Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2051 |
| ensemblid | ENSG00000106123.12 |
| hgncid | 3396 |
| symbol | EPHB6 |
| name | EPH receptor B6 |
| refseq_nuc | NM_004445.6 |
| refseq_prot | NP_004436.4 |
| ensembl_nuc | ENST00000652003.1 |
| ensembl_prot | ENSP00000498670.1 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 142855076 |
| end | 142871093 |
| strand | + |
| ver | v1.2 |
| region | chr7:142855076-142871093 |
| region5000 | chr7:142850076-142876093 |
| regionname0 | EPHB6_chr7_142855076_142871093 |
| regionname5000 | EPHB6_chr7_142850076_142876093 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1021 | 226 | 34 | 58 | 85 | 13 | 35 | 68 | EPHB6_chr7_142850076_142876093 | EPHB6 | MATEG others(1016): Show |
chr7 | 142850076 | 142876093 |
| a0002 | 0/0 | 1023 | 41 | 27 | 7 | 6 | 1 | 0 | 4 | EPHB6_chr7_142850076_142876093 | EPHB6 | MATEG others(1018): Show |
chr7 | 142850076 | 142876093 |
| a0003 | 0/0 | 1022 | 21 | 14 | 3 | 2 | 0 | 2 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | MATEG others(1017): Show |
chr7 | 142850076 | 142876093 |
| a0004 | 0/0 | 1022 | 18 | 16 | 1 | 1 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | MATEG others(1017): Show |
chr7 | 142850076 | 142876093 |
| a0005 | 0/0 | 1021 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | MATEG others(1016): Show |
chr7 | 142850076 | 142876093 |
| a0006 | 0/0 | 1021 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | MATEG others(1016): Show |
chr7 | 142850076 | 142876093 |
| a0007 | 0/0 | 1023 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | MATEG others(1018): Show |
chr7 | 142850076 | 142876093 |
| a0008 | 0/0 | 687 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | MATEG others(682): Show |
chr7 | 142850076 | 142876093 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3063 | 189 | 29 | 45 | 69 | 12 | 33 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3058): Show |
chr7 | 142850076 | 142876093 | ||
| a0001c0004 | 0/0 | 3063 | 16 | 0 | 7 | 9 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3058): Show |
chr7 | 142850076 | 142876093 | ||
| a0001c0007 | 0/0 | 3063 | 3 | 0 | 2 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3058): Show |
chr7 | 142850076 | 142876093 | ||
| a0001c0008 | 0/0 | 3063 | 3 | 3 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3058): Show |
chr7 | 142850076 | 142876093 | ||
| a0001c0009 | 0/0 | 3063 | 3 | 0 | 3 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3058): Show |
chr7 | 142850076 | 142876093 | ||
| a0001c0011 | 0/0 | 3063 | 2 | 0 | 0 | 2 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3058): Show |
chr7 | 142850076 | 142876093 | ||
| a0001c0012 | 0/0 | 3063 | 2 | 0 | 0 | 2 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3058): Show |
chr7 | 142850076 | 142876093 | ||
| a0001c0013 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3058): Show |
chr7 | 142850076 | 142876093 | ||
| a0001c0018 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3058): Show |
chr7 | 142850076 | 142876093 | ||
| a0001c0019 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3058): Show |
chr7 | 142850076 | 142876093 | ||
| a0001c0020 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3058): Show |
chr7 | 142850076 | 142876093 | ||
| a0001c0021 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3058): Show |
chr7 | 142850076 | 142876093 | ||
| a0001c0022 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3058): Show |
chr7 | 142850076 | 142876093 | ||
| a0001c0023 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 1 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3058): Show |
chr7 | 142850076 | 142876093 | ||
| a0001c0024 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3058): Show |
chr7 | 142850076 | 142876093 | ||
| a0002c0002 | 0/0 | 3069 | 40 | 26 | 7 | 6 | 1 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3064): Show |
chr7 | 142850076 | 142876093 | ||
| a0002c0015 | 0/0 | 3069 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3064): Show |
chr7 | 142850076 | 142876093 | ||
| a0003c0005 | 0/0 | 3066 | 11 | 10 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3061): Show |
chr7 | 142850076 | 142876093 | ||
| a0003c0006 | 0/0 | 3066 | 10 | 4 | 2 | 2 | 0 | 2 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3061): Show |
chr7 | 142850076 | 142876093 | ||
| a0004c0003 | 0/0 | 3066 | 17 | 16 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3061): Show |
chr7 | 142850076 | 142876093 | ||
| a0004c0017 | 0/0 | 3066 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3061): Show |
chr7 | 142850076 | 142876093 | ||
| a0005c0010 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3058): Show |
chr7 | 142850076 | 142876093 | ||
| a0006c0025 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3058): Show |
chr7 | 142850076 | 142876093 | ||
| a0007c0014 | 0/0 | 3069 | 1 | 0 | 0 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3064): Show |
chr7 | 142850076 | 142876093 | ||
| a0008c0016 | 0/0 | 3081 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | ATGGC others(3076): Show |
chr7 | 142850076 | 142876093 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3996 | 181 | 25 | 45 | 66 | 12 | 32 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0001c0001t0007 | 0/0 | 3996 | 4 | 4 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0001c0001t0008 | 0/0 | 3996 | 2 | 0 | 0 | 2 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0001c0001t0010 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0001c0001t0011 | 0/0 | 3996 | 1 | 0 | 0 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0001c0004t0001 | 0/0 | 3996 | 16 | 0 | 7 | 9 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0001c0007t0001 | 0/0 | 3996 | 3 | 0 | 2 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0001c0008t0006 | 0/0 | 3996 | 3 | 3 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0001c0009t0001 | 0/0 | 3996 | 3 | 0 | 3 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0001c0011t0001 | 0/0 | 3996 | 2 | 0 | 0 | 2 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0001c0012t0001 | 0/0 | 3996 | 2 | 0 | 0 | 2 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0001c0013t0001 | 0/0 | 3996 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0001c0018t0006 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0001c0019t0001 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0001c0020t0001 | 0/0 | 3996 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0001c0021t0001 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0001c0022t0001 | 0/0 | 3996 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0001c0023t0001 | 0/0 | 3996 | 1 | 0 | 0 | 0 | 1 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0001c0024t0001 | 0/0 | 3996 | 1 | 0 | 0 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0002c0002t0001 | 0/0 | 4002 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3997): Show |
chr7 | 142850076 | 142876093 |
| a0002c0002t0002 | 0/0 | 4001 | 23 | 18 | 4 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3996): Show |
chr7 | 142850076 | 142876093 |
| a0002c0002t0003 | 0/0 | 4001 | 11 | 3 | 2 | 5 | 1 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3996): Show |
chr7 | 142850076 | 142876093 |
| a0002c0002t0005 | 0/0 | 4001 | 5 | 5 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3996): Show |
chr7 | 142850076 | 142876093 |
| a0002c0015t0009 | 0/0 | 4001 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3996): Show |
chr7 | 142850076 | 142876093 |
| a0003c0005t0002 | 0/0 | 3998 | 11 | 10 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3993): Show |
chr7 | 142850076 | 142876093 |
| a0003c0006t0004 | 0/0 | 3999 | 10 | 4 | 2 | 2 | 0 | 2 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3994): Show |
chr7 | 142850076 | 142876093 |
| a0004c0003t0002 | 0/0 | 3998 | 17 | 16 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3993): Show |
chr7 | 142850076 | 142876093 |
| a0004c0017t0003 | 0/0 | 3998 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3993): Show |
chr7 | 142850076 | 142876093 |
| a0005c0010t0001 | 0/0 | 3996 | 2 | 2 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0006c0025t0001 | 0/0 | 3996 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3991): Show |
chr7 | 142850076 | 142876093 |
