001c0001t0001g0168 others(14): Show |
18 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.461+249_461+252del others(4): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797855 | |||||||
| chr12:47797855 | GGTGTGTG others(9): Show |
G | 7 | a0001c0001t0001g0075 a0001c0001t0002g0113 a0001c0001t0002g0114 others(4): Show |
7 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(4): Show |
intron_variant | MODIFIER | c.461+237_461+252del others(16): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797855 | |||||||
| chr12:47797895 | T | TGTGA | 3 | a0001c0001t0001g0017 a0001c0002t0003g0226 a0001c0002t0010g0025 |
5 | HG01516.hp1 HG03942.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.461+212_461+213ins others(4): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797895 | |||||||
| chr12:47797895 | T | TGTGTGTG others(1): Show |
12 | a0001c0001t0001g0188 a0001c0001t0004g0229 a0001c0001t0014g0161 others(9): Show |
13 | HG00280.hp2 HG00741.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.461+212_461+213ins others(8): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797895 | |||||||
| chr12:47797895 | T | TGTGTGTG others(3): Show |
4 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0002t0002g0062 others(1): Show |
4 | HG02257.hp1 HG02486.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.461+212_461+213ins others(10): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797895 | |||||||
| chr12:47797895 | T | TGTGTGTG others(3): Show |
1 | a0002c0006t0003g0259 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.461+212_461+213ins others(10): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797895 | |||||||
| chr12:47797895 | T | TGTGTGTG others(5): Show |
3 | a0001c0001t0001g0230 a0001c0002t0003g0158 a0004c0010t0016g0319 |
3 | HG02723.hp1 HG02809.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.461+212_461+213ins others(12): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797895 | |||||||
| chr12:47797895 | T | TGTGTGTG others(7): Show |
1 | a0004c0010t0001g0314 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.461+212_461+213ins others(14): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797895 | |||||||
| chr12:47797895 | T | TGTGTGTG others(7): Show |
5 | a0001c0001t0001g0228 a0001c0002t0001g0224 a0001c0002t0003g0016 others(2): Show |
6 | HG01074.hp1 HG02559.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.461+212_461+213ins others(14): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797895 | |||||||
| chr12:47797895 | T | TGTGTGTG others(9): Show |
3 | a0001c0001t0004g0026 a0001c0001t0004g0171 a0001c0001t0004g0172 |
4 | HG01109.hp1 HG02109.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.461+212_461+213ins others(16): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797895 | |||||||
| chr12:47797895 | T | TGTGTGTG others(11): Show |
1 | a0001c0001t0004g0222 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.461+212_461+213ins others(18): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797895 | |||||||
| chr12:47797897 | A | T | 2 | a0001c0001t0005g0199 a0001c0024t0006g0043 |
2 | HG01978.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.461+211T>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47797897 | |||||||
| chr12:47798027 | AGTGT | A | 3 | a0001c0003t0001g0276 a0001c0003t0001g0305 a0001c0003t0003g0326 |
3 | HG03516.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.461+77_461+80delAC others(2): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 5/25 | chr12 | 47798027 | |||||||
| chr12:47798234 | T | A | 1 | a0010c0022t0004g0244 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.350-15A>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 4/25 | chr12 | 47798234 | |||||||
| chr12:47798279 | A | C | 81 | a0001c0001t0001g0017 a0001c0001t0001g0050 a0001c0001t0001g0149 others(78): Show |
91 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.350-60T>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 4/25 | chr12 | 47798279 | |||||||
| chr12:47798461 | G | C | 1 | a0001c0001t0002g0115 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.349+101C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 4/25 | chr12 | 47798461 | |||||||
| chr12:47798468 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.349+94C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 4/25 | chr12 | 47798468 | |||||||
| chr12:47798469 | C | T | 1 | a0001c0001t0004g0163 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.349+93G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 4/25 | chr12 | 47798469 | |||||||
| chr12:47798986 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.71-14C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47798986 | |||||||
| chr12:47799039 | T | C | 1 | a0001c0001t0002g0295 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.71-67A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47799039 | |||||||
| chr12:47799058 | A | G | 16 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0165 others(13): Show |
18 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.71-86T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47799058 | |||||||
| chr12:47799060 | G | C | 13 | a0001c0001t0001g0149 a0001c0001t0001g0188 a0001c0001t0001g0328 others(10): Show |
14 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.71-88C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47799060 | |||||||
| chr12:47799103 | C | T | 1 | a0001c0002t0001g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.71-131G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47799103 | |||||||
| chr12:47799107 | T | C | 1 | a0001c0001t0005g0245 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.71-135A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47799107 | |||||||
| chr12:47799158 | T | C | 1 | a0001c0001t0005g0308 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.71-186A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47799158 | |||||||
| chr12:47799523 | G | A | 24 | a0001c0001t0001g0050 a0001c0001t0003g0060 a0001c0001t0003g0061 others(21): Show |
28 | HG00639.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.71-551C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47799523 | |||||||
| chr12:47799562 | T | C | 1 | a0001c0001t0002g0279 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.71-590A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47799562 | |||||||
| chr12:47799620 | C | T | 1 | a0001c0001t0004g0268 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.71-648G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47799620 | |||||||
| chr12:47799686 | G | A | 15 | a0001c0001t0001g0149 a0001c0001t0001g0188 a0001c0001t0001g0328 others(12): Show |
16 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.71-714C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47799686 | |||||||
| chr12:47799698 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.71-726A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47799698 | |||||||
| chr12:47799910 | G | T | 9 | a0001c0002t0003g0159 a0001c0002t0003g0220 a0001c0002t0003g0226 others(6): Show |
11 | HG00741.hp1 HG01081.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-938C>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47799910 | |||||||
| chr12:47799946 | C | T | 3 | a0001c0001t0003g0325 a0001c0001t0005g0212 a0001c0001t0005g0215 |
3 | HG02572.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.71-974G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47799946 | |||||||
| chr12:47800010 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0228 a0001c0001t0001g0230 others(3): Show |
7 | HG00280.hp2 HG03710.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.71-1038G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47800010 | |||||||
| chr12:47800118 | C | G | 1 | a0001c0003t0001g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.71-1146G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47800118 | |||||||
| chr12:47800364 | G | T | 1 | a0001c0001t0004g0019 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.71-1392C>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47800364 | |||||||
| chr12:47800547 | C | A | 8 | a0001c0001t0001g0149 a0001c0001t0008g0148 a0001c0003t0001g0160 others(5): Show |
8 | HG02257.hp2 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-1575G>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47800547 | |||||||
