Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1512 |
| ensemblid | ENSG00000103811.18 |
| hgncid | 2535 |
| symbol | CTSH |
| name | cathepsin H |
| refseq_nuc | NM_004390.5 |
| refseq_prot | NP_004381.2 |
| ensembl_nuc | ENST00000220166.10 |
| ensembl_prot | ENSP00000220166.6 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 78921058 |
| end | 78945046 |
| strand | - |
| ver | v1.2 |
| region | chr15:78921058-78945046 |
| region5000 | chr15:78916058-78950046 |
| regionname0 | CTSH_chr15_78921058_78945046 |
| regionname5000 | CTSH_chr15_78916058_78950046 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 335 | 277 | 71 | 35 | 153 | 2 | 14 | 115 | CTSH_chr15_78916058_78950046 | CTSH | MWATL others(330): Show |
chr15 | 78916058 | 78950046 |
| a0002 | 0/0 | 335 | 90 | 20 | 23 | 16 | 7 | 24 | 14 | CTSH_chr15_78916058_78950046 | CTSH | MWATL others(330): Show |
chr15 | 78916058 | 78950046 |
| a0003 | 0/0 | 335 | 23 | 0 | 5 | 9 | 5 | 4 | 6 | CTSH_chr15_78916058_78950046 | CTSH | MWATL others(330): Show |
chr15 | 78916058 | 78950046 |
| a0004 | 0/0 | 335 | 11 | 0 | 6 | 5 | 0 | 0 | 5 | CTSH_chr15_78916058_78950046 | CTSH | MWATL others(330): Show |
chr15 | 78916058 | 78950046 |
| a0005 | 0/0 | 335 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | MWATL others(330): Show |
chr15 | 78916058 | 78950046 |
| a0006 | 0/0 | 335 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | MWATL others(330): Show |
chr15 | 78916058 | 78950046 |
| a0007 | 0/0 | 335 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | MWATL others(330): Show |
chr15 | 78916058 | 78950046 |
| a0008 | 0/0 | 1 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | M | chr15 | 78916058 | 78950046 |
| a0009 | 0/0 | 335 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | MWATL others(330): Show |
chr15 | 78916058 | 78950046 |
| a0010 | 0/0 | 335 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | MWATL others(330): Show |
chr15 | 78916058 | 78950046 |
| a0011 | 0/0 | 335 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | MWATL others(330): Show |
chr15 | 78916058 | 78950046 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1005 | 142 | 46 | 20 | 65 | 1 | 10 | CTSH_chr15_78916058_78950046 | CTSH | ATGTG others(1000): Show |
chr15 | 78916058 | 78950046 | ||
| a0001c0002 | 1/0 | 1005 | 133 | 24 | 15 | 88 | 1 | 4 | CTSH_chr15_78916058_78950046 | CTSH | ATGTG others(1000): Show |
chr15 | 78916058 | 78950046 | ||
| a0001c0013 | 0/0 | 1005 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | ATGTG others(1000): Show |
chr15 | 78916058 | 78950046 | ||
| a0001c0014 | 0/1 | 1005 | 1 | 0 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | ATGTG others(1000): Show |
chr15 | 78916058 | 78950046 | ||
| a0002c0003 | 0/0 | 1005 | 83 | 14 | 22 | 16 | 7 | 24 | CTSH_chr15_78916058_78950046 | CTSH | ATGTG others(1000): Show |
chr15 | 78916058 | 78950046 | ||
| a0002c0006 | 0/0 | 1005 | 6 | 6 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | ATGTG others(1000): Show |
chr15 | 78916058 | 78950046 | ||
| a0002c0010 | 0/0 | 1005 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | ATGTG others(1000): Show |
chr15 | 78916058 | 78950046 | ||
| a0003c0004 | 0/0 | 1005 | 23 | 0 | 5 | 9 | 5 | 4 | CTSH_chr15_78916058_78950046 | CTSH | ATGTG others(1000): Show |
chr15 | 78916058 | 78950046 | ||
| a0004c0005 | 0/0 | 1005 | 11 | 0 | 6 | 5 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | ATGTG others(1000): Show |
chr15 | 78916058 | 78950046 | ||
| a0005c0007 | 0/0 | 1005 | 5 | 5 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | ATGTG others(1000): Show |
chr15 | 78916058 | 78950046 | ||
| a0006c0008 | 0/0 | 1005 | 3 | 1 | 2 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | ATGTG others(1000): Show |
chr15 | 78916058 | 78950046 | ||
| a0007c0011 | 0/0 | 1005 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | ATGTG others(1000): Show |
chr15 | 78916058 | 78950046 | ||
| a0008c0009 | 0/0 | 1005 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | ATGTA others(1000): Show |
chr15 | 78916058 | 78950046 | ||
| a0009c0015 | 0/0 | 1005 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | ATGTG others(1000): Show |
chr15 | 78916058 | 78950046 | ||
| a0010c0016 | 0/0 | 1005 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | ATGTG others(1000): Show |
chr15 | 78916058 | 78950046 | ||
| a0011c0012 | 0/0 | 1005 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | ATGTG others(1000): Show |
chr15 | 78916058 | 78950046 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2145 | 92 | 26 | 9 | 53 | 0 | 4 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0001c0001t0003 | 0/0 | 2145 | 4 | 3 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0001c0001t0004 | 0/0 | 2145 | 31 | 4 | 10 | 10 | 1 | 6 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0001c0001t0005 | 0/0 | 2145 | 6 | 4 | 0 | 2 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0001c0001t0008 | 0/0 | 2145 | 5 | 5 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0001c0001t0010 | 0/0 | 2145 | 2 | 2 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0001c0001t0013 | 0/0 | 2145 | 2 | 2 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0001c0002t0001 | 1/0 | 2145 | 60 | 19 | 4 | 33 | 0 | 3 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0001c0002t0003 | 0/0 | 2145 | 44 | 1 | 1 | 42 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0001c0002t0004 | 0/0 | 2145 | 3 | 0 | 0 | 3 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0001c0002t0005 | 0/0 | 2145 | 18 | 2 | 10 | 4 | 1 | 1 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0001c0002t0010 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0001c0002t0011 | 0/0 | 2145 | 3 | 0 | 0 | 3 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0001c0002t0016 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0001c0002t0018 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0001c0002t0019 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0001c0002t0020 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0001c0013t0002 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0001c0014t0004 | 0/1 | 2145 | 1 | 0 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0002c0003t0002 | 0/0 | 2145 | 66 | 13 | 16 | 15 | 6 | 16 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0002c0003t0006 | 0/0 | 2145 | 8 | 0 | 2 | 0 | 0 | 6 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0002c0003t0008 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0002c0003t0012 | 0/0 | 2145 | 3 | 1 | 1 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0002c0003t0014 | 0/0 | 2145 | 2 | 0 | 1 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0002c0003t0015 | 0/0 | 2145 | 2 | 0 | 1 | 0 | 1 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0002c0003t0021 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0002c0006t0002 | 0/0 | 2145 | 5 | 5 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0002c0006t0017 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0002c0010t0002 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0003c0004t0001 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0003c0004t0004 | 0/0 | 2145 | 5 | 0 | 0 | 5 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0003c0004t0005 | 0/0 | 2145 | 10 | 0 | 4 | 3 | 1 | 2 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0003c0004t0007 | 0/0 | 2145 | 6 | 0 | 1 | 0 | 4 | 1 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0003c0004t0009 | 0/0 | 2145 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0004c0005t0001 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0004c0005t0003 | 0/0 | 2145 | 10 | 0 | 5 | 5 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0005c0007t0001 | 0/0 | 2145 | 5 | 5 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0006c0008t0009 | 0/0 | 2145 | 3 | 1 | 2 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0007c0011t0002 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0008c0009t0002 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0009c0015t0001 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0010c0016t0001 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| a0011c0012t0002 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | AGTTG others(2140): Show |
chr15 | 78916058 | 78950046 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0016 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0003g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0004 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0007 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0017 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0005g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0008g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0008g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0008g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0010g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0010g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0001t0013g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0245 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0001 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0005g0003 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0005g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0005g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0005g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0005g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0005g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0005g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0005g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0005g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0005g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0010g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0011g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0011g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0011g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0016g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0018g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0019g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0002t0020g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0013t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0001c0014t0004g0250 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0012 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0020 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0047 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0006g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0006g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0006g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0006g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0006g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0006g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0006g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0006g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0008g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0012g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0012g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0012g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0014g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0014g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0015g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0015g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0003t0021g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0006t0002g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0006t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0006t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0006t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0006t0017g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0002c0010t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0003c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0003c0004t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0003c0004t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0003c0004t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0003c0004t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0003c0004t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0003c0004t0005g0013 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0003c0004t0005g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0003c0004t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0003c0004t0005g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0003c0004t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0003c0004t0005g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0003c0004t0005g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0003c0004t0007g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0003c0004t0007g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0003c0004t0007g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0003c0004t0007g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0003c0004t0007g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0003c0004t0009g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0004c0005t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0004c0005t0003g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0004c0005t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0004c0005t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0004c0005t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0004c0005t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0004c0005t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0005c0007t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0005c0007t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0005c0007t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0005c0007t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0005c0007t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0006c0008t0009g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0006c0008t0009g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0006c0008t0009g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0007c0011t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0008c0009t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0009c0015t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0010c0016t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| a0011c0012t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0003 | t0002 | g0047 | EUR | GBR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00099 | hp2 | a0002 | c0003 | t0002 | g0301 | EUR | GBR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00280 | hp1 | a0003 | c0004 | t0005 | g0060 | EUR | FIN | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00280 | hp2 | a0001 | c0002 | t0005 | g0003 | EUR | FIN | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00323 | hp1 | a0003 | c0004 | t0007 | g0062 | EUR | FIN | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00323 | hp2 | a0002 | c0003 | t0002 | g0299 | EUR | FIN | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00423 | hp2 | a0001 | c0002 | t0003 | g0118 | EAS | CHS | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | CHS | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | CHS | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | CHS | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | CHS | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00558 | hp2 | a0001 | c0002 | t0003 | g0123 | EAS | CHS | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00597 | hp2 | a0001 | c0002 | t0003 | g0106 | EAS | CHS | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00609 | hp1 | a0002 | c0003 | t0002 | g0304 | EAS | CHS | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00609 | hp2 | a0001 | c0002 | t0003 | g0138 | EAS | CHS | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CHS | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00642 | hp1 | a0002 | c0003 | t0014 | g0303 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00642 | hp2 | a0002 | c0003 | t0002 | g0262 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00673 | hp1 | a0001 | c0002 | t0003 | g0034 | EAS | CHS | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00733 | hp1 | a0001 | c0002 | t0005 | g0003 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00733 | hp2 | a0001 | c0002 | t0005 | g0239 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00735 | hp1 | a0001 | c0002 | t0005 | g0003 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00735 | hp2 | a0002 | c0003 | t0002 | g0275 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00738 | hp1 | a0003 | c0004 | t0005 | g0067 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00738 | hp2 | a0002 | c0003 | t0002 | g0021 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00741 | hp1 | a0003 | c0004 | t0005 | g0023 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG00741 | hp2 | a0003 | c0004 | t0007 | g0022 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01069 | hp1 | a0002 | c0003 | t0002 | g0046 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01074 | hp1 | a0006 | c0008 | t0009 | g0195 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01074 | hp2 | a0002 | c0003 | t0012 | g0298 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01081 | hp1 | a0002 | c0003 | t0002 | g0300 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0240 