Item | Value |
---|---|
geneid | 285141 |
ensemblid | ENSG00000204334.8 |
hgncid | 44395 |
symbol | ERICH2 |
name | glutamate rich 2 |
refseq_nuc | NM_001290030.2 |
refseq_prot | NP_001276959.1 |
ensembl_nuc | ENST00000697325.1 |
ensembl_prot | ENSP00000513252.1 |
mane_status | MANE Select |
chr | chr2 |
start | 170770378 |
end | 170798977 |
strand | + |
ver | v1.2 |
region | chr2:170770378-170798977 |
region5000 | chr2:170765378-170803977 |
regionname0 | ERICH2_chr2_170770378_170798977 |
regionname5000 | ERICH2_chr2_170765378_170803977 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 436 | 337 | 66 | 59 | 161 | 17 | 33 | 128 | ERICH2_chr2_170765378_170803977 | ERICH2 | MDTDI others(431): Show |
chr2 | 170765378 | 170803977 |
a0002 | 0/0 | 436 | 18 | 0 | 2 | 11 | 1 | 4 | 10 | ERICH2_chr2_170765378_170803977 | ERICH2 | MDTDI others(431): Show |
chr2 | 170765378 | 170803977 |
a0003 | 1/0 | 436 | 13 | 12 | 0 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | MDTDI others(431): Show |
chr2 | 170765378 | 170803977 |
a0004 | 0/0 | 438 | 9 | 6 | 1 | 0 | 0 | 2 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | MDTDI others(433): Show |
chr2 | 170765378 | 170803977 |
a0005 | 0/0 | 436 | 8 | 6 | 2 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | MDTDI others(431): Show |
chr2 | 170765378 | 170803977 |
a0006 | 0/0 | 436 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | MDTDI others(431): Show |
chr2 | 170765378 | 170803977 |
a0007 | 0/0 | 436 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | MDTDI others(431): Show |
chr2 | 170765378 | 170803977 |
a0008 | 0/0 | 436 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | MDTDI others(431): Show |
chr2 | 170765378 | 170803977 |
a0009 | 0/0 | 440 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | MDTDI others(435): Show |
chr2 | 170765378 | 170803977 |
a0010 | 0/0 | 436 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | MDTDI others(431): Show |
chr2 | 170765378 | 170803977 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1308 | 225 | 59 | 38 | 95 | 10 | 23 | ERICH2_chr2_170765378_170803977 | ERICH2 | ATGGA others(1303): Show |
chr2 | 170765378 | 170803977 | ||
a0001c0002 | 0/1 | 1308 | 108 | 6 | 21 | 66 | 7 | 7 | ERICH2_chr2_170765378_170803977 | ERICH2 | ATGGA others(1303): Show |
chr2 | 170765378 | 170803977 | ||
a0001c0007 | 0/0 | 1308 | 3 | 0 | 0 | 0 | 0 | 3 | ERICH2_chr2_170765378_170803977 | ERICH2 | ATGGA others(1303): Show |
chr2 | 170765378 | 170803977 | ||
a0001c0011 | 0/0 | 1308 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | ATGGA others(1303): Show |
chr2 | 170765378 | 170803977 | ||
a0002c0003 | 0/0 | 1308 | 18 | 0 | 2 | 11 | 1 | 4 | ERICH2_chr2_170765378_170803977 | ERICH2 | ATGGA others(1303): Show |
chr2 | 170765378 | 170803977 | ||
a0003c0004 | 1/0 | 1308 | 13 | 12 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | ATGGA others(1303): Show |
chr2 | 170765378 | 170803977 | ||
a0004c0006 | 0/0 | 1314 | 6 | 6 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | ATGGA others(1309): Show |
chr2 | 170765378 | 170803977 | ||
a0004c0008 | 0/0 | 1314 | 3 | 0 | 1 | 0 | 0 | 2 | ERICH2_chr2_170765378_170803977 | ERICH2 | ATGGA others(1309): Show |
chr2 | 170765378 | 170803977 | ||
a0005c0005 | 0/0 | 1308 | 7 | 5 | 2 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | ATGGA others(1303): Show |
chr2 | 170765378 | 170803977 | ||
a0005c0015 | 0/0 | 1308 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | ATGGA others(1303): Show |
chr2 | 170765378 | 170803977 | ||
a0006c0012 | 0/0 | 1308 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | ATGGA others(1303): Show |
chr2 | 170765378 | 170803977 | ||
a0007c0010 | 0/0 | 1308 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | ATGGA others(1303): Show |
chr2 | 170765378 | 170803977 | ||
a0008c0014 | 0/0 | 1308 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | ATGGA others(1303): Show |
chr2 | 170765378 | 170803977 | ||
a0009c0013 | 0/0 | 1320 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | ATGGA others(1315): Show |
chr2 | 170765378 | 170803977 | ||
a0010c0009 | 0/0 | 1308 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | ATGGA others(1303): Show |
chr2 | 170765378 | 170803977 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1698 | 225 | 59 | 38 | 95 | 10 | 23 | ERICH2_chr2_170765378_170803977 | ERICH2 | GTGGC others(1693): Show |
chr2 | 170765378 | 170803977 |
a0001c0002t0001 | 0/1 | 1698 | 107 | 6 | 21 | 65 | 7 | 7 | ERICH2_chr2_170765378_170803977 | ERICH2 | GTGGC others(1693): Show |
chr2 | 170765378 | 170803977 |
a0001c0002t0003 | 0/0 | 1698 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | GTGGC others(1693): Show |
chr2 | 170765378 | 170803977 |
a0001c0007t0001 | 0/0 | 1698 | 3 | 0 | 0 | 0 | 0 | 3 | ERICH2_chr2_170765378_170803977 | ERICH2 | GTGGC others(1693): Show |
chr2 | 170765378 | 170803977 |
a0001c0011t0001 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | GTGGC others(1693): Show |
chr2 | 170765378 | 170803977 |
a0002c0003t0001 | 0/0 | 1698 | 18 | 0 | 2 | 11 | 1 | 4 | ERICH2_chr2_170765378_170803977 | ERICH2 | GTGGC others(1693): Show |
chr2 | 170765378 | 170803977 |
a0003c0004t0001 | 1/0 | 1698 | 13 | 12 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | GTGGC others(1693): Show |
chr2 | 170765378 | 170803977 |
a0004c0006t0002 | 0/0 | 1704 | 6 | 6 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | GTGGC others(1699): Show |
chr2 | 170765378 | 170803977 |
a0004c0008t0001 | 0/0 | 1704 | 3 | 0 | 1 | 0 | 0 | 2 | ERICH2_chr2_170765378_170803977 | ERICH2 | GTGGC others(1699): Show |
chr2 | 170765378 | 170803977 |
a0005c0005t0001 | 0/0 | 1698 | 7 | 5 | 2 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | GTGGC others(1693): Show |
chr2 | 170765378 | 170803977 |
a0005c0015t0001 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | GTGGC others(1693): Show |
chr2 | 170765378 | 170803977 |
a0006c0012t0001 | 0/0 | 1698 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | GTGGC others(1693): Show |
chr2 | 170765378 | 170803977 |
a0007c0010t0001 | 0/0 | 1698 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | GTGGC others(1693): Show |
chr2 | 170765378 | 170803977 |
a0008c0014t0001 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | GTGGC others(1693): Show |
chr2 | 170765378 | 170803977 |
a0009c0013t0001 | 0/0 | 1710 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | GTGGC others(1705): Show |
chr2 | 170765378 | 170803977 |
a0010c0009t0001 | 0/0 | 1698 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | GTGGC others(1693): Show |