| chr12:47800630 | T | G | 3 | a0001c0003t0001g0276 a0001c0003t0001g0305 a0001c0003t0003g0326 |
3 | HG03516.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.70+1594A>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47800630 | |||||||
| chr12:47800652 | C | T | 18 | a0001c0002t0002g0045 a0001c0002t0004g0028 a0001c0002t0010g0256 others(15): Show |
22 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.70+1572G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47800652 | |||||||
| chr12:47800665 | T | A | 15 | a0001c0001t0001g0014 a0001c0001t0001g0165 a0001c0001t0001g0168 others(12): Show |
16 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.70+1559A>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47800665 | |||||||
| chr12:47800813 | A | G | 1 | a0001c0002t0001g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.70+1411T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47800813 | |||||||
| chr12:47800935 | T | C | 2 | a0001c0003t0001g0276 a0001c0003t0003g0326 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.70+1289A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47800935 | |||||||
| chr12:47800982 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.70+1242G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47800982 | |||||||
| chr12:47801051 | G | A | 1 | a0001c0001t0004g0175 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.70+1173C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47801051 | |||||||
| chr12:47801093 | T | C | 4 | a0001c0001t0002g0121 a0001c0001t0004g0027 a0001c0001t0004g0163 others(1): Show |
5 | HG02129.hp2 NA18940.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+1131A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47801093 | |||||||
| chr12:47801094 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.70+1130A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47801094 | |||||||
| chr12:47801100 | AAGCTCAG others(27): Show |
A | 1 | a0001c0005t0001g0191 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.70+1090_70+1123del others(34): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47801100 | |||||||
| chr12:47801174 | C | T | 52 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0165 others(49): Show |
58 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.70+1050G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47801174 | |||||||
| chr12:47801221 | T | C | 15 | a0001c0001t0001g0149 a0001c0001t0001g0188 a0001c0001t0001g0328 others(12): Show |
16 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.70+1003A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47801221 | |||||||
| chr12:47801269 | T | C | 24 | a0001c0001t0001g0050 a0001c0001t0003g0060 a0001c0001t0003g0061 others(21): Show |
28 | HG00639.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.70+955A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47801269 | |||||||
| chr12:47801286 | G | A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0030 others(24): Show |
37 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.70+938C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47801286 | |||||||
| chr12:47801473 | A | AT | 15 | a0001c0001t0001g0149 a0001c0001t0001g0188 a0001c0001t0001g0328 others(12): Show |
16 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.70+750dupA | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47801473 | |||||||
| chr12:47801565 | T | C | 91 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0050 others(88): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.70+659A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47801565 | |||||||
| chr12:47801641 | C | T | 91 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0050 others(88): Show |
102 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.70+583G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47801641 | |||||||
| chr12:47801668 | G | A | 49 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0165 others(46): Show |
55 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.70+556C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47801668 | |||||||
| chr12:47801778 | G | C | 1 | a0001c0001t0001g0237 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.70+446C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47801778 | |||||||
| chr12:47801873 | G | A | 1 | a0001c0002t0004g0028 | 2 | HG01123.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.70+351C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47801873 | |||||||
| chr12:47802090 | C | T | 20 | a0001c0001t0004g0175 a0001c0002t0001g0048 a0001c0002t0002g0045 others(17): Show |
24 | HG00140.hp2 HG00323.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.70+134G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47802090 | |||||||
| chr12:47802156 | G | C | 127 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0050 others(124): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.70+68C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 2/25 | chr12 | 47802156 | |||||||
| chr12:47802314 | G | C | 8 | a0001c0001t0004g0336 a0001c0002t0008g0195 a0001c0002t0012g0318 others(5): Show |
8 | HG02622.hp1 HG02896.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.20-40C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47802314 | |||||||
| chr12:47802557 | C | G | 2 | a0001c0001t0003g0065 a0001c0001t0003g0236 |
2 | HG00280.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.20-283G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47802557 | |||||||
| chr12:47802740 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.20-466C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47802740 | |||||||
| chr12:47803199 | G | A | 18 | a0001c0002t0001g0048 a0001c0002t0002g0045 a0001c0002t0004g0028 others(15): Show |
22 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.20-925C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47803199 | |||||||
| chr12:47803218 | G | A | 2 | a0001c0002t0001g0211 a0001c0003t0001g0305 |
2 | HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.20-944C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47803218 | |||||||
| chr12:47803305 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.20-1031C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47803305 | |||||||
| chr12:47803327 | C | T | 1 | a0001c0001t0002g0072 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.20-1053G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47803327 | |||||||
| chr12:47803424 | G | A | 25 | a0001c0001t0001g0050 a0001c0001t0003g0060 a0001c0001t0003g0061 others(22): Show |
29 | HG00639.hp1 HG00741.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.20-1150C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47803424 | |||||||
| chr12:47803454 | C | T | 1 | a0001c0004t0006g0041 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.20-1180G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47803454 | |||||||
| chr12:47803455 | G | A | 1 | a0001c0001t0001g0296 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.20-1181C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47803455 | |||||||
| chr12:47803457 | C | CTGCCCCT others(27): Show |
1 | a0001c0005t0001g0191 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.20-1217_20-1184dup others(34): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47803457 | |||||||
| chr12:47803520 | A | G | 1 | a0001c0001t0003g0325 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.20-1246T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47803520 | |||||||
| chr12:47803526 | A | G | 2 | a0002c0006t0001g0316 a0002c0006t0001g0317 |
2 | HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.20-1252T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47803526 | |||||||
| chr12:47803566 | T | C | 3 | a0001c0001t0003g0024 a0001c0001t0003g0217 a0001c0001t0003g0270 |
4 | HG02717.hp1 HG02818.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-1292A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47803566 | |||||||
| chr12:47803668 | T | G | 2 | a0001c0001t0005g0212 a0001c0001t0005g0215 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.20-1394A>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47803668 | |||||||