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01099 | hp1 | a0002 | c0003 | t0002 | g0047 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01106 | hp1 | a0002 | c0003 | t0002 | g0292 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0167 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0166 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01167 | hp2 | a0002 | c0003 | t0006 | g0283 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01168 | hp2 | a0002 | c0003 | t0002 | g0307 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0007 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0212 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01175 | hp2 | a0002 | c0003 | t0002 | g0268 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01192 | hp1 | a0002 | c0003 | t0002 | g0012 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01255 | hp1 | a0001 | c0001 | t0004 | g0017 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01255 | hp2 | a0002 | c0003 | t0021 | g0312 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01256 | hp1 | a0002 | c0003 | t0002 | g0289 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01257 | hp1 | a0003 | c0004 | t0005 | g0013 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01257 | hp2 | a0004 | c0005 | t0001 | g0115 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01258 | hp1 | a0003 | c0004 | t0005 | g0013 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01261 | hp1 | a0001 | c0002 | t0005 | g0156 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01261 | hp2 | a0001 | c0002 | t0005 | g0003 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01346 | hp1 | a0002 | c0003 | t0002 | g0253 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01358 | hp1 | a0001 | c0002 | t0005 | g0095 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01358 | hp2 | a0007 | c0011 | t0002 | g0308 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01361 | hp1 | a0002 | c0003 | t0002 | g0050 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01433 | hp1 | a0002 | c0003 | t0002 | g0050 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01433 | hp2 | a0006 | c0008 | t0009 | g0208 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01496 | hp1 | a0001 | c0002 | t0005 | g0158 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0249 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01515 | hp1 | a0003 | c0004 | t0007 | g0058 | EUR | IBS | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01515 | hp2 | a0002 | c0003 | t0002 | g0287 | EUR | IBS | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01517 | hp1 | a0002 | c0003 | t0002 | g0020 | EUR | IBS | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01517 | hp2 | a0003 | c0004 | t0007 | g0055 | EUR | IBS | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01884 | hp1 | a0001 | c0002 | t0003 | g0234 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01884 | hp2 | a0002 | c0003 | t0002 | g0267 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0159 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01891 | hp2 | a0002 | c0003 | t0002 | g0046 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01928 | hp1 | a0004 | c0005 | t0003 | g0114 | AMR | PEL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01928 | hp2 | a0001 | c0002 | t0005 | g0003 | AMR | PEL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01934 | hp1 | a0004 | c0005 | t0003 | g0006 | AMR | PEL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01934 | hp2 | a0001 | c0002 | t0005 | g0206 | AMR | PEL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | PEL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01943 | hp2 | a0004 | c0005 | t0003 | g0006 | AMR | PEL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | PEL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01975 | hp2 | a0002 | c0003 | t0006 | g0288 | AMR | PEL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01978 | hp2 | a0004 | c0005 | t0003 | g0006 | AMR | PEL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01981 | hp1 | a0001 | c0002 | t0005 | g0103 | AMR | PEL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01981 | hp2 | a0004 | c0005 | t0003 | g0006 | AMR | PEL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02004 | hp1 | a0002 | c0010 | t0002 | g0260 | AMR | PEL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02004 | hp2 | a0002 | c0003 | t0002 | g0021 | AMR | PEL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02015 | hp2 | a0003 | c0004 | t0005 | g0059 | EAS | KHV | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02027 | hp1 | a0001 | c0002 | t0018 | g0135 | EAS | KHV | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | KHV | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02040 | hp1 | a0002 | c0003 | t0002 | g0293 | EAS | KHV | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02040 | hp2 | a0003 | c0004 | t0004 | g0065 | EAS | KHV | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0105 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0155 | EAS | KHV | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02056 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | KHV | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02071 | hp1 | a0001 | c0002 | t0003 | g0137 | EAS | KHV | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | KHV | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | KHV | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02074 | hp2 | a0001 | c0002 | t0001 | g0126 | EAS | KHV | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02083 | hp2 | a0008 | c0009 | t0002 | g0252 | EAS | KHV | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | KHV | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02129 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | KHV | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02132 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | KHV | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | KHV | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02145 | hp1 | a0002 | c0006 | t0017 | g0054 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0235 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02155 | hp1 | a0001 | c0002 | t0003 | g0129 | EAS | CDX | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02155 | hp2 | a0001 | c0002 | t0003 | g0030 | EAS | CDX | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CDX | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02165 | hp2 | a0003 | c0004 | t0004 | g0063 | EAS | CDX | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02257 | hp1 | a0002 | c0003 | t0012 | g0296 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02257 | hp2 | a0001 | c0001 | t0013 | g0042 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02258 | hp1 | a0002 | c0003 | t0002 | g0266 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02280 | hp2 | a0002 | c0006 | t0002 | g0256 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02300 | hp1 | a0001 | c0001 | t0004 | g0185 | AMR | PEL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02300 | hp2 | a0001 | c0002 | t0003 | g0098 | AMR | PEL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02451 | hp2 | a0002 | c0003 | t0002 | g0264 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02572 | hp1 | a0002 | c0003 | t0002 | g0019 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02572 | hp2 | a0005 | c0007 | t0001 | g0071 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02602 | hp1 | a0003 | c0004 | t0007 | g0061 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02602 | hp2 | a0002 | c0003 | t0012 | g0295 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0244 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0052 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02647 | hp1 | a0009 | c0015 | t0001 | g0243 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02683 | hp1 | a0002 | c0003 | t0006 | g0297 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02698 | hp1 | a0002 | c0003 | t0006 | g0276 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02698 | hp2 | a0002 | c0003 | t0002 | g0045 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02723 | hp1 | a0002 | c0003 | t0002 | g0019 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0246 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0211 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0173 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0316 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02886 | hp2 | a0002 | c0006 | t0002 | g0255 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0146 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02895 | hp2 | a0002 | c0003 | t0002 | g0311 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0160 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0143 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0144 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02897 | hp2 | a0002 | c0003 | t0002 | g0272 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02922 | hp2 | a0005 | c0007 | t0001 | g0072 | AFR | ESN | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02965 | hp1 | a0002 | c0006 | t0002 | g0043 | AFR | ESN | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0150 | AFR | ESN | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | ESN | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | ESN | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0157 | AFR | ESN | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03017 | hp1 | a0002 | c0003 | t0002 | g0279 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0036 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0051 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03098 | hp1 | a0002 | c0003 | t0002 | g0019 | AFR | MSL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03098 | hp2 | a0001 | c0001 | t0010 | g0207 | AFR | MSL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03130 | hp1 | a0001 | c0002 | t0005 | g0232 | AFR | ESN | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03139 | hp1 | a0002 | c0006 | t0002 | g0043 | AFR | ESN | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03139 | hp2 | a0002 | c0003 | t0002 | g0259 | AFR | ESN | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03195 | hp1 | a0001 | c0002 | t0005 | g0233 | AFR | ESN | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0035 | AFR | ESN | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | MSL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03209 | hp2 | a0001 | c0002 | t0010 | g0145 | AFR | MSL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03225 | hp1 | a0005 | c0007 | t0001 | g0073 | AFR | MSL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03225 | hp2 | a0002 | c0003 | t0002 | g0265 | AFR | MSL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03486 | hp1 | a0002 | c0006 | t0002 | g0254 | AFR | MSL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03490 | hp1 | a0002 | c0003 | t0002 | g0282 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0168 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03491 | hp1 | a0002 | c0003 | t0002 | g0020 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03491 | hp2 | a0002 | c0003 | t0014 | g0290 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0036 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03492 | hp2 | a0002 | c0003 | t0002 | g0020 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03516 | hp1 | a0005 | c0007 | t0001 | g0075 | AFR | ESN | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | MSL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03579 | hp2 | a0002 | c0003 | t0002 | g0273 | AFR | MSL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03654 | hp1 | a0002 | c0003 | t0002 | g0012 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0079 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03688 | hp1 | a0002 | c0003 | t0002 | g0045 | SAS | STU | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03688 | hp2 | a0001 | c0001 | t0004 | g0152 | SAS | STU | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03704 | hp1 | a0002 | c0003 | t0002 | g0021 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0004 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03710 | hp1 | a0002 | c0003 | t0002 | g0294 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03710 | hp2 | a0002 | c0003 | t0002 | g0305 | SAS | PJL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03831 | hp1 | a0002 | c0003 | t0006 | g0281 | SAS | BEB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03831 | hp2 | a0002 | c0003 | t0002 | g0274 | SAS | BEB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0231 | SAS | BEB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03927 | hp1 | a0002 | c0003 | t0002 | g0257 | SAS | BEB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03927 | hp2 | a0002 | c0003 | t0006 | g0258 | SAS | BEB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG04115 | hp1 | a0003 | c0004 | t0009 | g0057 | SAS | STU | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG04115 | hp2 | a0002 | c0003 | t0002 | g0285 | SAS | STU | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG04184 | hp1 | a0002 | c0003 | t0002 | g0012 | SAS | BEB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG04184 | hp2 | a0002 | c0003 | t0006 | g0261 | SAS | BEB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG04199 | hp1 | a0001 | c0002 | t0005 | g0219 | SAS | STU | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG04199 | hp2 | a0003 | c0004 | t0005 | g0013 | SAS | STU | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG04204 | hp1 | a0002 | c0003 | t0002 | g0263 | SAS | STU | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG04204 | hp2 | a0002 | c0003 | t0006 | g0302 | SAS | STU | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0087 | SAS | STU | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | STU | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | YRI | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | YRI | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0172 | EAS | CHB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18747 | hp2 | a0001 | c0002 | t0016 | g0053 | EAS | CHB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | YRI | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18906 | hp2 | a0005 | c0007 | t0001 | g0074 | AFR | YRI | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18939 | hp2 | a0002 | c0003 | t0002 | g0313 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0188 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18942 | hp2 | a0001 | c0002 | t0003 | g0140 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0191 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18943 | hp2 | a0001 | c0002 | t0003 | g0130 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18944 | hp1 | a0002 | c0003 | t0002 | g0049 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18947 | hp1 | a0001 | c0002 | t0003 | g0121 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18947 | hp2 | a0002 | c0003 | t0002 | g0048 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18952 | hp1 | a0001 | c0002 | t0005 | g0134 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18953 | hp2 | a0010 | c0016 | t0001 | g0094 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18956 | hp2 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18959 | hp1 | a0001 | c0002 | t0003 | g0238 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18959 | hp2 | a0002 | c0003 | t0002 | g0310 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18960 | hp2 | a0001 | c0002 | t0003 | g0139 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18961 | hp1 | a0004 | c0005 | t0003 | g0101 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18962 | hp1 | a0001 | c0002 | t0003 | g0119 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18962 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18963 | hp1 | a0011 | c0012 | t0002 | g0309 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18964 | hp1 | a0003 | c0004 | t0004 | g0064 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18968 | hp1 | a0002 | c0003 | t0002 | g0048 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18969 | hp1 | a0001 | c0002 | t0003 | g0031 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18971 | hp2 | a0001 | c0002 | t0003 | g0032 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18973 | hp2 | a0002 | c0003 | t0008 | g0284 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18975 | hp2 | a0002 | c0003 | t0002 | g0277 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18977 | hp2 | a0001 | c0002 | t0005 | g0033 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0170 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18982 | hp1 | a0004 | c0005 | t0003 | g0110 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0128 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0127 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18984 | hp1 | a0001 | c0002 | t0003 | g0034 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18984 | hp2 | a0003 | c0004 | t0001 | g0056 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18986 | hp1 | a0001 | c0002 | t0003 | g0108 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18987 | hp1 | a0001 | c0002 | t0011 | g0112 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18987 | hp2 | a0001 | c0002 | t0004 | g0100 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18988 | hp1 | a0003 | c0004 | t0005 | g0070 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18990 | hp1 | a0001 | c0002 | t0005 | g0033 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18994 | hp2 | a0001 | c0002 | t0003 | g0122 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18995 | hp1 | a0002 | c0003 | t0002 | g0044 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18995 | hp2 | a0001 | c0002 | t0003 | g0107 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18998 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18998 | hp2 | a0004 | c0005 | t0003 | g0029 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19003 | hp2 | a0002 | c0003 | t0002 | g0269 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19004 | hp1 | a0001 | c0002 | t0011 | g0109 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19004 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19005 | hp1 | a0001 | c0002 | t0005 | g0132 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19010 | hp1 | a0001 | c0002 | t0003 | g0124 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19010 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19011 | hp2 | a0001 | c0002 | t0019 | g0131 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19012 | hp2 | a0001 | c0002 | t0003 | g0125 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | LWK | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | LWK | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | LWK | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | LWK | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19054 | hp1 | a0001 | c0002 | t0003 | g0120 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19054 | hp2 | a0003 | c0004 | t0005 | g0066 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19056 | hp1 | a0002 | c0003 | t0002 | g0012 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19056 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19057 | hp1 | a0004 | c0005 | t0003 | g0029 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19057 | hp2 | a0002 | c0003 | t0002 | g0278 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19060 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19063 | hp1 | a0001 | c0002 | t0004 | g0090 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19063 | hp2 | a0003 | c0004 | t0004 | g0068 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19065 | hp1 | a0001 | c0002 | t0003 | g0030 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19068 | hp2 | a0001 | c0002 | t0004 | g0092 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19070 | hp2 | a0001 | c0002 | t0003 | g0031 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19074 | hp1 | a0001 | c0002 | t0003 | g0085 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19077 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19077 | hp2 | a0002 | c0003 | t0002 | g0044 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19078 | hp1 | a0002 | c0003 | t0002 | g0270 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19078 | hp2 | a0001 | c0002 | t0003 | g0141 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19080 | hp1 | a0004 | c0005 | t0003 | g0113 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19080 | hp2 | a0001 | c0002 | t0003 | g0136 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19081 | hp1 | a0003 | c0004 | t0004 | g0069 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19087 | hp1 | a0001 | c0002 | t0003 | g0102 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19088 | hp1 | a0002 | c0003 | t0002 | g0049 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19088 | hp2 | a0001 | c0002 | t0011 | g0111 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19240 | hp1 | a0001 | c0013 | t0002 | g0315 | AFR | YRI | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA19240 | hp2 | a0001 | c0001 | t0008 | g0051 | AFR | YRI | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | ASW | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0037 | AFR | ASW | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0165 | EUR | TSI | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA20752 | hp2 | a0002 | c0003 | t0015 | g0271 | EUR | TSI | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA20805 | hp1 | a0002 | c0003 | t0002 | g0291 | EUR | TSI | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA20805 | hp2 | a0003 | c0004 | t0007 | g0022 | EUR | TSI | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA20905 | hp1 | a0003 | c0004 | t0005 | g0023 | SAS | GIH | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA20905 | hp2 | a0002 | c0003 | t0002 | g0306 | SAS | GIH | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01123 | hp1 | a0002 | c0003 | t0002 | g0286 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG01123 | hp2 | a0002 | c0003 | t0015 | g0280 | AMR | CLM | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02109 | hp1 | a0001 | c0002 | t0020 | g0175 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0241 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02486 | hp1 | a0006 | c0008 | t0009 | g0194 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0242 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0247 | AFR | ACB | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03471 | hp1 | a0001 | c0001 | t0008 | g0052 | AFR | MSL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG03471 | hp2 | a0001 | c0001 | t0013 | g0042 | AFR | MSL | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | USA | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | USA | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0236 | AFR | USA | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | LWK | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| NA21309 | hp2 | a0002 | c0003 | t0002 | g0314 | AFR | LWK | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| homoSapiens | chm13v2 | a0001 | c0014 | t0004 | g0250 | REF | REF | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0245 | REF | REF | CTSH_chr15_78916058_78950046 | CTSH | chr15 | 78916058 | 78950046 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:78925349 | G | A | 1 | a0004 | 11 | HG01257.hp2 HG01928.hp1 HG01934.hp1 others(8): Show |
missense_variant | MODERATE | c.791C>T | p.Thr264Ile | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/12 | 856/2145 | 791/1008 | 264/335 | chr15 | 78925349 | |||
| chr15:78931469 | T | C | 1 | a0009 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.530A>G | p.Asn177Ser | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/12 | 595/2145 | 530/1008 | 177/335 | chr15 | 78931469 | |||
| chr15:78932385 | T | C | 1 | a0006 | 3 | HG01074.hp1 HG01433.hp2 HG02486.hp1 |
missense_variant | MODERATE | c.479A>G | p.Lys160Arg | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 6/12 | 544/2145 | 479/1008 | 160/335 | chr15 | 78932385 | |||
| chr15:78937377 | G | A | 2 | a0007 a0010 |
2 | HG01358.hp2 NA18953.hp2 |
missense_variant | MODERATE | c.170C>T | p.Thr57Met | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/12 | 235/2145 | 170/1008 | 57/335 | chr15 | 78937377 | |||
| chr15:78937410 | T | A | 1 | a0011 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.137A>T | p.Tyr46Phe | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/12 | 202/2145 | 137/1008 | 46/335 | chr15 | 78937410 | |||
| chr15:78944905 | C | G | 4 | a0002 a0007 a0008 others(1): Show |
93 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(90): Show |
missense_variant | MODERATE | c.77G>C | p.Cys26Ser | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/12 | 142/2145 | 77/1008 | 26/335 | chr15 | 78944905 | |||
| chr15:78944915 | C | T | 1 | a0005 | 5 | HG02572.hp2 HG02922.hp2 HG03225.hp1 others(2): Show |
missense_variant | MODERATE | c.67G>A | p.Ala23Thr | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/12 | 132/2145 | 67/1008 | 23/335 | chr15 | 78944915 | |||
| chr15:78944951 | C | T | 1 | a0003 | 23 | HG00280.hp1 HG00323.hp1 HG00738.hp1 others(20): Show |
missense_variant | MODERATE | c.31G>A | p.Gly11Arg | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/12 | 96/2145 | 31/1008 | 11/335 | chr15 | 78944951 | |||
| chr15:78944977 | C | T | 1 | a0008 | 1 | HG02083.hp2 | stop_gained | HIGH | c.5G>A | p.Trp2* | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/12 | 70/2145 | 5/1008 | 2/335 | chr15 | 78944977 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:78932405 | C | T | 3 | a0001c0001 a0002c0010 a0006c0008 |
146 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(143): Show |
synonymous_variant | LOW | c.459G>A | p.Ala153Ala | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 6/12 | 524/2145 | 459/1008 | 153/335 | chr15 | 78932405 | |||
| chr15:78937403 | C | T | 2 | a0001c0013 a0002c0006 |
7 | HG02145.hp1 HG02280.hp2 HG02886.hp2 others(4): Show |
synonymous_variant | LOW | c.144G>A | p.Thr48Thr | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/12 | 209/2145 | 144/1008 | 48/335 | chr15 | 78937403 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:78921254 | C | T | 8 | a0001c0001t0003 a0001c0001t0008 a0001c0002t0003 others(5): Show |
69 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*876G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 12/12 | 876 | chr15 | 78921254 | ||||||
| chr15:78921268 | A | G | 1 | a0002c0003t0021 | 1 | HG01255.hp2 | 3_prime_UTR_variant | MODIFIER | c.*862T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 12/12 | 862 | chr15 | 78921268 | ||||||
| chr15:78921288 | C | T | 2 | a0002c0003t0014 a0003c0004t0007 |
8 | HG00323.hp1 HG00642.hp1 HG00741.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*842G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 12/12 | 842 | chr15 | 78921288 | ||||||
| chr15:78921308 | A | G | 1 | a0001c0002t0019 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*822T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 12/12 | 822 | chr15 | 78921308 | ||||||
| chr15:78921757 | C | T | 1 | a0001c0002t0011 | 3 | NA18987.hp1 NA19004.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*373G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 12/12 | 373 | chr15 | 78921757 | ||||||
| chr15:78921812 | G | A | 1 | a0001c0001t0013 | 2 | HG02257.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*318C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 12/12 | 318 | chr15 | 78921812 | ||||||
| chr15:78921837 | A | G | 1 | a0001c0002t0020 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*293T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 12/12 | 293 | chr15 | 78921837 | ||||||
| chr15:78921850 | C | T | 4 | a0001c0001t0004 a0001c0002t0004 a0002c0003t0015 others(1): Show |
41 | HG00438.hp1 HG01069.hp2 HG01106.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*280G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 12/12 | 280 | chr15 | 78921850 | ||||||
| chr15:78921873 | C | T | 7 | a0001c0001t0005 a0001c0002t0005 a0001c0002t0019 others(4): Show |
51 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*257G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 12/12 | 257 | chr15 | 78921873 | ||||||
| chr15:78921935 | C | T | 2 | a0001c0001t0010 a0001c0002t0010 |
3 | HG01891.hp1 HG03098.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*195G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 12/12 | 195 | chr15 | 78921935 | ||||||
| chr15:78921966 | C | T | 1 | a0001c0002t0018 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*164G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 12/12 | 164 | chr15 | 78921966 | ||||||
| chr15:78922050 | C | T | 2 | a0002c0003t0012 a0002c0003t0021 |
4 | HG01074.hp2 HG01255.hp2 HG02257.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*80G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 12/12 | 80 | chr15 | 78922050 | ||||||
| chr15:78922087 | G | A | 2 | a0003c0004t0009 a0006c0008t0009 |
4 | HG01074.hp1 HG01433.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*43C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 12/12 | 43 | chr15 | 78922087 | ||||||
| chr15:78944982 | C | A | 15 | a0001c0001t0008 a0001c0013t0002 a0002c0003t0002 others(12): Show |
99 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(96): Show |
5_prime_UTR_variant | MODIFIER | c.-1G>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/12 | 1 | chr15 | 78944982 | ||||||
| chr15:78944994 | G | T | 1 | a0002c0006t0017 | 1 | HG02145.hp1 | 5_prime_UTR_variant | MODIFIER | c.-13C>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/12 | 13 | chr15 | 78944994 | ||||||
| chr15:78944996 | C | T | 1 | a0001c0002t0016 | 1 | NA18747.hp2 | 5_prime_UTR_variant | MODIFIER | c.-15G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/12 | 15 | chr15 | 78944996 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:78922298 | G | A | 1 | a0001c0002t0001g0146 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.933-93C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 11/11 | chr15 | 78922298 | |||||||
| chr15:78922364 | C | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0177 a0001c0001t0001g0196 |
4 | NA18965.hp1 NA18973.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.933-159G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 11/11 | chr15 | 78922364 | |||||||
| chr15:78922413 | A | G | 1 | a0002c0003t0012g0295 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.933-208T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 11/11 | chr15 | 78922413 | |||||||
| chr15:78922479 | C | G | 12 | a0001c0002t0001g0037 a0001c0002t0001g0143 a0001c0002t0001g0144 others(9): Show |
13 | HG01496.hp2 HG02109.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.933-274G>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 11/11 | chr15 | 78922479 | |||||||
| chr15:78922526 | T | G | 83 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0040 others(80): Show |
118 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.933-321A>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 11/11 | chr15 | 78922526 | |||||||
| chr15:78922596 | C | A | 3 | a0001c0001t0010g0159 a0001c0001t0010g0207 a0001c0002t0010g0145 |
3 | HG01891.hp1 HG03098.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.933-391G>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 11/11 | chr15 | 78922596 | |||||||
| chr15:78922597 | G | A | 1 | a0001c0001t0001g0149 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.933-392C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 11/11 | chr15 | 78922597 | |||||||
| chr15:78922619 | C | G | 1 | a0003c0004t0001g0056 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.932+374G>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 11/11 | chr15 | 78922619 | |||||||
| chr15:78922639 | G | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0177 |
3 | NA18965.hp1 NA18973.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.932+354C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 11/11 | chr15 | 78922639 | |||||||
| chr15:78922778 | C | T | 29 | a0001c0001t0001g0024 a0001c0001t0001g0187 a0001c0001t0001g0201 others(26): Show |
43 | HG00438.hp2 HG00544.hp2 HG01361.hp2 others(40): Show |
intron_variant | MODIFIER | c.932+215G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 11/11 | chr15 | 78922778 | |||||||
| chr15:78922896 | T | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
80 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.932+97A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 11/11 | chr15 | 78922896 | |||||||
| chr15:78922905 | C | T | 30 | a0001c0001t0004g0004 a0001c0001t0004g0007 a0001c0001t0004g0017 others(27): Show |
40 | HG00438.hp1 HG01069.hp2 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.932+88G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 11/11 | chr15 | 78922905 | |||||||
| chr15:78922960 | C | G | 13 | a0001c0002t0001g0037 a0001c0002t0001g0143 a0001c0002t0001g0144 others(10): Show |
14 | HG01496.hp2 HG02109.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.932+33G>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 11/11 | chr15 | 78922960 | |||||||
| chr15:78922969 | A | C | 83 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0040 others(80): Show |
118 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.932+24T>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 11/11 | chr15 | 78922969 | |||||||
| chr15:78922984 | G | A | 1 | a0001c0002t0003g0106 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.932+9C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 11/11 | chr15 | 78922984 | |||||||
| chr15:78923209 | A | G | 1 | a0001c0001t0004g0152 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.807-91T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78923209 | |||||||
| chr15:78923226 | C | T | 40 | a0001c0001t0005g0008 a0001c0001t0005g0188 a0001c0002t0001g0105 others(37): Show |
52 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.807-108G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78923226 | |||||||
| chr15:78923392 | C | T | 1 | a0001c0002t0003g0032 | 2 | NA18956.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.807-274G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78923392 | |||||||
