Item | Value |
---|---|
geneid | 22950 |
ensemblid | ENSG00000163798.14 |
hgncid | 13813 |
symbol | SLC4A1AP |
name | solute carrier family 4 member 1 adaptor protein |
refseq_nuc | NM_018158.3 |
refseq_prot | NP_060628.3 |
ensembl_nuc | ENST00000326019.11 |
ensembl_prot | ENSP00000323837.7 |
mane_status | MANE Select |
chr | chr2 |
start | 27663889 |
end | 27694969 |
strand | + |
ver | v1.2 |
region | chr2:27663889-27694969 |
region5000 | chr2:27658889-27699969 |
regionname0 | SLC4A1AP_chr2_27663889_27694969 |
regionname5000 | SLC4A1AP_chr2_27658889_27699969 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 742 | 249 | 55 | 40 | 127 | 7 | 19 | 97 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | MADIL others(737): Show |
chr2 | 27658889 | 27699969 |
a0002 | 0/1 | 742 | 75 | 23 | 15 | 18 | 7 | 11 | 16 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | MADIL others(737): Show |
chr2 | 27658889 | 27699969 |
a0003 | 0/0 | 742 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | MADIL others(737): Show |
chr2 | 27658889 | 27699969 |
a0004 | 0/0 | 742 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | MADIL others(737): Show |
chr2 | 27658889 | 27699969 |
a0005 | 0/0 | 742 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | MADIL others(737): Show |
chr2 | 27658889 | 27699969 |
a0006 | 0/0 | 742 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | MADIL others(737): Show |
chr2 | 27658889 | 27699969 |
a0007 | 0/0 | 742 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | MADIL others(737): Show |
chr2 | 27658889 | 27699969 |
a0008 | 0/0 | 742 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | MADIL others(737): Show |
chr2 | 27658889 | 27699969 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2226 | 227 | 38 | 36 | 127 | 7 | 18 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | ATGGC others(2221): Show |
chr2 | 27658889 | 27699969 | ||
a0001c0003 | 0/0 | 2226 | 15 | 10 | 4 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | ATGGC others(2221): Show |
chr2 | 27658889 | 27699969 | ||
a0001c0005 | 0/0 | 2226 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | ATGGC others(2221): Show |
chr2 | 27658889 | 27699969 | ||
a0001c0006 | 0/0 | 2226 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | ATGGC others(2221): Show |
chr2 | 27658889 | 27699969 | ||
a0001c0007 | 0/0 | 2226 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | ATGGC others(2221): Show |
chr2 | 27658889 | 27699969 | ||
a0001c0013 | 0/0 | 2226 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | ATGGC others(2221): Show |
chr2 | 27658889 | 27699969 | ||
a0002c0002 | 0/1 | 2226 | 74 | 22 | 15 | 18 | 7 | 11 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | ATGGC others(2221): Show |
chr2 | 27658889 | 27699969 | ||
a0002c0008 | 0/0 | 2226 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | ATGGC others(2221): Show |
chr2 | 27658889 | 27699969 | ||
a0003c0004 | 0/0 | 2226 | 5 | 0 | 0 | 5 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | ATGGC others(2221): Show |
chr2 | 27658889 | 27699969 | ||
a0004c0012 | 0/0 | 2226 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | ATGGC others(2221): Show |
chr2 | 27658889 | 27699969 | ||
a0005c0010 | 0/0 | 2226 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | ATGGC others(2221): Show |
chr2 | 27658889 | 27699969 | ||
a0006c0009 | 0/0 | 2226 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | ATGGC others(2221): Show |
chr2 | 27658889 | 27699969 | ||
a0007c0014 | 0/0 | 2226 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | ATGGC others(2221): Show |
chr2 | 27658889 | 27699969 | ||
a0008c0011 | 0/0 | 2226 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | ATGGC others(2221): Show |
chr2 | 27658889 | 27699969 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2541 | 227 | 38 | 36 | 127 | 7 | 18 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | GGATT others(2536): Show |
chr2 | 27658889 | 27699969 |
a0001c0003t0001 | 0/0 | 2541 | 4 | 2 | 1 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | GGATT others(2536): Show |
chr2 | 27658889 | 27699969 |
a0001c0003t0002 | 0/0 | 2541 | 11 | 8 | 3 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | GGATT others(2536): Show |
chr2 | 27658889 | 27699969 |
a0001c0005t0001 | 0/0 | 2541 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | GGATT others(2536): Show |
chr2 | 27658889 | 27699969 |
a0001c0006t0001 | 0/0 | 2541 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | GGATT others(2536): Show |
chr2 | 27658889 | 27699969 |
a0001c0007t0001 | 0/0 | 2541 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | GGATT others(2536): Show |
chr2 | 27658889 | 27699969 |
a0001c0013t0001 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | GGATT others(2536): Show |
chr2 | 27658889 | 27699969 |
a0002c0002t0001 | 0/1 | 2541 | 74 | 22 | 15 | 18 | 7 | 11 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | GGATT others(2536): Show |
chr2 | 27658889 | 27699969 |
a0002c0008t0001 | 0/0 | 2541 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | GGATT others(2536): Show |
chr2 | 27658889 | 27699969 |
a0003c0004t0001 | 0/0 | 2541 | 5 | 0 | 0 | 5 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | GGATT others(2536): Show |
chr2 | 27658889 | 27699969 |
a0004c0012t0001 | 0/0 | 2541 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | GGATT others(2536): Show |
chr2 | 27658889 | 27699969 |
a0005c0010t0001 | 0/0 | 2541 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | GGATT others(2536): Show |
chr2 | 27658889 | 27699969 |
a0006c0009t0001 | 0/0 | 2541 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | GGATT others(2536): Show |
chr2 | 27658889 | 27699969 |
a0007c0014t0001 | 0/0 | 2541 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | GGATT others(2536): Show |
chr2 | 27658889 | 27699969 |
a0008c0011t0001 | 0/0 | 2541 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | GGATT others(2536): Show |
chr2 | 27658889 | 27699969 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 29 | 2 | 5 | 19 | 1 | 2 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 6 | 1 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0006 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0217 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0003t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0003t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0003t0002g0007 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0003t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0003t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0003t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0003t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0003t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0003t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0005t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0005t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0006t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0007t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0007t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0001c0013t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0004 | 0/0 | 5 | 0 | 0 | 3 | 1 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0198 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0002c0008t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0003c0004t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0003c0004t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0003c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0003c0004t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0003c0004t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0004c0012t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0005c0010t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0006c0009t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0007c0014t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
a0008c0011t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0118 | EUR | GBR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | GBR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0032 | EUR | GBR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0164 | EUR | FIN | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | FIN | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0147 | EUR | FIN | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00408 | hp2 | a0004 | c0012 | t0001 | g0216 | EAS | CHS | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00639 | hp2 | a0001 | c0003 | t0002 | g0045 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0111 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0025 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0188 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0191 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01099 | hp2 | a0005 | c0010 | t0001 | g0175 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0137 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01167 | hp1 | a0001 | c0003 | t0002 | g0007 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01169 | hp2 | a0001 | c0003 | t0002 | g0007 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0196 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0035 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0032 | AMR | CLM | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0230 | AMR | CLM | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0120 | AMR | CLM | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0190 | AMR | CLM | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01358 | hp1 | a0001 | c0003 | t0001 | g0019 | AMR | CLM | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | CLM | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0113 | AMR | CLM | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0143 | EUR | IBS | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0066 | EUR | IBS | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0004 | EUR | IBS | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0073 | EUR | IBS | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0119 | AFR | ACB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | PEL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02015 | hp2 | a0006 | c0009 | t0001 | g0004 | EAS | KHV | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | KHV | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0171 | AFR | ACB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02145 | hp2 | a0001 | c0013 | t0001 | g0055 | AFR | ACB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | CDX | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CDX | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CDX | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CDX | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0202 | AFR | ACB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0095 | AFR | ACB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0031 | AMR | PEL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02572 | hp1 | a0001 | c0007 | t0001 | g0037 | AFR | GWD | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | GWD | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02630 | hp2 | a0001 | c0003 | t0002 | g0007 | AFR | GWD | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02647 | hp1 | a0001 | c0007 | t0001 | g0038 | AFR | GWD | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0166 | AFR | GWD | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0210 | SAS | PJL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02698 | hp2 | a0001 | c0003 | t0001 | g0019 | SAS | PJL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0096 | AFR | GWD | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02717 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | GWD | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02723 | hp1 | a0001 | c0003 | t0002 | g0007 | AFR | GWD | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0172 | SAS | PJL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0211 | SAS | PJL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02818 | hp1 | a0001 | c0006 | t0001 | g0017 | AFR | GWD | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0100 | AFR | GWD | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0110 | AFR | GWD | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02922 | hp1 | a0001 | c0003 | t0002 | g0042 | AFR | ESN | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0081 | AFR | ESN | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0102 | AFR | ESN | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0187 | AFR | ESN | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | ESN | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0136 | AFR | ESN | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0142 | SAS | PJL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0203 | AFR | MSL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0020 | AFR | ESN | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0165 | AFR | ESN | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0098 | AFR | ESN | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | MSL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | MSL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03225 | hp1 | a0001 | c0003 | t0002 | g0039 | AFR | MSL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03486 | hp2 | a0001 | c0003 | t0002 | g0040 | AFR | MSL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0031 | SAS | PJL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0020 | AFR | ESN | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03540 | hp1 | a0001 | c0003 | t0002 | g0041 | AFR | GWD | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0140 | AFR | GWD | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03579 | hp2 | a0001 | c0006 | t0001 | g0017 | AFR | MSL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0112 | SAS | BEB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0138 | SAS | BEB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | BEB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0189 | SAS | BEB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0167 | SAS | STU | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | STU | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | YRI | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | YRI | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18940 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18941 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18964 | hp1 | a0007 | c0014 | t0001 | g0011 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18968 | hp1 | a0003 | c0004 | t0001 | g0212 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18982 | hp1 | a0003 | c0004 | t0001 | g0121 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18985 | hp2 | a0003 | c0004 | t0001 | g0036 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19000 | hp2 | a0003 | c0004 | t0001 | g0125 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19012 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19043 | hp2 | a0002 | c0008 | t0001 | g0097 | AFR | LWK | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19056 | hp1 | a0008 | c0011 | t0001 | g0003 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | YRI | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | ASW | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA20129 | hp2 | a0001 | c0003 | t0002 | g0018 | AFR | ASW | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0108 | EUR | TSI | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0199 | AMR | CLM | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02486 | hp2 | a0001 | c0003 | t0002 | g0018 | AFR | ACB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG02559 | hp2 | a0001 | c0005 | t0001 | g0057 | AFR | ACB | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | MSL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | MSL | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | USA | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | USA | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA18955 | hp2 | a0003 | c0004 | t0001 | g0002 | EAS | JPT | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | USA | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | USA | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | LWK | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
NA21309 | hp2 | a0001 | c0005 | t0001 | g0056 | AFR | LWK | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0198 | REF | REF | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0217 | REF | REF | SLC4A1AP_chr2_27658889_27699969 | SLC4A1AP | chr2 | 27658889 | 27699969 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:27664167 | C | A | 3 | a0002 a0005 a0006 |
76 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(73): Show |
missense_variant | MODERATE | c.253C>A | p.Pro85Thr | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 1/14 | 279/2541 | 253/2229 | 85/742 | chr2 | 27664167 | |||
chr2:27664293 | C | T | 1 | a0005 | 1 | HG01099.hp2 | missense_variant | MODERATE | c.379C>T | p.Arg127Cys | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 1/14 | 405/2541 | 379/2229 | 127/742 | chr2 | 27664293 | |||
chr2:27664492 | C | T | 1 | a0007 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.578C>T | p.Thr193Ile | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 1/14 | 604/2541 | 578/2229 | 193/742 | chr2 | 27664492 | |||
chr2:27675538 | G | A | 1 | a0008 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.1190G>A | p.Arg397Gln | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 6/14 | 1216/2541 | 1190/2229 | 397/742 | chr2 | 27675538 | |||
chr2:27677308 | A | G | 1 | a0006 | 1 | HG02015.hp2 | missense_variant | MODERATE | c.1358A>G | p.Asn453Ser | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 7/14 | 1384/2541 | 1358/2229 | 453/742 | chr2 | 27677308 | |||
chr2:27685230 | T | G | 1 | a0003 | 5 | NA18955.hp2 NA18968.hp1 NA18982.hp1 others(2): Show |
missense_variant | MODERATE | c.1907T>G | p.Met636Arg | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/14 | 1933/2541 | 1907/2229 | 636/742 | chr2 | 27685230 | |||
chr2:27694647 | T | A | 1 | a0004 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.2193T>A | p.Asp731Glu | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 14/14 | 2219/2541 | 2193/2229 | 731/742 | chr2 | 27694647 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:27663953 | G | T | 2 | a0001c0003 a0001c0007 |
17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
synonymous_variant | LOW | c.39G>T | p.Ser13Ser | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 1/14 | 65/2541 | 39/2229 | 13/742 | chr2 | 27663953 | |||
chr2:27663968 | G | T | 1 | a0001c0007 | 2 | HG02572.hp1 HG02647.hp1 |
synonymous_variant | LOW | c.54G>T | p.Gly18Gly | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 1/14 | 80/2541 | 54/2229 | 18/742 | chr2 | 27663968 | |||
chr2:27664211 | C | A | 1 | a0002c0008 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.297C>A | p.Pro99Pro | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 1/14 | 323/2541 | 297/2229 | 99/742 | chr2 | 27664211 | |||
chr2:27665273 | G | A | 1 | a0001c0005 | 2 | HG02559.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.837G>A | p.Glu279Glu | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/14 | 863/2541 | 837/2229 | 279/742 | chr2 | 27665273 | |||
chr2:27667296 | A | G | 1 | a0001c0013 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.888A>G | p.Glu296Glu | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 3/14 | 914/2541 | 888/2229 | 296/742 | chr2 | 27667296 | |||
chr2:27685108 | G | A | 1 | a0001c0006 | 2 | HG02818.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.1785G>A | p.Glu595Glu | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/14 | 1811/2541 | 1785/2229 | 595/742 | chr2 | 27685108 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:27694947 | C | A | 1 | a0001c0003t0002 | 11 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*264C>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 14/14 | 264 | chr2 | 27694947 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:27664738 | A | G | 1 | a0002c0002t0001g0233 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.663+161A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 1/13 | chr2 | 27664738 | |||||||
chr2:27664827 | G | A | 1 | a0001c0006t0001g0017 | 2 | HG02818.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.663+250G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 1/13 | chr2 | 27664827 | |||||||
chr2:27664903 | T | TA | 4 | a0001c0001t0001g0043 a0001c0003t0001g0019 a0001c0003t0001g0020 others(1): Show |
6 | HG01358.hp1 HG02698.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.664-180dupA | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 27664903 | ||||||
chr2:27664903 | T | TAA | 7 | a0001c0003t0002g0007 a0001c0003t0002g0018 a0001c0003t0002g0039 others(4): Show |
11 | HG01167.hp1 HG01169.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.664-181_664-180dup others(2): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 27664903 | ||||||
chr2:27664903 | TA | T | 8 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0227 others(5): Show |
8 | HG01168.hp1 HG01258.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.664-180delA | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 27664903 | ||||||
chr2:27665054 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.664-46C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 1/13 | chr2 | 27665054 | |||||||
chr2:27665380 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.859+85C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27665380 | |||||||
chr2:27665677 | G | C | 1 | a0001c0001t0001g0044 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.859+382G>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27665677 | |||||||
chr2:27665862 | T | C | 11 | a0001c0003t0001g0019 a0001c0003t0001g0020 a0001c0003t0002g0007 others(8): Show |
