Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4185 |
| ensemblid | ENSG00000073670.14 |
| hgncid | 189 |
| symbol | ADAM11 |
| name | ADAM metallopeptidase domain 11 |
| refseq_nuc | NM_002390.6 |
| refseq_prot | NP_002381.2 |
| ensembl_nuc | ENST00000200557.11 |
| ensembl_prot | ENSP00000200557.6 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 44758988 |
| end | 44781846 |
| strand | + |
| ver | v1.2 |
| region | chr17:44758988-44781846 |
| region5000 | chr17:44753988-44786846 |
| regionname0 | ADAM11_chr17_44758988_44781846 |
| regionname5000 | ADAM11_chr17_44753988_44786846 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 769 | 330 | 92 | 73 | 117 | 14 | 32 | 77 | ADAM11_chr17_44753988_44786846 | ADAM11 | MRLLR others(764): Show |
chr17 | 44753988 | 44786846 |
| a0002 | 0/0 | 769 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | MRLLR others(764): Show |
chr17 | 44753988 | 44786846 |
| a0003 | 0/0 | 769 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | MRLLR others(764): Show |
chr17 | 44753988 | 44786846 |
| a0004 | 0/0 | 769 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | MRLLR others(764): Show |
chr17 | 44753988 | 44786846 |
| a0005 | 0/0 | 769 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | MRLLR others(764): Show |
chr17 | 44753988 | 44786846 |
| a0006 | 0/0 | 769 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | MRLLR others(764): Show |
chr17 | 44753988 | 44786846 |
| a0007 | 0/0 | 769 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | MRLLR others(764): Show |
chr17 | 44753988 | 44786846 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2307 | 192 | 38 | 49 | 73 | 11 | 20 | ADAM11_chr17_44753988_44786846 | ADAM11 | ATGAG others(2302): Show |
chr17 | 44753988 | 44786846 | ||
| a0001c0002 | 0/0 | 2307 | 85 | 45 | 18 | 15 | 2 | 5 | ADAM11_chr17_44753988_44786846 | ADAM11 | ATGAG others(2302): Show |
chr17 | 44753988 | 44786846 | ||
| a0001c0003 | 1/0 | 2307 | 48 | 8 | 4 | 27 | 1 | 7 | ADAM11_chr17_44753988_44786846 | ADAM11 | ATGAG others(2302): Show |
chr17 | 44753988 | 44786846 | ||
| a0001c0004 | 0/0 | 2307 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | ATGAG others(2302): Show |
chr17 | 44753988 | 44786846 | ||
| a0001c0005 | 0/0 | 2307 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | ATGAG others(2302): Show |
chr17 | 44753988 | 44786846 | ||
| a0001c0007 | 0/0 | 2307 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | ATGAG others(2302): Show |
chr17 | 44753988 | 44786846 | ||
| a0001c0009 | 0/0 | 2307 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | ATGAG others(2302): Show |
chr17 | 44753988 | 44786846 | ||
| a0002c0011 | 0/0 | 2307 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | ATGAG others(2302): Show |
chr17 | 44753988 | 44786846 | ||
| a0003c0006 | 0/0 | 2307 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | ATGAG others(2302): Show |
chr17 | 44753988 | 44786846 | ||
| a0004c0008 | 0/0 | 2307 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | ATGAG others(2302): Show |
chr17 | 44753988 | 44786846 | ||
| a0005c0013 | 0/0 | 2307 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | ATGAG others(2302): Show |
chr17 | 44753988 | 44786846 | ||
| a0006c0010 | 0/0 | 2307 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | ATGAG others(2302): Show |
chr17 | 44753988 | 44786846 | ||
| a0007c0012 | 0/0 | 2307 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | ATGAG others(2302): Show |
chr17 | 44753988 | 44786846 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4615 | 161 | 27 | 46 | 57 | 11 | 19 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4610): Show |
chr17 | 44753988 | 44786846 |
| a0001c0001t0005 | 0/0 | 4615 | 11 | 10 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4610): Show |
chr17 | 44753988 | 44786846 |
| a0001c0001t0008 | 0/0 | 4615 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4610): Show |
chr17 | 44753988 | 44786846 |
| a0001c0001t0009 | 0/0 | 4614 | 5 | 0 | 2 | 2 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0001t0011 | 0/0 | 4615 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4610): Show |
chr17 | 44753988 | 44786846 |
| a0001c0001t0012 | 0/0 | 4615 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4610): Show |
chr17 | 44753988 | 44786846 |
| a0001c0001t0014 | 0/0 | 4615 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4610): Show |
chr17 | 44753988 | 44786846 |
| a0001c0001t0015 | 0/0 | 4615 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4610): Show |
chr17 | 44753988 | 44786846 |
| a0001c0001t0016 | 0/0 | 4615 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4610): Show |
chr17 | 44753988 | 44786846 |
| a0001c0001t0017 | 0/0 | 4614 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0001t0018 | 0/0 | 4614 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0001t0019 | 0/0 | 4614 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0001t0031 | 0/0 | 4615 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4610): Show |
chr17 | 44753988 | 44786846 |
| a0001c0002t0002 | 0/0 | 4614 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0002t0003 | 0/0 | 4614 | 37 | 18 | 7 | 7 | 2 | 3 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0002t0004 | 0/0 | 4614 | 17 | 7 | 3 | 7 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0002t0006 | 0/0 | 4614 | 11 | 9 | 2 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0002t0007 | 0/0 | 4614 | 8 | 8 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0002t0010 | 0/0 | 4615 | 3 | 1 | 1 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4610): Show |
chr17 | 44753988 | 44786846 |
| a0001c0002t0021 | 0/0 | 4614 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0002t0022 | 0/0 | 4614 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0002t0024 | 0/0 | 4615 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4610): Show |
chr17 | 44753988 | 44786846 |
| a0001c0002t0025 | 0/0 | 4614 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0002t0026 | 0/0 | 4614 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0002t0028 | 0/0 | 4614 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0002t0030 | 0/0 | 4614 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0002t0032 | 0/0 | 4614 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0003t0002 | 1/0 | 4614 | 43 | 8 | 4 | 23 | 1 | 6 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0003t0013 | 0/0 | 4614 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0003t0020 | 0/0 | 4614 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0003t0023 | 0/0 | 4615 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4610): Show |
chr17 | 44753988 | 44786846 |
| a0001c0003t0027 | 0/0 | 4614 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0004t0005 | 0/0 | 4615 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4610): Show |
chr17 | 44753988 | 44786846 |
| a0001c0005t0001 | 0/0 | 4615 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4610): Show |
chr17 | 44753988 | 44786846 |
| a0001c0007t0029 | 0/0 | 4614 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0001c0009t0008 | 0/0 | 4615 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4610): Show |
chr17 | 44753988 | 44786846 |
| a0002c0011t0001 | 0/0 | 4615 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4610): Show |
chr17 | 44753988 | 44786846 |
| a0003c0006t0001 | 0/0 | 4615 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4610): Show |
chr17 | 44753988 | 44786846 |
| a0004c0008t0003 | 0/0 | 4614 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| a0005c0013t0001 | 0/0 | 4615 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4610): Show |
chr17 | 44753988 | 44786846 |
| a0006c0010t0001 | 0/0 | 4615 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4610): Show |
chr17 | 44753988 | 44786846 |
| a0007c0012t0003 | 0/0 | 4614 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | AACCC others(4609): Show |
chr17 | 44753988 | 44786846 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 29 | 6 | 7 | 11 | 3 | 2 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0002 | 0/0 | 10 | 1 | 7 | 0 | 0 | 2 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0004 | 0/0 | 8 | 0 | 3 | 4 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0008 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0009 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0035 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0005g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0005g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0008g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0008g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0008g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0008g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0009g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0009g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0009g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0009g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0011g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0011g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0012g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0012g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0014g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0015g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0016g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0017g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0018g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0019g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0001t0031g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0005 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0034 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0006g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0006g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0007g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0007g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0007g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0007g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0007g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0010g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0010g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0010g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0021g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0022g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0024g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0025g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0026g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0028g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0030g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0002t0032g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0003 | 1/0 | 8 | 1 | 2 | 3 