| a0007c0014t0004 | 0/0 | 4002 | 1 | 0 | 0 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(3997): Show |
chr7 | 142850076 | 142876093 |
| a0008c0016t0004 | 0/0 | 4014 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | GGGCT others(4009): Show |
chr7 | 142850076 | 142876093 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 77 | 8 | 21 | 32 | 5 | 11 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0002 | 0/1 | 13 | 0 | 4 | 6 | 2 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0003 | 0/0 | 14 | 0 | 4 | 6 | 0 | 4 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0004 | 0/0 | 11 | 1 | 4 | 3 | 0 | 3 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0009 | 0/0 | 4 | 1 | 0 | 1 | 0 | 2 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0007g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0008g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0010g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0001t0011g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0004t0001g0001 | 0/0 | 10 | 0 | 6 | 4 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0004t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0004t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0004t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0004t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0007t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0008t0006g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0008t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0009t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0011t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0011t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0012t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0012t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0013t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0018t0006g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0019t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0020t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0021t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0022t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0023t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0001c0024t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0002g0011 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0002g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0003g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0003g0025 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0003g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0005g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0002t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0002c0015t0009g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0003c0005t0002g0006 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0003c0005t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0003c0005t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0003c0005t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0003c0005t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0003c0006t0004g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0003c0006t0004g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0003c0006t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0003c0006t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0003c0006t0004g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0003c0006t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0003c0006t0004g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0004c0003t0002g0005 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0004c0003t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0004c0003t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0004c0003t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0004c0003t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0004c0003t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0004c0003t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0004c0003t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0004c0003t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0004c0003t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0004c0017t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0005c0010t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0006c0025t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0007c0014t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| a0008c0016t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | GBR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00280 | hp1 | a0001 | c0023 | t0001 | g0001 | EUR | FIN | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00642 | hp2 | a0003 | c0005 | t0002 | g0006 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00735 | hp1 | a0004 | c0003 | t0002 | g0081 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG00741 | hp2 | a0001 | c0009 | t0001 | g0001 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01069 | hp1 | a0001 | c0009 | t0001 | g0001 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01070 | hp1 | a0003 | c0006 | t0004 | g0102 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01071 | hp1 | a0001 | c0009 | t0001 | g0001 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01071 | hp2 | a0003 | c0006 | t0004 | g0029 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01099 | hp1 | a0001 | c0013 | t0001 | g0009 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01106 | hp1 | a0002 | c0002 | t0003 | g0091 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01168 | hp1 | a0001 | c0007 | t0001 | g0007 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01169 | hp1 | a0001 | c0007 | t0001 | g0007 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01256 | hp1 | a0002 | c0002 | t0003 | g0093 | AMR | CLM | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0105 | AMR | CLM | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0011 | AMR | CLM | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01496 | hp1 | a0006 | c0025 | t0001 | g0002 | AMR | CLM | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | IBS | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01891 | hp1 | a0004 | c0003 | t0002 | g0079 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01928 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | PEL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01943 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PEL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0011 | AMR | PEL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01981 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PEL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01993 | hp1 | a0001 | c0004 | t0001 | g0061 | AMR | PEL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01993 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | PEL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02004 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | PEL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | KHV | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02055 | hp1 | a0002 | c0002 | t0005 | g0089 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02055 | hp2 | a0004 | c0003 | t0002 | g0084 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02145 | hp1 | a0002 | c0002 | t0005 | g0012 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02165 | hp1 | a0002 | c0002 | t0003 | g0094 | EAS | CDX | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02257 | hp1 | a0001 | c0018 | t0006 | g0086 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02258 | hp1 | a0002 | c0002 | t0005 | g0012 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02280 | hp2 | a0003 | c0006 | t0004 | g0018 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | PEL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02451 | hp1 | a0004 | c0003 | t0002 | g0005 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02451 | hp2 | a0002 | c0002 | t0005 | g0012 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02572 | hp1 | a0002 | c0015 | t0009 | g0087 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02572 | hp2 | a0003 | c0006 | t0004 | g0018 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02602 | hp1 | a0003 | c0006 | t0004 | g0103 | SAS | PJL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02615 | hp2 | a0003 | c0005 | t0002 | g0033 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02622 | hp2 | a0004 | c0003 | t0002 | g0005 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02630 | hp1 | a0003 | c0005 | t0002 | g0006 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0101 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02647 | hp1 | a0004 | c0003 | t0002 | g0005 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02647 | hp2 | a0002 | c0002 | t0003 | g0026 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02698 | hp2 | a0001 | c0024 | t0001 | g0001 | SAS | PJL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02717 | hp2 | a0004 | c0003 | t0002 | g0040 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02723 | hp1 | a0003 | c0006 | t0004 | g0018 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0073 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02818 | hp1 | a0002 | c0002 | t0003 | g0095 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02895 | hp2 | a0005 | c0010 | t0001 | g0019 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02896 | hp2 | a0003 | c0005 | t0002 | g0006 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02897 | hp1 | a0003 | c0005 | t0002 | g0006 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02897 | hp2 | a0005 | c0010 | t0001 | g0019 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | ESN | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02922 | hp2 | a0004 | c0003 | t0002 | g0114 | AFR | ESN | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02965 | hp1 | a0003 | c0005 | t0002 | g0031 | AFR | ESN | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02965 | hp2 | a0002 | c0002 | t0005 | g0012 | AFR | ESN | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02970 | hp2 | a0001 | c0008 | t0006 | g0088 | AFR | ESN | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0028 | AFR | ESN | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03041 | hp1 | a0004 | c0003 | t0002 | g0078 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0108 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0028 | AFR | ESN | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0106 | AFR | ESN | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03195 | hp1 | a0004 | c0003 | t0002 | g0005 | AFR | ESN | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03195 | hp2 | a0001 | c0008 | t0006 | g0024 | AFR | ESN | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03209 | hp1 | a0002 | c0002 | t0003 | g0026 | AFR | MSL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | MSL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0016 | AFR | MSL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03225 | hp2 | a0003 | c0005 | t0002 | g0034 | AFR | MSL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03453 | hp1 | a0003 | c0005 | t0002 | g0006 | AFR | MSL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0072 | AFR | MSL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0045 | AFR | MSL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03486 | hp2 | a0004 | c0003 | t0002 | g0083 | AFR | MSL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03492 | hp2 | a0001 | c0001 | t0011 | g0001 | SAS | PJL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0013 | AFR | ESN | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03516 | hp2 | a0003 | c0005 | t0002 | g0006 | AFR | ESN | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03540 | hp1 | a0004 | c0003 | t0002 | g0005 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03579 | hp1 | a0004 | c0003 | t0002 | g0005 | AFR | MSL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | STU | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03688 | hp2 | a0001 | c0007 | t0001 | g0007 | SAS | STU | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03704 | hp1 | a0003 | c0006 | t0004 | g0110 | SAS | PJL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03831 | hp2 | a0007 | c0014 | t0004 | g0048 | SAS | BEB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | STU | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0096 | AFR | YRI | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18612 | hp2 | a0003 | c0006 | t0004 | g0029 | EAS | CHB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0039 | AFR | YRI | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18940 | hp1 | a0001 | c0011 | t0001 | g0015 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18945 | hp2 | a0002 | c0002 | t0003 | g0017 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18954 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18957 | hp1 | a0002 | c0002 | t0003 | g0025 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18960 | hp2 | a0001 | c0012 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18963 | hp2 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18966 | hp2 | a0001 | c0021 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18974 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18979 | hp2 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18983 | hp1 | a0001 | c0001 | t0010 | g0054 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18984 | hp2 | a0001 | c0004 | t0001 | g0008 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18986 | hp2 | a0001 | c0004 | t0001 | g0008 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18989 | hp1 | a0001 | c0012 | t0001 | g0004 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18990 | hp1 | a0003 | c0006 | t0004 | g0041 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA18997 | hp2 | a0001 | c0022 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19000 | hp1 | a0001 | c0004 | t0001 | g0004 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19010 | hp1 | a0001 | c0011 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19030 | hp1 | a0003 | c0005 | t0002 | g0020 | AFR | LWK | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19030 | hp2 | a0003 | c0006 | t0004 | g0104 | AFR | LWK | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19043 | hp1 | a0001 | c0020 | t0001 | g0112 | AFR | LWK | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19054 | hp1 | a0004 | c0017 | t0003 | g0092 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19055 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19062 | hp1 | a0002 | c0002 | t0003 | g0017 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19079 | hp1 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19082 | hp2 | a0002 | c0002 | t0003 | g0017 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19084 | hp1 | a0001 | c0019 | t0001 | g0010 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19086 | hp2 | a0001 | c0004 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19090 | hp1 | a0001 | c0004 | t0001 | g0053 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19240 | hp1 | a0004 | c0003 | t0002 | g0115 | AFR | YRI | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0100 | AFR | YRI | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0014 | EUR | TSI | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA20752 | hp2 | a0002 | c0002 | t0003 | g0025 | EUR | TSI | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | TSI | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | GIH | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0047 | AMR | CLM | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG01123 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | CLM | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02109 | hp1 | a0004 | c0003 | t0002 | g0005 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0037 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02486 | hp1 | a0004 | c0003 | t0002 | g0082 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02486 | hp2 | a0001 | c0008 | t0006 | g0024 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG02559 | hp2 | a0003 | c0005 | t0002 | g0020 | AFR | ACB | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG03471 | hp2 | a0004 | c0003 | t0002 | g0005 | AFR | MSL | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG06807 | hp1 | a0008 | c0016 | t0004 | g0098 | AFR | USA | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| HG06807 | hp2 | a0001 | c0001 | t0007 | g0090 | AFR | USA | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | USA | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0002 | REF | REF | EPHB6_chr7_142850076_142876093 | EPHB6 | chr7 | 142850076 | 142876093 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:142864252 | G | A | 1 | a0005 | 2 | HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.452G>A | p.Arg151His | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 7/20 | 1193/3999 | 452/3069 | 151/1022 | chr7 | 142864252 | |||