17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.859+567T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27665862 | |||||||
chr2:27665870 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.859+575A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27665870 | |||||||
chr2:27665891 | A | C | 1 | a0001c0003t0001g0020 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.859+596A>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27665891 | |||||||
chr2:27666105 | T | G | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 |
3 | HG06807.hp2 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.859+810T>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666105 | |||||||
chr2:27666297 | G | C | 1 | a0001c0003t0001g0019 | 2 | HG01358.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.860-971G>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666297 | |||||||
chr2:27666349 | T | TCCA | 26 | a0001c0001t0001g0043 a0001c0001t0001g0101 a0001c0001t0001g0103 others(23): Show |
30 | HG00099.hp2 HG00738.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.860-916_860-914dup others(3): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 27666349 | ||||||
chr2:27666354 | C | CACCCACC others(1): Show |
6 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(3): Show |
6 | HG01192.hp1 HG01884.hp2 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.860-914_860-913ins others(8): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666354 | |||||||
chr2:27666355 | C | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(195): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.860-913C>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666355 | |||||||
chr2:27666356 | C | A | 26 | a0001c0001t0001g0043 a0001c0001t0001g0101 a0001c0001t0001g0103 others(23): Show |
30 | HG00099.hp2 HG00738.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.860-912C>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666356 | |||||||
chr2:27666359 | A | ACCAC | 41 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0030 others(38): Show |
58 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.860-907_860-906ins others(4): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 27666359 | ||||||
chr2:27666359 | A | ACCACC | 33 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0150 others(30): Show |
39 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.860-907_860-906ins others(5): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 27666359 | ||||||
chr2:27666359 | A | ACCACCC | 21 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0176 others(18): Show |
32 | HG00438.hp1 HG00741.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.860-907_860-906ins others(6): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 27666359 | ||||||
chr2:27666359 | A | C | 9 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 others(6): Show |
9 | HG00423.hp1 HG01192.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.860-909A>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666359 | |||||||
chr2:27666360 | C | CCA | 15 | a0001c0001t0001g0028 a0001c0001t0001g0089 a0001c0001t0001g0090 others(12): Show |
16 | HG00140.hp1 HG01168.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.860-907_860-906ins others(2): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 27666360 | ||||||
chr2:27666361 | C | CA | 23 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0026 others(20): Show |
32 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(29): Show |
intron_variant | MODIFIER | c.860-907_860-906ins others(1): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666361 | |||||||
chr2:27666362 | C | A | 43 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0013 others(40): Show |
85 | HG00323.hp1 HG00544.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.860-906C>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666362 | |||||||
chr2:27666362 | C | G | 1 | a0002c0002t0001g0203 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.860-906C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666362 | |||||||
chr2:27666363 | C | G | 1 | a0002c0002t0001g0202 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.860-905C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666363 | |||||||
chr2:27666364 | C | A | 1 | a0001c0001t0001g0049 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.860-904C>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666364 | |||||||
chr2:27666365 | C | A | 1 | a0001c0001t0001g0021 | 2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.860-903C>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666365 | |||||||
chr2:27666367 | C | G | 9 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0231 others(6): Show |
13 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.860-901C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666367 | |||||||
chr2:27666368 | C | G | 1 | a0002c0002t0001g0199 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.860-900C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666368 | |||||||
chr2:27666369 | C | G | 1 | a0001c0003t0001g0019 | 2 | HG01358.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.860-899C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666369 | |||||||
chr2:27666371 | CA | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0046 others(11): Show |
17 | HG01069.hp2 HG01256.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.860-896delA | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666371 | |||||||
chr2:27666372 | A | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(213): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.860-896A>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666372 | |||||||
chr2:27666374 | C | G | 1 | a0001c0001t0001g0149 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.860-894C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666374 | |||||||
chr2:27666377 | G | A | 1 | a0002c0002t0001g0230 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.860-891G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666377 | |||||||
chr2:27666503 | T | C | 1 | a0001c0003t0002g0042 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.860-765T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666503 | |||||||
chr2:27666619 | G | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0050 |
4 | NA18966.hp2 NA18968.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.860-649G>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666619 | |||||||
chr2:27666679 | A | G | 3 | a0001c0001t0001g0197 a0001c0001t0001g0214 a0001c0001t0001g0221 |
3 | HG01074.hp2 HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.860-589A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666679 | |||||||
chr2:27666694 | T | TA | 5 | a0001c0001t0001g0051 a0001c0001t0001g0075 a0001c0001t0001g0089 others(2): Show |
5 | HG01346.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.860-570dupA | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 27666694 | ||||||
chr2:27666855 | CTA | C | 12 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0148 others(9): Show |
13 | HG00099.hp2 HG00323.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.860-397_860-396del others(2): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 27666855 | ||||||
chr2:27666868 | TATA | T | 2 | a0001c0003t0001g0019 a0001c0003t0001g0020 |
4 | HG01358.hp1 HG02698.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.860-399_860-397del others(3): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666868 | |||||||
chr2:27666869 | ATAT | A | 16 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0001g0075 others(13): Show |
20 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.860-397_860-395del others(3): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 27666869 | ||||||
chr2:27666871 | A | T | 1 | a0001c0001t0001g0218 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.860-397A>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666871 | |||||||
chr2:27666871 | ATT | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
290 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.860-385_860-384del others(2): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | 27666871 | ||||||
chr2:27666874 | T | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.860-394T>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666874 | |||||||
chr2:27666875 | T | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.860-393T>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666875 | |||||||
chr2:27666891 | C | T | 6 | a0001c0003t0002g0007 a0001c0003t0002g0018 a0001c0003t0002g0039 others(3): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.860-377C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27666891 | |||||||
chr2:27667034 | A | T | 1 | a0001c0003t0001g0020 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.860-234A>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27667034 | |||||||
chr2:27667103 | T | C | 4 | a0001c0003t0001g0019 a0001c0003t0001g0020 a0001c0007t0001g0037 others(1): Show |
6 | HG01358.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.860-165T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 2/13 | chr2 | 27667103 | |||||||
chr2:27667414 | A | G | 1 | a0001c0006t0001g0017 | 2 | HG02818.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.982+24A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 3/13 | chr2 | 27667414 | |||||||
chr2:27667634 | G | A | 10 | a0001c0003t0001g0019 a0001c0003t0001g0020 a0001c0003t0002g0007 others(7): Show |
16 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.982+244G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 3/13 | chr2 | 27667634 | |||||||
chr2:27667943 | G | T | 1 | a0001c0003t0002g0041 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.982+553G>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 3/13 | chr2 | 27667943 | |||||||
chr2:27667965 | A | G | 1 | a0001c0001t0001g0043 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.982+575A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 3/13 | chr2 | 27667965 | |||||||
chr2:27668041 | G | C | 1 | a0001c0001t0001g0204 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.982+651G>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 3/13 | chr2 | 27668041 | |||||||
chr2:27668146 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.983-697A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 3/13 | chr2 | 27668146 | |||||||
chr2:27668153 | C | CT | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0214 others(2): Show |
6 | HG01074.hp2 HG02559.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.983-677dupT | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | 27668153 | ||||||
chr2:27668371 | C | T | 6 | a0001c0003t0002g0007 a0001c0003t0002g0018 a0001c0003t0002g0039 others(3): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-472C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 3/13 | chr2 | 27668371 | |||||||
chr2:27668419 | G | A | 6 | a0001c0003t0002g0007 a0001c0003t0002g0018 a0001c0003t0002g0039 others(3): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.983-424G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 3/13 | chr2 | 27668419 | |||||||