| chr12:47803755 | T | C | 1 | a0001c0004t0006g0131 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.20-1481A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47803755 | |||||||
| chr12:47804089 | C | T | 3 | a0001c0003t0001g0276 a0001c0003t0001g0305 a0001c0003t0003g0326 |
3 | HG03516.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.20-1815G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47804089 | |||||||
| chr12:47804162 | T | C | 1 | a0009c0027t0002g0335 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.20-1888A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47804162 | |||||||
| chr12:47804216 | G | A | 5 | a0001c0001t0001g0132 a0001c0001t0001g0153 a0001c0001t0001g0154 others(2): Show |
5 | HG01123.hp1 HG01261.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.20-1942C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47804216 | |||||||
| chr12:47804442 | C | G | 8 | a0001c0001t0002g0331 a0001c0001t0002g0334 a0001c0001t0005g0199 others(5): Show |
8 | NA18954.hp1 NA18956.hp2 NA18971.hp2 others(5): Show |
intron_variant | MODIFIER | c.20-2168G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47804442 | |||||||
| chr12:47804451 | G | T | 7 | a0001c0002t0008g0195 a0001c0002t0012g0318 a0001c0009t0003g0320 others(4): Show |
7 | HG02896.hp1 HG02922.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.20-2177C>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47804451 | |||||||
| chr12:47804524 | GA | G | 76 | a0001c0001t0001g0014 a0001c0001t0001g0050 a0001c0001t0001g0165 others(73): Show |
85 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.20-2251delT | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47804524 | |||||||
| chr12:47804524 | GAA | G | 11 | a0001c0001t0001g0149 a0001c0001t0008g0148 a0001c0003t0001g0029 others(8): Show |
12 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.20-2252_20-2251del others(2): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47804524 | |||||||
| chr12:47804603 | G | A | 25 | a0001c0001t0001g0050 a0001c0001t0003g0060 a0001c0001t0003g0061 others(22): Show |
29 | HG00639.hp1 HG00741.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.20-2329C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47804603 | |||||||
| chr12:47804625 | C | T | 7 | a0001c0002t0008g0195 a0001c0002t0012g0318 a0001c0009t0003g0320 others(4): Show |
7 | HG02896.hp1 HG02922.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.20-2351G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47804625 | |||||||
| chr12:47804661 | C | G | 3 | a0001c0003t0001g0276 a0001c0003t0001g0305 a0001c0003t0003g0326 |
3 | HG03516.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.20-2387G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47804661 | |||||||
| chr12:47804777 | T | C | 1 | a0001c0001t0002g0116 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.20-2503A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47804777 | |||||||
| chr12:47804963 | C | T | 7 | a0001c0002t0008g0195 a0001c0002t0012g0318 a0001c0009t0003g0320 others(4): Show |
7 | HG02896.hp1 HG02922.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.20-2689G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47804963 | |||||||
| chr12:47805073 | A | AT | 37 | a0001c0001t0001g0014 a0001c0001t0001g0165 a0001c0001t0001g0168 others(34): Show |
42 | HG00140.hp2 HG00323.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.20-2800dupA | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47805073 | |||||||
| chr12:47805073 | AT | A | 14 | a0001c0001t0001g0017 a0001c0001t0001g0228 a0001c0001t0001g0230 others(11): Show |
15 | HG00280.hp2 HG02895.hp2 HG02896.hp1 others(12): Show |
intron_variant | MODIFIER | c.20-2800delA | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47805073 | |||||||
| chr12:47805217 | G | T | 1 | a0001c0001t0004g0163 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.20-2943C>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47805217 | |||||||
| chr12:47805259 | G | T | 75 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0050 others(72): Show |
85 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.20-2985C>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47805259 | |||||||
| chr12:47805261 | T | G | 57 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0050 others(54): Show |
63 | HG00280.hp2 HG00639.hp1 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.20-2987A>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47805261 | |||||||
| chr12:47805344 | A | G | 1 | a0001c0001t0001g0309 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.20-3070T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47805344 | |||||||
| chr12:47805389 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.20-3115C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47805389 | |||||||
| chr12:47805526 | C | T | 11 | a0001c0001t0001g0149 a0001c0001t0008g0148 a0001c0003t0001g0029 others(8): Show |
12 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.20-3252G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47805526 | |||||||
| chr12:47805956 | A | C | 27 | a0001c0001t0001g0050 a0001c0001t0003g0060 a0001c0001t0003g0061 others(24): Show |
32 | HG00639.hp1 HG00741.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.20-3682T>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47805956 | |||||||
| chr12:47806223 | A | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0030 others(37): Show |
50 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.20-3949T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47806223 | |||||||
| chr12:47806273 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0228 a0001c0001t0001g0230 others(3): Show |
7 | HG00280.hp2 HG03710.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.20-3999G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47806273 | |||||||
| chr12:47806300 | C | T | 1 | a0001c0001t0004g0336 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.20-4026G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47806300 | |||||||
| chr12:47806558 | G | A | 14 | a0001c0001t0001g0014 a0001c0001t0001g0165 a0001c0001t0001g0168 others(11): Show |
15 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.20-4284C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47806558 | |||||||
| chr12:47806592 | G | A | 9 | a0001c0001t0005g0212 a0001c0001t0005g0215 a0001c0002t0008g0195 others(6): Show |
9 | HG02895.hp2 HG02896.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.20-4318C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47806592 | |||||||
| chr12:47806621 | G | A | 2 | a0001c0001t0003g0068 a0001c0002t0012g0318 |
2 | NA19000.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.20-4347C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47806621 | |||||||
| chr12:47806668 | G | A | 14 | a0001c0001t0001g0014 a0001c0001t0001g0165 a0001c0001t0001g0168 others(11): Show |
15 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.20-4394C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47806668 | |||||||
| chr12:47806733 | A | G | 11 | a0001c0001t0001g0014 a0001c0001t0001g0165 a0001c0001t0001g0168 others(8): Show |
12 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.20-4459T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47806733 | |||||||
| chr12:47806795 | T | G | 7 | a0001c0001t0004g0056 a0001c0001t0007g0008 a0001c0001t0007g0009 others(4): Show |
9 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.20-4521A>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47806795 | |||||||
| chr12:47806853 | C | T | 2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | NA18964.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.20-4579G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47806853 | |||||||
| chr12:47806866 | GCTCCCAA others(2): Show |
G | 11 | a0001c0001t0001g0014 a0001c0001t0001g0165 a0001c0001t0001g0168 others(8): Show |
12 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.20-4601_20-4593del others(9): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47806866 | |||||||
| chr12:47806912 | A | C | 37 | a0001c0001t0001g0137 a0001c0001t0001g0202 a0001c0001t0001g0203 others(34): Show |
41 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.20-4638T>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47806912 | |||||||
| chr12:47806945 | C | CT | 28 | a0001c0001t0001g0050 a0001c0001t0001g0143 a0001c0001t0001g0145 others(25): Show |