| chr15:78923478 | A | G | 92 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0040 others(89): Show |
128 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.807-360T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78923478 | |||||||
| chr15:78923581 | A | G | 1 | a0002c0003t0006g0297 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.807-463T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78923581 | |||||||
| chr15:78923584 | C | T | 1 | a0002c0003t0002g0289 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.807-466G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78923584 | |||||||
| chr15:78923621 | A | G | 3 | a0002c0003t0002g0044 a0002c0003t0002g0048 a0002c0003t0002g0313 |
5 | NA18939.hp2 NA18947.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.807-503T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78923621 | |||||||
| chr15:78923720 | G | A | 1 | a0002c0003t0008g0284 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.807-602C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78923720 | |||||||
| chr15:78923845 | A | C | 1 | a0003c0004t0007g0022 | 2 | HG00741.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.807-727T>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78923845 | |||||||
| chr15:78923896 | A | C | 1 | a0003c0004t0004g0068 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.807-778T>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78923896 | |||||||
| chr15:78923908 | G | A | 2 | a0001c0002t0003g0127 a0001c0002t0003g0136 |
2 | NA18983.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.807-790C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78923908 | |||||||
| chr15:78923930 | C | T | 1 | a0002c0003t0002g0044 | 2 | NA18995.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.807-812G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78923930 | |||||||
| chr15:78923979 | G | A | 11 | a0001c0002t0001g0037 a0001c0002t0001g0150 a0001c0002t0001g0157 others(8): Show |
12 | HG01496.hp2 HG02109.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.807-861C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78923979 | |||||||
| chr15:78924043 | C | G | 83 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0178 others(80): Show |
116 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.807-925G>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924043 | |||||||
| chr15:78924077 | T | TG | 29 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0153 others(26): Show |
38 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.807-960dupC | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924077 | |||||||
| chr15:78924096 | CG | C | 83 | a0001c0001t0001g0009 a0001c0001t0001g0039 a0001c0001t0001g0147 others(80): Show |
109 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.807-979delC | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924096 | |||||||
| chr15:78924096 | CGG | C | 34 | a0001c0001t0001g0104 a0001c0001t0001g0189 a0001c0001t0001g0220 others(31): Show |
46 | HG00544.hp2 HG01074.hp1 HG01361.hp1 others(43): Show |
intron_variant | MODIFIER | c.807-980_807-979del others(2): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924096 | |||||||
| chr15:78924096 | CGGG | C | 51 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0082 others(48): Show |
72 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.807-981_807-979del others(3): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924096 | |||||||
| chr15:78924097 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.807-979C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924097 | |||||||
| chr15:78924098 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.807-980C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924098 | |||||||
| chr15:78924101 | G | C | 1 | a0002c0003t0002g0267 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.807-983C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924101 | |||||||
| chr15:78924101 | G | GGGGGGGG others(10): Show |
1 | a0001c0002t0001g0105 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.807-984_807-983ins others(17): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924101 | |||||||
| chr15:78924102 | G | A | 1 | a0001c0002t0001g0236 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.807-984C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924102 | |||||||
| chr15:78924102 | G | C | 2 | a0001c0001t0004g0166 a0001c0002t0019g0131 |
2 | HG01109.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.807-984C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924102 | |||||||
| chr15:78924102 | G | GGGGGGAG others(8): Show |
1 | a0005c0007t0001g0071 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.807-985_807-984ins others(15): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924102 | |||||||
| chr15:78924102 | G | GGGGGGGA others(9): Show |
1 | a0002c0003t0002g0259 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.807-985_807-984ins others(16): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924102 | |||||||
| chr15:78924102 | G | T | 39 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0082 others(36): Show |
60 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.807-984C>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924102 | |||||||
| chr15:78924103 | G | C | 32 | a0001c0001t0001g0147 a0001c0001t0001g0179 a0001c0001t0001g0200 others(29): Show |
48 | HG00280.hp2 HG00733.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.807-985C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924103 | |||||||
| chr15:78924104 | G | C | 1 | a0002c0003t0002g0292 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.807-986C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924104 | |||||||
| chr15:78924204 | A | G | 1 | a0001c0001t0004g0160 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.807-1086T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924204 | |||||||
| chr15:78924385 | A | G | 28 | a0001c0001t0001g0011 a0001c0001t0001g0176 a0001c0001t0001g0179 others(25): Show |
35 | HG01109.hp1 HG01496.hp2 HG02258.hp1 others(32): Show |
intron_variant | MODIFIER | c.806+949T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924385 | |||||||
| chr15:78924437 | CAGGG | C | 7 | a0001c0002t0003g0098 a0004c0005t0001g0115 a0004c0005t0003g0006 others(4): Show |
11 | HG01257.hp2 HG01928.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.806+893_806+896del others(4): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924437 | |||||||
| chr15:78924461 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.806+873G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924461 | |||||||
| chr15:78924483 | C | T | 1 | a0001c0002t0003g0120 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.806+851G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924483 | |||||||
| chr15:78924658 | C | T | 1 | a0002c0003t0002g0273 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.806+676G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924658 | |||||||
| chr15:78924686 | A | G | 1 | a0004c0005t0003g0110 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.806+648T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924686 | |||||||
| chr15:78924692 | A | AT | 136 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(133): Show |
181 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.806+641dupA | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924692 | |||||||
| chr15:78924705 | T | C | 2 | a0002c0003t0006g0261 a0002c0003t0006g0302 |
2 | HG04184.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.806+629A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924705 | |||||||
| chr15:78924707 | T | G | 1 | a0001c0001t0001g0217 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.806+627A>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924707 | |||||||
| chr15:78924783 | A | G | 2 | a0001c0002t0001g0143 a0001c0002t0001g0144 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.806+551T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924783 | |||||||
| chr15:78924802 | G | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0222 others(6): Show |
13 | HG01109.hp1 HG02055.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.806+532C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924802 | |||||||
| chr15:78924821 | C | T | 1 | a0002c0003t0002g0282 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.806+513G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924821 | |||||||
| chr15:78924843 | C | T | 3 | a0001c0002t0001g0005 a0001c0002t0001g0089 a0010c0016t0001g0094 |
6 | NA18940.hp2 NA18946.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.806+491G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924843 | |||||||
| chr15:78924852 | C | CT | 22 | a0001c0001t0001g0024 a0001c0001t0001g0142 a0001c0001t0001g0251 others(19): Show |
26 | HG00280.hp1 HG01123.hp1 HG01361.hp2 others(23): Show |
intron_variant | MODIFIER | c.806+481dupA | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924852 | |||||||
| chr15:78924852 | C | CTTT | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.806+479_806+481dup others(3): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924852 | |||||||
| chr15:78924852 | CT | C | 8 | a0001c0001t0010g0159 a0001c0001t0010g0207 a0001c0002t0001g0146 others(5): Show |
9 | HG01891.hp1 HG02145.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.806+481delA | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924852 | |||||||
| chr15:78924893 | G | A | 1 | a0001c0001t0004g0171 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.806+441C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924893 | |||||||
| chr15:78924948 | G | A | 3 | a0001c0002t0001g0005 a0001c0002t0001g0089 a0010c0016t0001g0094 |
6 | NA18940.hp2 NA18946.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.806+386C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924948 | |||||||
| chr15:78924987 | C | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(60): Show |
81 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.806+347G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78924987 | |||||||
| chr15:78925005 | G | GT | 62 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0222 others(59): Show |
86 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.806+328dupA | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78925005 | |||||||
| chr15:78925005 | G | T | 1 | a0001c0002t0003g0125 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.806+329C>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78925005 | |||||||
| chr15:78925058 | T | G | 64 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(61): Show |
82 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.806+276A>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78925058 | |||||||
| chr15:78925128 | T | A | 4 | a0003c0004t0009g0057 a0006c0008t0009g0194 a0006c0008t0009g0195 others(1): Show |
4 | HG01074.hp1 HG01433.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.806+206A>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78925128 | |||||||
| chr15:78925208 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.806+126G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78925208 | |||||||
| chr15:78925232 | A | G | 1 | a0003c0004t0004g0068 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.806+102T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78925232 | |||||||
| chr15:78925264 | G | A | 31 | a0001c0001t0001g0024 a0001c0001t0003g0182 a0001c0002t0001g0005 others(28): Show |
43 | HG00438.hp2 HG00544.hp2 HG01361.hp2 others(40): Show |
intron_variant | MODIFIER | c.806+70C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78925264 | |||||||
| chr15:78925289 | A | G | 65 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(62): Show |
83 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.806+45T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 10/11 | chr15 | 78925289 | |||||||
| chr15:78925466 | A | T | 11 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0222 others(8): Show |
15 | HG01109.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.700-26T>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78925466 | |||||||
| chr15:78925481 | C | T | 1 | a0001c0002t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.700-41G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78925481 | |||||||
| chr15:78925558 | A | G | 62 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(59): Show |
80 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.700-118T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78925558 | |||||||
| chr15:78925650 | C | A | 1 | a0001c0002t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.700-210G>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78925650 | |||||||
| chr15:78925650 | C | T | 44 | a0001c0002t0001g0133 a0001c0002t0003g0001 a0001c0002t0003g0030 others(41): Show |
62 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.700-210G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78925650 | |||||||
| chr15:78926154 | T | C | 1 | a0001c0013t0002g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.700-714A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78926154 | |||||||
| chr15:78926165 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.700-725C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78926165 | |||||||
| chr15:78926228 | C | T | 1 | a0001c0002t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.700-788G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78926228 | |||||||
| chr15:78926350 | C | T | 1 | a0001c0002t0001g0247 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.700-910G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78926350 | |||||||
| chr15:78926351 | C | T | 1 | a0003c0004t0005g0060 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.700-911G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78926351 | |||||||
| chr15:78926362 | G | C | 1 | a0001c0002t0018g0135 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.700-922C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78926362 | |||||||
| chr15:78926431 | C | T | 57 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(54): Show |
75 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.700-991G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78926431 | |||||||
| chr15:78926486 | G | A | 32 | a0001c0001t0001g0024 a0001c0001t0003g0182 a0001c0002t0001g0005 others(29): Show |
44 | HG00438.hp2 HG00544.hp2 HG01361.hp2 others(41): Show |
intron_variant | MODIFIER | c.700-1046C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78926486 | |||||||
| chr15:78926577 | T | C | 1 | a0001c0001t0001g0190 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.699+1136A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78926577 | |||||||
| chr15:78926642 | A | G | 13 | a0001c0002t0001g0037 a0001c0002t0001g0143 a0001c0002t0001g0144 others(10): Show |
14 | HG01496.hp2 HG02109.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.699+1071T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78926642 | |||||||
| chr15:78926652 | C | T | 60 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(57): Show |
78 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.699+1061G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78926652 | |||||||
| chr15:78926772 | G | A | 3 | a0001c0001t0001g0251 a0001c0002t0001g0241 a0001c0002t0001g0242 |
3 | HG02109.hp2 HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.699+941C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78926772 | |||||||
| chr15:78926838 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(57): Show |
78 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.699+875C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78926838 | |||||||
| chr15:78926846 | C | T | 30 | a0001c0002t0001g0041 a0001c0002t0001g0105 a0001c0002t0001g0236 others(27): Show |
39 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.699+867G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78926846 | |||||||
| chr15:78926938 | C | T | 1 | a0001c0002t0001g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.699+775G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78926938 | |||||||
| chr15:78926990 | G | A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(58): Show |
79 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.699+723C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78926990 | |||||||
| chr15:78927007 | G | T | 2 | a0001c0002t0005g0219 a0001c0002t0005g0239 |
2 | HG00733.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.699+706C>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78927007 | |||||||
| chr15:78927010 | A | T | 1 | a0001c0002t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.699+703T>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78927010 | |||||||
| chr15:78927016 | C | T | 1 | a0001c0002t0003g0127 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.699+697G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78927016 | |||||||
| chr15:78927030 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(58): Show |
79 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.699+683G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78927030 | |||||||