chr2:27668544 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.983-299G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 3/13 | chr2 | 27668544 | |||||||
chr2:27668586 | A | T | 1 | a0001c0003t0001g0019 | 2 | HG01358.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.983-257A>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 3/13 | chr2 | 27668586 | |||||||
chr2:27668602 | A | G | 1 | a0002c0002t0001g0146 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.983-241A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 3/13 | chr2 | 27668602 | |||||||
chr2:27668747 | A | G | 1 | a0001c0006t0001g0017 | 2 | HG02818.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.983-96A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 3/13 | chr2 | 27668747 | |||||||
chr2:27668826 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.983-17C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 3/13 | chr2 | 27668826 | |||||||
chr2:27669156 | A | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(38): Show |
84 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1044-92A>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 4/13 | chr2 | 27669156 | |||||||
chr2:27669407 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1183+20T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27669407 | |||||||
chr2:27669457 | T | C | 6 | a0001c0003t0002g0007 a0001c0003t0002g0018 a0001c0003t0002g0039 others(3): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1183+70T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27669457 | |||||||
chr2:27669591 | C | T | 2 | a0001c0007t0001g0037 a0001c0007t0001g0038 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1183+204C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27669591 | |||||||
chr2:27669613 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1183+226C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27669613 | |||||||
chr2:27669659 | C | CT | 10 | a0001c0003t0001g0019 a0001c0003t0001g0020 a0001c0003t0002g0007 others(7): Show |
16 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1183+278dupT | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27669659 | ||||||
chr2:27669809 | G | C | 1 | a0001c0001t0001g0080 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1183+422G>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27669809 | |||||||
chr2:27669827 | T | A | 84 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0001g0075 others(81): Show |
108 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.1183+440T>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27669827 | |||||||
chr2:27669925 | G | A | 1 | a0001c0003t0001g0020 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1183+538G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27669925 | |||||||
chr2:27669956 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1183+569C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27669956 | |||||||
chr2:27670051 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1183+664C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27670051 | |||||||
chr2:27670235 | T | G | 1 | a0002c0002t0001g0164 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1183+848T>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27670235 | |||||||
chr2:27670275 | G | C | 7 | a0002c0002t0001g0014 a0002c0002t0001g0025 a0002c0002t0001g0081 others(4): Show |
10 | HG00738.hp2 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1183+888G>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27670275 | |||||||
chr2:27670279 | T | C | 1 | a0002c0002t0001g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1183+892T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27670279 | |||||||
chr2:27670298 | G | A | 7 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0079 others(4): Show |
9 | HG00733.hp2 HG01109.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.1183+911G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27670298 | |||||||
chr2:27670397 | A | G | 1 | a0002c0002t0001g0232 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1183+1010A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27670397 | |||||||
chr2:27670466 | A | C | 1 | a0001c0001t0001g0107 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1183+1079A>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27670466 | |||||||
chr2:27670631 | C | T | 2 | a0001c0003t0001g0019 a0001c0003t0001g0020 |
4 | HG01358.hp1 HG02698.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1183+1244C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27670631 | |||||||
chr2:27670662 | C | T | 6 | a0001c0003t0002g0007 a0001c0003t0002g0018 a0001c0003t0002g0039 others(3): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1183+1275C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27670662 | |||||||
chr2:27670682 | C | G | 1 | a0001c0001t0001g0023 | 2 | NA18964.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1183+1295C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27670682 | |||||||
chr2:27670720 | G | A | 6 | a0001c0003t0002g0007 a0001c0003t0002g0018 a0001c0003t0002g0039 others(3): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1183+1333G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27670720 | |||||||
chr2:27670803 | T | C | 62 | a0001c0001t0001g0101 a0001c0001t0001g0109 a0001c0003t0002g0042 others(59): Show |
79 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.1183+1416T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27670803 | |||||||
chr2:27670852 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1183+1465C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27670852 | |||||||
chr2:27670873 | T | A | 3 | a0001c0001t0001g0197 a0001c0001t0001g0214 a0001c0001t0001g0221 |
3 | HG01074.hp2 HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1183+1486T>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27670873 | |||||||
chr2:27670922 | C | CT | 41 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(38): Show |
83 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1183+1554dupT | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27670922 | ||||||
chr2:27670922 | CT | C | 23 | a0001c0001t0001g0026 a0001c0001t0001g0051 a0001c0001t0001g0052 others(20): Show |
25 | HG00733.hp2 HG01167.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.1183+1554delT | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27670922 | ||||||
chr2:27670926 | T | TC | 1 | a0001c0001t0001g0013 | 3 | NA18966.hp2 NA18968.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1183+1539_1183+154 others(5): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27670926 | |||||||
chr2:27670927 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1183+1540T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27670927 | |||||||
chr2:27670945 | A | ATGGAGTC others(18): Show |
6 | a0001c0003t0002g0007 a0001c0003t0002g0018 a0001c0003t0002g0039 others(3): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1183+1565_1183+158 others(29): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27670945 | ||||||
chr2:27671385 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1183+1998C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27671385 | |||||||
chr2:27671576 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1183+2189C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27671576 | |||||||
chr2:27671702 | T | G | 1 | a0002c0002t0001g0095 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1183+2315T>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27671702 | |||||||
chr2:27671910 | T | G | 8 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0001g0075 others(5): Show |
8 | HG01346.hp2 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1183+2523T>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27671910 | |||||||
chr2:27672151 | C | G | 1 | a0001c0006t0001g0017 | 2 | HG02818.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1183+2764C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27672151 | |||||||
chr2:27672206 | C | T | 8 | a0002c0002t0001g0032 a0002c0002t0001g0108 a0002c0002t0001g0113 others(5): Show |
9 | HG00140.hp2 HG01099.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1183+2819C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27672206 | |||||||
chr2:27672211 | A | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0223 |
2 | HG02559.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1183+2824A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27672211 | |||||||
chr2:27672218 | C | G | 1 | a0001c0003t0001g0019 | 2 | HG01358.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1183+2831C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27672218 | |||||||
chr2:27672335 | T | TTTC | 20 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0001g0075 others(17): Show |
27 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.1183+2949_1183+295 others(7): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27672335 | ||||||
chr2:27672341 | G | T | 2 | a0001c0007t0001g0037 a0001c0007t0001g0038 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1183+2954G>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27672341 | |||||||
chr2:27672356 | A | G | 1 | a0001c0003t0001g0020 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1183+2969A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27672356 | |||||||
chr2:27672378 | G | C | 1 | a0002c0002t0001g0196 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1183+2991G>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27672378 | |||||||
chr2:27672410 | T | A | 1 | a0001c0001t0001g0151 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1183+3023T>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27672410 | |||||||
chr2:27673000 | C | T | 1 | a0002c0002t0001g0196 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1184-2532C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27673000 | |||||||
chr2:27673036 | GA | G | 60 | a0001c0001t0001g0101 a0002c0002t0001g0004 a0002c0002t0001g0009 others(57): Show |
77 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(74): Show |
intron_variant | MODIFIER | c.1184-2495delA | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27673036 | |||||||
chr2:27673047 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1184-2485G>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27673047 | |||||||
chr2:27673107 | C | G | 3 | a0001c0001t0001g0053 a0001c0001t0001g0078 a0001c0001t0001g0085 |
3 | HG02723.hp2 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1184-2425C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27673107 | |||||||
chr2:27673216 | A | T | 5 | a0001c0001t0001g0148 a0001c0001t0001g0197 a0001c0001t0001g0213 others(2): Show |
5 | HG01074.hp2 HG01884.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184-2316A>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27673216 | |||||||
chr2:27673302 | T | TTC | 8 | a0001c0003t0001g0019 a0002c0002t0001g0029 a0002c0002t0001g0035 others(5): Show |