32 | HG00639.hp1 HG00741.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.20-4672dupA | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47806945 | |||||||
| chr12:47806945 | C | CTT | 7 | a0001c0002t0008g0195 a0001c0002t0012g0318 a0001c0009t0003g0320 others(4): Show |
7 | HG02896.hp1 HG02922.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.20-4673_20-4672dup others(2): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47806945 | |||||||
| chr12:47806961 | A | G | 24 | a0001c0001t0001g0050 a0001c0001t0003g0060 a0001c0001t0003g0061 others(21): Show |
28 | HG00639.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.20-4687T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47806961 | |||||||
| chr12:47806982 | C | T | 1 | a0001c0002t0002g0062 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.20-4708G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47806982 | |||||||
| chr12:47807050 | C | A | 23 | a0001c0001t0001g0050 a0001c0001t0003g0060 a0001c0001t0003g0061 others(20): Show |
27 | HG00639.hp1 HG00741.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.20-4776G>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47807050 | |||||||
| chr12:47807121 | G | A | 1 | a0001c0002t0002g0062 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.20-4847C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47807121 | |||||||
| chr12:47807156 | T | A | 1 | a0001c0001t0004g0336 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.20-4882A>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47807156 | |||||||
| chr12:47807191 | C | T | 1 | a0001c0004t0006g0007 | 2 | HG03017.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.20-4917G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47807191 | |||||||
| chr12:47807220 | G | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0202 a0001c0001t0001g0203 others(1): Show |
4 | HG02258.hp1 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.20-4946C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47807220 | |||||||
| chr12:47807276 | A | G | 37 | a0001c0001t0001g0137 a0001c0001t0001g0202 a0001c0001t0001g0203 others(34): Show |
41 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.20-5002T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47807276 | |||||||
| chr12:47807397 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0145 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.20-5123C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47807397 | |||||||
| chr12:47807452 | T | C | 1 | a0001c0025t0004g0071 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.20-5178A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47807452 | |||||||
| chr12:47807534 | C | T | 24 | a0001c0001t0001g0050 a0001c0001t0003g0060 a0001c0001t0003g0061 others(21): Show |
28 | HG00639.hp1 HG00741.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.20-5260G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47807534 | |||||||
| chr12:47807672 | G | A | 35 | a0001c0001t0001g0137 a0001c0001t0001g0202 a0001c0001t0001g0203 others(32): Show |
39 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.20-5398C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47807672 | |||||||
| chr12:47808118 | G | A | 3 | a0001c0019t0001g0302 a0002c0013t0001g0303 a0002c0013t0002g0304 |
3 | HG02559.hp1 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.20-5844C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47808118 | |||||||
| chr12:47808263 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(245): Show |
282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.20-5989A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47808263 | |||||||
| chr12:47808264 | G | A | 36 | a0001c0001t0001g0137 a0001c0001t0001g0202 a0001c0001t0001g0203 others(33): Show |
40 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.20-5990C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47808264 | |||||||
| chr12:47808325 | C | T | 1 | a0001c0002t0001g0211 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.20-6051G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47808325 | |||||||
| chr12:47808473 | C | A | 1 | a0001c0003t0001g0160 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.20-6199G>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47808473 | |||||||
| chr12:47808522 | C | T | 1 | a0001c0002t0001g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.20-6248G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47808522 | |||||||
| chr12:47808735 | C | T | 3 | a0001c0019t0001g0302 a0002c0013t0001g0303 a0002c0013t0002g0304 |
3 | HG02559.hp1 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.20-6461G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47808735 | |||||||
| chr12:47808825 | GTCCACAC others(6): Show |
G | 1 | a0001c0001t0003g0122 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.20-6564_20-6552del others(13): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47808825 | |||||||
| chr12:47808840 | A | G | 1 | a0001c0001t0003g0122 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.20-6566T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47808840 | |||||||
| chr12:47808843 | T | G | 1 | a0001c0001t0003g0122 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.20-6569A>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47808843 | |||||||
| chr12:47808844 | T | G | 1 | a0001c0001t0003g0122 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.20-6570A>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47808844 | |||||||
| chr12:47808845 | T | G | 1 | a0001c0001t0003g0122 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.20-6571A>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47808845 | |||||||
| chr12:47808913 | C | G | 1 | a0001c0002t0001g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.20-6639G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47808913 | |||||||
| chr12:47808986 | C | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0228 a0001c0001t0001g0230 others(3): Show |
7 | HG00280.hp2 HG03710.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.20-6712G>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47808986 | |||||||
| chr12:47809002 | C | G | 2 | a0001c0001t0005g0322 a0001c0001t0005g0323 |
2 | NA18953.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.20-6728G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47809002 | |||||||
| chr12:47809018 | G | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0228 a0001c0001t0001g0230 others(3): Show |
7 | HG00280.hp2 HG03710.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.20-6744C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47809018 | |||||||
| chr12:47809049 | C | T | 1 | a0001c0007t0006g0306 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.20-6775G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47809049 | |||||||
| chr12:47809057 | C | T | 1 | a0008c0023t0001g0174 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.20-6783G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47809057 | |||||||
| chr12:47809158 | C | T | 18 | a0001c0002t0001g0048 a0001c0002t0002g0045 a0001c0002t0004g0028 others(15): Show |
22 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.20-6884G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47809158 | |||||||
| chr12:47809404 | T | G | 1 | a0001c0001t0001g0227 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.20-7130A>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47809404 | |||||||
| chr12:47809680 | C | T | 1 | a0001c0001t0004g0080 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.20-7406G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47809680 | |||||||
| chr12:47809715 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0328 |
2 | HG02055.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.20-7441G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47809715 | |||||||
| chr12:47809763 | G | C | 7 | a0001c0002t0008g0195 a0001c0002t0012g0318 a0001c0009t0003g0320 others(4): Show |
7 | HG02896.hp1 HG02922.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.20-7489C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47809763 | |||||||
| chr12:47809813 | C | T | 1 | a0001c0002t0001g0211 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.20-7539G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47809813 | |||||||
