Item | Value |
---|---|
geneid | 8748 |
ensemblid | ENSG00000134007.5 |
hgncid | 199 |
symbol | ADAM20 |
name | ADAM metallopeptidase domain 20 |
refseq_nuc | NM_003814.5 |
refseq_prot | NP_003805.4 |
ensembl_nuc | ENST00000256389.5 |
ensembl_prot | ENSP00000256389.3 |
mane_status | MANE Select |
chr | chr14 |
start | 70522358 |
end | 70535004 |
strand | - |
ver | v1.2 |
region | chr14:70522358-70535004 |
region5000 | chr14:70517358-70540004 |
regionname0 | ADAM20_chr14_70522358_70535004 |
regionname5000 | ADAM20_chr14_70517358_70540004 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 726 | 380 | 77 | 69 | 182 | 12 | 38 | 138 | ADAM20_chr14_70517358_70540004 | ADAM20 | MAVGE others(721): Show |
chr14 | 70517358 | 70540004 |
a0002 | 0/0 | 726 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | MAVGE others(721): Show |
chr14 | 70517358 | 70540004 |
a0003 | 0/0 | 726 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | ADAM20_chr14_70517358_70540004 | ADAM20 | MAVGE others(721): Show |
chr14 | 70517358 | 70540004 |
a0004 | 0/0 | 726 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | MAVGE others(721): Show |
chr14 | 70517358 | 70540004 |
a0005 | 0/0 | 726 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | MAVGE others(721): Show |
chr14 | 70517358 | 70540004 |
a0006 | 0/0 | 726 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 | MAVGE others(721): Show |
chr14 | 70517358 | 70540004 |
a0007 | 0/0 | 697 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 | MAVGE others(692): Show |
chr14 | 70517358 | 70540004 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2178 | 352 | 66 | 65 | 170 | 11 | 38 | ADAM20_chr14_70517358_70540004 | ADAM20 | ATGGC others(2173): Show |
chr14 | 70517358 | 70540004 | ||
a0001c0002 | 0/0 | 2178 | 26 | 9 | 4 | 12 | 1 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | ATGGC others(2173): Show |
chr14 | 70517358 | 70540004 | ||
a0001c0006 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | ATGGC others(2173): Show |
chr14 | 70517358 | 70540004 | ||
a0001c0010 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | ATGGC others(2173): Show |
chr14 | 70517358 | 70540004 | ||
a0002c0003 | 0/0 | 2178 | 8 | 8 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | ATGGC others(2173): Show |
chr14 | 70517358 | 70540004 | ||
a0003c0004 | 0/0 | 2178 | 6 | 0 | 0 | 6 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | ATGGC others(2173): Show |
chr14 | 70517358 | 70540004 | ||
a0004c0005 | 0/0 | 2178 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | ATGGC others(2173): Show |
chr14 | 70517358 | 70540004 | ||
a0005c0009 | 0/0 | 2178 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | ATGGC others(2173): Show |
chr14 | 70517358 | 70540004 | ||
a0006c0007 | 0/0 | 2178 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | ATGGC others(2173): Show |
chr14 | 70517358 | 70540004 | ||
a0007c0008 | 0/0 | 2216 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | ATGGC others(2211): Show |
chr14 | 70517358 | 70540004 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2784 | 244 | 52 | 57 | 95 | 10 | 28 | ADAM20_chr14_70517358_70540004 | ADAM20 | AGTGT others(2779): Show |
chr14 | 70517358 | 70540004 |
a0001c0001t0002 | 0/0 | 2784 | 98 | 8 | 8 | 74 | 1 | 7 | ADAM20_chr14_70517358_70540004 | ADAM20 | AGTGT others(2779): Show |
chr14 | 70517358 | 70540004 |
a0001c0001t0004 | 0/0 | 2784 | 9 | 6 | 0 | 0 | 0 | 3 | ADAM20_chr14_70517358_70540004 | ADAM20 | AGTGT others(2779): Show |
chr14 | 70517358 | 70540004 |
a0001c0001t0005 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | AGTGT others(2779): Show |
chr14 | 70517358 | 70540004 |
a0001c0002t0003 | 0/0 | 2784 | 26 | 9 | 4 | 12 | 1 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | AGTGT others(2779): Show |
chr14 | 70517358 | 70540004 |
a0001c0006t0002 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | AGTGT others(2779): Show |
chr14 | 70517358 | 70540004 |
a0001c0010t0001 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | AGTGT others(2779): Show |
chr14 | 70517358 | 70540004 |
a0002c0003t0001 | 0/0 | 2784 | 8 | 8 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | AGTGT others(2779): Show |
chr14 | 70517358 | 70540004 |
a0003c0004t0001 | 0/0 | 2784 | 5 | 0 | 0 | 5 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | AGTGT others(2779): Show |
chr14 | 70517358 | 70540004 |
a0003c0004t0002 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | AGTGT others(2779): Show |
chr14 | 70517358 | 70540004 |
a0004c0005t0001 | 0/0 | 2784 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | AGTGT others(2779): Show |
chr14 | 70517358 | 70540004 |
a0005c0009t0001 | 0/0 | 2784 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | AGTGT others(2779): Show |
chr14 | 70517358 | 70540004 |
a0006c0007t0002 | 0/0 | 2784 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | AGTGT others(2779): Show |
chr14 | 70517358 | 70540004 |
a0007c0008t0003 | 0/0 | 2822 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | AGTGT others(2817): Show |
chr14 | 70517358 | 70540004 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 85 | 4 | 15 | 50 | 4 | 11 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0003 | 0/0 | 32 | 2 | 9 | 15 | 0 | 6 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0006 | 0/1 | 19 | 0 | 12 | 0 | 4 | 2 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0007 | 0/0 | 11 | 8 | 2 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0008 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0009 | 0/0 | 8 | 1 | 3 | 3 | 1 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0010 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0021 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0002g0002 | 0/0 | 56 | 1 | 7 | 42 | 1 | 5 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0002g0005 | 0/0 | 22 | 0 | 1 | 20 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0002g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0002g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0004g0012 | 0/0 | 4 | 1 | 0 | 0 | 0 | 3 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0004g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0001t0005g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0002t0003g0004 | 0/0 | 24 | 9 | 3 | 11 | 1 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0002t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0006t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0001c0010t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0002c0003t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0002c0003t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0002c0003t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0002c0003t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0002c0003t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0003c0004t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0003c0004t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0003c0004t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0004c0005t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0005c0009t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0006c0007t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