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0013g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0013g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0020g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0023g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0003t0027g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0004t0005g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0004t0005g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0005t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0007t0029g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0001c0009t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0002c0011t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0003c0006t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0004c0008t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0005c0013t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0006c0010t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| a0007c0012t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0003 | g0141 | EUR | GBR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | GBR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00140 | hp1 | a0001 | c0003 | t0002 | g0017 | EUR | GBR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | GBR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | FIN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00323 | hp1 | a0001 | c0002 | t0003 | g0140 | EUR | FIN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | FIN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00544 | hp2 | a0001 | c0009 | t0008 | g0001 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00558 | hp1 | a0001 | c0007 | t0029 | g0192 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00597 | hp2 | a0001 | c0003 | t0002 | g0016 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00609 | hp2 | a0001 | c0002 | t0003 | g0171 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00621 | hp1 | a0001 | c0001 | t0031 | g0007 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00621 | hp2 | a0001 | c0002 | t0004 | g0005 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00639 | hp1 | a0001 | c0002 | t0004 | g0005 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00639 | hp2 | a0001 | c0002 | t0003 | g0012 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00673 | hp1 | a0002 | c0011 | t0001 | g0011 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG00733 | hp2 | a0001 | c0002 | t0004 | g0005 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01074 | hp1 | a0001 | c0002 | t0010 | g0163 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0162 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01109 | hp1 | a0001 | c0004 | t0005 | g0227 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01167 | hp1 | a0001 | c0003 | t0002 | g0003 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01167 | hp2 | a0001 | c0002 | t0006 | g0029 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01168 | hp2 | a0001 | c0002 | t0003 | g0173 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01169 | hp1 | a0001 | c0002 | t0003 | g0174 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01169 | hp2 | a0001 | c0002 | t0006 | g0029 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0031 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0148 | AMR | PUR | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0175 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01261 | hp1 | a0001 | c0005 | t0001 | g0004 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01261 | hp2 | a0001 | c0001 | t0009 | g0002 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01358 | hp1 | a0001 | c0002 | t0003 | g0177 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01361 | hp2 | a0001 | c0002 | t0003 | g0172 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01433 | hp1 | a0001 | c0002 | t0028 | g0122 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01496 | hp1 | a0001 | c0001 | t0009 | g0002 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | IBS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0217 | EUR | IBS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01884 | hp1 | a0001 | c0002 | t0003 | g0186 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01884 | hp2 | a0001 | c0002 | t0003 | g0189 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01891 | hp2 | a0001 | c0002 | t0006 | g0131 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01943 | hp2 | a0001 | c0003 | t0002 | g0003 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01952 | hp1 | a0003 | c0006 | t0001 | g0200 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01978 | hp1 | a0001 | c0002 | t0025 | g0005 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01993 | hp1 | a0001 | c0002 | t0022 | g0012 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02004 | hp1 | a0001 | c0003 | t0002 | g0019 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02004 | hp2 | a0001 | c0002 | t0004 | g0212 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02015 | hp1 | a0001 | c0002 | t0004 | g0214 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02055 | hp1 | a0001 | c0003 | t0002 | g0045 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0169 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02056 | hp2 | a0001 | c0001 | t0008 | g0112 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02071 | hp1 | a0001 | c0001 | t0009 | g0089 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02080 | hp1 | a0001 | c0001 | t0009 | g0043 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02080 | hp2 | a0001 | c0001 | t0011 | g0118 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02083 | hp2 | a0001 | c0003 | t0002 | g0037 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02129 | hp1 | a0001 | c0002 | t0004 | g0198 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02129 | hp2 | a0001 | c0003 | t0002 | g0190 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02132 | hp1 | a0001 | c0003 | t0002 | g0038 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02132 | hp2 | a0001 | c0001 | t0017 | g0001 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02135 | hp2 | a0001 | c0003 | t0002 | g0046 | EAS | KHV | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02145 | hp1 | a0001 | c0002 | t0007 | g0193 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02148 | hp2 | a0001 | c0002 | t0030 | g0166 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CDX | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02155 | hp2 | a0001 | c0003 | t0002 | g0018 | EAS | CDX | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02165 | hp2 | a0004 | c0008 | t0003 | g0182 | EAS | CDX | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02258 | hp2 | a0001 | c0002 | t0007 | g0191 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02300 | hp2 | a0001 | c0003 | t0002 | g0017 | AMR | PEL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02451 | hp1 | a0001 | c0002 | t0021 | g0196 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02451 | hp2 | a0001 | c0002 | t0003 | g0181 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02572 | hp2 | a0001 | c0002 | t0010 | g0168 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02602 | hp1 | a0001 | c0003 | t0002 | g0018 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0220 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02615 | hp2 | a0001 | c0002 | t0006 | g0145 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02622 | hp1 | a0001 | c0002 | t0003 | g0013 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02622 | hp2 | a0001 | c0002 | t0006 | g0143 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02630 | hp1 | a0001 | c0002 | t0003 | g0013 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02630 | hp2 | a0001 | c0002 | t0024 | g0195 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02647 | hp2 | a0001 | c0002 | t0003 | g0013 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02723 | hp2 | a0001 | c0002 | t0007 | g0136 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02735 | hp1 | a0001 | c0002 | t0003 | g0012 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02738 | hp2 | a0001 | c0001 | t0009 | g0010 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02809 | hp1 | a0005 | c0013 | t0001 | g0009 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02809 | hp2 | a0001 | c0002 | t0006 | g0142 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02818 | hp1 | a0001 | c0002 | t0003 | g0031 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02818 | hp2 | a0001 | c0002 | t0006 | g0144 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0030 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02896 | hp1 | a0001 | c0002 | t0003 | g0180 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0015 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02965 | hp2 | a0001 | c0002 | t0003 | g0176 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02970 | hp1 | a0001 | c0002 | t0007 | g0032 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0197 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02976 | hp2 | a0001 | c0002 | t0006 | g0028 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03017 | hp2 | a0001 | c0002 | t0003 | g0139 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03041 | hp1 | a0001 | c0002 | t0004 | g0015 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03098 | hp1 | a0001 | c0002 | t0003 | g0223 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03098 | hp2 | a0001 | c0001 | t0005 | g0219 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03130 | hp1 | a0001 | c0002 | t0004 | g0208 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03130 | hp2 | a0001 | c0003 | t0002 | g0053 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03139 | hp1 | a0001 | c0003 | t0002 | g0061 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03139 | hp2 | a0001 | c0002 | t0003 | g0167 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03195 | hp1 | a0001 | c0002 | t0006 | g0160 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03195 | hp2 | a0001 | c0002 | t0004 | g0015 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03209 | hp2 | a0001 | c0002 | t0004 | g0034 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03225 | hp2 | a0001 | c0003 | t0002 | g0060 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03453 | hp1 | a0001 | c0002 | t0006 | g0157 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03453 | hp2 | a0001 | c0003 | t0002 | g0225 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03486 | hp1 | a0001 | c0002 | t0007 | g0179 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03486 | hp2 | a0001 | c0002 | t0003 | g0014 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03492 | hp2 | a0001 | c0003 | t0002 | g0019 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03516 | hp1 | a0001 | c0003 | t0002 | g0003 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0149 | AFR | ESN | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0151 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03540 | hp2 | a0001 | c0002 | t0007 | g0032 | AFR | GWD | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03579 | hp1 | a0001 | c0004 | t0005 | g0228 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0132 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03654 | hp2 | a0001 | c0002 | t0032 | g0216 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03669 | hp2 | a0001 | c0002 | t0003 | g0183 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03710 | hp2 | a0001 | c0003 | t0002 | g0003 | SAS | PJL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03834 | hp1 | a0001 | c0002 | t0026 | g0085 | SAS | BEB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03927 | hp2 | a0001 | c0003 | t0002 | g0178 | SAS | BEB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG04204 | hp2 | a0001 | c0003 | t0002 | g0097 | SAS | STU | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0147 | AFR | YRI | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18747 | hp2 | a0001 | c0002 | t0004 | g0005 | EAS | CHB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18906 | hp2 | a0001 | c0002 | t0003 | g0185 | AFR | YRI | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18940 | hp1 | a0001 | c0003 | t0002 | g0059 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18941 | hp1 | a0001 | c0003 | t0002 | g0052 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18942 | hp2 | a0001 | c0003 | t0002 | g0058 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18946 | hp2 | a0001 | c0003 | t0002 | g0048 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18948 | hp1 | a0001 | c0003 | t0002 | g0050 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18956 | hp1 | a0001 | c0001 | t0014 | g0106 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18962 | hp2 | a0001 | c0001 | t0018 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18964 | hp1 | a0001 | c0002 | t0003 | g0138 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18967 | hp1 | a0001 | c0003 | t0002 | g0042 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18971 | hp1 | a0001 | c0003 | t0002 | g0051 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18973 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18973 | hp2 | a0001 | c0002 | t0003 | g0137 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18980 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18984 | hp2 | a0001 | c0002 | t0004 | g0213 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18987 | hp2 | a0001 | c0002 | t0010 | g0164 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18994 | hp1 | a0001 | c0001 | t0019 | g0072 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA18994 | hp2 | a0001 | c0003 | t0020 | g0041 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19000 | hp2 | a0001 | c0002 | t0003 | g0184 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19002 | hp1 | a0001 | c0001 | t0012 | g0023 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19002 | hp2 | a0001 | c0001 | t0016 | g0063 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19004 | hp1 | a0001 | c0001 | t0012 | g0007 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19004 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19005 | hp2 | a0001 | c0003 | t0002 | g0020 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19010 | hp1 | a0001 | c0003 | t0002 | g0056 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19030 | hp1 | a0001 | c0002 | t0003 | g0161 | AFR | LWK | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19030 | hp2 | a0001 | c0001 | t0015 | g0226 | AFR | LWK | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19043 | hp2 | a0001 | c0002 | t0006 | g0028 | AFR | LWK | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19057 | hp2 | a0006 | c0010 | t0001 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19062 | hp1 | a0001 | c0002 | t0003 | g0188 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19062 | hp2 | a0001 | c0003 | t0002 | g0040 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19063 | hp2 | a0001 | c0002 | t0004 | g0005 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19064 | hp2 | a0001 | c0003 | t0013 | g0016 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19067 | hp2 | a0001 | c0003 | t0002 | g0057 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19068 | hp2 | a0001 | c0003 | t0002 | g0039 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19079 | hp1 | a0001 | c0001 | t0008 | g0124 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19079 | hp2 | a0001 | c0001 | t0008 | g0099 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19081 | hp2 | a0001 | c0003 | t0023 | g0036 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19085 | hp2 | a0001 | c0003 | t0013 | g0054 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19087 | hp1 | a0001 | c0003 | t0002 | g0020 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19087 | hp2 | a0001 | c0002 | t0003 | g0129 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19088 | hp2 | a0001 | c0001 | t0011 | g0065 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19089 | hp1 | a0001 | c0003 | t0002 | g0055 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19090 | hp1 | a0001 | c0002 | t0004 | g0034 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19090 | hp2 | a0001 | c0001 | t0008 | g0023 | EAS | JPT | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA19240 | hp2 | a0001 | c0002 | t0004 | g0146 | AFR | YRI | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0014 | AFR | ASW | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA20129 | hp2 | a0001 | c0002 | t0004 | g0215 | AFR | ASW | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | TSI | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA20905 | hp1 | a0001 | c0003 | t0027 | g0003 | SAS | GIH | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA20905 | hp2 | a0001 | c0003 | t0002 | g0170 | SAS | GIH | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0014 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02486 | hp1 | a0001 | c0003 | t0002 | g0044 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0159 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02559 | hp1 | a0001 | c0002 | t0003 | g0165 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0158 | AFR | MSL | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | USA | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| HG06807 | hp2 | a0001 | c0002 | t0003 | g0187 | AFR | USA | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA20300 | hp2 | a0001 | c0002 | t0007 | g0194 | AFR | USA | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA21309 | hp1 | a0001 | c0002 | t0007 | g0209 | AFR | LWK | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| NA21309 | hp2 | a0007 | c0012 | t0003 | g0128 | AFR | LWK | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0035 | REF | REF | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0002 | g0003 | REF | REF | ADAM11_chr17_44753988_44786846 | ADAM11 | chr17 | 44753988 | 44786846 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44772292 | G | A | 1 | a0003 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.569G>A | p.Arg190Gln | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 7/27 | 781/4614 | 569/2310 | 190/769 | chr17 | 44772292 | |||
| chr17:44773288 | A | G | 1 | a0007 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.853A>G | p.Ile285Val | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/27 | 1065/4614 | 853/2310 | 285/769 | chr17 | 44773288 | |||
| chr17:44774568 | A | T | 1 | a0002 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.1154A>T | p.His385Leu | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 13/27 | 1366/4614 | 1154/2310 | 385/769 | chr17 | 44774568 | |||
| chr17:44774577 | C | T | 1 | a0004 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.1163C>T | p.Ser388Leu | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 13/27 | 1375/4614 | 1163/2310 | 388/769 | chr17 | 44774577 | |||
| chr17:44777715 | C | T | 1 | a0006 | 1 | NA19057.hp2 | missense_variant | MODERATE | c.1922C>T | p.Ala641Val | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 23/27 | 2134/4614 | 1922/2310 | 641/769 | chr17 | 44777715 | |||
| chr17:44777720 | G | A | 1 | a0005 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.1927G>A | p.Gly643Ser | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 23/27 | 2139/4614 | 1927/2310 | 643/769 | chr17 | 44777720 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44759765 | C | T | 1 | a0001c0004 | 2 | HG01109.hp1 HG03579.hp1 |
synonymous_variant | LOW | c.105C>T | p.Gly35Gly | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/27 | 317/4614 | 105/2310 | 35/769 | chr17 | 44759765 | |||
| chr17:44770027 | G | A | 1 | a0001c0005 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.360G>A | p.Glu120Glu | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/27 | 572/4614 | 360/2310 | 120/769 | chr17 | 44770027 | |||
| chr17:44770048 | C | T | 1 | a0005c0013 | 1 | HG02809.hp1 | splice_region_variant&synonymous_variant | LOW | c.381C>T | p.Thr127Thr | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/27 | 593/4614 | 381/2310 | 127/769 | chr17 | 44770048 | |||
| chr17:44774361 | C | T | 8 | a0001c0001 a0001c0004 a0001c0005 others(5): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
synonymous_variant | LOW | c.1059C>T | p.His353His | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 12/27 | 1271/4614 | 1059/2310 | 353/769 | chr17 | 44774361 | |||
| chr17:44775236 | G | T | 8 | a0001c0001 a0001c0004 a0001c0005 others(5): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
synonymous_variant | LOW | c.1245G>T | p.Ser415Ser | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 15/27 | 1457/4614 | 1245/2310 | 415/769 | chr17 | 44775236 | |||
| chr17:44775242 | T | C | 12 | a0001c0001 a0001c0002 a0001c0004 others(9): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(284): Show |
synonymous_variant | LOW | c.1251T>C | p.Cys417Cys | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 15/27 | 1463/4614 | 1251/2310 | 417/769 | chr17 | 44775242 | |||
| chr17:44777242 | T | C | 8 | a0001c0001 a0001c0004 a0001c0005 others(5): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
synonymous_variant | LOW | c.1758T>C | p.Ser586Ser | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 21/27 | 1970/4614 | 1758/2310 | 586/769 | chr17 | 44777242 | |||
| chr17:44777590 | G | A | 1 | a0001c0009 | 1 | HG00544.hp2 | synonymous_variant | LOW | c.1890G>A | p.Glu630Glu | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 22/27 | 2102/4614 | 1890/2310 | 630/769 | chr17 | 44777590 | |||
| chr17:44778053 | G | A | 1 | a0001c0007 | 1 | HG00558.hp1 | synonymous_variant | LOW | c.2172G>A | p.Thr724Thr | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 24/27 | 2384/4614 | 2172/2310 | 724/769 | chr17 | 44778053 | |||
| chr17:44778186 | T | C | 8 | a0001c0001 a0001c0004 a0001c0005 others(5): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
synonymous_variant | LOW | c.2220T>C | p.Ile740Ile | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/27 | 2432/4614 | 2220/2310 | 740/769 | chr17 | 44778186 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44759006 | C | T | 1 | a0001c0002t0032 | 1 | HG03654.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-194C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 1/27 | chr17 | 44759006 | |||||||
| chr17:44779794 | C | T | 1 | a0001c0001t0031 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*40C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 40 | chr17 | 44779794 | ||||||
| chr17:44779807 | C | T | 1 | a0001c0002t0030 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*53C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 53 | chr17 | 44779807 | ||||||
| chr17:44780062 | G | A | 20 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(17): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*308G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 308 | chr17 | 44780062 | ||||||