| chr12:47810030 | T | G | 1 | a0001c0001t0002g0144 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.20-7756A>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810030 | |||||||
| chr12:47810059 | G | C | 1 | a0001c0001t0001g0288 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.20-7785C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810059 | |||||||
| chr12:47810225 | C | T | 1 | a0001c0002t0001g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.20-7951G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810225 | |||||||
| chr12:47810228 | G | C | 8 | a0001c0001t0001g0149 a0001c0001t0008g0148 a0001c0003t0001g0160 others(5): Show |
8 | HG02257.hp2 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.20-7954C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810228 | |||||||
| chr12:47810241 | C | T | 1 | a0002c0006t0003g0315 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.20-7967G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810241 | |||||||
| chr12:47810446 | G | A | 5 | a0001c0001t0004g0022 a0001c0001t0004g0140 a0001c0001t0004g0171 others(2): Show |
6 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-8172C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810446 | |||||||
| chr12:47810471 | G | A | 26 | a0001c0001t0001g0050 a0001c0001t0003g0060 a0001c0001t0003g0061 others(23): Show |
30 | HG00639.hp1 HG00741.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.20-8197C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810471 | |||||||
| chr12:47810640 | A | G | 12 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0165 others(9): Show |
14 | HG01168.hp1 HG01169.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.20-8366T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810640 | |||||||
| chr12:47810673 | T | C | 67 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0137 others(64): Show |
73 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.20-8399A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810673 | |||||||
| chr12:47810716 | C | G | 18 | a0001c0002t0001g0048 a0001c0002t0002g0045 a0001c0002t0004g0028 others(15): Show |
22 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.20-8442G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810716 | |||||||
| chr12:47810737 | G | A | 1 | a0001c0002t0001g0136 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.20-8463C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810737 | |||||||
| chr12:47810802 | AGGTCTCT others(11): Show |
A | 3 | a0001c0019t0001g0302 a0002c0013t0001g0303 a0002c0013t0002g0304 |
3 | HG02559.hp1 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.20-8546_20-8529del others(18): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810802 | |||||||
| chr12:47810804 | G | GTC | 58 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0033 others(55): Show |
65 | HG00423.hp2 HG00639.hp1 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.20-8532_20-8531dup others(2): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810804 | |||||||
| chr12:47810804 | G | GTCTC | 27 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(24): Show |
35 | HG00733.hp1 HG00735.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.20-8534_20-8531dup others(4): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810804 | |||||||
| chr12:47810804 | G | GTCTCTC | 19 | a0001c0001t0001g0001 a0001c0001t0001g0123 a0001c0001t0001g0192 others(16): Show |
19 | HG01081.hp2 HG01255.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.20-8536_20-8531dup others(6): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810804 | |||||||
| chr12:47810804 | G | GTCTCTCT others(1): Show |
6 | a0001c0001t0001g0142 a0001c0001t0001g0185 a0001c0001t0002g0176 others(3): Show |
6 | HG00621.hp1 HG00642.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-8538_20-8531dup others(8): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810804 | |||||||
| chr12:47810804 | G | GTCTCTCT others(3): Show |
2 | a0001c0001t0001g0038 a0001c0002t0010g0025 |
2 | HG01516.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.20-8540_20-8531dup others(10): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810804 | |||||||
| chr12:47810804 | G | GTCTCTCT others(7): Show |
1 | a0001c0002t0010g0025 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.20-8544_20-8531dup others(14): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810804 | |||||||
| chr12:47810804 | G | GTCTCTCT others(9): Show |
1 | a0001c0002t0003g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.20-8546_20-8531dup others(16): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810804 | |||||||
| chr12:47810804 | GTC | G | 29 | a0001c0001t0001g0138 a0001c0001t0001g0143 a0001c0001t0001g0145 others(26): Show |
29 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.20-8532_20-8531del others(2): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810804 | |||||||
| chr12:47810804 | GTCTC | G | 60 | a0001c0001t0001g0036 a0001c0001t0001g0066 a0001c0001t0001g0067 others(57): Show |
67 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.20-8534_20-8531del others(4): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810804 | |||||||
| chr12:47810804 | GTCTCTC | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0241 a0001c0001t0001g0266 others(6): Show |
12 | HG00558.hp1 HG02055.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.20-8536_20-8531del others(6): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810804 | |||||||
| chr12:47810804 | GTCTCTCT others(1): Show |
G | 6 | a0001c0001t0001g0181 a0001c0001t0002g0079 a0001c0001t0002g0088 others(3): Show |
6 | HG01934.hp2 HG02071.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.20-8538_20-8531del others(8): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810804 | |||||||
| chr12:47810804 | GTCTCTCT others(3): Show |
G | 20 | a0001c0001t0002g0282 a0001c0001t0003g0037 a0001c0001t0004g0080 others(17): Show |
24 | HG00140.hp2 HG00323.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.20-8540_20-8531del others(10): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810804 | |||||||
| chr12:47810804 | GTCTCTCT others(5): Show |
G | 11 | a0001c0001t0001g0149 a0001c0001t0008g0148 a0001c0003t0001g0029 others(8): Show |
12 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.20-8542_20-8531del others(12): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810804 | |||||||
| chr12:47810804 | GTCTCTCT others(7): Show |
G | 1 | a0001c0001t0004g0336 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.20-8544_20-8531del others(14): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810804 | |||||||
| chr12:47810814 | CTCTCTCT others(27): Show |
C | 28 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0165 others(25): Show |
30 | HG00280.hp2 HG01168.hp1 HG01169.hp2 others(27): Show |
intron_variant | MODIFIER | c.20-8574_20-8541del others(34): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810814 | |||||||
| chr12:47810816 | CTCTCTCT others(25): Show |
C | 39 | a0001c0001t0001g0137 a0001c0001t0001g0202 a0001c0001t0001g0203 others(36): Show |
43 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.20-8574_20-8543del others(32): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810816 | |||||||
| chr12:47810822 | C | G | 3 | a0001c0019t0001g0302 a0002c0013t0001g0303 a0002c0013t0002g0304 |
3 | HG02559.hp1 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.20-8548G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810822 | |||||||
| chr12:47810842 | C | A | 2 | a0004c0010t0001g0314 a0004c0010t0016g0319 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.20-8568G>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810842 | |||||||
| chr12:47810844 | C | A | 19 | a0001c0001t0002g0269 a0001c0002t0001g0048 a0001c0002t0002g0045 others(16): Show |
23 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.20-8570G>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810844 | |||||||
| chr12:47810848 | A | C | 1 | a0001c0001t0001g0280 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.20-8574T>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810848 | |||||||
| chr12:47810880 | C | T | 1 | a0001c0002t0010g0025 | 2 | HG01516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.20-8606G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47810880 | |||||||