11 | HG01106.hp2 HG01123.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1184-2208_1184-220 others(6): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673302 | ||||||
chr2:27673302 | TTCTC | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0145 |
3 | HG01981.hp1 HG02559.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1184-2210_1184-220 others(8): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673302 | ||||||
chr2:27673333 | C | CT | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1184-2196dupT | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673333 | ||||||
chr2:27673400 | T | TTCCC | 42 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(39): Show |
62 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.1184-2090_1184-208 others(8): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673400 | ||||||
chr2:27673400 | T | TTCCCTCC others(1): Show |
3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0205 |
3 | HG02056.hp1 HG02738.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.1184-2094_1184-208 others(12): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673400 | ||||||
chr2:27673400 | TTCCC | T | 25 | a0001c0001t0001g0028 a0001c0001t0001g0046 a0001c0001t0001g0048 others(22): Show |
26 | HG00280.hp2 HG00738.hp1 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.1184-2090_1184-208 others(8): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673400 | ||||||
chr2:27673400 | TTCCCTCC others(1): Show |
T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(96): Show |
159 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1184-2094_1184-208 others(12): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673400 | ||||||
chr2:27673400 | TTCCCTCC others(5): Show |
T | 10 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0074 others(7): Show |
11 | HG01358.hp1 HG01516.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1184-2098_1184-208 others(16): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673400 | ||||||
chr2:27673400 | TTCCCTCC others(9): Show |
T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0049 a0001c0001t0001g0071 others(1): Show |
5 | HG02559.hp1 HG03453.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184-2102_1184-208 others(20): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673400 | ||||||
chr2:27673400 | TTCCCTCC others(13): Show |
T | 3 | a0001c0001t0001g0090 a0001c0003t0001g0020 a0001c0005t0001g0057 |
4 | HG01168.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184-2106_1184-208 others(24): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673400 | ||||||
chr2:27673419 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1184-2113C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27673419 | |||||||
chr2:27673434 | CCCTCCCT others(5): Show |
C | 4 | a0002c0002t0001g0146 a0002c0002t0001g0190 a0002c0002t0001g0196 others(1): Show |
4 | HG01192.hp1 HG01346.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1184-2094_1184-208 others(16): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673434 | ||||||
chr2:27673438 | C | CCCTCCCT others(5): Show |
3 | a0001c0001t0001g0034 a0001c0001t0001g0158 a0001c0001t0001g0181 |
3 | NA18959.hp2 NA19009.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.1184-2087_1184-208 others(16): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673438 | ||||||
chr2:27673438 | CCCTCCCT others(1): Show |
C | 3 | a0001c0001t0001g0010 a0001c0003t0002g0042 a0002c0002t0001g0233 |
3 | HG02056.hp2 HG02922.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1184-2090_1184-208 others(12): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673438 | ||||||
chr2:27673442 | C | G | 1 | a0001c0001t0001g0046 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1184-2090C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27673442 | |||||||
chr2:27673442 | CCCTT | C | 7 | a0001c0001t0001g0026 a0001c0003t0002g0007 a0001c0003t0002g0018 others(4): Show |
10 | HG00639.hp2 HG00733.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1184-2072_1184-206 others(8): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673442 | ||||||
chr2:27673446 | T | C | 3 | a0001c0001t0001g0002 a0001c0001t0001g0134 a0001c0003t0002g0007 |
4 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184-2086T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27673446 | |||||||
chr2:27673683 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1184-1849G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27673683 | |||||||
chr2:27673753 | G | C | 1 | a0001c0001t0001g0103 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1184-1779G>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27673753 | |||||||
chr2:27673769 | C | G | 11 | a0001c0003t0001g0019 a0001c0003t0001g0020 a0001c0003t0002g0007 others(8): Show |
17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1184-1763C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27673769 | |||||||
chr2:27673932 | C | G | 1 | a0001c0003t0002g0042 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1184-1600C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27673932 | |||||||
chr2:27673976 | A | C | 1 | a0001c0003t0001g0020 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1184-1556A>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27673976 | |||||||
chr2:27673990 | T | TTG | 11 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0044 others(8): Show |
13 | HG00408.hp1 HG01069.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.1184-1502_1184-150 others(6): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673990 | ||||||
chr2:27673990 | TTG | T | 21 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0026 others(18): Show |
23 | HG00642.hp2 HG00733.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1184-1502_1184-150 others(6): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673990 | ||||||
chr2:27673990 | TTGTG | T | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(79): Show |
105 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.1184-1504_1184-150 others(8): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673990 | ||||||
chr2:27673990 | TTGTGTG | T | 11 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0053 others(8): Show |
11 | HG00639.hp1 HG02486.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1184-1506_1184-150 others(10): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673990 | ||||||
chr2:27673990 | TTGTGTGT others(1): Show |
T | 4 | a0001c0001t0001g0075 a0001c0001t0001g0183 a0001c0007t0001g0037 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1184-1508_1184-150 others(12): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673990 | ||||||
chr2:27673990 | TTGTGTGT others(3): Show |
T | 13 | a0001c0001t0001g0023 a0001c0001t0001g0051 a0001c0001t0001g0071 others(10): Show |
15 | HG01346.hp2 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1184-1510_1184-150 others(14): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673990 | ||||||
chr2:27673990 | TTGTGTGT others(5): Show |
T | 3 | a0001c0003t0001g0019 a0001c0003t0001g0020 a0002c0002t0001g0230 |
5 | HG01258.hp2 HG01358.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1184-1512_1184-150 others(16): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673990 | ||||||
chr2:27673990 | TTGTGTGT others(7): Show |
T | 54 | a0001c0001t0001g0101 a0001c0003t0002g0007 a0001c0003t0002g0018 others(51): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.1184-1514_1184-150 others(18): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673990 | ||||||
chr2:27673990 | TTGTGTGT others(11): Show |
T | 3 | a0001c0001t0001g0186 a0001c0001t0001g0219 a0002c0002t0001g0120 |
3 | HG00423.hp1 HG01261.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.1184-1518_1184-150 others(22): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27673990 | ||||||
chr2:27674000 | G | A | 1 | a0001c0007t0001g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1184-1532G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27674000 | |||||||
chr2:27674255 | G | C | 1 | a0001c0001t0001g0221 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1184-1277G>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27674255 | |||||||
chr2:27674463 | A | G | 11 | a0001c0003t0001g0019 a0001c0003t0001g0020 a0001c0003t0002g0007 others(8): Show |
17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1184-1069A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27674463 | |||||||
chr2:27674580 | AT | A | 11 | a0001c0003t0001g0019 a0001c0003t0001g0020 a0001c0003t0002g0007 others(8): Show |
17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1184-943delT | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27674580 | ||||||
chr2:27674698 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1184-834C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27674698 | |||||||
chr2:27674713 | A | AT | 12 | a0001c0001t0001g0022 a0001c0001t0001g0053 a0001c0001t0001g0067 others(9): Show |
13 | HG00733.hp1 HG01256.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1184-804dupT | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27674713 | ||||||
chr2:27674768 | G | A | 11 | a0001c0003t0001g0019 a0001c0003t0001g0020 a0001c0003t0002g0007 others(8): Show |
17 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1184-764G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27674768 | |||||||
chr2:27674819 | C | T | 8 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0001g0075 others(5): Show |
8 | HG01346.hp2 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1184-713C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27674819 | |||||||
chr2:27674900 | C | T | 1 | a0001c0003t0001g0020 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1184-632C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27674900 | |||||||
chr2:27674968 | G | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(78): Show |
107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1184-564G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27674968 | |||||||
chr2:27674993 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1184-539T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27674993 | |||||||
chr2:27675124 | G | T | 1 | a0001c0001t0001g0227 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1184-408G>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27675124 | |||||||
chr2:27675153 | C | A | 2 | a0001c0007t0001g0037 a0001c0007t0001g0038 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1184-379C>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27675153 | |||||||
chr2:27675449 | T | C | 1 | a0001c0003t0001g0020 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1184-83T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | chr2 | 27675449 | |||||||
chr2:27675489 | CT | C | 3 | a0001c0001t0001g0067 a0001c0001t0001g0152 a0001c0001t0001g0156 |
3 | HG01256.hp1 NA19001.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1184-37delT | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 27675489 | ||||||