| chr17:44780149 | C | T | 20 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(17): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*395C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 395 | chr17 | 44780149 | ||||||
| chr17:44780176 | T | A | 1 | a0001c0001t0014 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*422T>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 422 | chr17 | 44780176 | ||||||
| chr17:44780209 | C | T | 2 | a0001c0001t0012 a0001c0001t0014 |
3 | NA18956.hp1 NA19002.hp1 NA19004.hp1 |
3_prime_UTR_variant | MODIFIER | c.*455C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 455 | chr17 | 44780209 | ||||||
| chr17:44780214 | A | T | 1 | a0001c0001t0014 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*460A>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 460 | chr17 | 44780214 | ||||||
| chr17:44780225 | G | A | 2 | a0001c0001t0015 a0001c0003t0020 |
2 | NA18994.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*471G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 471 | chr17 | 44780225 | ||||||
| chr17:44780237 | G | T | 1 | a0001c0007t0029 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*483G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 483 | chr17 | 44780237 | ||||||
| chr17:44780255 | A | T | 1 | a0001c0001t0019 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*501A>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 501 | chr17 | 44780255 | ||||||
| chr17:44780298 | G | C | 1 | a0001c0001t0014 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*544G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 544 | chr17 | 44780298 | ||||||
| chr17:44780323 | A | C | 1 | a0001c0001t0014 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*569A>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 569 | chr17 | 44780323 | ||||||
| chr17:44780385 | C | A | 1 | a0001c0001t0016 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*631C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 631 | chr17 | 44780385 | ||||||
| chr17:44780425 | T | G | 1 | a0001c0002t0021 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*671T>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 671 | chr17 | 44780425 | ||||||
| chr17:44780556 | C | CG | 17 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(14): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*810dupG | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 811 | INFO_REALIGN_3_PRIME | chr17 | 44780556 | |||||
| chr17:44780556 | C | G | 1 | a0001c0001t0018 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*802C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 802 | chr17 | 44780556 | ||||||
| chr17:44780562 | G | C | 1 | a0001c0002t0022 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*808G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 808 | chr17 | 44780562 | ||||||
| chr17:44780562 | G | GC | 2 | a0001c0001t0011 a0001c0001t0014 |
3 | HG02080.hp2 NA18956.hp1 NA19088.hp2 |
3_prime_UTR_variant | MODIFIER | c.*808_*809insC | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 809 | chr17 | 44780562 | ||||||
| chr17:44780577 | T | C | 4 | a0001c0002t0004 a0001c0002t0021 a0001c0002t0025 others(1): Show |
20 | HG00621.hp2 HG00639.hp1 HG00733.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*823T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 823 | chr17 | 44780577 | ||||||
| chr17:44780947 | T | C | 20 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0008 others(17): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
3_prime_UTR_variant | MODIFIER | c.*1193T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 1193 | chr17 | 44780947 | ||||||
| chr17:44780978 | C | T | 3 | a0001c0001t0008 a0001c0001t0017 a0001c0009t0008 |
6 | HG00544.hp2 HG02056.hp2 HG02132.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1224C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 1224 | chr17 | 44780978 | ||||||
| chr17:44780991 | G | A | 1 | a0001c0002t0006 | 11 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1237G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 1237 | chr17 | 44780991 | ||||||
| chr17:44781126 | A | C | 4 | a0001c0002t0007 a0001c0002t0024 a0001c0002t0028 others(1): Show |
11 | HG00558.hp1 HG01433.hp1 HG02145.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1372A>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 1372 | chr17 | 44781126 | ||||||
| chr17:44781210 | C | A | 4 | a0001c0002t0004 a0001c0002t0021 a0001c0002t0025 others(1): Show |
20 | HG00621.hp2 HG00639.hp1 HG00733.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1456C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 1456 | chr17 | 44781210 | ||||||
| chr17:44781287 | G | A | 3 | a0001c0001t0005 a0001c0001t0015 a0001c0004t0005 |
14 | HG01109.hp1 HG01243.hp2 HG02486.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1533G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 1533 | chr17 | 44781287 | ||||||
| chr17:44781385 | C | T | 1 | a0001c0003t0027 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1631C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 1631 | chr17 | 44781385 | ||||||
| chr17:44781433 | G | A | 1 | a0001c0002t0021 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1679G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 1679 | chr17 | 44781433 | ||||||
| chr17:44781582 | C | T | 13 | a0001c0002t0003 a0001c0002t0004 a0001c0002t0006 others(10): Show |
84 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1828C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 1828 | chr17 | 44781582 | ||||||
| chr17:44781739 | C | T | 1 | a0001c0003t0013 | 2 | NA19064.hp2 NA19085.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1985C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 1985 | chr17 | 44781739 | ||||||
| chr17:44781796 | G | A | 1 | a0001c0002t0026 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2042G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 27/27 | 2042 | chr17 | 44781796 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:44760112 | C | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(207): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.237+215C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44760112 | |||||||
| chr17:44760332 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.237+435C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44760332 | |||||||
| chr17:44760436 | A | G | 2 | a0001c0004t0005g0227 a0001c0004t0005g0228 |
2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.237+539A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44760436 | |||||||
| chr17:44760708 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.237+811G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44760708 | |||||||
| chr17:44760973 | C | T | 1 | a0001c0001t0015g0226 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.237+1076C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44760973 | |||||||
| chr17:44761183 | CTG | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(85): Show |
137 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.237+1289_237+1290d others(4): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44761183 | ||||||
| chr17:44761383 | C | G | 1 | a0001c0003t0002g0225 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.237+1486C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761383 | |||||||
| chr17:44761486 | T | G | 5 | a0001c0003t0002g0037 a0001c0003t0002g0038 a0001c0003t0002g0039 others(2): Show |
5 | HG02083.hp2 HG02132.hp1 NA19062.hp2 others(2): Show |
intron_variant | MODIFIER | c.237+1589T>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761486 | |||||||
| chr17:44761525 | T | A | 1 | a0007c0012t0003g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.237+1628T>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761525 | |||||||
| chr17:44761535 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.237+1638C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761535 | |||||||
| chr17:44761593 | T | A | 1 | a0001c0001t0016g0063 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.237+1696T>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761593 | |||||||
| chr17:44761603 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.237+1706G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761603 | |||||||
| chr17:44761679 | G | A | 1 | a0001c0001t0011g0065 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.237+1782G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761679 | |||||||
| chr17:44761692 | G | C | 1 | a0001c0001t0016g0063 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.237+1795G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761692 | |||||||
| chr17:44761698 | T | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(167): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.237+1801T>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761698 | |||||||
| chr17:44761749 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.237+1852G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761749 | |||||||
| chr17:44761824 | GT | G | 40 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0033 others(37): Show |
57 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.237+1928delT | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761824 | |||||||
| chr17:44761899 | C | A | 1 | a0001c0001t0016g0063 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.237+2002C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761899 | |||||||
| chr17:44761948 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.237+2051G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44761948 | |||||||
| chr17:44762051 | C | T | 2 | a0001c0001t0015g0226 a0007c0012t0003g0128 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.237+2154C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44762051 | |||||||
| chr17:44762082 | C | T | 2 | a0001c0002t0021g0196 a0001c0003t0002g0197 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.237+2185C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44762082 | |||||||
| chr17:44762137 | G | A | 1 | a0001c0002t0004g0198 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.237+2240G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44762137 | |||||||
| chr17:44762183 | C | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(207): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.237+2286C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44762183 | |||||||
| chr17:44762373 | C | G | 1 | a0001c0003t0002g0061 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.237+2476C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44762373 | |||||||
| chr17:44762628 | G | A | 2 | a0001c0001t0015g0226 a0007c0012t0003g0128 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.237+2731G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44762628 | |||||||
| chr17:44762778 | A | G | 2 | a0001c0002t0021g0196 a0001c0003t0002g0197 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.237+2881A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44762778 | |||||||
| chr17:44762917 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.237+3020G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44762917 | |||||||