| chr12:47811021 | A | G | 44 | a0001c0001t0001g0137 a0001c0001t0001g0188 a0001c0001t0001g0202 others(41): Show |
48 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.19+8746T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47811021 | |||||||
| chr12:47811106 | C | T | 1 | a0001c0001t0005g0245 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.19+8661G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47811106 | |||||||
| chr12:47811183 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.19+8584T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47811183 | |||||||
| chr12:47811282 | G | A | 26 | a0001c0001t0001g0050 a0001c0001t0003g0060 a0001c0001t0003g0061 others(23): Show |
30 | HG00639.hp1 HG00741.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.19+8485C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47811282 | |||||||
| chr12:47811484 | G | A | 36 | a0001c0001t0001g0137 a0001c0001t0001g0202 a0001c0001t0001g0203 others(33): Show |
40 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.19+8283C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47811484 | |||||||
| chr12:47811524 | C | G | 2 | a0001c0001t0005g0199 a0001c0020t0005g0200 |
2 | NA18956.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.19+8243G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47811524 | |||||||
| chr12:47811575 | C | A | 1 | a0002c0013t0002g0304 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.19+8192G>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47811575 | |||||||
| chr12:47811575 | C | T | 18 | a0001c0002t0001g0048 a0001c0002t0002g0045 a0001c0002t0004g0028 others(15): Show |
22 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.19+8192G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47811575 | |||||||
| chr12:47811663 | C | T | 1 | a0001c0002t0001g0277 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.19+8104G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47811663 | |||||||
| chr12:47811741 | C | T | 1 | a0010c0022t0004g0244 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.19+8026G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47811741 | |||||||
| chr12:47812047 | C | T | 1 | a0001c0002t0010g0025 | 2 | HG01516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.19+7720G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47812047 | |||||||
| chr12:47812110 | C | G | 3 | a0001c0019t0001g0302 a0002c0013t0001g0303 a0002c0013t0002g0304 |
3 | HG02559.hp1 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.19+7657G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47812110 | |||||||
| chr12:47812195 | A | G | 1 | a0001c0003t0009g0147 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.19+7572T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47812195 | |||||||
| chr12:47812232 | T | C | 3 | a0001c0001t0001g0329 a0001c0001t0003g0169 a0001c0001t0003g0170 |
3 | HG01346.hp2 HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.19+7535A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47812232 | |||||||
| chr12:47812313 | T | C | 208 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0014 others(205): Show |
231 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.19+7454A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47812313 | |||||||
| chr12:47812356 | C | T | 1 | a0001c0003t0001g0029 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.19+7411G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47812356 | |||||||
| chr12:47812559 | G | C | 1 | a0001c0002t0001g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.19+7208C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47812559 | |||||||
| chr12:47812583 | C | G | 1 | a0001c0001t0002g0331 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.19+7184G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47812583 | |||||||
| chr12:47812643 | G | A | 5 | a0001c0001t0004g0022 a0001c0001t0004g0140 a0001c0001t0004g0171 others(2): Show |
6 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+7124C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47812643 | |||||||
| chr12:47812752 | G | C | 1 | a0001c0001t0001g0123 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.19+7015C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47812752 | |||||||
| chr12:47812915 | A | C | 1 | a0001c0003t0003g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.19+6852T>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47812915 | |||||||
| chr12:47812916 | A | C | 2 | a0001c0001t0003g0135 a0001c0002t0001g0136 |
2 | HG02723.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.19+6851T>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47812916 | |||||||
| chr12:47813027 | G | A | 1 | a0001c0002t0012g0318 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.19+6740C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47813027 | |||||||
| chr12:47813070 | C | A | 1 | a0001c0002t0001g0211 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.19+6697G>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47813070 | |||||||
| chr12:47813434 | G | A | 14 | a0001c0001t0001g0149 a0001c0001t0008g0148 a0001c0003t0001g0029 others(11): Show |
15 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.19+6333C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47813434 | |||||||
| chr12:47813469 | C | A | 1 | a0001c0001t0004g0336 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.19+6298G>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47813469 | |||||||
| chr12:47813670 | T | C | 29 | a0001c0001t0001g0138 a0001c0001t0001g0149 a0001c0001t0001g0192 others(26): Show |
30 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.19+6097A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47813670 | |||||||
| chr12:47813677 | CGAG | C | 17 | a0001c0002t0001g0048 a0001c0002t0002g0045 a0001c0002t0004g0028 others(14): Show |
21 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.19+6087_19+6089del others(3): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47813677 | |||||||
| chr12:47813714 | G | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0228 a0001c0001t0001g0230 others(3): Show |
7 | HG00280.hp2 HG03710.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+6053C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47813714 | |||||||
| chr12:47813745 | G | A | 1 | a0001c0001t0002g0297 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.19+6022C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47813745 | |||||||
| chr12:47813817 | G | A | 21 | a0001c0001t0001g0050 a0001c0001t0003g0060 a0001c0001t0003g0061 others(18): Show |
25 | HG00639.hp1 HG00741.hp1 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.19+5950C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47813817 | |||||||
| chr12:47813892 | G | A | 1 | a0001c0001t0003g0218 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.19+5875C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47813892 | |||||||
| chr12:47813947 | T | C | 8 | a0001c0003t0001g0276 a0001c0003t0001g0305 a0001c0003t0003g0326 others(5): Show |
8 | HG02896.hp1 HG02922.hp2 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.19+5820A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47813947 | |||||||
| chr12:47813952 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.19+5815G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47813952 | |||||||
| chr12:47814015 | G | T | 1 | a0001c0001t0002g0094 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.19+5752C>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47814015 | |||||||
| chr12:47814029 | A | G | 1 | a0001c0004t0006g0156 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.19+5738T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47814029 | |||||||
| chr12:47814167 | G | A | 26 | a0001c0001t0001g0050 a0001c0001t0001g0309 a0001c0001t0001g0310 others(23): Show |
30 | HG00639.hp1 HG00741.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.19+5600C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47814167 | |||||||
| chr12:47814179 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.19+5588G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47814179 | |||||||
| chr12:47814206 | C | T | 2 | a0001c0002t0013g0047 a0001c0002t0013g0134 |
2 | HG00140.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.19+5561G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47814206 | |||||||