| chr15:78927035 | C | G | 13 | a0001c0002t0001g0037 a0001c0002t0001g0143 a0001c0002t0001g0144 others(10): Show |
14 | HG01496.hp2 HG02109.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.699+678G>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78927035 | |||||||
| chr15:78927050 | T | C | 2 | a0002c0003t0012g0298 a0002c0003t0021g0312 |
2 | HG01074.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.699+663A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78927050 | |||||||
| chr15:78927081 | C | T | 70 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(67): Show |
92 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.699+632G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78927081 | |||||||
| chr15:78927190 | C | T | 1 | a0001c0001t0005g0008 | 4 | HG02622.hp2 HG02809.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.699+523G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78927190 | |||||||
| chr15:78927215 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.699+498G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78927215 | |||||||
| chr15:78927216 | G | A | 45 | a0001c0001t0001g0226 a0001c0002t0001g0133 a0001c0002t0003g0001 others(42): Show |
63 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.699+497C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78927216 | |||||||
| chr15:78927268 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.699+445C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78927268 | |||||||
| chr15:78927319 | G | A | 2 | a0001c0002t0001g0146 a0001c0002t0010g0145 |
2 | HG02895.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.699+394C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78927319 | |||||||
| chr15:78927665 | C | T | 1 | a0001c0002t0001g0133 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.699+48G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78927665 | |||||||
| chr15:78927712 | C | T | 1 | a0003c0004t0005g0066 | 1 | NA19054.hp2 | splice_donor_variant&intron_variant | HIGH | c.699+1G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 9/11 | chr15 | 78927712 | |||||||
| chr15:78927843 | G | A | 1 | a0001c0001t0005g0191 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.631-62C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78927843 | |||||||
| chr15:78928003 | G | C | 60 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(57): Show |
78 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.631-222C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928003 | |||||||
| chr15:78928005 | T | A | 1 | a0001c0002t0001g0041 | 2 | NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.631-224A>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928005 | |||||||
| chr15:78928084 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.631-303C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928084 | |||||||
| chr15:78928120 | G | A | 1 | a0003c0004t0005g0066 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.631-339C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928120 | |||||||
| chr15:78928174 | A | AGGCAGGA others(8): Show |
29 | a0001c0001t0001g0016 a0001c0001t0001g0142 a0001c0001t0003g0035 others(26): Show |
46 | HG00438.hp1 HG01069.hp2 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.631-408_631-394dup others(15): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928174 | |||||||
| chr15:78928191 | G | C | 29 | a0001c0001t0001g0016 a0001c0001t0001g0142 a0001c0001t0003g0035 others(26): Show |
46 | HG00438.hp1 HG01069.hp2 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.631-410C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928191 | |||||||
| chr15:78928207 | A | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(121): Show |
165 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(162): Show |
intron_variant | MODIFIER | c.631-426T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928207 | |||||||
| chr15:78928225 | A | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(57): Show |
78 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.631-444T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928225 | |||||||
| chr15:78928244 | G | A | 69 | a0001c0001t0001g0082 a0001c0001t0001g0147 a0001c0002t0001g0231 others(66): Show |
85 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.631-463C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928244 | |||||||
| chr15:78928296 | G | A | 6 | a0001c0002t0001g0037 a0001c0002t0001g0143 a0001c0002t0001g0144 others(3): Show |
7 | HG02572.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.631-515C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928296 | |||||||
| chr15:78928333 | C | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-552G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928333 | |||||||
| chr15:78928337 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-556C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928337 | |||||||
| chr15:78928338 | C | CG | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-558dupC | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928338 | |||||||
| chr15:78928341 | T | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-560A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928341 | |||||||
| chr15:78928342 | A | G | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-561T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928342 | |||||||
| chr15:78928352 | G | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-571C>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928352 | |||||||
| chr15:78928353 | C | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-572G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928353 | |||||||
| chr15:78928357 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-576C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928357 | |||||||
| chr15:78928360 | T | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-579A>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928360 | |||||||
| chr15:78928363 | A | G | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-582T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928363 | |||||||
| chr15:78928365 | T | G | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-584A>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928365 | |||||||
| chr15:78928370 | G | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-589C>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928370 | |||||||
| chr15:78928371 | T | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-590A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928371 | |||||||
| chr15:78928377 | C | T | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-596G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928377 | |||||||
| chr15:78928380 | G | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-599C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928380 | |||||||
| chr15:78928382 | T | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-601A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928382 | |||||||
| chr15:78928393 | T | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-612A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928393 | |||||||
| chr15:78928394 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-613C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928394 | |||||||
| chr15:78928395 | T | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-614A>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928395 | |||||||
| chr15:78928410 | T | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-629A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928410 | |||||||
| chr15:78928413 | A | AAAAC | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-633_631-632ins others(4): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928413 | |||||||
| chr15:78928416 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-635C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928416 | |||||||
| chr15:78928422 | T | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-641A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928422 | |||||||
| chr15:78928444 | T | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-663A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928444 | |||||||
| chr15:78928446 | C | G | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.631-665G>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928446 | |||||||
| chr15:78928463 | G | T | 1 | a0001c0001t0004g0152 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.631-682C>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928463 | |||||||
| chr15:78928513 | C | T | 1 | a0001c0002t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.631-732G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928513 | |||||||
| chr15:78928543 | C | T | 29 | a0001c0001t0001g0016 a0001c0001t0001g0142 a0001c0001t0003g0035 others(26): Show |
46 | HG00438.hp1 HG01069.hp2 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.631-762G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928543 | |||||||
| chr15:78928556 | C | CT | 3 | a0003c0004t0001g0056 a0003c0004t0005g0059 a0003c0004t0005g0070 |
3 | HG02015.hp2 NA18984.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.631-776dupA | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928556 | |||||||
| chr15:78928559 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.631-778G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928559 | |||||||
| chr15:78928564 | C | CA | 9 | a0001c0002t0001g0231 a0002c0003t0002g0021 a0002c0003t0002g0253 others(6): Show |
11 | HG00323.hp2 HG00735.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.631-784dupT | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928564 | |||||||
| chr15:78928564 | CA | C | 55 | a0001c0002t0001g0037 a0001c0002t0001g0126 a0001c0002t0001g0133 others(52): Show |
72 | HG00558.hp2 HG00597.hp2 HG01167.hp2 others(69): Show |
intron_variant | MODIFIER | c.631-784delT | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928564 | |||||||
| chr15:78928564 | CAA | C | 9 | a0001c0001t0004g0167 a0001c0001t0004g0211 a0001c0002t0001g0143 others(6): Show |
10 | HG01106.hp2 HG01496.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.631-785_631-784del others(2): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928564 | |||||||
| chr15:78928564 | CAAA | C | 25 | a0001c0001t0001g0251 a0001c0001t0004g0004 a0001c0001t0004g0007 others(22): Show |
40 | HG00438.hp1 HG00438.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.631-786_631-784del others(3): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928564 | |||||||
| chr15:78928564 | CAAAA | C | 80 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0142 others(77): Show |
106 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.631-787_631-784del others(4): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928564 | |||||||
| chr15:78928564 | CAAAAA | C | 8 | a0001c0001t0004g0160 a0001c0002t0001g0096 a0001c0002t0001g0241 others(5): Show |
8 | HG01515.hp1 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.631-788_631-784del others(5): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928564 | |||||||
| chr15:78928584 | AAAAAAG | A | 62 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(59): Show |
84 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.631-809_631-804del others(6): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928584 | |||||||
| chr15:78928585 | AAAAAGAA others(3): Show |
A | 1 | a0001c0001t0001g0193 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.631-814_631-805del others(10): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928585 | |||||||
| chr15:78928590 | G | A | 1 | a0001c0002t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.631-809C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928590 | |||||||
| chr15:78928598 | A | G | 2 | a0005c0007t0001g0073 a0005c0007t0001g0074 |
2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.630+814T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928598 | |||||||
| chr15:78928650 | G | T | 45 | a0001c0002t0001g0126 a0001c0002t0001g0133 a0001c0002t0003g0001 others(42): Show |
63 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.630+762C>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928650 | |||||||
| chr15:78928735 | G | A | 1 | a0004c0005t0003g0114 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.630+677C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928735 | |||||||
| chr15:78928787 | A | C | 14 | a0001c0002t0001g0037 a0001c0002t0001g0143 a0001c0002t0001g0144 others(11): Show |
15 | HG01496.hp2 HG02109.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.630+625T>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928787 | |||||||
| chr15:78928857 | G | A | 3 | a0001c0001t0001g0248 a0001c0002t0001g0146 a0001c0002t0010g0145 |
3 | HG01243.hp1 HG02895.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.630+555C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78928857 | |||||||
| chr15:78929014 | G | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
77 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.630+398C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78929014 | |||||||
| chr15:78929062 | A | C | 1 | a0001c0001t0001g0225 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.630+350T>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78929062 | |||||||
| chr15:78929064 | T | C | 1 | a0001c0001t0004g0169 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.630+348A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78929064 | |||||||
| chr15:78929104 | G | A | 1 | a0001c0002t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.630+308C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78929104 | |||||||
| chr15:78929320 | G | A | 1 | a0002c0003t0002g0300 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.630+92C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78929320 | |||||||
| chr15:78929320 | G | C | 31 | a0001c0001t0001g0016 a0001c0001t0001g0142 a0001c0001t0001g0251 others(28): Show |
48 | HG00438.hp1 HG01069.hp2 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.630+92C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78929320 | |||||||
| chr15:78929383 | G | A | 6 | a0001c0001t0001g0248 a0001c0001t0008g0051 a0001c0001t0008g0052 others(3): Show |
8 | HG01243.hp1 HG02630.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.630+29C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 8/11 | chr15 | 78929383 | |||||||
| chr15:78929554 | G | A | 1 | a0001c0002t0003g0136 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.549-61C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78929554 | |||||||
| chr15:78929563 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.549-70G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78929563 | |||||||
| chr15:78929564 | G | A | 2 | a0001c0002t0005g0156 a0001c0002t0005g0158 |
2 | HG01261.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.549-71C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78929564 | |||||||
| chr15:78929565 | T | C | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
78 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.549-72A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78929565 | |||||||
| chr15:78929568 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.549-75G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78929568 | |||||||
| chr15:78929571 | G | A | 1 | a0002c0003t0002g0301 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.549-78C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78929571 | |||||||
| chr15:78929625 | G | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02486.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.549-132C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78929625 | |||||||
| chr15:78929807 | A | G | 76 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(73): Show |
100 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.549-314T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78929807 | |||||||
| chr15:78929923 | G | A | 2 | a0004c0005t0003g0029 a0004c0005t0003g0101 |
3 | NA18961.hp1 NA18998.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.549-430C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78929923 | |||||||
| chr15:78929929 | C | T | 32 | a0001c0001t0003g0182 a0001c0002t0001g0005 a0001c0002t0001g0014 others(29): Show |
43 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.549-436G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78929929 | |||||||
| chr15:78930161 | C | T | 1 | a0005c0007t0001g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.549-668G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78930161 | |||||||
| chr15:78930162 | G | A | 32 | a0001c0001t0003g0182 a0001c0002t0001g0005 a0001c0002t0001g0014 others(29): Show |
43 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.549-669C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78930162 | |||||||
| chr15:78930181 | T | C | 1 | a0001c0002t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.549-688A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78930181 | |||||||
| chr15:78930187 | G | C | 16 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0222 others(13): Show |