| chr17:44762925 | G | C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0033 a0001c0001t0001g0199 others(11): Show |
22 | HG00323.hp2 HG00673.hp2 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.237+3028G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44762925 | |||||||
| chr17:44762969 | C | CA | 21 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0070 others(18): Show |
25 | HG00609.hp1 HG01074.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.237+3089dupA | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44762969 | ||||||
| chr17:44762969 | C | CAA | 34 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0033 others(31): Show |
51 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.237+3088_237+3089d others(4): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44762969 | ||||||
| chr17:44763150 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG02109.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.237+3253C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44763150 | |||||||
| chr17:44763494 | AG | A | 3 | a0001c0002t0003g0129 a0001c0002t0003g0137 a0001c0002t0003g0138 |
3 | NA18964.hp1 NA18973.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.237+3599delG | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44763494 | ||||||
| chr17:44763565 | C | T | 7 | a0001c0002t0007g0032 a0001c0002t0007g0136 a0001c0002t0007g0191 others(4): Show |
8 | HG00558.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.237+3668C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44763565 | |||||||
| chr17:44763721 | CT | C | 9 | a0001c0001t0001g0074 a0001c0001t0001g0130 a0001c0001t0001g0199 others(6): Show |
9 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(6): Show |
intron_variant | MODIFIER | c.237+3837delT | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44763721 | ||||||
| chr17:44763747 | C | T | 1 | a0001c0003t0002g0190 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.237+3850C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44763747 | |||||||
| chr17:44763757 | C | T | 3 | a0001c0001t0005g0219 a0001c0001t0005g0220 a0001c0003t0002g0225 |
3 | HG02615.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.237+3860C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44763757 | |||||||
| chr17:44763799 | C | G | 1 | a0001c0001t0001g0205 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.237+3902C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44763799 | |||||||
| chr17:44763878 | A | G | 1 | a0001c0003t0002g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.237+3981A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44763878 | |||||||
| chr17:44763931 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.237+4034G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44763931 | |||||||
| chr17:44763948 | C | T | 1 | a0001c0003t0002g0059 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.237+4051C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44763948 | |||||||
| chr17:44764012 | C | T | 1 | a0001c0002t0003g0189 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.237+4115C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764012 | |||||||
| chr17:44764081 | C | A | 2 | a0001c0002t0004g0015 a0001c0002t0004g0208 |
4 | HG02922.hp1 HG03041.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.237+4184C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764081 | |||||||
| chr17:44764156 | T | A | 1 | a0001c0001t0016g0063 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.237+4259T>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764156 | |||||||
| chr17:44764262 | C | A | 9 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0131 others(6): Show |
11 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.237+4365C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764262 | |||||||
| chr17:44764390 | G | C | 1 | a0001c0002t0004g0146 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.237+4493G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764390 | |||||||
| chr17:44764476 | C | A | 1 | a0001c0001t0016g0063 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.237+4579C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764476 | |||||||
| chr17:44764610 | G | A | 3 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 |
3 | HG00140.hp2 HG01361.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.237+4713G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764610 | |||||||
| chr17:44764711 | A | T | 1 | a0001c0001t0016g0063 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.237+4814A>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764711 | |||||||
| chr17:44764743 | C | A | 1 | a0001c0001t0016g0063 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.237+4846C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764743 | |||||||
| chr17:44764745 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.237+4848T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764745 | |||||||
| chr17:44764847 | C | T | 41 | a0001c0002t0002g0175 a0001c0002t0003g0012 a0001c0002t0003g0013 others(38): Show |
47 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.238-4871C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44764847 | |||||||
| chr17:44765151 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.238-4567T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44765151 | |||||||
| chr17:44765229 | G | A | 7 | a0001c0001t0001g0150 a0001c0001t0005g0030 a0001c0001t0005g0132 others(4): Show |
8 | HG01243.hp2 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.238-4489G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44765229 | |||||||
| chr17:44765278 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(91): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.238-4440C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44765278 | |||||||
| chr17:44765439 | C | G | 1 | a0001c0001t0008g0124 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.238-4279C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44765439 | |||||||
| chr17:44765533 | A | T | 1 | a0001c0002t0006g0160 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.238-4185A>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44765533 | |||||||
| chr17:44765610 | C | CT | 23 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0081 others(20): Show |
27 | HG00558.hp1 HG02145.hp1 HG02165.hp1 others(24): Show |
intron_variant | MODIFIER | c.238-4085dupT | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44765610 | ||||||
| chr17:44765610 | C | CTT | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(67): Show |
119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.238-4086_238-4085d others(4): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44765610 | ||||||
| chr17:44765610 | C | CTTT | 24 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0073 others(21): Show |
27 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.238-4087_238-4085d others(5): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44765610 | ||||||
| chr17:44765610 | C | CTTTT | 20 | a0001c0002t0002g0175 a0001c0002t0003g0031 a0001c0002t0003g0129 others(17): Show |
21 | HG00099.hp1 HG00609.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.238-4088_238-4085d others(6): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44765610 | ||||||
| chr17:44765610 | C | CTTTTT | 20 | a0001c0001t0001g0150 a0001c0001t0005g0030 a0001c0001t0005g0132 others(17): Show |
25 | HG01243.hp2 HG01358.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.238-4089_238-4085d others(7): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44765610 | ||||||
| chr17:44765610 | C | CTTTTTT | 6 | a0001c0001t0005g0151 a0001c0002t0003g0185 a0001c0002t0003g0186 others(3): Show |
6 | HG01884.hp1 HG03195.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.238-4090_238-4085d others(8): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44765610 | ||||||
| chr17:44765610 | CTTTTT | C | 6 | a0001c0001t0001g0080 a0001c0001t0001g0204 a0001c0002t0004g0015 others(3): Show |
9 | HG01433.hp2 HG02273.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.238-4089_238-4085d others(7): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44765610 | ||||||
| chr17:44765610 | CTTTTTT | C | 39 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0033 others(36): Show |
55 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.238-4090_238-4085d others(8): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44765610 | ||||||
| chr17:44765648 | T | G | 1 | a0001c0001t0016g0063 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.238-4070T>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44765648 | |||||||
| chr17:44765661 | C | T | 1 | a0001c0002t0002g0175 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.238-4057C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44765661 | |||||||
| chr17:44765673 | T | G | 3 | a0001c0001t0001g0086 a0001c0001t0001g0113 a0001c0001t0001g0114 |
3 | HG00438.hp2 NA19000.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.238-4045T>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44765673 | |||||||
| chr17:44765779 | C | T | 11 | a0001c0001t0001g0150 a0001c0001t0005g0030 a0001c0001t0005g0132 others(8): Show |
12 | HG01243.hp2 HG02280.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.238-3939C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44765779 | |||||||
| chr17:44766143 | C | T | 1 | a0001c0003t0002g0056 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.238-3575C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766143 | |||||||
| chr17:44766188 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.238-3530G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766188 | |||||||
| chr17:44766430 | C | T | 1 | a0001c0002t0006g0144 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.238-3288C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766430 | |||||||
| chr17:44766479 | T | G | 1 | a0001c0001t0016g0063 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.238-3239T>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766479 | |||||||
| chr17:44766528 | G | A | 2 | a0001c0004t0005g0227 a0001c0004t0005g0228 |
2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.238-3190G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766528 | |||||||
| chr17:44766553 | T | A | 1 | a0001c0001t0016g0063 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.238-3165T>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766553 | |||||||
| chr17:44766561 | C | T | 2 | a0001c0001t0005g0219 a0001c0001t0005g0220 |
2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.238-3157C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766561 | |||||||
| chr17:44766566 | C | G | 7 | a0001c0002t0007g0032 a0001c0002t0007g0136 a0001c0002t0007g0191 others(4): Show |
8 | HG00558.hp1 HG02145.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.238-3152C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766566 | |||||||
| chr17:44766594 | C | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG03041.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.238-3124C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766594 | |||||||
| chr17:44766745 | C | T | 1 | a0001c0001t0008g0112 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.238-2973C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766745 | |||||||