| chr7:142864293 | C | CCCT | 2 | a0002 a0007 |
42 | HG01106.hp1 HG01123.hp1 HG01256.hp1 others(39): Show |
disruptive_inframe_insertion | MODERATE | c.519_521dupCTC | p.Ser174dup | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 7/20 | 1263/3999 | 522/3069 | 174/1022 | INFO_REALIGN_3_PRIME | chr7 | 142864293 | ||
| chr7:142864293 | CCCT | C | 3 | a0001 a0005 a0006 |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
disruptive_inframe_deletion | MODERATE | c.519_521delCTC | p.Ser174del | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 7/20 | 1260/3999 | 519/3069 | 173/1022 | INFO_REALIGN_3_PRIME | chr7 | 142864293 | ||
| chr7:142865497 | G | GGCTTCTG others(8): Show |
1 | a0008 | 1 | HG06807.hp1 | conservative_inframe_insertion | MODERATE | c.976_990dupTCTGCTGG others(7): Show |
p.Ser326_Ala330dup | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 8/20 | 1732/3999 | 991/3069 | 331/1022 | INFO_REALIGN_3_PRIME | chr7 | 142865497 | ||
| chr7:142865498 | G | T | 5 | a0001 a0002 a0004 others(2): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
missense_variant | MODERATE | c.973G>T | p.Ala325Ser | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 8/20 | 1714/3999 | 973/3069 | 325/1022 | chr7 | 142865498 | |||
| chr7:142865523 | C | T | 1 | a0001 | 3 | HG01168.hp1 HG01169.hp1 HG03688.hp2 |
missense_variant | MODERATE | c.998C>T | p.Ser333Leu | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 8/20 | 1739/3999 | 998/3069 | 333/1022 | chr7 | 142865523 | |||
| chr7:142866073 | G | A | 1 | a0002 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1219G>A | p.Val407Met | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 9/20 | 1960/3999 | 1219/3069 | 407/1022 | chr7 | 142866073 | |||
| chr7:142866247 | A | G | 1 | a0001 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.1393A>G | p.Asn465Asp | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 9/20 | 2134/3999 | 1393/3069 | 465/1022 | chr7 | 142866247 | |||
| chr7:142866514 | G | A | 1 | a0001 | 2 | NA18960.hp2 NA18989.hp1 |
missense_variant | MODERATE | c.1496G>A | p.Ser499Asn | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 10/20 | 2237/3999 | 1496/3069 | 499/1022 | chr7 | 142866514 | |||
| chr7:142867052 | C | G | 1 | a0001 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.1734C>G | p.Phe578Leu | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 11/20 | 2475/3999 | 1734/3069 | 578/1022 | chr7 | 142867052 | |||
| chr7:142868297 | A | C | 1 | a0008 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1975A>C | p.Ile659Leu | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 14/20 | 2716/3999 | 1975/3069 | 659/1022 | chr7 | 142868297 | |||
| chr7:142868304 | A | G | 1 | a0008 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1982A>G | p.Glu661Gly | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 14/20 | 2723/3999 | 1982/3069 | 661/1022 | chr7 | 142868304 | |||
| chr7:142868306 | C | A | 1 | a0008 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1984C>A | p.Leu662Ile | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 14/20 | 2725/3999 | 1984/3069 | 662/1022 | chr7 | 142868306 | |||
| chr7:142868315 | G | A | 1 | a0008 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1993G>A | p.Glu665Lys | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 14/20 | 2734/3999 | 1993/3069 | 665/1022 | chr7 | 142868315 | |||
| chr7:142868330 | T | G | 1 | a0008 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.2008T>G | p.Tyr670Asp | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 14/20 | 2749/3999 | 2008/3069 | 670/1022 | chr7 | 142868330 | |||
| chr7:142868500 | G | T | 1 | a0008 | 1 | HG06807.hp1 | stop_gained | HIGH | c.2047G>T | p.Gly683* | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 15/20 | 2788/3999 | 2047/3069 | 683/1022 | chr7 | 142868500 | |||
| chr7:142868978 | G | A | 1 | a0006 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.2291G>A | p.Arg764Gln | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 16/20 | 3032/3999 | 2291/3069 | 764/1022 | chr7 | 142868978 | |||
| chr7:142870891 | C | T | 1 | a0001 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.3056C>T | p.Ser1019Leu | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 20/20 | 3797/3999 | 3056/3069 | 1019/1022 | chr7 | 142870891 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:142863989 | C | T | 1 | a0001c0009 | 3 | HG00741.hp2 HG01069.hp1 HG01071.hp1 |
synonymous_variant | LOW | c.189C>T | p.Asp63Asp | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 7/20 | 930/3999 | 189/3069 | 63/1022 | chr7 | 142863989 | |||
| chr7:142864028 | T | C | 1 | a0001c0013 | 1 | HG01099.hp1 | synonymous_variant | LOW | c.228T>C | p.His76His | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 7/20 | 969/3999 | 228/3069 | 76/1022 | chr7 | 142864028 | |||
| chr7:142864253 | C | T | 1 | a0003c0005 | 11 | HG00642.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
synonymous_variant | LOW | c.453C>T | p.Arg151Arg | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 7/20 | 1194/3999 | 453/3069 | 151/1022 | chr7 | 142864253 | |||
| chr7:142864295 | C | A | 1 | a0003c0005 | 11 | HG00642.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
synonymous_variant | LOW | c.495C>A | p.Pro165Pro | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 7/20 | 1236/3999 | 495/3069 | 165/1022 | chr7 | 142864295 | |||
| chr7:142864325 | T | C | 1 | a0001c0011 | 2 | NA18940.hp1 NA19010.hp1 |
synonymous_variant | LOW | c.525T>C | p.Ser175Ser | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 7/20 | 1266/3999 | 525/3069 | 175/1022 | chr7 | 142864325 | |||
| chr7:142864367 | G | A | 1 | a0001c0007 | 3 | HG01168.hp1 HG01169.hp1 HG03688.hp2 |
synonymous_variant | LOW | c.567G>A | p.Gln189Gln | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 7/20 | 1308/3999 | 567/3069 | 189/1022 | chr7 | 142864367 | |||
| chr7:142864424 | C | T | 1 | a0006c0025 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.624C>T | p.Arg208Arg | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 7/20 | 1365/3999 | 624/3069 | 208/1022 | chr7 | 142864424 | |||
| chr7:142864649 | C | T | 1 | a0001c0008 | 3 | HG02486.hp2 HG02970.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.849C>T | p.Pro283Pro | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 7/20 | 1590/3999 | 849/3069 | 283/1022 | chr7 | 142864649 | |||
| chr7:142865545 | C | T | 1 | a0001c0004 | 16 | HG01123.hp2 HG01928.hp2 HG01943.hp1 others(13): Show |
synonymous_variant | LOW | c.1020C>T | p.His340His | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 8/20 | 1761/3999 | 1020/3069 | 340/1022 | chr7 | 142865545 | |||
| chr7:142866111 | C | T | 1 | a0001c0024 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.1257C>T | p.Ser419Ser | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 9/20 | 1998/3999 | 1257/3069 | 419/1022 | chr7 | 142866111 | |||
| chr7:142866914 | C | T | 1 | a0001c0022 | 1 | NA18997.hp2 | synonymous_variant | LOW | c.1596C>T | p.Asp532Asp | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 11/20 | 2337/3999 | 1596/3069 | 532/1022 | chr7 | 142866914 | |||
| chr7:142867630 | A | G | 22 | a0001c0001 a0001c0004 a0001c0007 others(19): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
synonymous_variant | LOW | c.1773A>G | p.Pro591Pro | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 12/20 | 2514/3999 | 1773/3069 | 591/1022 | chr7 | 142867630 | |||
| chr7:142868021 | A | G | 22 | a0001c0001 a0001c0004 a0001c0007 others(19): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
synonymous_variant | LOW | c.1890A>G | p.Thr630Thr | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 13/20 | 2631/3999 | 1890/3069 | 630/1022 | chr7 | 142868021 | |||
| chr7:142868311 | C | A | 1 | a0008c0016 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.1989C>A | p.Ala663Ala | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 14/20 | 2730/3999 | 1989/3069 | 663/1022 | chr7 | 142868311 | |||