| chr12:47814290 | T | C | 7 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0003g0024 others(4): Show |
8 | HG02145.hp2 HG02717.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.19+5477A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47814290 | |||||||
| chr12:47814313 | T | G | 1 | a0001c0001t0005g0219 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.19+5454A>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47814313 | |||||||
| chr12:47814361 | A | T | 26 | a0001c0001t0001g0050 a0001c0001t0001g0309 a0001c0001t0001g0310 others(23): Show |
30 | HG00639.hp1 HG00741.hp1 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.19+5406T>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47814361 | |||||||
| chr12:47814463 | G | A | 2 | a0004c0010t0001g0314 a0004c0010t0016g0319 |
2 | HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.19+5304C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47814463 | |||||||
| chr12:47814494 | T | G | 49 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0137 others(46): Show |
55 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.19+5273A>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47814494 | |||||||
| chr12:47814585 | T | C | 129 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(126): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.19+5182A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47814585 | |||||||
| chr12:47814637 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0124 |
2 | HG03831.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.19+5130A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47814637 | |||||||
| chr12:47814692 | C | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0228 a0001c0001t0001g0230 others(3): Show |
7 | HG00280.hp2 HG03710.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+5075G>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47814692 | |||||||
| chr12:47814763 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.19+5004C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47814763 | |||||||
| chr12:47814811 | C | T | 1 | a0001c0001t0005g0046 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.19+4956G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47814811 | |||||||
| chr12:47814844 | C | G | 19 | a0001c0001t0001g0138 a0001c0001t0001g0149 a0001c0001t0001g0192 others(16): Show |
20 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.19+4923G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47814844 | |||||||
| chr12:47814917 | G | A | 5 | a0001c0001t0001g0138 a0001c0001t0001g0192 a0001c0001t0003g0193 others(2): Show |
5 | HG02717.hp2 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+4850C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47814917 | |||||||
| chr12:47814956 | T | C | 1 | a0001c0001t0002g0128 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.19+4811A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47814956 | |||||||
| chr12:47814993 | G | A | 4 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(1): Show |
4 | HG00423.hp1 HG00597.hp1 HG00609.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+4774C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47814993 | |||||||
| chr12:47815016 | A | G | 5 | a0001c0001t0004g0022 a0001c0001t0004g0140 a0001c0001t0004g0171 others(2): Show |
6 | HG01109.hp1 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.19+4751T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47815016 | |||||||
| chr12:47815382 | G | T | 17 | a0001c0002t0001g0048 a0001c0002t0002g0045 a0001c0002t0004g0028 others(14): Show |
21 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.19+4385C>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47815382 | |||||||
| chr12:47815880 | G | A | 17 | a0001c0002t0001g0048 a0001c0002t0002g0045 a0001c0002t0004g0028 others(14): Show |
21 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.19+3887C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47815880 | |||||||
| chr12:47815893 | A | AT | 122 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(119): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.19+3873dupA | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47815893 | |||||||
| chr12:47815893 | A | ATT | 6 | a0001c0001t0001g0228 a0001c0001t0002g0331 a0001c0001t0005g0204 others(3): Show |
6 | HG01106.hp1 HG01433.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.19+3872_19+3873dup others(2): Show |
HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47815893 | |||||||
| chr12:47815893 | AT | A | 8 | a0001c0001t0001g0145 a0001c0001t0001g0301 a0001c0001t0004g0272 others(5): Show |
8 | HG01257.hp1 HG02896.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.19+3873delA | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47815893 | |||||||
| chr12:47815917 | A | T | 3 | a0001c0003t0001g0276 a0001c0003t0001g0305 a0001c0003t0003g0326 |
3 | HG03516.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.19+3850T>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47815917 | |||||||
| chr12:47815952 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.19+3815G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47815952 | |||||||
| chr12:47816017 | G | A | 1 | a0001c0001t0003g0325 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.19+3750C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47816017 | |||||||
| chr12:47816077 | A | G | 2 | a0001c0001t0002g0063 a0001c0001t0002g0077 |
2 | HG00673.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.19+3690T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47816077 | |||||||
| chr12:47816251 | C | T | 1 | a0001c0002t0003g0158 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.19+3516G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47816251 | |||||||
| chr12:47816367 | T | G | 5 | a0001c0001t0001g0033 a0001c0001t0001g0298 a0001c0001t0001g0299 others(2): Show |
6 | HG02135.hp1 HG02523.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.19+3400A>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47816367 | |||||||
| chr12:47816535 | T | A | 17 | a0001c0002t0001g0048 a0001c0002t0002g0045 a0001c0002t0004g0028 others(14): Show |
21 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.19+3232A>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47816535 | |||||||
| chr12:47816752 | G | A | 1 | a0001c0002t0003g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.19+3015C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47816752 | |||||||
| chr12:47816844 | G | A | 14 | a0001c0001t0001g0017 a0001c0001t0001g0228 a0001c0001t0001g0230 others(11): Show |
15 | HG00280.hp2 HG02451.hp2 HG02896.hp1 others(12): Show |
intron_variant | MODIFIER | c.19+2923C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47816844 | |||||||
| chr12:47816908 | G | A | 7 | a0001c0002t0008g0195 a0001c0002t0012g0318 a0001c0009t0003g0320 others(4): Show |
7 | HG02896.hp1 HG02922.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+2859C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47816908 | |||||||
| chr12:47816935 | G | C | 1 | a0001c0003t0001g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.19+2832C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47816935 | |||||||
| chr12:47816961 | A | C | 1 | a0001c0002t0001g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.19+2806T>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47816961 | |||||||
| chr12:47816964 | G | T | 1 | a0001c0001t0003g0076 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.19+2803C>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47816964 | |||||||
| chr12:47816995 | T | C | 6 | a0001c0001t0001g0034 a0001c0005t0001g0020 a0001c0005t0001g0021 others(3): Show |
9 | NA18956.hp1 NA18961.hp2 NA18975.hp2 others(6): Show |
intron_variant | MODIFIER | c.19+2772A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47816995 | |||||||
| chr12:47817004 | C | T | 19 | a0001c0001t0001g0233 a0001c0001t0003g0232 a0001c0001t0004g0056 others(16): Show |
22 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.19+2763G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47817004 | |||||||
| chr12:47817020 | C | T | 1 | a0001c0003t0003g0326 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.19+2747G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47817020 | |||||||