| chr17:44766746 | G | A | 2 | a0001c0001t0005g0219 a0001c0001t0005g0220 |
2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.238-2972G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766746 | |||||||
| chr17:44766795 | T | A | 1 | a0001c0001t0016g0063 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.238-2923T>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766795 | |||||||
| chr17:44766869 | A | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(140): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.238-2849A>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44766869 | |||||||
| chr17:44767097 | A | C | 1 | a0001c0002t0003g0184 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.238-2621A>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44767097 | |||||||
| chr17:44767213 | G | A | 1 | a0001c0002t0004g0146 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.238-2505G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44767213 | |||||||
| chr17:44767354 | C | CA | 45 | a0001c0001t0001g0033 a0001c0001t0001g0081 a0001c0001t0001g0088 others(42): Show |
53 | HG00408.hp1 HG00438.hp2 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.238-2341dupA | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44767354 | ||||||
| chr17:44767354 | CA | C | 19 | a0001c0001t0001g0026 a0001c0001t0001g0066 a0001c0001t0001g0084 others(16): Show |
20 | HG00099.hp1 HG01168.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.238-2341delA | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | INFO_REALIGN_3_PRIME | chr17 | 44767354 | ||||||
| chr17:44767685 | G | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG00280.hp2 HG03704.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.238-2033G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44767685 | |||||||
| chr17:44767896 | C | T | 2 | a0001c0001t0015g0226 a0007c0012t0003g0128 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.238-1822C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44767896 | |||||||
| chr17:44767909 | G | C | 3 | a0001c0001t0001g0082 a0001c0001t0001g0117 a0001c0001t0016g0063 |
3 | NA18975.hp2 NA18984.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.238-1809G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44767909 | |||||||
| chr17:44767979 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.238-1739A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44767979 | |||||||
| chr17:44767997 | T | C | 1 | a0003c0006t0001g0200 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.238-1721T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44767997 | |||||||
| chr17:44768067 | G | T | 1 | a0001c0003t0002g0061 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.238-1651G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768067 | |||||||
| chr17:44768085 | A | G | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0222 |
3 | HG01255.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.238-1633A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768085 | |||||||
| chr17:44768168 | A | G | 4 | a0001c0001t0001g0068 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | HG00408.hp2 HG00544.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.238-1550A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768168 | |||||||
| chr17:44768180 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.238-1538A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768180 | |||||||
| chr17:44768216 | A | G | 1 | a0001c0003t0002g0053 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.238-1502A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768216 | |||||||
| chr17:44768266 | A | G | 1 | a0001c0002t0006g0144 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.238-1452A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768266 | |||||||
| chr17:44768326 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(91): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.238-1392G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768326 | |||||||
| chr17:44768509 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.238-1209G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768509 | |||||||
| chr17:44768657 | G | T | 1 | a0001c0001t0014g0106 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.238-1061G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768657 | |||||||
| chr17:44768737 | G | T | 3 | a0001c0003t0002g0039 a0001c0003t0002g0040 a0001c0003t0023g0036 |
3 | NA19062.hp2 NA19068.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.238-981G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768737 | |||||||
| chr17:44768761 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.238-957C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768761 | |||||||
| chr17:44768780 | A | G | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG03041.hp2 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.238-938A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768780 | |||||||
| chr17:44768824 | C | A | 1 | a0001c0002t0004g0212 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.238-894C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768824 | |||||||
| chr17:44768937 | C | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0033 others(21): Show |
34 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.238-781C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768937 | |||||||
| chr17:44768963 | G | T | 1 | a0001c0002t0030g0166 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.238-755G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768963 | |||||||
| chr17:44768981 | C | T | 1 | a0001c0002t0004g0146 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.238-737C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44768981 | |||||||
| chr17:44769040 | T | C | 1 | a0001c0003t0002g0044 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.238-678T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44769040 | |||||||
| chr17:44769063 | A | T | 1 | a0001c0003t0002g0059 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.238-655A>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44769063 | |||||||
| chr17:44769145 | G | A | 1 | a0001c0002t0003g0189 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.238-573G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44769145 | |||||||
| chr17:44769261 | G | A | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(207): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.238-457G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44769261 | |||||||
| chr17:44769472 | G | A | 1 | a0001c0002t0003g0139 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.238-246G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44769472 | |||||||
| chr17:44769521 | C | T | 2 | a0001c0001t0015g0226 a0007c0012t0003g0128 |
2 | NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.238-197C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44769521 | |||||||
| chr17:44769626 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(207): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.238-92T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44769626 | |||||||
| chr17:44769655 | C | G | 1 | a0001c0003t0002g0061 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.238-63C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44769655 | |||||||
| chr17:44769660 | C | G | 1 | a0001c0002t0006g0029 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.238-58C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44769660 | |||||||
| chr17:44769665 | C | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(90): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.238-53C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 2/26 | chr17 | 44769665 | |||||||
| chr17:44769861 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.314+67G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 3/26 | chr17 | 44769861 | |||||||
| chr17:44769943 | C | G | 1 | a0001c0003t0002g0061 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.315-39C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 3/26 | chr17 | 44769943 | |||||||
| chr17:44770070 | C | G | 41 | a0001c0002t0002g0175 a0001c0002t0003g0012 a0001c0002t0003g0013 others(38): Show |
47 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.381+22C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770070 | |||||||
| chr17:44770288 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.381+240C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770288 | |||||||
| chr17:44770400 | C | T | 15 | a0001c0001t0001g0150 a0001c0001t0005g0030 a0001c0001t0005g0132 others(12): Show |
16 | HG01109.hp1 HG01243.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.381+352C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770400 | |||||||
| chr17:44770488 | T | TC | 13 | a0001c0001t0001g0047 a0001c0003t0002g0016 a0001c0003t0002g0017 others(10): Show |
14 | HG00140.hp1 HG00597.hp1 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.381+451dupC | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr17 | 44770488 | ||||||
| chr17:44770488 | TC | T | 24 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0033 others(21): Show |
35 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.381+451delC | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr17 | 44770488 | ||||||
| chr17:44770490 | C | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(164): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.381+442C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770490 | |||||||
| chr17:44770495 | CCCCCG | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(84): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.381+452_381+456del others(5): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr17 | 44770495 | ||||||
| chr17:44770496 | C | G | 53 | a0001c0002t0002g0175 a0001c0002t0003g0012 a0001c0002t0003g0013 others(50): Show |
63 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.381+448C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770496 | |||||||
| chr17:44770497 | C | T | 1 | a0001c0001t0001g0009 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.381+449C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770497 | |||||||
| chr17:44770497 | CCCG | C | 67 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(64): Show |
81 | HG00099.hp1 HG00323.hp1 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.381+452_381+454del others(3): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr17 | 44770497 | ||||||
| chr17:44770499 | CG | C | 4 | a0001c0001t0015g0226 a0001c0002t0007g0193 a0001c0002t0032g0216 others(1): Show |
4 | HG02145.hp1 HG03654.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.381+452delG | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770499 | |||||||
| chr17:44770500 | G | C | 15 | a0001c0001t0001g0150 a0001c0001t0005g0030 a0001c0001t0005g0132 others(12): Show |
16 | HG01109.hp1 HG01243.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.381+452G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770500 | |||||||
| chr17:44770501 | C | G | 5 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(2): Show |