| chr7:142868616 | C | T | 1 | a0004c0003 | 17 | HG00735.hp1 HG01891.hp1 HG02055.hp2 others(14): Show |
synonymous_variant | LOW | c.2163C>T | p.Ala721Ala | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 15/20 | 2904/3999 | 2163/3069 | 721/1022 | chr7 | 142868616 | |||
| chr7:142868700 | G | A | 1 | a0001c0018 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.2247G>A | p.Thr749Thr | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 15/20 | 2988/3999 | 2247/3069 | 749/1022 | chr7 | 142868700 | |||
| chr7:142869075 | G | A | 1 | a0001c0019 | 1 | NA19084.hp1 | synonymous_variant | LOW | c.2388G>A | p.Ser796Ser | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 16/20 | 3129/3999 | 2388/3069 | 796/1022 | chr7 | 142869075 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:142855114 | G | A | 2 | a0002c0002t0003 a0004c0017t0003 |
12 | HG01106.hp1 HG01256.hp1 HG02165.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-703G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/20 | 8114 | chr7 | 142855114 | ||||||
| chr7:142855157 | C | A | 1 | a0002c0002t0005 | 5 | HG02055.hp1 HG02145.hp1 HG02258.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-660C>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/20 | 8071 | chr7 | 142855157 | ||||||
| chr7:142855211 | G | C | 5 | a0001c0001t0007 a0001c0008t0006 a0001c0018t0006 others(2): Show |
14 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-606G>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/20 | 8017 | chr7 | 142855211 | ||||||
| chr7:142855241 | T | A | 5 | a0001c0001t0007 a0001c0008t0006 a0001c0018t0006 others(2): Show |
14 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-576T>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/20 | 7987 | chr7 | 142855241 | ||||||
| chr7:142855246 | G | A | 5 | a0001c0001t0007 a0001c0008t0006 a0001c0018t0006 others(2): Show |
14 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-571G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/20 | 7982 | chr7 | 142855246 | ||||||
| chr7:142855352 | G | C | 1 | a0001c0001t0010 | 1 | NA18983.hp1 | 5_prime_UTR_variant | MODIFIER | c.-465G>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/20 | 7876 | chr7 | 142855352 | ||||||
| chr7:142855372 | C | A | 1 | a0001c0001t0011 | 1 | HG03492.hp2 | 5_prime_UTR_variant | MODIFIER | c.-445C>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/20 | 7856 | chr7 | 142855372 | ||||||
| chr7:142861133 | A | G | 29 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0008 others(26): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
5_prime_UTR_variant | MODIFIER | c.-350A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 2/20 | 2095 | chr7 | 142861133 | ||||||
| chr7:142862078 | C | A | 2 | a0001c0008t0006 a0001c0018t0006 |
4 | HG02257.hp1 HG02486.hp2 HG02970.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-235C>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 3/20 | 1150 | chr7 | 142862078 | ||||||
| chr7:142863183 | G | A | 1 | a0001c0001t0008 | 2 | NA18979.hp2 NA19055.hp1 |
5_prime_UTR_variant | MODIFIER | c.-45G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 5/20 | 45 | chr7 | 142863183 | ||||||
| chr7:142871017 | TC | T | 7 | a0002c0002t0002 a0002c0002t0003 a0002c0002t0005 others(4): Show |
69 | HG00642.hp2 HG00735.hp1 HG01106.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*116delC | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 20/20 | 116 | INFO_REALIGN_3_PRIME | chr7 | 142871017 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:142855480 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-432+95T>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142855480 | |||||||
| chr7:142855561 | G | A | 6 | a0001c0001t0001g0032 a0003c0005t0002g0006 a0003c0005t0002g0020 others(3): Show |
12 | HG00642.hp2 HG02258.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-432+176G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142855561 | |||||||
| chr7:142855886 | C | T | 8 | a0002c0002t0003g0017 a0002c0002t0003g0025 a0002c0002t0003g0026 others(5): Show |
12 | HG01106.hp1 HG01256.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.-432+501C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142855886 | |||||||
| chr7:142855933 | T | A | 1 | a0002c0002t0002g0096 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-432+548T>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142855933 | |||||||
| chr7:142855955 | G | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-432+570G>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142855955 | |||||||
| chr7:142856027 | T | C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(11): Show |
30 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.-432+642T>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142856027 | |||||||
| chr7:142856121 | C | T | 8 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0008t0006g0024 others(5): Show |
14 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-432+736C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142856121 | |||||||
| chr7:142856383 | A | G | 11 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(8): Show |
27 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(24): Show |
intron_variant | MODIFIER | c.-432+998A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142856383 | |||||||
| chr7:142856516 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(102): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-432+1131A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142856516 | |||||||
| chr7:142856558 | A | G | 8 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0008t0006g0024 others(5): Show |
14 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-432+1173A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142856558 | |||||||
| chr7:142856617 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-432+1232A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142856617 | |||||||
| chr7:142856665 | C | T | 16 | a0001c0001t0001g0032 a0001c0001t0001g0080 a0003c0005t0002g0006 others(13): Show |
29 | HG00642.hp2 HG00735.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.-432+1280C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142856665 | |||||||
| chr7:142856775 | G | A | 1 | a0002c0002t0002g0045 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-432+1390G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142856775 | |||||||
| chr7:142856861 | A | G | 9 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0008t0006g0024 others(6): Show |
15 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-432+1476A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142856861 | |||||||
| chr7:142856864 | T | A | 16 | a0001c0001t0001g0032 a0001c0001t0001g0080 a0003c0005t0002g0006 others(13): Show |
29 | HG00642.hp2 HG00735.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.-432+1479T>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142856864 | |||||||
| chr7:142856930 | A | G | 2 | a0001c0001t0001g0111 a0001c0020t0001g0112 |
2 | HG02622.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-432+1545A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142856930 | |||||||
| chr7:142857050 | C | T | 1 | a0001c0001t0007g0090 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-432+1665C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142857050 | |||||||
| chr7:142857083 | G | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(102): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-432+1698G>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142857083 | |||||||
| chr7:142857114 | G | T | 8 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0008t0006g0024 others(5): Show |
14 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-432+1729G>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142857114 | |||||||
| chr7:142857141 | T | C | 8 | a0001c0001t0007g0016 a0001c0001t0007g0090 a0001c0008t0006g0024 others(5): Show |
14 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-432+1756T>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142857141 | |||||||
| chr7:142857157 | C | T | 1 | a0002c0002t0002g0039 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-432+1772C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142857157 | |||||||