a0007c0008t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0003 | g0004 | EUR | GBR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00642 | hp1 | a0004 | c0005 | t0001 | g0020 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00733 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00735 | hp2 | a0004 | c0005 | t0001 | g0020 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01074 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01099 | hp2 | a0004 | c0005 | t0001 | g0020 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01192 | hp2 | a0001 | c0002 | t0003 | g0092 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01346 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0057 | EUR | IBS | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01884 | hp1 | a0002 | c0003 | t0001 | g0034 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01884 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02145 | hp2 | a0002 | c0003 | t0001 | g0036 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02258 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02258 | hp2 | a0002 | c0003 | t0001 | g0086 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02451 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02622 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02723 | hp1 | a0002 | c0003 | t0001 | g0034 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0059 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02896 | hp1 | a0005 | c0009 | t0001 | g0051 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02970 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03041 | hp1 | a0002 | c0003 | t0001 | g0036 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03098 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03209 | hp2 | a0001 | c0006 | t0002 | g0048 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03579 | hp2 | a0002 | c0003 | t0001 | g0087 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | STU | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | STU | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | BEB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0012 | SAS | STU | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18940 | hp1 | a0001 | c0002 | t0003 | g0093 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18942 | hp2 | a0003 | c0004 | t0001 | g0019 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18948 | hp1 | a0006 | c0007 | t0002 | g0049 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18953 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18956 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18963 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18965 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18967 | hp2 | a0007 | c0008 | t0003 | g0091 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18969 | hp1 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18973 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18975 | hp2 | a0003 | c0004 | t0001 | g0031 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18981 | hp1 | a0003 | c0004 | t0001 | g0019 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18981 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18984 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18985 | hp2 | a0003 | c0004 | t0001 | g0019 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18988 | hp2 | a0003 | c0004 | t0001 | g0031 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18989 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18995 | hp1 | a0003 | c0004 | t0002 | g0041 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19030 | hp1 | a0001 | c0002 | t0003 | g0004 | AFR | LWK | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19030 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | LWK | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0055 | AFR | LWK | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19058 | hp2 | a0001 | c0001 | t0005 | g0069 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19066 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19086 | hp2 | a0001 | c0002 | t0003 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA19240 | hp2 | a0002 | c0003 | t0001 | g0035 | AFR | YRI | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ASW | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ASW | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02109 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG02559 | hp2 | a0002 | c0003 | t0001 | g0035 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | USA | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA21309 | hp1 | a0001 | c0010 | t0001 | g0070 | AFR | LWK | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0006 | REF | REF | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | ADAM20_chr14_70517358_70540004 | ADAM20 | chr14 | 70517358 | 70540004 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:70522609 | G | A | 1 | a0006 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.2149C>T | p.Arg717Cys | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 2533/2784 | 2149/2181 | 717/726 | chr14 | 70522609 | |||
chr14:70522703 | T | TAATCCTT others(31): Show |
1 | a0007 | 1 | NA18967.hp2 | frameshift_variant | HIGH | c.2017_2054dupGATAGT others(32): Show |
p.Asn686fs | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 2438/2784 | 2054/2181 | 685/726 | chr14 | 70522703 | |||
chr14:70523134 | C | T | 1 | a0003 | 6 | NA18942.hp2 NA18975.hp2 NA18981.hp1 others(3): Show |
missense_variant | MODERATE | c.1624G>A | p.Gly542Ser | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 2008/2784 | 1624/2181 | 542/726 | chr14 | 70523134 | |||
chr14:70523230 | T | C | 1 | a0002 | 8 | HG01884.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
missense_variant | MODERATE | c.1528A>G | p.Asn510Asp | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 1912/2784 | 1528/2181 | 510/726 | chr14 | 70523230 | |||