5 | HG02258.hp1 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+453C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770501 | |||||||
| chr17:44770502 | C | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(84): Show |
136 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.381+454C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770502 | |||||||
| chr17:44770503 | C | G | 3 | a0001c0004t0005g0227 a0001c0004t0005g0228 a0007c0012t0003g0128 |
3 | HG01109.hp1 HG03579.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.381+455C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770503 | |||||||
| chr17:44770580 | C | A | 1 | a0001c0002t0003g0183 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.381+532C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770580 | |||||||
| chr17:44770726 | T | C | 85 | a0001c0001t0001g0150 a0001c0001t0005g0030 a0001c0001t0005g0132 others(82): Show |
102 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.381+678T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770726 | |||||||
| chr17:44770820 | A | C | 5 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 others(2): Show |
5 | HG02258.hp1 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-764A>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770820 | |||||||
| chr17:44770872 | TG | T | 3 | a0001c0001t0001g0123 a0001c0001t0014g0106 a0001c0003t0002g0039 |
3 | NA18956.hp1 NA18987.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.382-709delG | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr17 | 44770872 | ||||||
| chr17:44770952 | T | C | 2 | a0001c0002t0028g0122 a0001c0007t0029g0192 |
2 | HG00558.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.382-632T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44770952 | |||||||
| chr17:44771152 | T | G | 1 | a0001c0001t0001g0201 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.382-432T>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44771152 | |||||||
| chr17:44771279 | G | A | 5 | a0001c0003t0002g0037 a0001c0003t0002g0038 a0001c0003t0002g0039 others(2): Show |
5 | HG02083.hp2 HG02132.hp1 NA19062.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-305G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44771279 | |||||||
| chr17:44771297 | C | CA | 45 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0024 others(42): Show |
62 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.382-269dupA | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr17 | 44771297 | ||||||
| chr17:44771297 | CA | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(98): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.382-269delA | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | INFO_REALIGN_3_PRIME | chr17 | 44771297 | ||||||
| chr17:44771336 | C | T | 1 | a0001c0002t0004g0146 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.382-248C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44771336 | |||||||
| chr17:44771557 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.382-27G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 4/26 | chr17 | 44771557 | |||||||
| chr17:44771726 | C | T | 15 | a0001c0001t0001g0150 a0001c0001t0005g0030 a0001c0001t0005g0132 others(12): Show |
16 | HG01109.hp1 HG01243.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.468-30C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 5/26 | chr17 | 44771726 | |||||||
| chr17:44771990 | G | GCCCCAGC others(11): Show |
1 | a0001c0003t0020g0041 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.543+170_543+187dup others(18): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 6/26 | INFO_REALIGN_3_PRIME | chr17 | 44771990 | ||||||
| chr17:44772135 | C | T | 1 | a0001c0003t0002g0060 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.544-132C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 6/26 | chr17 | 44772135 | |||||||
| chr17:44772353 | G | T | 1 | a0001c0003t0002g0197 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.610+20G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 7/26 | chr17 | 44772353 | |||||||
| chr17:44772545 | G | A | 1 | a0001c0001t0005g0148 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.678+79G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 8/26 | chr17 | 44772545 | |||||||
| chr17:44772577 | G | A | 2 | a0001c0001t0005g0158 a0001c0001t0005g0159 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.678+111G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 8/26 | chr17 | 44772577 | |||||||
| chr17:44772843 | C | T | 1 | a0001c0002t0028g0122 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.679-14C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 8/26 | chr17 | 44772843 | |||||||
| chr17:44772984 | T | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0006 others(71): Show |
108 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.754-30T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 9/26 | chr17 | 44772984 | |||||||
| chr17:44773165 | C | T | 1 | a0001c0002t0003g0186 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.825+80C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 10/26 | chr17 | 44773165 | |||||||
| chr17:44773573 | T | G | 11 | a0001c0001t0005g0030 a0001c0001t0005g0132 a0001c0001t0005g0147 others(8): Show |
12 | HG01109.hp1 HG01243.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.992+146T>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44773573 | |||||||
| chr17:44773706 | G | A | 1 | a0001c0002t0003g0177 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.992+279G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44773706 | |||||||
| chr17:44773749 | T | G | 3 | a0001c0001t0001g0027 a0001c0001t0001g0130 a0001c0001t0001g0134 |
4 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.992+322T>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44773749 | |||||||
| chr17:44773803 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(133): Show |
200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.992+376A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44773803 | |||||||
| chr17:44773816 | C | T | 1 | a0001c0002t0032g0216 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.992+389C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44773816 | |||||||
| chr17:44773822 | G | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0117 a0001c0001t0016g0063 |
3 | NA18975.hp2 NA18984.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.992+395G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44773822 | |||||||
| chr17:44773883 | G | C | 9 | a0001c0002t0007g0032 a0001c0002t0007g0136 a0001c0002t0007g0191 others(6): Show |
10 | HG00558.hp1 HG01433.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.993-412G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44773883 | |||||||
| chr17:44773936 | C | T | 1 | a0001c0002t0004g0215 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.993-359C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44773936 | |||||||
| chr17:44774042 | G | C | 6 | a0001c0002t0003g0129 a0001c0002t0003g0137 a0001c0002t0003g0138 others(3): Show |
6 | HG01074.hp1 HG01358.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.993-253G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44774042 | |||||||
| chr17:44774097 | A | AAAAAAG | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.993-188_993-183dup others(6): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | INFO_REALIGN_3_PRIME | chr17 | 44774097 | ||||||
| chr17:44774134 | G | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(133): Show |
200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.993-161G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44774134 | |||||||
| chr17:44774135 | G | T | 1 | a0001c0007t0029g0192 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.993-160G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44774135 | |||||||
| chr17:44774266 | G | A | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(133): Show |
200 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.993-29G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 11/26 | chr17 | 44774266 | |||||||
| chr17:44774693 | C | T | 59 | a0001c0002t0002g0175 a0001c0002t0003g0012 a0001c0002t0003g0013 others(56): Show |
68 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(65): Show |
splice_region_variant&intron_variant | LOW | c.1169-5C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 13/26 | chr17 | 44774693 | |||||||
| chr17:44774777 | A | G | 1 | a0001c0001t0014g0106 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1220+28A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 14/26 | chr17 | 44774777 | |||||||
| chr17:44774846 | C | A | 1 | a0001c0003t0002g0052 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1220+97C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 14/26 | chr17 | 44774846 | |||||||
| chr17:44774894 | C | A | 1 | a0001c0003t0002g0061 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1220+145C>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 14/26 | chr17 | 44774894 | |||||||
| chr17:44775043 | A | ATGGGAGC others(28): Show |
1 | a0001c0001t0001g0202 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1221-168_1221-134d others(37): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 14/26 | INFO_REALIGN_3_PRIME | chr17 | 44775043 | ||||||
| chr17:44775081 | A | G | 2 | a0001c0002t0006g0028 a0001c0002t0006g0131 |
3 | HG01891.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1221-131A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 14/26 | chr17 | 44775081 | |||||||
| chr17:44775780 | C | G | 35 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0033 others(32): Show |
46 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.1485+104C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 17/26 | chr17 | 44775780 | |||||||
| chr17:44775793 | G | A | 1 | a0001c0003t0002g0052 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1485+117G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 17/26 | chr17 | 44775793 | |||||||
| chr17:44775878 | A | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
198 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1485+202A>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 17/26 | chr17 | 44775878 | |||||||
| chr17:44775879 | G | C | 1 | a0001c0001t0001g0202 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1485+203G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 17/26 | chr17 | 44775879 | |||||||
| chr17:44775888 | G | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0156 |
2 | HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1485+212G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 17/26 | chr17 | 44775888 | |||||||
| chr17:44775965 | G | A | 11 | a0001c0002t0004g0005 a0001c0002t0004g0015 a0001c0002t0004g0034 others(8): Show |
18 | HG00621.hp2 HG00639.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.1486-162G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 17/26 | chr17 | 44775965 | |||||||
| chr17:44776058 | G | T | 1 | a0001c0001t0001g0104 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1486-69G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 17/26 | chr17 | 44776058 | |||||||
| chr17:44776059 | A | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1486-68A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 17/26 | chr17 | 44776059 | |||||||