| chr7:142857245 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-432+1860G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142857245 | |||||||
| chr7:142857320 | G | A | 1 | a0002c0002t0003g0091 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-432+1935G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142857320 | |||||||
| chr7:142857489 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(53): Show |
183 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.-432+2104G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142857489 | |||||||
| chr7:142857692 | C | T | 1 | a0002c0002t0002g0039 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-432+2307C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142857692 | |||||||
| chr7:142857813 | G | A | 1 | a0004c0017t0003g0092 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-432+2428G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142857813 | |||||||
| chr7:142858131 | A | C | 1 | a0001c0001t0001g0076 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-432+2746A>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142858131 | |||||||
| chr7:142858159 | A | G | 2 | a0001c0001t0001g0010 a0001c0019t0001g0010 |
4 | NA18950.hp1 NA18974.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.-432+2774A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142858159 | |||||||
| chr7:142858261 | A | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0075 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-431-2791A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142858261 | |||||||
| chr7:142858286 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-431-2766T>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142858286 | |||||||
| chr7:142858346 | A | G | 3 | a0004c0003t0002g0082 a0004c0003t0002g0083 a0004c0003t0002g0084 |
3 | HG02055.hp2 HG02486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-431-2706A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142858346 | |||||||
| chr7:142858423 | CT | C | 29 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0044 others(26): Show |
46 | HG00621.hp1 HG00735.hp1 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.-431-2599delT | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 142858423 | ||||||
| chr7:142858423 | CTT | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(79): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.-431-2600_-431-259 others(6): Show |
EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 142858423 | ||||||
| chr7:142858423 | CTTT | C | 8 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0052 others(5): Show |
11 | HG01167.hp1 HG01255.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.-431-2601_-431-259 others(7): Show |
EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 142858423 | ||||||
| chr7:142858570 | G | A | 1 | a0002c0002t0003g0093 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-431-2482G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142858570 | |||||||
| chr7:142858581 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-431-2471A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142858581 | |||||||
| chr7:142858583 | A | C | 8 | a0001c0001t0001g0027 a0001c0001t0001g0071 a0001c0001t0001g0109 others(5): Show |
9 | HG01123.hp1 HG02300.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-431-2469A>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142858583 | |||||||
| chr7:142858592 | C | T | 1 | a0002c0002t0002g0101 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-431-2460C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142858592 | |||||||
| chr7:142858602 | A | ATT | 11 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0021 others(8): Show |
26 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(23): Show |
intron_variant | MODIFIER | c.-431-2434_-431-243 others(6): Show |
EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 142858602 | ||||||
| chr7:142858602 | A | ATTT | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(63): Show |
197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.-431-2435_-431-243 others(7): Show |
EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 142858602 | ||||||
| chr7:142858602 | A | ATTTT | 11 | a0001c0001t0001g0015 a0001c0001t0001g0038 a0001c0001t0001g0067 others(8): Show |
12 | HG00642.hp1 HG01123.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.-431-2436_-431-243 others(8): Show |
EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 142858602 | ||||||
| chr7:142858602 | A | ATTTTT | 3 | a0003c0005t0002g0006 a0003c0005t0002g0020 a0003c0005t0002g0031 |
9 | HG00642.hp2 HG02559.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-431-2437_-431-243 others(9): Show |
EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 142858602 | ||||||
| chr7:142858602 | AT | A | 8 | a0002c0002t0002g0013 a0002c0002t0002g0028 a0002c0002t0002g0045 others(5): Show |
12 | HG01070.hp1 HG01256.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.-431-2433delT | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 142858602 | ||||||
| chr7:142858661 | C | T | 3 | a0001c0001t0001g0066 a0002c0002t0002g0039 a0002c0002t0002g0072 |
3 | HG02148.hp2 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-431-2391C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142858661 | |||||||
| chr7:142858675 | T | C | 6 | a0004c0003t0002g0005 a0004c0003t0002g0040 a0004c0003t0002g0078 others(3): Show |
13 | HG00735.hp1 HG02109.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-431-2377T>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142858675 | |||||||
| chr7:142858742 | G | A | 1 | a0002c0015t0009g0087 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-431-2310G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142858742 | |||||||
| chr7:142858871 | G | A | 8 | a0002c0002t0005g0012 a0002c0002t0005g0089 a0002c0015t0009g0087 others(5): Show |
17 | HG00642.hp2 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-431-2181G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142858871 | |||||||
| chr7:142859145 | GTTCCT | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(93): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-431-1904_-431-190 others(9): Show |
EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 142859145 | ||||||
| chr7:142859229 | C | G | 1 | a0002c0002t0002g0037 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-431-1823C>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142859229 | |||||||
| chr7:142859274 | C | T | 1 | a0002c0002t0002g0096 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-431-1778C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142859274 | |||||||
| chr7:142859317 | T | C | 1 | a0002c0002t0002g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-431-1735T>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142859317 | |||||||
| chr7:142859424 | T | C | 12 | a0002c0002t0002g0077 a0002c0002t0003g0017 a0002c0002t0003g0025 others(9): Show |
19 | HG01106.hp1 HG01256.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.-431-1628T>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142859424 | |||||||
| chr7:142859625 | A | AT | 7 | a0002c0002t0002g0011 a0002c0002t0002g0106 a0003c0005t0002g0006 others(4): Show |
16 | HG00642.hp2 HG01361.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.-431-1417dupT | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr7 | 142859625 | ||||||
| chr7:142859650 | T | C | 1 | a0002c0002t0002g0045 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-431-1402T>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142859650 | |||||||
| chr7:142859664 | C | A | 1 | a0001c0004t0001g0053 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-431-1388C>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142859664 | |||||||
| chr7:142859983 | A | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0043 a0001c0001t0001g0069 |
5 | HG01515.hp1 HG02738.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.-431-1069A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142859983 | |||||||
| chr7:142860128 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-431-924T>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142860128 | |||||||
| chr7:142860279 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-431-773T>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142860279 | |||||||