chr2:27676051 | T | G | 6 | a0001c0003t0002g0007 a0001c0003t0002g0018 a0001c0003t0002g0039 others(3): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1344+359T>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 6/13 | chr2 | 27676051 | |||||||
chr2:27676178 | GA | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0099 |
5 | NA18960.hp2 NA18989.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.1344+493delA | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 27676178 | ||||||
chr2:27676362 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1344+670G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 6/13 | chr2 | 27676362 | |||||||
chr2:27676611 | C | T | 2 | a0001c0003t0001g0019 a0001c0003t0001g0020 |
4 | HG01358.hp1 HG02698.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345-684C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 6/13 | chr2 | 27676611 | |||||||
chr2:27676620 | G | A | 8 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0001g0075 others(5): Show |
8 | HG01346.hp2 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1345-675G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 6/13 | chr2 | 27676620 | |||||||
chr2:27676659 | T | TA | 6 | a0001c0001t0001g0152 a0001c0001t0001g0185 a0001c0001t0001g0200 others(3): Show |
6 | HG02486.hp1 HG03130.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-623dupA | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 27676659 | ||||||
chr2:27676759 | A | G | 20 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0001g0075 others(17): Show |
27 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.1345-536A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 6/13 | chr2 | 27676759 | |||||||
chr2:27676767 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1345-528T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 6/13 | chr2 | 27676767 | |||||||
chr2:27676808 | T | C | 19 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0001g0075 others(16): Show |
26 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.1345-487T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 6/13 | chr2 | 27676808 | |||||||
chr2:27676829 | C | CA | 8 | a0001c0001t0001g0015 a0001c0001t0001g0094 a0001c0001t0001g0117 others(5): Show |
10 | HG01433.hp2 HG02074.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1345-448dupA | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 27676829 | ||||||
chr2:27676829 | CA | C | 92 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): Show |
118 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.1345-448delA | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 27676829 | ||||||
chr2:27676836 | A | C | 2 | a0001c0003t0001g0019 a0001c0003t0001g0020 |
4 | HG01358.hp1 HG02698.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1345-459A>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 6/13 | chr2 | 27676836 | |||||||
chr2:27676941 | C | T | 1 | a0001c0007t0001g0038 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1345-354C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 6/13 | chr2 | 27676941 | |||||||
chr2:27677133 | A | G | 1 | a0001c0003t0001g0019 | 2 | HG01358.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1345-162A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 6/13 | chr2 | 27677133 | |||||||
chr2:27677164 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1345-131A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 6/13 | chr2 | 27677164 | |||||||
chr2:27677648 | A | T | 1 | a0001c0001t0001g0209 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1415-90A>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 7/13 | chr2 | 27677648 | |||||||
chr2:27677702 | A | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0134 a0001c0001t0001g0155 |
3 | HG01361.hp1 HG01433.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1415-36A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 7/13 | chr2 | 27677702 | |||||||
chr2:27678092 | C | T | 3 | a0001c0001t0001g0132 a0001c0001t0001g0149 a0001c0001t0001g0160 |
3 | HG03831.hp2 HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1601+168C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27678092 | |||||||
chr2:27678271 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1601+347G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27678271 | |||||||
chr2:27678385 | C | T | 10 | a0001c0003t0001g0019 a0001c0003t0001g0020 a0001c0003t0002g0007 others(7): Show |
16 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1601+461C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27678385 | |||||||
chr2:27678433 | C | T | 1 | a0002c0008t0001g0097 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1601+509C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27678433 | |||||||
chr2:27678517 | A | C | 1 | a0001c0001t0001g0070 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1601+593A>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27678517 | |||||||
chr2:27678532 | CA | C | 10 | a0001c0003t0001g0019 a0001c0003t0001g0020 a0001c0003t0002g0007 others(7): Show |
16 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1601+618delA | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 27678532 | ||||||
chr2:27678633 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1601+709C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27678633 | |||||||
chr2:27678688 | A | G | 1 | a0002c0002t0001g0191 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1601+764A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27678688 | |||||||
chr2:27678758 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1601+834A>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27678758 | |||||||
chr2:27678837 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1601+913G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27678837 | |||||||
chr2:27678861 | C | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(38): Show |
84 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1601+937C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27678861 | |||||||
chr2:27678868 | T | A | 1 | a0001c0001t0001g0105 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1601+944T>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27678868 | |||||||
chr2:27678904 | G | A | 3 | a0001c0001t0001g0091 a0001c0001t0001g0104 a0001c0001t0001g0215 |
3 | NA18939.hp1 NA18974.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1601+980G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27678904 | |||||||
chr2:27678948 | C | G | 4 | a0001c0003t0001g0019 a0001c0003t0001g0020 a0001c0007t0001g0037 others(1): Show |
6 | HG01358.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1601+1024C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27678948 | |||||||
chr2:27679252 | G | A | 10 | a0001c0003t0001g0019 a0001c0003t0001g0020 a0001c0003t0002g0007 others(7): Show |
16 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.1601+1328G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27679252 | |||||||
chr2:27679320 | C | T | 3 | a0001c0001t0001g0053 a0001c0001t0001g0078 a0001c0001t0001g0085 |
3 | HG02723.hp2 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1601+1396C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27679320 | |||||||
chr2:27679321 | G | A | 1 | a0001c0001t0001g0026 | 2 | HG00733.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1601+1397G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27679321 | |||||||
chr2:27679377 | C | T | 7 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0001g0075 others(4): Show |
7 | HG01346.hp2 HG01891.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1601+1453C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27679377 | |||||||
chr2:27679401 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1601+1477G>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27679401 | |||||||
chr2:27679425 | A | C | 1 | a0001c0001t0001g0201 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1601+1501A>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27679425 | |||||||
chr2:27679635 | A | G | 5 | a0001c0001t0001g0051 a0001c0001t0001g0075 a0001c0001t0001g0089 others(2): Show |
5 | HG01346.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1601+1711A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27679635 | |||||||
chr2:27679742 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1601+1818C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27679742 | |||||||
chr2:27679746 | G | T | 1 | a0001c0003t0001g0020 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1601+1822G>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27679746 | |||||||
chr2:27679822 | C | T | 5 | a0001c0001t0001g0051 a0001c0001t0001g0075 a0001c0001t0001g0089 others(2): Show |
5 | HG01346.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.1601+1898C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27679822 | |||||||
chr2:27679847 | C | T | 1 | a0001c0003t0001g0020 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1601+1923C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27679847 | |||||||
chr2:27679857 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1601+1933T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27679857 | |||||||
chr2:27679885 | C | G | 1 | a0001c0001t0001g0090 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1601+1961C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27679885 | |||||||
chr2:27679904 | G | A | 1 | a0001c0003t0001g0020 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1601+1980G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27679904 | |||||||
chr2:27680040 | G | A | 4 | a0001c0003t0002g0018 a0001c0003t0002g0039 a0001c0003t0002g0040 others(1): Show |
5 | HG02486.hp2 HG03225.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1601+2116G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27680040 | |||||||
chr2:27680120 | C | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(78): Show |
107 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1602-2128C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27680120 | |||||||
chr2:27680300 | T | A | 1 | a0001c0006t0001g0017 | 2 | HG02818.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1602-1948T>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27680300 | |||||||
chr2:27680786 | A | AAAC | 6 | a0001c0001t0001g0192 a0001c0001t0001g0197 a0001c0001t0001g0214 others(3): Show |
7 | HG01074.hp2 HG01884.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.1602-1430_1602-142 others(7): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 27680786 | ||||||
chr2:27680786 | AAAC | A | 65 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(62): Show |
82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.1602-1430_1602-142 others(7): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 27680786 | ||||||
chr2:27680786 | AAACAACA others(2): Show |
A | 12 | a0001c0001t0001g0201 a0001c0003t0001g0019 a0001c0003t0001g0020 others(9): Show |
18 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.1602-1436_1602-142 others(13): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 27680786 | ||||||