chr14:70523238 | G | C | 1 | a0004 | 3 | HG00642.hp1 HG00735.hp2 HG01099.hp2 |
missense_variant | MODERATE | c.1520C>G | p.Thr507Arg | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 1904/2784 | 1520/2181 | 507/726 | chr14 | 70523238 | |||
chr14:70523882 | T | G | 1 | a0005 | 1 | HG02896.hp1 | missense_variant | MODERATE | c.876A>C | p.Gln292His | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 1260/2784 | 876/2181 | 292/726 | chr14 | 70523882 | |||
chr14:70524933 | A | C | 3 | a0001 a0003 a0006 |
101 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(98): Show |
splice_region_variant | LOW | c.-176T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | chr14 | 70524933 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:70522676 | C | G | 1 | a0001c0006 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.2082G>C | p.Leu694Leu | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 2466/2784 | 2082/2181 | 694/726 | chr14 | 70522676 | |||
chr14:70523045 | T | C | 2 | a0001c0002 a0007c0008 |
27 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
synonymous_variant | LOW | c.1713A>G | p.Val571Val | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 2097/2784 | 1713/2181 | 571/726 | chr14 | 70523045 | |||
chr14:70523681 | G | A | 2 | a0001c0002 a0007c0008 |
27 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
synonymous_variant | LOW | c.1077C>T | p.Cys359Cys | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 1461/2784 | 1077/2181 | 359/726 | chr14 | 70523681 | |||
chr14:70524284 | T | C | 1 | a0001c0010 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.474A>G | p.Val158Val | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 858/2784 | 474/2181 | 158/726 | chr14 | 70524284 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:70522368 | A | C | 1 | a0001c0001t0005 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*209T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 209 | chr14 | 70522368 | ||||||
chr14:70522458 | C | T | 1 | a0001c0001t0004 | 9 | HG02723.hp2 HG02818.hp2 HG02895.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*119G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 119 | chr14 | 70522458 | ||||||
chr14:70534947 | G | C | 2 | a0001c0002t0003 a0007c0008t0003 |
27 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-327C>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/2 | chr14 | 70534947 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:70524971 | G | T | 1 | a0001c0001t0004g0055 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-176-38C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70524971 | |||||||
chr14:70524988 | A | G | 5 | a0002c0003t0001g0034 a0002c0003t0001g0035 a0002c0003t0001g0036 others(2): Show |
8 | HG01884.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-176-55T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70524988 | |||||||
chr14:70525089 | A | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0030 |
10 | HG00280.hp1 HG00738.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-176-156T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525089 | |||||||
chr14:70525089 | A | T | 1 | a0001c0001t0004g0012 | 4 | HG02895.hp1 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-156T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525089 | |||||||
chr14:70525150 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-176-217G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525150 | |||||||
chr14:70525216 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0030 |
10 | HG00280.hp1 HG00738.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-176-283A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525216 | |||||||
chr14:70525286 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-176-353T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525286 | |||||||
chr14:70525517 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-176-584C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525517 | |||||||
chr14:70525540 | A | G | 5 | a0001c0001t0001g0085 a0001c0002t0003g0004 a0001c0002t0003g0092 others(2): Show |
28 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.-176-607T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525540 | |||||||
chr14:70525703 | C | T | 1 | a0001c0001t0004g0012 | 4 | HG02895.hp1 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-770G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525703 | |||||||
chr14:70525770 | TC | T | 3 | a0001c0001t0004g0022 a0001c0001t0004g0055 a0001c0001t0004g0059 |
5 | HG02723.hp2 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176-838delG | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525770 | |||||||
chr14:70525857 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-176-924C>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525857 | |||||||
chr14:70525898 | A | C | 2 | a0001c0001t0001g0089 a0001c0001t0004g0012 |
5 | HG02145.hp1 HG02895.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176-965T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525898 | |||||||
chr14:70525943 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0004g0012 |
5 | HG02145.hp1 HG02895.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176-1010G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525943 | |||||||
chr14:70525992 | T | C | 30 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0018 others(27): Show |
132 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.-176-1059A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525992 | |||||||
chr14:70526496 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-176-1563A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526496 | |||||||
chr14:70526545 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-176-1612C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526545 | |||||||
chr14:70526602 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-176-1669T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526602 | |||||||
chr14:70526699 | G | A | 1 | a0002c0003t0001g0087 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-176-1766C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526699 | |||||||
chr14:70526772 | G | T | 4 | a0002c0003t0001g0035 a0002c0003t0001g0036 a0002c0003t0001g0086 others(1): Show |
6 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-176-1839C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526772 | |||||||