21 | HG01109.hp1 HG02055.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.549-694C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78930187 | |||||||
| chr15:78930300 | T | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(188): Show |
263 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(260): Show |
intron_variant | MODIFIER | c.549-807A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78930300 | |||||||
| chr15:78930351 | C | T | 3 | a0002c0003t0002g0262 a0002c0003t0002g0279 a0002c0003t0015g0280 |
3 | HG00642.hp2 HG01123.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.549-858G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78930351 | |||||||
| chr15:78930386 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.549-893C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78930386 | |||||||
| chr15:78930395 | C | T | 45 | a0001c0002t0001g0126 a0001c0002t0001g0133 a0001c0002t0003g0001 others(42): Show |
63 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.549-902G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78930395 | |||||||
| chr15:78930396 | G | A | 6 | a0001c0001t0001g0040 a0001c0001t0001g0223 a0001c0001t0001g0224 others(3): Show |
7 | HG02055.hp2 HG02451.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.549-903C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78930396 | |||||||
| chr15:78930451 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.549-958G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78930451 | |||||||
| chr15:78930514 | G | A | 33 | a0001c0001t0003g0182 a0001c0002t0001g0005 a0001c0002t0001g0014 others(30): Show |
44 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.548+937C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78930514 | |||||||
| chr15:78930537 | A | AAAAT | 9 | a0001c0001t0001g0222 a0001c0001t0010g0159 a0001c0002t0001g0126 others(6): Show |
9 | HG01891.hp1 HG02074.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.548+910_548+913dup others(4): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78930537 | |||||||
| chr15:78930537 | AAAAT | A | 113 | a0001c0001t0001g0016 a0001c0001t0001g0248 a0001c0001t0001g0251 others(110): Show |
154 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.548+910_548+913del others(4): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78930537 | |||||||
| chr15:78930537 | AAAATAAA others(1): Show |
A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
78 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.548+906_548+913del others(8): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78930537 | |||||||
| chr15:78930573 | A | T | 45 | a0001c0002t0001g0126 a0001c0002t0001g0133 a0001c0002t0003g0001 others(42): Show |
63 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.548+878T>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78930573 | |||||||
| chr15:78930582 | C | T | 70 | a0001c0002t0001g0231 a0002c0003t0002g0012 a0002c0003t0002g0019 others(67): Show |
86 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.548+869G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78930582 | |||||||
| chr15:78930926 | G | A | 1 | a0003c0004t0005g0066 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.548+525C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78930926 | |||||||
| chr15:78931063 | T | C | 1 | a0001c0002t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.548+388A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78931063 | |||||||
| chr15:78931103 | G | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(55): Show |
77 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.548+348C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78931103 | |||||||
| chr15:78931108 | C | T | 1 | a0005c0007t0001g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.548+343G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78931108 | |||||||
| chr15:78931246 | C | A | 1 | a0001c0001t0001g0223 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.548+205G>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78931246 | |||||||
| chr15:78931248 | T | C | 3 | a0006c0008t0009g0194 a0006c0008t0009g0195 a0006c0008t0009g0208 |
3 | HG01074.hp1 HG01433.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.548+203A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78931248 | |||||||
| chr15:78931300 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.548+151T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78931300 | |||||||
| chr15:78931339 | G | A | 241 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(238): Show |
323 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(320): Show |
intron_variant | MODIFIER | c.548+112C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78931339 | |||||||
| chr15:78931385 | T | G | 1 | a0001c0001t0001g0222 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.548+66A>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78931385 | |||||||
| chr15:78931386 | G | A | 2 | a0001c0002t0001g0241 a0001c0002t0001g0242 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.548+65C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78931386 | |||||||
| chr15:78931412 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.548+39T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78931412 | |||||||
| chr15:78931437 | G | A | 1 | a0002c0003t0014g0303 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.548+14C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 7/11 | chr15 | 78931437 | |||||||
| chr15:78931563 | C | T | 1 | a0001c0002t0011g0109 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.493-57G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 6/11 | chr15 | 78931563 | |||||||
| chr15:78931796 | G | A | 3 | a0001c0001t0004g0036 a0001c0001t0004g0168 a0001c0001t0004g0211 |
4 | HG02738.hp1 HG03017.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.493-290C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 6/11 | chr15 | 78931796 | |||||||
| chr15:78931863 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.493-357G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 6/11 | chr15 | 78931863 | |||||||
| chr15:78931888 | C | A | 1 | a0001c0002t0001g0235 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.493-382G>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 6/11 | chr15 | 78931888 | |||||||
| chr15:78931980 | T | A | 27 | a0001c0001t0001g0016 a0001c0001t0003g0035 a0001c0001t0003g0161 others(24): Show |
43 | HG00438.hp1 HG01069.hp2 HG01099.hp2 others(40): Show |
intron_variant | MODIFIER | c.492+392A>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 6/11 | chr15 | 78931980 | |||||||
| chr15:78932087 | C | T | 2 | a0001c0002t0001g0084 a0001c0002t0001g0099 |
2 | HG00438.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.492+285G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 6/11 | chr15 | 78932087 | |||||||
| chr15:78932088 | G | A | 11 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0222 others(8): Show |
15 | HG01109.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.492+284C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 6/11 | chr15 | 78932088 | |||||||
| chr15:78932105 | C | T | 45 | a0001c0002t0001g0126 a0001c0002t0001g0133 a0001c0002t0003g0001 others(42): Show |
63 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.492+267G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 6/11 | chr15 | 78932105 | |||||||
| chr15:78932108 | C | T | 13 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0039 others(10): Show |
18 | HG00621.hp1 HG00673.hp2 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.492+264G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 6/11 | chr15 | 78932108 | |||||||
| chr15:78932167 | T | C | 45 | a0001c0002t0001g0126 a0001c0002t0001g0133 a0001c0002t0003g0001 others(42): Show |
63 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.492+205A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 6/11 | chr15 | 78932167 | |||||||
| chr15:78932341 | C | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(128): Show |
175 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.492+31G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 6/11 | chr15 | 78932341 | |||||||
| chr15:78932342 | G | A | 2 | a0002c0003t0002g0272 a0002c0003t0002g0311 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.492+30C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 6/11 | chr15 | 78932342 | |||||||
| chr15:78932352 | G | A | 1 | a0001c0002t0020g0175 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.492+20C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 6/11 | chr15 | 78932352 | |||||||
| chr15:78932495 | T | C | 4 | a0001c0002t0001g0244 a0001c0002t0001g0246 a0001c0002t0001g0249 others(1): Show |
4 | HG01496.hp2 HG02622.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.406-37A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78932495 | |||||||
| chr15:78932505 | G | A | 1 | a0003c0004t0001g0056 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.406-47C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78932505 | |||||||
| chr15:78932541 | C | T | 2 | a0001c0002t0010g0145 a0003c0004t0004g0069 |
2 | HG03209.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.406-83G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78932541 | |||||||
| chr15:78932552 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.406-94A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78932552 | |||||||
| chr15:78932582 | C | T | 8 | a0001c0002t0001g0241 a0001c0002t0001g0242 a0001c0013t0002g0315 others(5): Show |
9 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.406-124G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78932582 | |||||||
| chr15:78932590 | T | C | 9 | a0001c0001t0001g0251 a0001c0002t0001g0241 a0001c0002t0001g0242 others(6): Show |
10 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.406-132A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78932590 | |||||||
| chr15:78932621 | GGCCCTGT others(29): Show |
G | 1 | a0001c0001t0001g0251 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.406-199_406-164del others(36): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78932621 | |||||||
| chr15:78932650 | GCTCGCAA others(29): Show |
G | 2 | a0001c0002t0001g0241 a0001c0002t0001g0242 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.406-228_406-193del others(36): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78932650 | |||||||
| chr15:78932683 | G | C | 31 | a0001c0002t0001g0005 a0001c0002t0001g0014 a0001c0002t0001g0015 others(28): Show |
42 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.406-225C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78932683 | |||||||
| chr15:78932949 | C | CA | 181 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(178): Show |
249 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(246): Show |
intron_variant | MODIFIER | c.406-492_406-491ins others(1): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78932949 | |||||||
| chr15:78933082 | C | A | 1 | a0005c0007t0001g0075 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.406-624G>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78933082 | |||||||
| chr15:78933368 | C | T | 46 | a0001c0001t0013g0042 a0001c0002t0001g0126 a0001c0002t0001g0133 others(43): Show |
65 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.406-910G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78933368 | |||||||
| chr15:78933420 | G | T | 4 | a0002c0003t0002g0277 a0002c0003t0002g0278 a0008c0009t0002g0252 others(1): Show |
4 | HG02083.hp2 NA18963.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.406-962C>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78933420 | |||||||
| chr15:78933471 | CT | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(188): Show |
263 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(260): Show |
intron_variant | MODIFIER | c.406-1014delA | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78933471 | |||||||
| chr15:78933559 | G | C | 1 | a0001c0013t0002g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.406-1101C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78933559 | |||||||
| chr15:78933606 | G | A | 1 | a0002c0003t0002g0304 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.406-1148C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78933606 | |||||||
| chr15:78933904 | C | T | 1 | a0002c0003t0002g0274 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.405+1074G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78933904 | |||||||
| chr15:78934099 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.405+879G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78934099 | |||||||
| chr15:78934149 | T | C | 2 | a0002c0003t0002g0305 a0002c0003t0002g0314 |
2 | HG03710.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.405+829A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78934149 | |||||||
| chr15:78934185 | C | G | 1 | a0002c0003t0006g0276 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.405+793G>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78934185 | |||||||
| chr15:78934186 | G | A | 4 | a0002c0006t0002g0043 a0002c0006t0002g0255 a0002c0006t0002g0256 others(1): Show |
5 | HG02145.hp1 HG02280.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.405+792C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78934186 | |||||||
| chr15:78934343 | C | A | 1 | a0002c0003t0002g0019 | 3 | HG02572.hp1 HG02723.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.405+635G>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78934343 | |||||||
| chr15:78934371 | G | A | 1 | a0003c0004t0009g0057 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.405+607C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78934371 | |||||||
| chr15:78934380 | C | G | 1 | a0005c0007t0001g0071 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.405+598G>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78934380 | |||||||
| chr15:78934629 | G | A | 1 | a0001c0002t0001g0247 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.405+349C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78934629 | |||||||
| chr15:78934721 | G | A | 1 | a0002c0003t0002g0266 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.405+257C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78934721 | |||||||
| chr15:78934769 | A | C | 32 | a0001c0001t0003g0182 a0001c0002t0001g0005 a0001c0002t0001g0014 others(29): Show |
43 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.405+209T>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78934769 | |||||||
| chr15:78934953 | A | T | 1 | a0003c0004t0009g0057 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.405+25T>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 5/11 | chr15 | 78934953 | |||||||
| chr15:78935120 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0013g0042 |
3 | HG02257.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.301-38G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 4/11 | chr15 | 78935120 | |||||||
| chr15:78935634 | G | T | 1 | a0001c0001t0001g0181 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.300+46C>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 4/11 | chr15 | 78935634 | |||||||
| chr15:78935673 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG03130.hp2 | splice_region_variant&intron_variant | LOW | c.300+7A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 4/11 | chr15 | 78935673 | |||||||
| chr15:78935915 | A | G | 59 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(56): Show |
78 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.230-165T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78935915 | |||||||
| chr15:78935960 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.230-210A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78935960 | |||||||
| chr15:78935974 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.230-224C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78935974 | |||||||
| chr15:78936029 | A | G | 68 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(65): Show |
90 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.230-279T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936029 | |||||||
| chr15:78936054 | G | A | 10 | a0001c0002t0001g0015 a0001c0002t0001g0025 a0001c0002t0001g0076 others(7): Show |
13 | HG00544.hp2 HG02027.hp2 NA18948.hp2 others(10): Show |
intron_variant | MODIFIER | c.230-304C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936054 | |||||||
| chr15:78936113 | T | C | 1 | a0001c0001t0004g0169 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.230-363A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936113 | |||||||
| chr15:78936180 | CT | C | 141 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0038 others(138): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.230-431delA | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936180 | |||||||
| chr15:78936180 | CTT | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(109): Show |
153 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(150): Show |
intron_variant | MODIFIER | c.230-432_230-431del others(2): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936180 | |||||||
| chr15:78936180 | CTTT | C | 7 | a0001c0001t0001g0204 a0001c0002t0001g0242 a0001c0002t0003g0108 others(4): Show |