| chr7:142860375 | C | T | 29 | a0001c0008t0006g0024 a0001c0008t0006g0088 a0001c0018t0006g0086 others(26): Show |
44 | HG00735.hp1 HG01123.hp1 HG01261.hp1 others(41): Show |
intron_variant | MODIFIER | c.-431-677C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142860375 | |||||||
| chr7:142860436 | G | A | 1 | a0001c0001t0010g0054 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-431-616G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142860436 | |||||||
| chr7:142860557 | C | G | 2 | a0002c0002t0003g0026 a0002c0002t0003g0095 |
3 | HG02647.hp2 HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-431-495C>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142860557 | |||||||
| chr7:142860592 | A | G | 29 | a0001c0008t0006g0024 a0001c0008t0006g0088 a0001c0018t0006g0086 others(26): Show |
44 | HG00735.hp1 HG01123.hp1 HG01261.hp1 others(41): Show |
intron_variant | MODIFIER | c.-431-460A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142860592 | |||||||
| chr7:142860733 | G | A | 1 | a0001c0001t0001g0023 | 2 | NA18997.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-431-319G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142860733 | |||||||
| chr7:142860770 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-431-282C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 1/19 | chr7 | 142860770 | |||||||
| chr7:142861228 | G | A | 1 | a0002c0002t0002g0037 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-297+42G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 2/19 | chr7 | 142861228 | |||||||
| chr7:142861342 | ATCCTATA others(3): Show |
A | 29 | a0001c0008t0006g0024 a0001c0008t0006g0088 a0001c0018t0006g0086 others(26): Show |
44 | HG00735.hp1 HG01123.hp1 HG01261.hp1 others(41): Show |
intron_variant | MODIFIER | c.-297+158_-297+167d others(12): Show |
EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr7 | 142861342 | ||||||
| chr7:142861401 | G | C | 10 | a0004c0003t0002g0005 a0004c0003t0002g0040 a0004c0003t0002g0078 others(7): Show |
17 | HG00735.hp1 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.-297+215G>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 2/19 | chr7 | 142861401 | |||||||
| chr7:142861643 | C | A | 29 | a0001c0008t0006g0024 a0001c0008t0006g0088 a0001c0018t0006g0086 others(26): Show |
44 | HG00735.hp1 HG01123.hp1 HG01261.hp1 others(41): Show |
intron_variant | MODIFIER | c.-296-374C>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 2/19 | chr7 | 142861643 | |||||||
| chr7:142861820 | A | C | 1 | a0002c0002t0002g0073 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-296-197A>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 2/19 | chr7 | 142861820 | |||||||
| chr7:142861870 | T | A | 1 | a0004c0003t0002g0082 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-296-147T>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 2/19 | chr7 | 142861870 | |||||||
| chr7:142862292 | A | G | 12 | a0002c0002t0002g0077 a0002c0002t0003g0017 a0002c0002t0003g0025 others(9): Show |
19 | HG01106.hp1 HG01256.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.-180+159A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 3/19 | chr7 | 142862292 | |||||||
| chr7:142862394 | G | T | 1 | a0001c0001t0001g0042 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-180+261G>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 3/19 | chr7 | 142862394 | |||||||
| chr7:142862414 | A | C | 3 | a0001c0008t0006g0024 a0001c0008t0006g0088 a0001c0018t0006g0086 |
4 | HG02257.hp1 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-180+281A>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 3/19 | chr7 | 142862414 | |||||||
| chr7:142862427 | C | A | 12 | a0002c0002t0001g0046 a0002c0002t0002g0013 a0002c0002t0002g0028 others(9): Show |
16 | HG01123.hp1 HG01261.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-180+294C>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 3/19 | chr7 | 142862427 | |||||||
| chr7:142862899 | A | G | 2 | a0001c0001t0001g0064 a0001c0001t0001g0067 |
2 | HG00642.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.-102+66A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 4/19 | chr7 | 142862899 | |||||||
| chr7:142862943 | G | C | 13 | a0002c0002t0001g0046 a0002c0002t0002g0013 a0002c0002t0002g0028 others(10): Show |
17 | HG01123.hp1 HG01261.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-102+110G>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 4/19 | chr7 | 142862943 | |||||||
| chr7:142863024 | G | A | 2 | a0002c0002t0002g0011 a0002c0002t0002g0106 |
5 | HG01361.hp2 HG01952.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-101-103G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 4/19 | chr7 | 142863024 | |||||||
| chr7:142863034 | A | G | 2 | a0002c0002t0002g0011 a0002c0002t0002g0106 |
5 | HG01361.hp2 HG01952.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-101-93A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 4/19 | chr7 | 142863034 | |||||||
| chr7:142863071 | A | G | 1 | a0002c0002t0002g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-101-56A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 4/19 | chr7 | 142863071 | |||||||
| chr7:142863497 | T | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.101-134T>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 5/19 | chr7 | 142863497 | |||||||
| chr7:142863533 | C | T | 12 | a0002c0002t0001g0046 a0002c0002t0002g0013 a0002c0002t0002g0028 others(9): Show |
16 | HG01123.hp1 HG01261.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.101-98C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 5/19 | chr7 | 142863533 | |||||||
| chr7:142863555 | G | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(124): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.101-76G>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 5/19 | chr7 | 142863555 | |||||||
| chr7:142863619 | A | G | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | HG00639.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.101-12A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 5/19 | chr7 | 142863619 | |||||||
| chr7:142863750 | C | A | 1 | a0001c0001t0001g0055 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.165+55C>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 6/19 | chr7 | 142863750 | |||||||
| chr7:142863778 | C | T | 2 | a0003c0006t0004g0103 a0007c0014t0004g0048 |
2 | HG02602.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.165+83C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 6/19 | chr7 | 142863778 | |||||||
| chr7:142863919 | G | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(117): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.166-47G>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 6/19 | chr7 | 142863919 | |||||||
| chr7:142864779 | G | A | 9 | a0002c0002t0002g0077 a0002c0002t0003g0017 a0002c0002t0003g0025 others(6): Show |
13 | HG01106.hp1 HG01256.hp1 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.949+30G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 7/19 | chr7 | 142864779 | |||||||
| chr7:142864981 | C | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(76): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.949+232C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 7/19 | chr7 | 142864981 | |||||||
| chr7:142865093 | G | A | 2 | a0002c0002t0002g0011 a0002c0002t0002g0106 |
5 | HG01361.hp2 HG01952.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.949+344G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 7/19 | chr7 | 142865093 | |||||||
| chr7:142865330 | A | C | 1 | a0001c0020t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.950-145A>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 7/19 | chr7 | 142865330 | |||||||
| chr7:142865789 | C | G | 17 | a0002c0002t0001g0046 a0002c0002t0002g0013 a0002c0002t0002g0028 others(14): Show |
27 | HG00642.hp2 HG01123.hp1 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.1105+159C>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 8/19 | chr7 | 142865789 | |||||||
| chr7:142866335 | C | G | 1 | a0001c0001t0001g0085 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1462+19C>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 9/19 | chr7 | 142866335 | |||||||