chr14:70526800 | A | G | 1 | a0001c0001t0001g0014 | 4 | NA18957.hp2 NA18971.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-1867T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526800 | |||||||
chr14:70526854 | T | G | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1921A>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526854 | |||||||
chr14:70526855 | G | A | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1922C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526855 | |||||||
chr14:70526863 | C | A | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1930G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526863 | |||||||
chr14:70526869 | C | A | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1936G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526869 | |||||||
chr14:70526874 | A | T | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1941T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526874 | |||||||
chr14:70526875 | G | C | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1942C>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526875 | |||||||
chr14:70526894 | T | G | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1961A>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526894 | |||||||
chr14:70526906 | A | G | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1973T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526906 | |||||||
chr14:70526907 | G | C | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1974C>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526907 | |||||||
chr14:70526908 | G | T | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1975C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526908 | |||||||
chr14:70526916 | C | T | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1983G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526916 | |||||||
chr14:70526917 | T | C | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1984A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526917 | |||||||
chr14:70526918 | G | T | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1985C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526918 | |||||||
chr14:70526922 | A | T | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1989T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526922 | |||||||
chr14:70526933 | G | T | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2000C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526933 | |||||||
chr14:70526935 | G | T | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2002C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526935 | |||||||
chr14:70526939 | C | A | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2006G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526939 | |||||||
chr14:70526940 | A | C | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2007T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526940 | |||||||
chr14:70526941 | A | T | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2008T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526941 | |||||||
chr14:70526942 | C | A | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2009G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526942 | |||||||
chr14:70526942 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-176-2009G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526942 | |||||||
chr14:70526998 | A | T | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2065T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526998 | |||||||
chr14:70527000 | G | A | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2067C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527000 | |||||||
chr14:70527005 | T | A | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2072A>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527005 | |||||||
chr14:70527019 | C | A | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2086G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527019 | |||||||
chr14:70527033 | A | T | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2100T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527033 | |||||||
chr14:70527040 | T | A | 1 | a0001c0001t0002g0047 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2107A>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527040 | |||||||
chr14:70527238 | A | T | 4 | a0001c0002t0003g0004 a0001c0002t0003g0092 a0001c0002t0003g0093 others(1): Show |
27 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-176-2305T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527238 | |||||||
chr14:70527323 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-176-2390C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527323 | |||||||
chr14:70527397 | C | G | 2 | a0001c0001t0001g0067 a0001c0001t0001g0079 |
2 | HG03654.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-176-2464G>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527397 | |||||||
chr14:70527516 | T | C | 3 | a0001c0001t0001g0027 a0001c0001t0001g0058 a0001c0001t0001g0074 |
4 | HG01243.hp1 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-2583A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527516 | |||||||
chr14:70527640 | A | G | 4 | a0001c0001t0004g0012 a0001c0001t0004g0022 a0001c0001t0004g0055 others(1): Show |
9 | HG02723.hp2 HG02818.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-176-2707T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527640 | |||||||
chr14:70527732 | TG | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0024 others(2): Show |
19 | HG01243.hp2 HG01433.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-176-2800delC | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527732 | |||||||
chr14:70527763 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-176-2830G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527763 | |||||||
chr14:70527861 | T | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0024 others(2): Show |
19 | HG01243.hp2 HG01433.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-176-2928A>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527861 | |||||||
chr14:70527894 | C | T | 56 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(53): Show |
208 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.-176-2961G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527894 | |||||||
chr14:70527913 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0030 |
10 | HG00280.hp1 HG00738.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-176-2980A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527913 | |||||||