| chr12:47817037 | T | C | 1 | a0001c0002t0008g0195 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.19+2730A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47817037 | |||||||
| chr12:47817175 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0228 a0001c0001t0001g0230 others(3): Show |
7 | HG00280.hp2 HG03710.hp2 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.19+2592G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47817175 | |||||||
| chr12:47817275 | T | G | 52 | a0001c0001t0001g0050 a0001c0001t0001g0137 a0001c0001t0001g0138 others(49): Show |
58 | HG00639.hp1 HG00741.hp1 HG01074.hp1 others(55): Show |
intron_variant | MODIFIER | c.19+2492A>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47817275 | |||||||
| chr12:47817554 | T | C | 5 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(2): Show |
5 | HG02572.hp2 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.19+2213A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47817554 | |||||||
| chr12:47817570 | G | A | 1 | a0001c0001t0007g0049 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.19+2197C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47817570 | |||||||
| chr12:47817602 | T | G | 13 | a0001c0001t0001g0017 a0001c0001t0001g0228 a0001c0001t0001g0230 others(10): Show |
14 | HG00280.hp2 HG02896.hp1 HG02922.hp2 others(11): Show |
intron_variant | MODIFIER | c.19+2165A>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47817602 | |||||||
| chr12:47817723 | G | A | 61 | a0001c0001t0001g0017 a0001c0001t0001g0050 a0001c0001t0001g0137 others(58): Show |
67 | HG00280.hp2 HG00639.hp1 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.19+2044C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47817723 | |||||||
| chr12:47817745 | A | G | 4 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(1): Show |
4 | HG02572.hp2 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.19+2022T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47817745 | |||||||
| chr12:47817858 | C | A | 8 | a0001c0001t0001g0017 a0001c0001t0001g0196 a0001c0001t0001g0227 others(5): Show |
9 | HG00280.hp2 HG03710.hp2 HG04184.hp1 others(6): Show |
intron_variant | MODIFIER | c.19+1909G>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47817858 | |||||||
| chr12:47817895 | A | G | 1 | a0005c0015t0003g0162 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.19+1872T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47817895 | |||||||
| chr12:47817999 | A | T | 88 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0038 others(85): Show |
99 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.19+1768T>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47817999 | |||||||
| chr12:47818011 | C | G | 2 | a0001c0001t0001g0328 a0001c0002t0001g0211 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.19+1756G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47818011 | |||||||
| chr12:47818012 | T | C | 2 | a0001c0001t0001g0328 a0001c0002t0001g0211 |
2 | HG02055.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.19+1755A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47818012 | |||||||
| chr12:47818188 | C | G | 61 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0001g0138 others(58): Show |
63 | HG00140.hp2 HG00642.hp2 HG00738.hp1 others(60): Show |
intron_variant | MODIFIER | c.19+1579G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47818188 | |||||||
| chr12:47818197 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(45): Show |
61 | HG00597.hp2 HG00642.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.19+1570C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47818197 | |||||||
| chr12:47818230 | A | G | 114 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(111): Show |
127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.19+1537T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47818230 | |||||||
| chr12:47818314 | T | C | 1 | a0001c0004t0006g0131 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.19+1453A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47818314 | |||||||
| chr12:47818361 | T | C | 1 | a0001c0003t0001g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.19+1406A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47818361 | |||||||
| chr12:47818599 | G | A | 17 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(14): Show |
18 | HG01081.hp1 HG01099.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.19+1168C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47818599 | |||||||
| chr12:47818749 | G | A | 20 | a0001c0001t0001g0050 a0001c0001t0004g0042 a0001c0001t0004g0051 others(17): Show |
21 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.19+1018C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47818749 | |||||||
| chr12:47818887 | G | C | 2 | a0001c0001t0005g0322 a0001c0001t0005g0323 |
2 | NA18953.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.19+880C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47818887 | |||||||
| chr12:47818936 | C | T | 14 | a0001c0001t0001g0050 a0001c0001t0004g0042 a0001c0001t0004g0051 others(11): Show |
15 | HG00323.hp2 HG00639.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.19+831G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47818936 | |||||||
| chr12:47819079 | C | T | 1 | a0001c0001t0012g0059 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.19+688G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47819079 | |||||||
| chr12:47819081 | C | A | 1 | a0001c0001t0001g0324 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.19+686G>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47819081 | |||||||
| chr12:47819162 | G | C | 3 | a0001c0001t0003g0325 a0001c0002t0001g0327 a0001c0003t0003g0326 |
3 | HG02451.hp2 HG02572.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.19+605C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47819162 | |||||||
| chr12:47819163 | G | A | 1 | a0001c0001t0001g0328 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.19+604C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47819163 | |||||||
| chr12:47819164 | G | T | 75 | a0001c0001t0001g0036 a0001c0001t0001g0066 a0001c0001t0001g0067 others(72): Show |
82 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.19+603C>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47819164 | |||||||
| chr12:47819369 | G | C | 1 | a0001c0001t0001g0329 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.19+398C>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47819369 | |||||||
| chr12:47819452 | A | G | 3 | a0001c0001t0003g0060 a0001c0001t0003g0061 a0001c0002t0002g0062 |
3 | HG02257.hp1 HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.19+315T>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47819452 | |||||||
| chr12:47819495 | T | C | 1 | a0001c0001t0003g0330 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.19+272A>G | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47819495 | |||||||
| chr12:47819528 | G | A | 5 | a0001c0001t0002g0331 a0001c0001t0002g0334 a0001c0001t0005g0332 others(2): Show |
5 | NA18954.hp1 NA18971.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.19+239C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47819528 | |||||||
| chr12:47819533 | C | T | 1 | a0001c0001t0012g0059 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.19+234G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47819533 | |||||||
| chr12:47819603 | C | G | 24 | a0001c0001t0001g0050 a0001c0001t0004g0042 a0001c0001t0004g0051 others(21): Show |
29 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.19+164G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47819603 | |||||||
| chr12:47819620 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | HG02145.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.19+147G>A | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47819620 | |||||||
| chr12:47819692 | C | G | 2 | a0001c0001t0001g0036 a0001c0001t0003g0037 |
2 | HG00597.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.19+75G>C | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47819692 | |||||||
| chr12:47819710 | G | A | 1 | a0001c0001t0004g0336 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.19+57C>T | HDAC7 | ENSG00000061273.18 | transcript | ENST00000080059.12 | protein_coding | 1/25 | chr12 | 47819710 |