7 | HG00558.hp2 HG01257.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.230-433_230-431del others(3): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936180 | |||||||
| chr15:78936186 | T | C | 1 | a0001c0002t0010g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.230-436A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936186 | |||||||
| chr15:78936187 | T | C | 1 | a0001c0002t0001g0146 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.230-437A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936187 | |||||||
| chr15:78936300 | G | C | 6 | a0001c0013t0002g0315 a0002c0006t0002g0043 a0002c0006t0002g0254 others(3): Show |
7 | HG02145.hp1 HG02280.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.230-550C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936300 | |||||||
| chr15:78936322 | C | A | 1 | a0002c0003t0002g0262 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.230-572G>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936322 | |||||||
| chr15:78936531 | C | T | 1 | a0001c0001t0013g0042 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.230-781G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936531 | |||||||
| chr15:78936538 | C | T | 1 | a0010c0016t0001g0094 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.229+780G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936538 | |||||||
| chr15:78936618 | G | T | 3 | a0002c0003t0002g0257 a0002c0003t0002g0263 a0002c0003t0002g0274 |
3 | HG03831.hp2 HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.229+700C>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936618 | |||||||
| chr15:78936621 | G | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | NA19070.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.229+697C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936621 | |||||||
| chr15:78936631 | GTTTCT | G | 11 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0222 others(8): Show |
15 | HG01109.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.229+682_229+686del others(5): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936631 | |||||||
| chr15:78936675 | G | C | 47 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0002t0001g0126 others(44): Show |
65 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.229+643C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936675 | |||||||
| chr15:78936778 | C | T | 2 | a0001c0002t0001g0241 a0001c0002t0001g0242 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.229+540G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936778 | |||||||
| chr15:78936857 | A | G | 266 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(263): Show |
358 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(355): Show |
intron_variant | MODIFIER | c.229+461T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936857 | |||||||
| chr15:78936890 | A | G | 35 | a0001c0001t0001g0016 a0001c0001t0001g0142 a0001c0001t0003g0035 others(32): Show |
56 | HG00280.hp2 HG00438.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.229+428T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936890 | |||||||
| chr15:78936909 | G | A | 31 | a0001c0002t0001g0005 a0001c0002t0001g0014 a0001c0002t0001g0015 others(28): Show |
42 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.229+409C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936909 | |||||||
| chr15:78936918 | C | T | 1 | a0002c0003t0002g0264 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.229+400G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936918 | |||||||
| chr15:78936921 | G | A | 2 | a0001c0001t0004g0172 a0001c0001t0004g0212 |
2 | HG01175.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.229+397C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78936921 | |||||||
| chr15:78937009 | C | T | 1 | a0002c0003t0002g0273 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.229+309G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78937009 | |||||||
| chr15:78937014 | C | G | 4 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0153 others(1): Show |
4 | HG01243.hp2 HG01346.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.229+304G>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78937014 | |||||||
| chr15:78937067 | G | C | 6 | a0001c0013t0002g0315 a0002c0006t0002g0043 a0002c0006t0002g0254 others(3): Show |
7 | HG02145.hp1 HG02280.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.229+251C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78937067 | |||||||
| chr15:78937120 | G | A | 9 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0177 others(6): Show |
12 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(9): Show |
intron_variant | MODIFIER | c.229+198C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78937120 | |||||||
| chr15:78937127 | C | T | 1 | a0001c0002t0003g0125 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.229+191G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78937127 | |||||||
| chr15:78937147 | G | A | 1 | a0001c0001t0004g0155 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.229+171C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78937147 | |||||||
| chr15:78937302 | A | G | 35 | a0001c0001t0001g0016 a0001c0001t0001g0142 a0001c0001t0003g0035 others(32): Show |
56 | HG00280.hp2 HG00438.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.229+16T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 3/11 | chr15 | 78937302 | |||||||
| chr15:78937430 | C | T | 1 | a0001c0002t0001g0236 | 1 | NA20300.hp2 | splice_region_variant&intron_variant | LOW | c.124-7G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78937430 | |||||||
| chr15:78937451 | C | A | 1 | a0001c0001t0001g0230 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.124-28G>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78937451 | |||||||
| chr15:78937609 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.124-186C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78937609 | |||||||
| chr15:78937615 | T | A | 1 | a0001c0002t0001g0077 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.124-192A>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78937615 | |||||||
| chr15:78937617 | TGGCCAGA others(3): Show |
T | 41 | a0001c0002t0001g0041 a0001c0002t0001g0105 a0001c0002t0001g0235 others(38): Show |
47 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.124-204_124-195del others(10): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78937617 | |||||||
| chr15:78937650 | G | C | 2 | a0001c0002t0001g0241 a0001c0002t0001g0242 |
2 | HG02109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.124-227C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78937650 | |||||||
| chr15:78937750 | A | G | 31 | a0001c0002t0001g0005 a0001c0002t0001g0014 a0001c0002t0001g0015 others(28): Show |
42 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.124-327T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78937750 | |||||||
| chr15:78937767 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.124-344G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78937767 | |||||||
| chr15:78938046 | G | GT | 47 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0002t0001g0126 others(44): Show |
65 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.124-624dupA | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78938046 | |||||||
| chr15:78938047 | T | G | 105 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(102): Show |
149 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.124-624A>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78938047 | |||||||
| chr15:78938225 | C | T | 47 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0018 others(44): Show |
61 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.124-802G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78938225 | |||||||
| chr15:78938368 | C | CA | 42 | a0001c0001t0001g0104 a0001c0001t0001g0205 a0001c0001t0008g0051 others(39): Show |
50 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.123+771dupT | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78938368 | |||||||
| chr15:78938368 | CA | C | 6 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0224 others(3): Show |
6 | HG02965.hp2 HG03834.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+771delT | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78938368 | |||||||
| chr15:78938380 | A | T | 1 | a0001c0001t0001g0213 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.123+760T>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78938380 | |||||||
| chr15:78938395 | G | T | 65 | a0001c0001t0001g0016 a0001c0001t0001g0142 a0001c0001t0003g0035 others(62): Show |
97 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.123+745C>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78938395 | |||||||
| chr15:78938517 | A | G | 14 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0002t0003g0030 others(11): Show |
15 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.123+623T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78938517 | |||||||
| chr15:78938627 | A | G | 240 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0040 others(237): Show |
318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.123+513T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78938627 | |||||||
| chr15:78938663 | T | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(55): Show |
77 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.123+477A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78938663 | |||||||
| chr15:78938704 | G | T | 32 | a0001c0001t0001g0016 a0001c0001t0003g0035 a0001c0001t0003g0161 others(29): Show |
52 | HG00280.hp2 HG00438.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.123+436C>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78938704 | |||||||
| chr15:78938717 | C | T | 31 | a0001c0002t0001g0005 a0001c0002t0001g0014 a0001c0002t0001g0015 others(28): Show |
42 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.123+423G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78938717 | |||||||
| chr15:78938801 | T | C | 1 | a0002c0003t0002g0268 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.123+339A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78938801 | |||||||
| chr15:78938838 | G | GT | 5 | a0001c0001t0004g0155 a0001c0002t0001g0077 a0001c0002t0001g0241 others(2): Show |
5 | HG02056.hp1 HG02109.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.123+301dupA | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78938838 | |||||||
| chr15:78938838 | GT | G | 71 | a0001c0002t0001g0231 a0002c0003t0002g0012 a0002c0003t0002g0019 others(68): Show |
87 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.123+301delA | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78938838 | |||||||
| chr15:78938858 | A | G | 1 | a0001c0002t0003g0118 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.123+282T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78938858 | |||||||
| chr15:78938861 | A | C | 142 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(139): Show |
201 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(198): Show |
intron_variant | MODIFIER | c.123+279T>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78938861 | |||||||
| chr15:78939099 | G | A | 2 | a0002c0003t0002g0272 a0002c0003t0002g0311 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.123+41C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78939099 | |||||||
| chr15:78939136 | T | C | 35 | a0001c0002t0001g0041 a0001c0002t0001g0105 a0001c0002t0001g0235 others(32): Show |
40 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(37): Show |
splice_region_variant&intron_variant | LOW | c.123+4A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 2/11 | chr15 | 78939136 | |||||||
| chr15:78939176 | A | G | 122 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0002t0001g0126 others(119): Show |
156 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(153): Show |
splice_region_variant&intron_variant | LOW | c.92-5T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78939176 | |||||||
| chr15:78939181 | G | GA | 75 | a0001c0002t0001g0146 a0001c0002t0001g0231 a0001c0002t0001g0241 others(72): Show |
91 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.92-11dupT | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78939181 | |||||||
| chr15:78939184 | A | AG | 47 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0002t0001g0126 others(44): Show |
65 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.92-14_92-13insC | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78939184 | |||||||
| chr15:78939274 | A | G | 122 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0002t0001g0126 others(119): Show |
156 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.92-103T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78939274 | |||||||
| chr15:78939455 | C | T | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | NA19070.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.92-284G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78939455 | |||||||
| chr15:78939616 | G | A | 1 | a0001c0001t0001g0221 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.92-445C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78939616 | |||||||
| chr15:78939784 | G | C | 58 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(55): Show |
77 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.92-613C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78939784 | |||||||
| chr15:78939837 | C | T | 10 | a0001c0002t0011g0109 a0001c0002t0011g0111 a0001c0002t0011g0112 others(7): Show |
14 | HG01257.hp2 HG01928.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.92-666G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78939837 | |||||||
| chr15:78939861 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01243.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.92-690G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78939861 | |||||||
| chr15:78939933 | G | GT | 3 | a0001c0001t0013g0042 a0001c0002t0001g0241 a0001c0002t0001g0242 |
4 | HG02109.hp2 HG02257.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-763dupA | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78939933 | |||||||
| chr15:78939970 | C | G | 1 | a0008c0009t0002g0252 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.92-799G>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78939970 | |||||||
| chr15:78939977 | A | G | 74 | a0001c0001t0008g0051 a0001c0001t0008g0052 a0001c0001t0008g0316 others(71): Show |
92 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.92-806T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78939977 | |||||||
| chr15:78939988 | T | C | 74 | a0001c0001t0008g0051 a0001c0001t0008g0052 a0001c0001t0008g0316 others(71): Show |
92 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.92-817A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78939988 | |||||||
| chr15:78940183 | AT | A | 71 | a0001c0002t0001g0231 a0002c0003t0002g0012 a0002c0003t0002g0019 others(68): Show |
87 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.92-1013delA | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78940183 | |||||||
| chr15:78940217 | T | A | 1 | a0001c0001t0004g0007 | 4 | HG01167.hp1 HG01169.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-1046A>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78940217 | |||||||
| chr15:78940358 | C | T | 71 | a0001c0002t0001g0231 a0002c0003t0002g0012 a0002c0003t0002g0019 others(68): Show |
87 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.92-1187G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78940358 | |||||||
| chr15:78940429 | A | T | 1 | a0001c0001t0004g0152 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.92-1258T>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78940429 | |||||||
| chr15:78940434 | A | C | 1 | a0001c0001t0004g0007 | 4 | HG01167.hp1 HG01169.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-1263T>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78940434 | |||||||
| chr15:78940521 | G | C | 47 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0002t0001g0126 others(44): Show |
65 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.92-1350C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78940521 | |||||||
| chr15:78940528 | A | T | 2 | a0001c0002t0001g0025 a0001c0002t0001g0083 |
3 | HG00544.hp2 NA18953.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.92-1357T>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78940528 | |||||||
| chr15:78940537 | CA | C | 92 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0149 others(89): Show |
113 | HG00280.hp1 HG00323.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.92-1367delT | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78940537 | |||||||
| chr15:78940537 | CAA | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
198 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(195): Show |
intron_variant | MODIFIER | c.92-1368_92-1367del others(2): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78940537 | |||||||
| chr15:78940578 | C | A | 1 | a0001c0002t0001g0236 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-1407G>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78940578 | |||||||
| chr15:78940883 | T | C | 74 | a0001c0001t0008g0051 a0001c0001t0008g0052 a0001c0001t0008g0316 others(71): Show |