chr14:70528043 | T | G | 1 | a0001c0001t0002g0038 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-176-3110A>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528043 | |||||||
chr14:70528048 | T | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0083 |
7 | HG01109.hp2 HG01175.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.-176-3115A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528048 | |||||||
chr14:70528055 | T | A | 1 | a0002c0003t0001g0087 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-176-3122A>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528055 | |||||||
chr14:70528105 | G | T | 47 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(44): Show |
188 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.-176-3172C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528105 | |||||||
chr14:70528116 | A | G | 2 | a0001c0001t0002g0040 a0001c0001t0002g0044 |
2 | NA18952.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-176-3183T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528116 | |||||||
chr14:70528198 | A | G | 4 | a0001c0002t0003g0004 a0001c0002t0003g0092 a0001c0002t0003g0093 others(1): Show |
27 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-176-3265T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528198 | |||||||
chr14:70528220 | T | C | 1 | a0001c0002t0003g0093 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-176-3287A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528220 | |||||||
chr14:70528280 | G | A | 1 | a0007c0008t0003g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-176-3347C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528280 | |||||||
chr14:70528281 | A | G | 1 | a0007c0008t0003g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-176-3348T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528281 | |||||||
chr14:70528282 | G | C | 1 | a0001c0001t0001g0026 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-176-3349C>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528282 | |||||||
chr14:70528282 | G | T | 1 | a0007c0008t0003g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-176-3349C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528282 | |||||||
chr14:70528413 | CCTTTTCA others(4): Show |
C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0030 |
10 | HG00280.hp1 HG00738.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-176-3491_-176-348 others(15): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528413 | |||||||
chr14:70528525 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-176-3592C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528525 | |||||||
chr14:70528582 | G | A | 1 | a0004c0005t0001g0020 | 3 | HG00642.hp1 HG00735.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.-176-3649C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528582 | |||||||
chr14:70528632 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0030 |
10 | HG00280.hp1 HG00738.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-176-3699T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528632 | |||||||
chr14:70528677 | A | G | 19 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0013 others(16): Show |
101 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.-176-3744T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528677 | |||||||
chr14:70528929 | CAA | C | 2 | a0001c0001t0001g0089 a0001c0001t0004g0012 |
5 | HG02145.hp1 HG02895.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176-3998_-176-399 others(6): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528929 | |||||||
chr14:70528985 | T | C | 1 | a0005c0009t0001g0051 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-176-4052A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528985 | |||||||
chr14:70528988 | A | T | 1 | a0001c0002t0003g0092 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-176-4055T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528988 | |||||||
chr14:70529059 | G | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0024 others(6): Show |
24 | HG01243.hp2 HG01433.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.-176-4126C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529059 | |||||||
chr14:70529108 | T | C | 1 | a0005c0009t0001g0051 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-176-4175A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529108 | |||||||
chr14:70529167 | T | C | 45 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0018 others(42): Show |
178 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.-176-4234A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529167 | |||||||
chr14:70529194 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-176-4261G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529194 | |||||||
chr14:70529214 | C | A | 1 | a0007c0008t0003g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-176-4281G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529214 | |||||||
chr14:70529215 | A | T | 1 | a0007c0008t0003g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-176-4282T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529215 | |||||||
chr14:70529350 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-176-4417A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529350 | |||||||
chr14:70529388 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0088 |
7 | HG00621.hp1 HG01069.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.-176-4455A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529388 | |||||||
chr14:70529544 | T | C | 4 | a0001c0001t0001g0027 a0001c0001t0001g0058 a0001c0001t0001g0073 others(1): Show |
5 | HG01243.hp1 HG02976.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176-4611A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529544 | |||||||
chr14:70529764 | G | A | 1 | a0001c0001t0004g0012 | 4 | HG02895.hp1 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-4831C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529764 | |||||||
chr14:70529835 | C | A | 1 | a0007c0008t0003g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-176-4902G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529835 | |||||||
chr14:70529851 | A | T | 35 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0018 others(32): Show |
140 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.-176-4918T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529851 | |||||||
chr14:70529865 | T | C | 2 | a0001c0001t0004g0022 a0001c0001t0004g0059 |
4 | HG02723.hp2 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+4932A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529865 | |||||||