| chr7:142866355 | C | T | 12 | a0002c0002t0002g0077 a0002c0002t0003g0017 a0002c0002t0003g0025 others(9): Show |
19 | HG01106.hp1 HG01256.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.1462+39C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 9/19 | chr7 | 142866355 | |||||||
| chr7:142866402 | C | T | 10 | a0004c0003t0002g0005 a0004c0003t0002g0040 a0004c0003t0002g0078 others(7): Show |
17 | HG00735.hp1 HG01891.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1463-79C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 9/19 | chr7 | 142866402 | |||||||
| chr7:142866615 | A | G | 3 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0020t0001g0112 |
3 | HG02622.hp1 NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1587+10A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 10/19 | chr7 | 142866615 | |||||||
| chr7:142866762 | T | G | 1 | a0002c0002t0002g0037 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1588-144T>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 10/19 | chr7 | 142866762 | |||||||
| chr7:142867099 | G | A | 38 | a0002c0002t0001g0046 a0002c0002t0002g0011 a0002c0002t0002g0013 others(35): Show |
59 | HG00735.hp1 HG01106.hp1 HG01123.hp1 others(56): Show |
intron_variant | MODIFIER | c.1750+31G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 11/19 | chr7 | 142867099 | |||||||
| chr7:142867424 | T | G | 13 | a0001c0001t0001g0056 a0002c0002t0002g0077 a0002c0002t0003g0017 others(10): Show |
20 | HG01106.hp1 HG01256.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.1751-184T>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 11/19 | chr7 | 142867424 | |||||||
| chr7:142867449 | C | T | 1 | a0002c0015t0009g0087 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1751-159C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 11/19 | chr7 | 142867449 | |||||||
| chr7:142867502 | C | T | 1 | a0001c0004t0001g0061 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1751-106C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 11/19 | chr7 | 142867502 | |||||||
| chr7:142867514 | G | C | 1 | a0001c0001t0001g0057 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1751-94G>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 11/19 | chr7 | 142867514 | |||||||
| chr7:142867534 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1751-74T>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 11/19 | chr7 | 142867534 | |||||||
| chr7:142867892 | G | A | 14 | a0002c0002t0002g0011 a0002c0002t0002g0077 a0002c0002t0002g0106 others(11): Show |
24 | HG01106.hp1 HG01256.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1866-105G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 12/19 | chr7 | 142867892 | |||||||
| chr7:142867910 | G | A | 12 | a0002c0002t0001g0046 a0002c0002t0002g0013 a0002c0002t0002g0028 others(9): Show |
16 | HG01123.hp1 HG01261.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1866-87G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 12/19 | chr7 | 142867910 | |||||||
| chr7:142867988 | G | A | 12 | a0002c0002t0001g0046 a0002c0002t0002g0013 a0002c0002t0002g0028 others(9): Show |
16 | HG01123.hp1 HG01261.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.1866-9G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 12/19 | chr7 | 142867988 | |||||||
| chr7:142868073 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1918+24G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 13/19 | chr7 | 142868073 | |||||||
| chr7:142868365 | AGCAGGGC others(8): Show |
A | 1 | a0008c0016t0004g0098 | 1 | HG06807.hp1 | splice_region_variant&intron_variant | LOW | c.2038+7_2038+21delC others(14): Show |
EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr7 | 142868365 | ||||||
| chr7:142868383 | A | G | 1 | a0008c0016t0004g0098 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2038+23A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 14/19 | chr7 | 142868383 | |||||||
| chr7:142868394 | G | C | 1 | a0008c0016t0004g0098 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2038+34G>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 14/19 | chr7 | 142868394 | |||||||
| chr7:142868403 | T | A | 1 | a0008c0016t0004g0098 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2038+43T>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 14/19 | chr7 | 142868403 | |||||||
| chr7:142868408 | G | C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(39): Show |
149 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.2038+48G>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 14/19 | chr7 | 142868408 | |||||||
| chr7:142868447 | G | A | 1 | a0003c0006t0004g0104 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2039-45G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 14/19 | chr7 | 142868447 | |||||||
| chr7:142868846 | G | A | 36 | a0002c0002t0002g0011 a0002c0002t0002g0013 a0002c0002t0002g0028 others(33): Show |
57 | HG00735.hp1 HG01106.hp1 HG01123.hp1 others(54): Show |
intron_variant | MODIFIER | c.2286+107G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 15/19 | chr7 | 142868846 | |||||||
| chr7:142868886 | G | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.2287-88G>C | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 15/19 | chr7 | 142868886 | |||||||
| chr7:142868897 | G | A | 1 | a0003c0005t0002g0033 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2287-77G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 15/19 | chr7 | 142868897 | |||||||
| chr7:142868906 | T | A | 7 | a0002c0002t0002g0077 a0002c0002t0003g0017 a0002c0002t0003g0025 others(4): Show |
10 | HG01106.hp1 HG01256.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.2287-68T>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 15/19 | chr7 | 142868906 | |||||||
| chr7:142868907 | A | G | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(122): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.2287-67A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 15/19 | chr7 | 142868907 | |||||||
| chr7:142868929 | CCT | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(80): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.2287-44_2287-43del others(2): Show |
EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 15/19 | chr7 | 142868929 | |||||||
| chr7:142869175 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2460+28C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 16/19 | chr7 | 142869175 | |||||||
| chr7:142869247 | C | A | 1 | a0004c0003t0002g0078 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2460+100C>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 16/19 | chr7 | 142869247 | |||||||
| chr7:142869339 | C | T | 1 | a0004c0003t0002g0115 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2460+192C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 16/19 | chr7 | 142869339 | |||||||
| chr7:142869473 | C | T | 5 | a0003c0005t0002g0006 a0003c0005t0002g0020 a0003c0005t0002g0031 others(2): Show |
11 | HG00642.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.2460+326C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 16/19 | chr7 | 142869473 | |||||||
| chr7:142869636 | C | T | 1 | a0002c0002t0002g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2461-181C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 16/19 | chr7 | 142869636 | |||||||
| chr7:142870050 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2610+84G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 17/19 | chr7 | 142870050 | |||||||
| chr7:142870100 | C | T | 1 | a0004c0003t0002g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2611-114C>T | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 17/19 | chr7 | 142870100 | |||||||
| chr7:142870174 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2611-40A>G | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 17/19 | chr7 | 142870174 | |||||||
| chr7:142870189 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(77): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.2611-25G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 17/19 | chr7 | 142870189 | |||||||
| chr7:142870765 | G | A | 11 | a0002c0002t0002g0013 a0002c0002t0002g0028 a0002c0002t0002g0039 others(8): Show |
15 | HG01123.hp1 HG01261.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.2961-31G>A | EPHB6 | ENSG00000106123.12 | transcript | ENST00000652003.1 | protein_coding | 19/19 | chr7 | 142870765 |