chr2:27680838 | T | TA | 7 | a0001c0001t0001g0068 a0001c0001t0001g0149 a0001c0003t0001g0019 others(4): Show |
8 | HG01358.hp1 HG02145.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1602-1395dupA | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | 27680838 | ||||||
chr2:27681091 | A | G | 1 | a0002c0002t0001g0168 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1602-1157A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27681091 | |||||||
chr2:27681256 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1602-992T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27681256 | |||||||
chr2:27681620 | G | C | 1 | a0001c0006t0001g0017 | 2 | HG02818.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1602-628G>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27681620 | |||||||
chr2:27682024 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1602-224A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27682024 | |||||||
chr2:27682077 | C | G | 1 | a0001c0003t0001g0019 | 2 | HG01358.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1602-171C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27682077 | |||||||
chr2:27682121 | A | G | 2 | a0001c0007t0001g0037 a0001c0007t0001g0038 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1602-127A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 8/13 | chr2 | 27682121 | |||||||
chr2:27682521 | ATTCT | A | 48 | a0001c0001t0001g0101 a0002c0002t0001g0004 a0002c0002t0001g0009 others(45): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.1713+165_1713+168d others(6): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 27682521 | ||||||
chr2:27682531 | T | C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0213 |
2 | HG02622.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1713+172T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 9/13 | chr2 | 27682531 | |||||||
chr2:27682617 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0049 |
3 | NA18906.hp2 NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1713+258C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 9/13 | chr2 | 27682617 | |||||||
chr2:27682644 | C | T | 6 | a0002c0002t0001g0014 a0002c0002t0001g0025 a0002c0002t0001g0081 others(3): Show |
9 | HG00738.hp2 HG02280.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1713+285C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 9/13 | chr2 | 27682644 | |||||||
chr2:27682789 | T | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0178 |
2 | HG03490.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1713+430T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 9/13 | chr2 | 27682789 | |||||||
chr2:27683778 | C | A | 1 | a0002c0002t0001g0196 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1714-1259C>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 9/13 | chr2 | 27683778 | |||||||
chr2:27683847 | T | C | 10 | a0001c0003t0001g0019 a0001c0003t0002g0007 a0001c0003t0002g0018 others(7): Show |
15 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1714-1190T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 9/13 | chr2 | 27683847 | |||||||
chr2:27684051 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1714-986C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 9/13 | chr2 | 27684051 | |||||||
chr2:27684124 | C | T | 1 | a0002c0002t0001g0233 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1714-913C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 9/13 | chr2 | 27684124 | |||||||
chr2:27684288 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0229 |
2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1714-749C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 9/13 | chr2 | 27684288 | |||||||
chr2:27684427 | C | CA | 11 | a0001c0001t0001g0086 a0001c0001t0001g0149 a0001c0003t0002g0007 others(8): Show |
15 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1714-593dupA | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 27684427 | ||||||
chr2:27684427 | CA | C | 8 | a0001c0001t0001g0129 a0001c0001t0001g0133 a0001c0001t0001g0152 others(5): Show |
8 | HG00423.hp1 HG01515.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714-593delA | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 27684427 | ||||||
chr2:27684535 | T | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0094 others(1): Show |
6 | HG00609.hp1 NA18970.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.1714-502T>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 9/13 | chr2 | 27684535 | |||||||
chr2:27684556 | T | C | 1 | a0001c0001t0001g0028 | 2 | HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1714-481T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 9/13 | chr2 | 27684556 | |||||||
chr2:27684577 | T | C | 3 | a0001c0001t0001g0114 a0001c0001t0001g0145 a0001c0001t0001g0229 |
3 | HG01981.hp1 HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1714-460T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 9/13 | chr2 | 27684577 | |||||||
chr2:27684606 | A | G | 7 | a0001c0003t0002g0007 a0001c0003t0002g0018 a0001c0003t0002g0039 others(4): Show |
11 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.1714-431A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 9/13 | chr2 | 27684606 | |||||||
chr2:27684761 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1714-276C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 9/13 | chr2 | 27684761 | |||||||
chr2:27684950 | G | A | 8 | a0001c0003t0001g0019 a0001c0003t0002g0007 a0001c0003t0002g0018 others(5): Show |
13 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1714-87G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 9/13 | chr2 | 27684950 | |||||||
chr2:27684961 | C | T | 8 | a0001c0003t0001g0019 a0001c0003t0002g0007 a0001c0003t0002g0018 others(5): Show |
13 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1714-76C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 9/13 | chr2 | 27684961 | |||||||
chr2:27685348 | G | A | 1 | a0001c0013t0001g0055 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1954+71G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27685348 | |||||||
chr2:27685598 | G | C | 3 | a0001c0001t0001g0114 a0001c0001t0001g0145 a0001c0001t0001g0229 |
3 | HG01981.hp1 HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1954+321G>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27685598 | |||||||
chr2:27685741 | G | T | 18 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0001g0075 others(15): Show |
25 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.1954+464G>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27685741 | |||||||
chr2:27685776 | T | C | 1 | a0001c0006t0001g0017 | 2 | HG02818.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1954+499T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27685776 | |||||||
chr2:27685800 | A | G | 1 | a0001c0006t0001g0017 | 2 | HG02818.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1954+523A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27685800 | |||||||
chr2:27685837 | T | C | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0231 |
3 | HG02486.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1954+560T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27685837 | |||||||
chr2:27686039 | T | C | 8 | a0001c0003t0001g0019 a0001c0003t0002g0007 a0001c0003t0002g0018 others(5): Show |
13 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1954+762T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27686039 | |||||||
chr2:27686162 | G | A | 1 | a0002c0002t0001g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1954+885G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27686162 | |||||||
chr2:27686233 | A | G | 1 | a0001c0003t0002g0040 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1954+956A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27686233 | |||||||
chr2:27686364 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1954+1087C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27686364 | |||||||
chr2:27686504 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1954+1227C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27686504 | |||||||
chr2:27686702 | A | C | 1 | a0002c0002t0001g0141 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1955-1232A>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27686702 | |||||||
chr2:27686874 | T | C | 1 | a0001c0003t0001g0019 | 2 | HG01358.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1955-1060T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27686874 | |||||||
chr2:27686904 | G | A | 1 | a0001c0003t0001g0019 | 2 | HG01358.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1955-1030G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27686904 | |||||||
chr2:27687055 | C | G | 8 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0001g0075 others(5): Show |
8 | HG01346.hp2 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1955-879C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27687055 | |||||||
chr2:27687239 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1955-695G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27687239 | |||||||
chr2:27687348 | C | T | 6 | a0001c0003t0002g0007 a0001c0003t0002g0018 a0001c0003t0002g0039 others(3): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.1955-586C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27687348 | |||||||
chr2:27687411 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1955-523T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27687411 | |||||||
chr2:27687428 | A | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0082 |
3 | HG00733.hp2 HG01167.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1955-506A>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27687428 | |||||||
chr2:27687565 | T | G | 1 | a0001c0001t0001g0177 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1955-369T>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27687565 | |||||||
chr2:27687617 | A | G | 1 | a0002c0002t0001g0100 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1955-317A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27687617 | |||||||
chr2:27687693 | A | G | 9 | a0001c0003t0001g0019 a0001c0003t0001g0020 a0001c0003t0002g0007 others(6): Show |
15 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1955-241A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27687693 | |||||||
chr2:27687839 | A | C | 39 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(36): Show |
82 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.1955-95A>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27687839 | |||||||
chr2:27687921 | T | C | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0231 |
3 | HG02486.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1955-13T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 10/13 | chr2 | 27687921 | |||||||
chr2:27688079 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2041+59A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 11/13 | chr2 | 27688079 | |||||||