chr14:70529913 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-177+4884A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529913 | |||||||
chr14:70529932 | C | T | 3 | a0001c0001t0001g0026 a0001c0001t0001g0053 a0001c0001t0001g0054 |
4 | HG02615.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177+4865G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529932 | |||||||
chr14:70529938 | T | G | 1 | a0007c0008t0003g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+4859A>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529938 | |||||||
chr14:70529939 | G | T | 1 | a0007c0008t0003g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+4858C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529939 | |||||||
chr14:70529940 | T | A | 1 | a0007c0008t0003g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+4857A>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529940 | |||||||
chr14:70530021 | G | A | 1 | a0001c0001t0004g0012 | 4 | HG02895.hp1 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+4776C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530021 | |||||||
chr14:70530053 | C | T | 1 | a0001c0001t0004g0055 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-177+4744G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530053 | |||||||
chr14:70530064 | C | A | 1 | a0002c0003t0001g0087 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-177+4733G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530064 | |||||||
chr14:70530132 | T | A | 1 | a0001c0001t0001g0026 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-177+4665A>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530132 | |||||||
chr14:70530183 | T | C | 1 | a0001c0001t0002g0042 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-177+4614A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530183 | |||||||
chr14:70530249 | G | A | 1 | a0001c0001t0002g0043 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-177+4548C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530249 | |||||||
chr14:70530436 | A | G | 1 | a0001c0001t0002g0046 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-177+4361T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530436 | |||||||
chr14:70530472 | T | G | 1 | a0007c0008t0003g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+4325A>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530472 | |||||||
chr14:70530579 | G | A | 1 | a0001c0001t0002g0017 | 3 | HG02451.hp2 HG02809.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+4218C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530579 | |||||||
chr14:70530591 | G | A | 2 | a0001c0001t0002g0045 a0001c0001t0002g0050 |
2 | NA18946.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.-177+4206C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530591 | |||||||
chr14:70530690 | A | C | 1 | a0001c0001t0001g0001 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-177+4107T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530690 | |||||||
chr14:70530712 | C | T | 1 | a0005c0009t0001g0051 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-177+4085G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530712 | |||||||
chr14:70530843 | A | C | 1 | a0007c0008t0003g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+3954T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530843 | |||||||
chr14:70530845 | A | C | 1 | a0007c0008t0003g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+3952T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530845 | |||||||
chr14:70530846 | G | T | 1 | a0007c0008t0003g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+3951C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530846 | |||||||
chr14:70530851 | G | T | 1 | a0001c0001t0002g0002 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-177+3946C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530851 | |||||||
chr14:70530855 | A | C | 1 | a0007c0008t0003g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+3942T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530855 | |||||||
chr14:70530856 | C | G | 1 | a0007c0008t0003g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+3941G>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530856 | |||||||
chr14:70530857 | A | C | 1 | a0007c0008t0003g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+3940T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530857 | |||||||
chr14:70530859 | A | T | 1 | a0007c0008t0003g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+3938T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530859 | |||||||
chr14:70530865 | A | T | 1 | a0007c0008t0003g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+3932T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530865 | |||||||
chr14:70530965 | G | C | 38 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0018 others(35): Show |
146 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.-177+3832C>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530965 | |||||||
chr14:70531071 | T | C | 4 | a0001c0002t0003g0004 a0001c0002t0003g0092 a0001c0002t0003g0093 others(1): Show |
27 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-177+3726A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531071 | |||||||
chr14:70531190 | C | G | 3 | a0001c0001t0004g0022 a0001c0001t0004g0055 a0001c0001t0004g0059 |
5 | HG02723.hp2 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-177+3607G>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531190 | |||||||
chr14:70531337 | T | A | 2 | a0002c0003t0001g0035 a0002c0003t0001g0036 |
4 | HG02145.hp2 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177+3460A>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531337 | |||||||
chr14:70531346 | A | G | 3 | a0001c0001t0004g0022 a0001c0001t0004g0055 a0001c0001t0004g0059 |
5 | HG02723.hp2 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-177+3451T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531346 | |||||||
chr14:70531413 | G | C | 1 | a0001c0001t0001g0021 | 3 | HG01074.hp2 HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-177+3384C>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531413 | |||||||
chr14:70531579 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-177+3218G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531579 | |||||||
chr14:70531605 | T | TA | 2 | a0002c0003t0001g0035 a0002c0003t0001g0036 |
4 | HG02145.hp2 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177+3191dupT | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531605 | |||||||