92 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.92-1712A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78940883 | |||||||
| chr15:78940907 | C | T | 1 | a0002c0003t0015g0271 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.92-1736G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78940907 | |||||||
| chr15:78940913 | T | C | 74 | a0001c0001t0008g0051 a0001c0001t0008g0052 a0001c0001t0008g0316 others(71): Show |
92 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.92-1742A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78940913 | |||||||
| chr15:78941067 | A | T | 2 | a0002c0003t0002g0269 a0002c0003t0002g0270 |
2 | NA19003.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.92-1896T>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941067 | |||||||
| chr15:78941152 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.92-1981G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941152 | |||||||
| chr15:78941155 | CGTGGCTC others(359): Show |
C | 1 | a0001c0001t0001g0220 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.92-2350_92-1985del | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941155 | |||||||
| chr15:78941284 | A | G | 74 | a0001c0001t0008g0051 a0001c0001t0008g0052 a0001c0001t0008g0316 others(71): Show |
92 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.92-2113T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941284 | |||||||
| chr15:78941360 | G | A | 1 | a0002c0003t0002g0273 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.92-2189C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941360 | |||||||
| chr15:78941410 | C | T | 57 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(54): Show |
76 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.92-2239G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941410 | |||||||
| chr15:78941411 | G | A | 2 | a0001c0001t0003g0035 a0001c0001t0003g0161 |
3 | HG02970.hp2 HG03195.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.92-2240C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941411 | |||||||
| chr15:78941422 | T | TA | 117 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0016 others(114): Show |
149 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.92-2252dupT | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941422 | |||||||
| chr15:78941422 | T | TAA | 80 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(77): Show |
98 | HG00544.hp1 HG00597.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.92-2253_92-2252dup others(2): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941422 | |||||||
| chr15:78941422 | T | TAAA | 10 | a0001c0001t0001g0039 a0001c0001t0001g0104 a0001c0001t0001g0149 others(7): Show |
10 | HG00423.hp1 HG02135.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.92-2254_92-2252dup others(3): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941422 | |||||||
| chr15:78941422 | TA | T | 28 | a0001c0002t0001g0231 a0001c0002t0003g0108 a0002c0003t0002g0012 others(25): Show |
31 | HG00323.hp2 HG00609.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.92-2252delT | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941422 | |||||||
| chr15:78941438 | A | T | 3 | a0001c0002t0001g0240 a0001c0002t0005g0219 a0001c0002t0005g0239 |
3 | HG00733.hp2 HG01081.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.92-2267T>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941438 | |||||||
| chr15:78941451 | T | A | 34 | a0001c0002t0001g0041 a0001c0002t0001g0105 a0001c0002t0001g0235 others(31): Show |
37 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.92-2280A>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941451 | |||||||
| chr15:78941651 | C | G | 1 | a0001c0001t0001g0223 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.92-2480G>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941651 | |||||||
| chr15:78941721 | G | A | 1 | a0001c0002t0003g0098 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.92-2550C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941721 | |||||||
| chr15:78941730 | G | A | 6 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0028 others(3): Show |
9 | HG00558.hp1 HG01361.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.92-2559C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941730 | |||||||
| chr15:78941731 | G | C | 1 | a0001c0002t0001g0246 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.92-2560C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941731 | |||||||
| chr15:78941781 | A | G | 74 | a0001c0001t0008g0051 a0001c0001t0008g0052 a0001c0001t0008g0316 others(71): Show |
92 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.92-2610T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941781 | |||||||
| chr15:78941782 | T | C | 309 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(306): Show |
407 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(404): Show |
intron_variant | MODIFIER | c.92-2611A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941782 | |||||||
| chr15:78941795 | C | CA | 85 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0001t0001g0215 others(82): Show |
103 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.92-2625dupT | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941795 | |||||||
| chr15:78941795 | CA | C | 7 | a0001c0001t0001g0151 a0001c0002t0001g0080 a0001c0002t0001g0081 others(4): Show |
7 | HG03041.hp1 HG03130.hp1 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-2625delT | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941795 | |||||||
| chr15:78941926 | T | C | 74 | a0001c0001t0008g0051 a0001c0001t0008g0052 a0001c0001t0008g0316 others(71): Show |
92 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.92-2755A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78941926 | |||||||
| chr15:78942036 | A | T | 71 | a0001c0002t0001g0231 a0002c0003t0002g0012 a0002c0003t0002g0019 others(68): Show |
87 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.91+2855T>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942036 | |||||||
| chr15:78942042 | G | C | 79 | a0001c0001t0008g0051 a0001c0001t0008g0052 a0001c0001t0008g0316 others(76): Show |
98 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.91+2849C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942042 | |||||||
| chr15:78942128 | T | C | 39 | a0001c0001t0001g0149 a0001c0001t0001g0217 a0001c0001t0001g0218 others(36): Show |
44 | HG00280.hp1 HG00323.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.91+2763A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942128 | |||||||
| chr15:78942163 | C | T | 1 | a0001c0002t0001g0150 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.91+2728G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942163 | |||||||
| chr15:78942215 | C | CT | 15 | a0001c0001t0008g0051 a0001c0001t0008g0052 a0001c0001t0008g0316 others(12): Show |
21 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.91+2675dupA | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942215 | |||||||
| chr15:78942215 | CT | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(202): Show |
279 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.91+2675delA | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942215 | |||||||
| chr15:78942215 | CTT | C | 16 | a0001c0001t0001g0011 a0001c0001t0001g0040 a0001c0001t0001g0221 others(13): Show |
20 | HG01109.hp1 HG02055.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.91+2674_91+2675del others(2): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942215 | |||||||
| chr15:78942243 | G | T | 296 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(293): Show |
390 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(387): Show |
intron_variant | MODIFIER | c.91+2648C>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942243 | |||||||
| chr15:78942250 | C | T | 2 | a0001c0002t0001g0146 a0001c0002t0010g0145 |
2 | HG02895.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.91+2641G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942250 | |||||||
| chr15:78942362 | A | G | 2 | a0001c0002t0001g0143 a0001c0002t0001g0144 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.91+2529T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942362 | |||||||
| chr15:78942369 | C | T | 1 | a0005c0007t0001g0071 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.91+2522G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942369 | |||||||
| chr15:78942431 | T | G | 1 | a0001c0002t0001g0079 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.91+2460A>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942431 | |||||||
| chr15:78942457 | C | G | 1 | a0001c0013t0002g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.91+2434G>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942457 | |||||||
| chr15:78942482 | G | C | 47 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0002t0001g0126 others(44): Show |
65 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.91+2409C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942482 | |||||||
| chr15:78942521 | C | T | 1 | a0002c0003t0002g0262 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.91+2370G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942521 | |||||||
| chr15:78942522 | A | G | 71 | a0001c0002t0001g0231 a0002c0003t0002g0012 a0002c0003t0002g0019 others(68): Show |
87 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.91+2369T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942522 | |||||||
| chr15:78942615 | G | A | 26 | a0001c0002t0001g0041 a0001c0002t0001g0105 a0001c0002t0001g0235 others(23): Show |
31 | HG00280.hp1 HG00323.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.91+2276C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942615 | |||||||
| chr15:78942797 | C | T | 8 | a0001c0001t0008g0051 a0001c0001t0008g0052 a0001c0001t0008g0316 others(5): Show |
11 | HG02145.hp1 HG02280.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.91+2094G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942797 | |||||||
| chr15:78942819 | C | G | 310 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(307): Show |
408 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(405): Show |
intron_variant | MODIFIER | c.91+2072G>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942819 | |||||||
| chr15:78942906 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.91+1985T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942906 | |||||||
| chr15:78942952 | T | C | 8 | a0001c0001t0008g0051 a0001c0001t0008g0052 a0001c0001t0008g0316 others(5): Show |
11 | HG02145.hp1 HG02280.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.91+1939A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78942952 | |||||||
| chr15:78943049 | G | A | 1 | a0001c0002t0001g0247 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.91+1842C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78943049 | |||||||
| chr15:78943083 | A | G | 1 | a0002c0003t0006g0261 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.91+1808T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78943083 | |||||||
| chr15:78943104 | T | C | 72 | a0001c0001t0001g0248 a0001c0002t0001g0231 a0002c0003t0002g0012 others(69): Show |
88 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.91+1787A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78943104 | |||||||
| chr15:78943238 | G | C | 8 | a0001c0001t0008g0051 a0001c0001t0008g0052 a0001c0001t0008g0316 others(5): Show |
11 | HG02145.hp1 HG02280.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.91+1653C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78943238 | |||||||
| chr15:78943251 | CTGTT | C | 30 | a0001c0002t0001g0041 a0001c0002t0001g0105 a0001c0002t0001g0235 others(27): Show |
35 | HG00280.hp1 HG00323.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.91+1636_91+1639del others(4): Show |
CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78943251 | |||||||
| chr15:78943331 | C | G | 8 | a0001c0001t0008g0051 a0001c0001t0008g0052 a0001c0001t0008g0316 others(5): Show |
11 | HG02145.hp1 HG02280.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.91+1560G>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78943331 | |||||||
| chr15:78943486 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.91+1405A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78943486 | |||||||
| chr15:78943519 | C | G | 1 | a0002c0003t0002g0259 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.91+1372G>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78943519 | |||||||
| chr15:78943534 | A | G | 8 | a0001c0001t0008g0051 a0001c0001t0008g0052 a0001c0001t0008g0316 others(5): Show |
11 | HG02145.hp1 HG02280.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.91+1357T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78943534 | |||||||
| chr15:78943627 | T | A | 1 | a0003c0004t0005g0070 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.91+1264A>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78943627 | |||||||
| chr15:78943721 | A | G | 48 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0002t0001g0126 others(45): Show |
66 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.91+1170T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78943721 | |||||||
| chr15:78943838 | C | T | 1 | a0001c0013t0002g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.91+1053G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78943838 | |||||||
| chr15:78943841 | G | A | 1 | a0001c0002t0003g0238 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.91+1050C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78943841 | |||||||
| chr15:78943854 | A | T | 1 | a0001c0013t0002g0315 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.91+1037T>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78943854 | |||||||
| chr15:78943875 | G | C | 2 | a0001c0002t0001g0240 a0001c0002t0005g0239 |
2 | HG00733.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.91+1016C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78943875 | |||||||
| chr15:78943884 | T | C | 1 | a0001c0002t0001g0249 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.91+1007A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78943884 | |||||||
| chr15:78943963 | G | C | 4 | a0002c0006t0002g0043 a0002c0006t0002g0255 a0002c0006t0002g0256 others(1): Show |
5 | HG02145.hp1 HG02280.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.91+928C>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78943963 | |||||||
| chr15:78943995 | T | C | 3 | a0001c0001t0013g0042 a0001c0002t0001g0241 a0001c0002t0001g0242 |
4 | HG02109.hp2 HG02257.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+896A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78943995 | |||||||
| chr15:78944007 | G | A | 1 | a0002c0003t0002g0050 | 2 | HG01361.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.91+884C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78944007 | |||||||
| chr15:78944069 | A | AC | 11 | a0001c0001t0001g0104 a0001c0002t0001g0076 a0001c0002t0001g0077 others(8): Show |
11 | HG01981.hp1 HG02055.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.91+821dupG | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78944069 | |||||||
| chr15:78944123 | G | T | 308 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(305): Show |
406 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(403): Show |
intron_variant | MODIFIER | c.91+768C>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78944123 | |||||||
| chr15:78944238 | G | A | 5 | a0002c0006t0002g0043 a0002c0006t0002g0254 a0002c0006t0002g0255 others(2): Show |
6 | HG02145.hp1 HG02280.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.91+653C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78944238 | |||||||
| chr15:78944298 | G | A | 1 | a0001c0001t0001g0018 | 3 | NA18956.hp1 NA19058.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.91+593C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78944298 | |||||||
| chr15:78944473 | G | A | 72 | a0001c0001t0001g0251 a0002c0003t0002g0012 a0002c0003t0002g0019 others(69): Show |
88 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.91+418C>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78944473 | |||||||
| chr15:78944591 | A | G | 76 | a0002c0003t0002g0012 a0002c0003t0002g0019 a0002c0003t0002g0020 others(73): Show |
93 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.91+300T>C | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78944591 | |||||||
| chr15:78944649 | T | C | 1 | a0002c0003t0002g0314 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.91+242A>G | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78944649 | |||||||
| chr15:78944772 | TC | T | 34 | a0001c0001t0001g0024 a0001c0001t0001g0082 a0001c0002t0001g0005 others(31): Show |
46 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.91+118delG | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78944772 | |||||||
| chr15:78944815 | C | T | 1 | a0002c0003t0002g0253 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.91+76G>A | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78944815 | |||||||
| chr15:78944838 | C | A | 76 | a0002c0003t0002g0012 a0002c0003t0002g0019 a0002c0003t0002g0020 others(73): Show |
93 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.91+53G>T | CTSH | ENSG00000103811.18 | transcript | ENST00000220166.10 | protein_coding | 1/11 | chr15 | 78944838 |