| chr17:44776326 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(91): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1566+119C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 18/26 | chr17 | 44776326 | |||||||
| chr17:44776473 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1566+266C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 18/26 | chr17 | 44776473 | |||||||
| chr17:44776550 | C | G | 35 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0033 others(32): Show |
46 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.1567-195C>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 18/26 | chr17 | 44776550 | |||||||
| chr17:44776582 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1567-163G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 18/26 | chr17 | 44776582 | |||||||
| chr17:44776685 | G | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0033 others(32): Show |
46 | HG00323.hp2 HG00642.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.1567-60G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 18/26 | chr17 | 44776685 | |||||||
| chr17:44776687 | G | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0130 others(3): Show |
10 | HG02055.hp2 HG02647.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.1567-58G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 18/26 | chr17 | 44776687 | |||||||
| chr17:44776840 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(91): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1617+45G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 19/26 | chr17 | 44776840 | |||||||
| chr17:44777134 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(91): Show |
147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1682-32G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 20/26 | chr17 | 44777134 | |||||||
| chr17:44777421 | G | C | 1 | a0001c0001t0008g0099 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1782-61G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 21/26 | chr17 | 44777421 | |||||||
| chr17:44777630 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1901+29G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 22/26 | chr17 | 44777630 | |||||||
| chr17:44777694 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA19063.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.1902-1G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 22/26 | chr17 | 44777694 | |||||||
| chr17:44777880 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.2070+17T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 23/26 | chr17 | 44777880 | |||||||
| chr17:44778092 | G | T | 1 | a0001c0003t0002g0051 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2185+26G>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 24/26 | chr17 | 44778092 | |||||||
| chr17:44778104 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(139): Show |
207 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.2185+38T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 24/26 | chr17 | 44778104 | |||||||
| chr17:44778378 | A | G | 3 | a0001c0001t0001g0025 a0001c0001t0001g0103 a0001c0001t0001g0121 |
4 | HG00733.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2276+136A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778378 | |||||||
| chr17:44778563 | G | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(126): Show |
193 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.2276+321G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778563 | |||||||
| chr17:44778586 | C | T | 2 | a0001c0001t0001g0202 a0007c0012t0003g0128 |
2 | NA19063.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2276+344C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778586 | |||||||
| chr17:44778615 | G | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.2276+373G>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778615 | |||||||
| chr17:44778646 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2276+404G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778646 | |||||||
| chr17:44778650 | C | T | 8 | a0001c0001t0001g0009 a0001c0001t0001g0210 a0001c0001t0001g0211 others(5): Show |
10 | HG00642.hp2 HG01069.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.2276+408C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778650 | |||||||
| chr17:44778688 | C | CA | 6 | a0001c0001t0001g0206 a0001c0003t0002g0020 a0001c0003t0002g0040 others(3): Show |
7 | HG01175.hp1 HG02135.hp2 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.2276+471dupA | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr17 | 44778688 | ||||||
| chr17:44778688 | C | CAAAAAAA others(12): Show |
1 | a0001c0002t0010g0164 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2276+461_2276+462i others(21): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr17 | 44778688 | ||||||
| chr17:44778688 | CA | C | 9 | a0001c0001t0001g0199 a0001c0002t0004g0015 a0001c0002t0004g0034 others(6): Show |
12 | HG00323.hp2 HG02015.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.2276+471delA | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr17 | 44778688 | ||||||
| chr17:44778688 | CAA | C | 16 | a0001c0002t0004g0005 a0001c0002t0004g0146 a0001c0002t0004g0198 others(13): Show |
22 | HG00621.hp2 HG00639.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.2276+470_2276+471d others(4): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr17 | 44778688 | ||||||
| chr17:44778688 | CAAAAAAA others(4): Show |
C | 1 | a0007c0012t0003g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2276+461_2276+471d others(13): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr17 | 44778688 | ||||||
| chr17:44778713 | A | AAAAAAAA others(13): Show |
2 | a0001c0002t0003g0162 a0001c0002t0024g0195 |
2 | HG01081.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2276+471_2276+472i others(22): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | |||||||
| chr17:44778713 | A | AAAAAAAA others(12): Show |
1 | a0001c0002t0028g0122 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2276+471_2276+472i others(21): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | |||||||
| chr17:44778713 | A | AAAAAAAA others(11): Show |
2 | a0001c0002t0003g0188 a0001c0002t0007g0194 |
2 | NA19062.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2276+471_2276+472i others(20): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | |||||||
| chr17:44778713 | A | AAAAAAAA others(10): Show |
8 | a0001c0002t0002g0175 a0001c0002t0003g0012 a0001c0002t0003g0139 others(5): Show |
10 | HG00323.hp1 HG00639.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.2276+471_2276+472i others(19): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | |||||||
| chr17:44778713 | A | AAAAAAAA others(9): Show |
1 | a0001c0002t0007g0179 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2276+471_2276+472i others(18): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | |||||||
| chr17:44778713 | A | AAAAAAAA others(8): Show |
3 | a0001c0002t0003g0031 a0001c0002t0003g0137 a0001c0002t0003g0177 |
4 | HG01243.hp1 HG01358.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2276+471_2276+472i others(17): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | |||||||
| chr17:44778713 | A | AAAAAAAA others(7): Show |
12 | a0001c0002t0003g0013 a0001c0002t0003g0129 a0001c0002t0003g0138 others(9): Show |
14 | HG00099.hp1 HG00609.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.2276+471_2276+472i others(16): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | |||||||
| chr17:44778713 | A | AAAAAAAA others(6): Show |
8 | a0001c0002t0003g0014 a0001c0002t0003g0161 a0001c0002t0003g0169 others(5): Show |
10 | HG00558.hp1 HG01074.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.2276+471_2276+472i others(15): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | |||||||
| chr17:44778713 | A | AAAAAAAA others(5): Show |
2 | a0001c0002t0003g0173 a0001c0002t0003g0180 |
2 | HG01168.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2276+471_2276+472i others(14): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | |||||||
| chr17:44778713 | A | AAAAAAAA others(4): Show |
1 | a0001c0002t0003g0174 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2276+471_2276+472i others(13): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | |||||||
| chr17:44778713 | A | AAAAAAAA others(3): Show |
2 | a0001c0002t0003g0186 a0001c0002t0007g0191 |
2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2276+471_2276+472i others(12): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | |||||||
| chr17:44778713 | A | AAAAG | 15 | a0001c0001t0001g0009 a0001c0001t0001g0101 a0001c0001t0001g0210 others(12): Show |
17 | HG00642.hp2 HG01069.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2276+471_2276+472i others(6): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | |||||||
| chr17:44778713 | A | AAAG | 29 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(26): Show |
37 | HG00621.hp1 HG00642.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.2276+471_2276+472i others(5): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | |||||||
| chr17:44778713 | A | AAG | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(66): Show |
114 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.2276+471_2276+472i others(4): Show |
ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | |||||||
| chr17:44778713 | A | AG | 4 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0154 others(1): Show |
4 | HG01070.hp1 HG01884.hp2 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.2276+472dupG | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | INFO_REALIGN_3_PRIME | chr17 | 44778713 | ||||||
| chr17:44778713 | A | G | 29 | a0001c0001t0005g0159 a0001c0002t0003g0181 a0001c0002t0003g0187 others(26): Show |
38 | HG00621.hp2 HG00639.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.2276+471A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778713 | |||||||
| chr17:44778714 | G | A | 1 | a0001c0001t0014g0106 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2276+472G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778714 | |||||||
| chr17:44778814 | A | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG00408.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.2277-408A>G | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778814 | |||||||
| chr17:44778989 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(132): Show |
199 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.2277-233T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44778989 | |||||||
| chr17:44779082 | T | C | 9 | a0001c0002t0006g0028 a0001c0002t0006g0029 a0001c0002t0006g0131 others(6): Show |
11 | HG01167.hp2 HG01169.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.2277-140T>C | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 25/26 | chr17 | 44779082 | |||||||
| chr17:44779253 | C | T | 1 | a0001c0001t0014g0106 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2294+14C>T | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 26/26 | chr17 | 44779253 | |||||||
| chr17:44779348 | G | A | 1 | a0001c0002t0003g0183 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2294+109G>A | ADAM11 | ENSG00000073670.14 | transcript | ENST00000200557.11 | protein_coding | 26/26 | chr17 | 44779348 |