chr14:70531629 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-177+3168C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531629 | |||||||
chr14:70531680 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-177+3117G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531680 | |||||||
chr14:70531685 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-177+3112C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531685 | |||||||
chr14:70531861 | T | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0024 others(2): Show |
19 | HG01243.hp2 HG01433.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-177+2936A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531861 | |||||||
chr14:70531946 | T | C | 1 | a0001c0001t0001g0025 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-177+2851A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531946 | |||||||
chr14:70532015 | A | C | 1 | a0007c0008t0003g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+2782T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532015 | |||||||
chr14:70532033 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-177+2764G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532033 | |||||||
chr14:70532116 | G | A | 38 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0018 others(35): Show |
146 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.-177+2681C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532116 | |||||||
chr14:70532203 | T | C | 2 | a0001c0001t0002g0046 a0001c0001t0002g0047 |
2 | NA18997.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.-177+2594A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532203 | |||||||
chr14:70532231 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0024 others(2): Show |
19 | HG01243.hp2 HG01433.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-177+2566T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532231 | |||||||
chr14:70532257 | T | C | 1 | a0001c0001t0004g0012 | 4 | HG02895.hp1 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+2540A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532257 | |||||||
chr14:70532307 | C | T | 4 | a0001c0002t0003g0004 a0001c0002t0003g0092 a0001c0002t0003g0093 others(1): Show |
27 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-177+2490G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532307 | |||||||
chr14:70532378 | C | A | 38 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0018 others(35): Show |
146 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.-177+2419G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532378 | |||||||
chr14:70532378 | C | G | 2 | a0001c0001t0001g0011 a0001c0001t0001g0032 |
7 | HG02523.hp1 NA18952.hp1 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.-177+2419G>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532378 | |||||||
chr14:70532453 | A | C | 1 | a0001c0001t0004g0012 | 4 | HG02895.hp1 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+2344T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532453 | |||||||
chr14:70532521 | A | C | 16 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0023 others(13): Show |
93 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-177+2276T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532521 | |||||||
chr14:70532534 | T | G | 1 | a0001c0001t0001g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-177+2263A>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532534 | |||||||
chr14:70532589 | C | T | 1 | a0001c0001t0004g0012 | 4 | HG02895.hp1 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+2208G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532589 | |||||||
chr14:70532608 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-177+2189A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532608 | |||||||
chr14:70532672 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0030 |
10 | HG00280.hp1 HG00738.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-177+2125G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532672 | |||||||
chr14:70532760 | T | G | 35 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0018 others(32): Show |
140 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.-177+2037A>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532760 | |||||||
chr14:70532826 | A | C | 1 | a0001c0001t0002g0039 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-177+1971T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532826 | |||||||
chr14:70532885 | A | AAT | 3 | a0001c0001t0004g0022 a0001c0001t0004g0055 a0001c0001t0004g0059 |
5 | HG02723.hp2 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-177+1910_-177+191 others(6): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532885 | |||||||
chr14:70532979 | C | T | 4 | a0001c0002t0003g0004 a0001c0002t0003g0092 a0001c0002t0003g0093 others(1): Show |
27 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-177+1818G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532979 | |||||||
chr14:70533042 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG03710.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-177+1755C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533042 | |||||||
chr14:70533151 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0052 |
5 | HG01433.hp2 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177+1646C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533151 | |||||||
chr14:70533156 | T | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0081 others(2): Show |
25 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.-177+1641A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533156 | |||||||
chr14:70533508 | C | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0024 others(6): Show |
24 | HG01243.hp2 HG01433.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.-177+1289G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533508 | |||||||
chr14:70533716 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-177+1081T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533716 | |||||||
chr14:70533756 | T | A | 1 | a0001c0001t0001g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-177+1041A>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533756 | |||||||
chr14:70533763 | T | TA | 3 | a0001c0001t0001g0009 a0001c0001t0004g0022 a0001c0001t0004g0059 |
12 | HG00280.hp1 HG00738.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.-177+1033_-177+103 others(5): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533763 | |||||||
chr14:70533764 | T | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0004g0022 others(1): Show |