chr2:27688117 | G | A | 1 | a0002c0002t0001g0110 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2041+97G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 11/13 | chr2 | 27688117 | |||||||
chr2:27688153 | G | A | 1 | a0002c0002t0001g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2041+133G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 11/13 | chr2 | 27688153 | |||||||
chr2:27689050 | T | C | 3 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0231 |
3 | HG02486.hp1 HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2109+283T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27689050 | |||||||
chr2:27689111 | T | TTTTA | 7 | a0002c0002t0001g0014 a0002c0002t0001g0025 a0002c0002t0001g0081 others(4): Show |
10 | HG00738.hp2 HG02280.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.2109+365_2109+368d others(6): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 27689111 | ||||||
chr2:27689192 | G | A | 1 | a0002c0002t0001g0189 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2109+425G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27689192 | |||||||
chr2:27689196 | G | A | 6 | a0001c0003t0002g0007 a0001c0003t0002g0018 a0001c0003t0002g0039 others(3): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.2109+429G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27689196 | |||||||
chr2:27689284 | A | G | 1 | a0001c0003t0002g0042 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2109+517A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27689284 | |||||||
chr2:27689371 | G | A | 17 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0001g0075 others(14): Show |
24 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.2109+604G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27689371 | |||||||
chr2:27689514 | C | G | 2 | a0002c0002t0001g0095 a0002c0002t0001g0100 |
2 | HG02280.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.2109+747C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27689514 | |||||||
chr2:27689898 | A | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0229 |
2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2109+1131A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27689898 | |||||||
chr2:27689909 | A | G | 4 | a0001c0001t0001g0090 a0001c0001t0001g0128 a0001c0001t0001g0131 others(1): Show |
4 | HG00280.hp2 HG01069.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.2109+1142A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27689909 | |||||||
chr2:27689935 | C | T | 8 | a0001c0003t0001g0019 a0001c0003t0001g0020 a0001c0003t0002g0007 others(5): Show |
14 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.2109+1168C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27689935 | |||||||
chr2:27689978 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2109+1211A>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27689978 | |||||||
chr2:27690111 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2109+1344G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27690111 | |||||||
chr2:27690321 | T | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(37): Show |
83 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.2109+1554T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27690321 | |||||||
chr2:27690348 | C | T | 6 | a0001c0003t0002g0007 a0001c0003t0002g0018 a0001c0003t0002g0039 others(3): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.2109+1581C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27690348 | |||||||
chr2:27690381 | C | T | 1 | a0001c0003t0001g0020 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2109+1614C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27690381 | |||||||
chr2:27690545 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2109+1778G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27690545 | |||||||
chr2:27690695 | C | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0127 a0001c0001t0001g0154 others(4): Show |
12 | HG01074.hp1 HG01106.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.2109+1928C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27690695 | |||||||
chr2:27690731 | C | T | 2 | a0002c0002t0001g0112 a0002c0002t0001g0210 |
2 | HG02698.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2109+1964C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27690731 | |||||||
chr2:27690742 | A | T | 1 | a0002c0002t0001g0142 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2109+1975A>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27690742 | |||||||
chr2:27690793 | G | A | 1 | a0005c0010t0001g0175 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2109+2026G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27690793 | |||||||
chr2:27690873 | C | G | 1 | a0001c0006t0001g0017 | 2 | HG02818.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2109+2106C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27690873 | |||||||
chr2:27690973 | A | G | 1 | a0001c0001t0001g0063 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2109+2206A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27690973 | |||||||
chr2:27691295 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2110-2390T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27691295 | |||||||
chr2:27691514 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2110-2171T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27691514 | |||||||
chr2:27691583 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2110-2102T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27691583 | |||||||
chr2:27691592 | C | CT | 5 | a0001c0001t0001g0109 a0001c0001t0001g0149 a0001c0006t0001g0017 others(2): Show |
7 | HG02300.hp2 HG02818.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.2110-2076dupT | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 27691592 | ||||||
chr2:27691592 | CT | C | 14 | a0001c0001t0001g0053 a0001c0001t0001g0076 a0001c0001t0001g0078 others(11): Show |
19 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.2110-2076delT | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 27691592 | ||||||
chr2:27691602 | T | C | 8 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0001g0075 others(5): Show |
8 | HG01346.hp2 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2110-2083T>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27691602 | |||||||
chr2:27691662 | C | T | 2 | a0001c0007t0001g0037 a0001c0007t0001g0038 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.2110-2023C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27691662 | |||||||
chr2:27691710 | C | G | 2 | a0002c0002t0001g0102 a0002c0002t0001g0119 |
2 | HG01884.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2110-1975C>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27691710 | |||||||
chr2:27691746 | C | T | 1 | a0001c0003t0001g0019 | 2 | HG01358.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.2110-1939C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27691746 | |||||||
chr2:27691965 | TTC | T | 2 | a0001c0003t0001g0019 a0001c0003t0001g0020 |
4 | HG01358.hp1 HG02698.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2110-1700_2110-169 others(6): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 27691965 | ||||||
chr2:27691965 | TTCTCTC | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 |
3 | HG06807.hp2 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2110-1704_2110-169 others(10): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 27691965 | ||||||
chr2:27692059 | T | A | 1 | a0001c0001t0001g0225 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2110-1626T>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27692059 | |||||||
chr2:27692138 | A | G | 17 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0001g0075 others(14): Show |
24 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.2110-1547A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27692138 | |||||||
chr2:27692677 | G | C | 1 | a0001c0001t0001g0058 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2110-1008G>C | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27692677 | |||||||
chr2:27692752 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2110-933C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27692752 | |||||||
chr2:27692792 | A | G | 61 | a0001c0001t0001g0101 a0001c0003t0002g0042 a0002c0002t0001g0004 others(58): Show |
78 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.2110-893A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27692792 | |||||||
chr2:27692927 | G | GATTT | 6 | a0001c0003t0002g0007 a0001c0003t0002g0018 a0001c0003t0002g0039 others(3): Show |
10 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.2110-734_2110-731d others(6): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 27692927 | ||||||
chr2:27692927 | G | GATTTATT others(9): Show |
1 | a0001c0003t0001g0020 | 2 | HG03139.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2110-746_2110-731d others(18): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 27692927 | ||||||
chr2:27693118 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2110-567G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27693118 | |||||||
chr2:27693124 | A | ATTTTGCA others(14): Show |
17 | a0001c0001t0001g0051 a0001c0001t0001g0071 a0001c0001t0001g0075 others(14): Show |
24 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.2110-550_2110-549i others(23): Show |
SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 27693124 | ||||||
chr2:27693224 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2110-461G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27693224 | |||||||
chr2:27693236 | A | AT | 42 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(39): Show |
87 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.2110-433dupT | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 27693236 | ||||||
chr2:27693397 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2110-288A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 12/13 | chr2 | 27693397 | |||||||
chr2:27694040 | C | T | 1 | a0001c0006t0001g0017 | 2 | HG02818.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2179+286C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 13/13 | chr2 | 27694040 | |||||||
chr2:27694136 | C | T | 1 | a0002c0002t0001g0096 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2179+382C>T | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 13/13 | chr2 | 27694136 | |||||||
chr2:27694340 | G | A | 2 | a0001c0007t0001g0037 a0001c0007t0001g0038 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.2180-294G>A | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 13/13 | chr2 | 27694340 | |||||||
chr2:27694444 | A | G | 7 | a0001c0003t0002g0007 a0001c0003t0002g0018 a0001c0003t0002g0039 others(4): Show |
11 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.2180-190A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 13/13 | chr2 | 27694444 | |||||||
chr2:27694501 | A | G | 2 | a0002c0002t0001g0140 a0002c0002t0001g0187 |
2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2180-133A>G | SLC4A1AP | ENSG00000163798.14 | transcript | ENST00000326019.11 | protein_coding | 13/13 | chr2 | 27694501 |