14 | HG00280.hp1 HG00738.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.-177+1033A>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533764 | |||||||
chr14:70533765 | A | T | 1 | a0001c0001t0001g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-177+1032T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533765 | |||||||
chr14:70533776 | A | AC | 2 | a0001c0001t0001g0010 a0001c0001t0001g0088 |
7 | HG00621.hp1 HG01069.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.-177+1020dupG | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533776 | |||||||
chr14:70533848 | T | C | 38 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0018 others(35): Show |
146 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.-177+949A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533848 | |||||||
chr14:70534061 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-177+736G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534061 | |||||||
chr14:70534062 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-177+735C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534062 | |||||||
chr14:70534074 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01081.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-177+723G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534074 | |||||||
chr14:70534082 | C | CA | 12 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0015 others(9): Show |
54 | HG00609.hp2 HG00621.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.-177+714dupT | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534082 | |||||||
chr14:70534082 | C | CAA | 4 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0083 others(1): Show |
6 | HG01257.hp1 HG02071.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-177+713_-177+714d others(4): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534082 | |||||||
chr14:70534082 | CA | C | 5 | a0001c0001t0001g0027 a0001c0001t0001g0056 a0001c0001t0001g0057 others(2): Show |
6 | HG01243.hp1 HG01517.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-177+714delT | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534082 | |||||||
chr14:70534082 | CAAA | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0052 |
6 | HG02559.hp1 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-177+712_-177+714d others(5): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534082 | |||||||
chr14:70534082 | CAAAA | C | 9 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0024 others(6): Show |
29 | HG01069.hp2 HG01243.hp2 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.-177+711_-177+714d others(6): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534082 | |||||||
chr14:70534082 | CAAAAA | C | 12 | a0001c0001t0001g0053 a0001c0001t0002g0005 a0001c0001t0002g0013 others(9): Show |
38 | HG00438.hp2 HG00558.hp2 HG01258.hp2 others(35): Show |
intron_variant | MODIFIER | c.-177+710_-177+714d others(7): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534082 | |||||||
chr14:70534082 | CAAAAAA | C | 8 | a0001c0001t0002g0002 a0001c0001t0002g0037 a0001c0001t0002g0038 others(5): Show |
63 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-177+709_-177+714d others(8): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534082 | |||||||
chr14:70534093 | A | C | 1 | a0001c0001t0001g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-177+704T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534093 | |||||||
chr14:70534104 | AAAAAC | A | 5 | a0001c0001t0001g0026 a0001c0002t0003g0004 a0001c0002t0003g0092 others(2): Show |
23 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.-177+688_-177+692d others(7): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534104 | |||||||
chr14:70534105 | AAAAC | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0088 a0001c0002t0003g0004 |
7 | HG00621.hp1 HG02615.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-177+688_-177+691d others(6): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534105 | |||||||
chr14:70534107 | A | C | 3 | a0001c0001t0001g0001 a0001c0001t0002g0005 a0002c0003t0001g0086 |
4 | HG02258.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+690T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534107 | |||||||
chr14:70534107 | AAC | A | 2 | a0001c0001t0001g0009 a0001c0001t0004g0012 |
9 | HG00738.hp1 HG01106.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-177+688_-177+689d others(4): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534107 | |||||||
chr14:70534109 | C | A | 1 | a0001c0001t0001g0021 | 3 | HG01074.hp2 HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-177+688G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534109 | |||||||
chr14:70534117 | C | G | 1 | a0001c0001t0002g0038 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-177+680G>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534117 | |||||||
chr14:70534125 | C | G | 1 | a0001c0001t0004g0055 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-177+672G>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534125 | |||||||
chr14:70534191 | T | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0053 a0001c0001t0001g0054 |
4 | HG02615.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177+606A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534191 | |||||||
chr14:70534300 | C | G | 38 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0018 others(35): Show |
146 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.-177+497G>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534300 | |||||||
chr14:70534383 | G | A | 42 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0018 others(39): Show |
173 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.-177+414C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534383 | |||||||
chr14:70534505 | C | T | 28 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0024 others(25): Show |
125 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.-177+292G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534505 | |||||||
chr14:70534546 | A | G | 1 | a0001c0001t0002g0037 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-177+251T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534546 | |||||||
chr14:70534716 | A | G | 1 | a0001c0001t0004g0012 | 4 | HG02895.hp1 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+81T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534716 | |||||||
chr14:70534753 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-177+44A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534753 |