chr2 | 170765378 | 170803977 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 27 | 0 | 5 | 20 | 1 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0003 | 0/0 | 19 | 0 | 4 | 12 | 2 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0005 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0006 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0008 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0009 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0010 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0051 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0001 | 0/0 | 51 | 4 | 7 | 37 | 1 | 2 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0007 | 0/0 | 8 | 0 | 5 | 0 | 3 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0012 | 0/0 | 5 | 0 | 1 | 0 | 2 | 2 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0002t0003g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0007t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0007t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0001c0011t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0002c0003t0001g0004 | 0/0 | 11 | 0 | 1 | 8 | 0 | 2 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0002c0003t0001g0013 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0002c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0002c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0002c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0002c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0003c0004t0001g0011 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0003c0004t0001g0038 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0003c0004t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0003c0004t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0003c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0003c0004t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0003c0004t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0004c0006t0002g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0004c0006t0002g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0004c0006t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0004c0006t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0004c0008t0001g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0004c0008t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0005c0005t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0005c0005t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0005c0005t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0005c0005t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0005c0005t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0005c0005t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0005c0015t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0006c0012t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0007c0010t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0008c0014t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0009c0013t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
a0010c0009t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0085 | EUR | GBR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0012 | EUR | GBR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0012 | EUR | GBR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | GBR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | FIN | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | FIN | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | FIN | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0121 | EUR | FIN | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00423 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | CHS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | CHS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00621 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | CHS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00733 | hp2 | a0005 | c0005 | t0001 | g0059 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0035 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01071 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01074 | hp1 | a0004 | c0008 | t0001 | g0077 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0035 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01168 | hp1 | a0002 | c0003 | t0001 | g0013 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0087 | AMR | CLM | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01261 | hp2 | a0005 | c0005 | t0001 | g0058 | AMR | CLM | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01361 | hp1 | a0007 | c0010 | t0001 | g0023 | AMR | CLM | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01361 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | CLM | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | CLM | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | IBS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0007 | EUR | IBS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01516 | hp2 | a0002 | c0003 | t0001 | g0013 | EUR | IBS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0007 | EUR | IBS | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | PEL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PEL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02027 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | KHV | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02055 | hp2 | a0003 | c0004 | t0001 | g0011 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | KHV | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0091 | EAS | KHV | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02145 | hp1 | a0003 | c0004 | t0001 | g0011 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CDX | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0075 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02258 | hp1 | a0008 | c0014 | t0001 | g0127 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02280 | hp1 | a0003 | c0004 | t0001 | g0038 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02451 | hp2 | a0001 | c0011 | t0001 | g0124 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0054 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02622 | hp2 | a0003 | c0004 | t0001 | g0071 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02647 | hp1 | a0004 | c0006 | t0002 | g0045 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02683 | hp1 | a0002 | c0003 | t0001 | g0113 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02735 | hp1 | a0001 | c0007 | t0001 | g0112 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02809 | hp1 | a0004 | c0006 | t0002 | g0046 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02818 | hp1 | a0003 | c0004 | t0001 | g0011 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02886 | hp1 | a0003 | c0004 | t0001 | g0011 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02895 | hp2 | a0005 | c0005 | t0001 | g0057 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02896 | hp1 | a0003 | c0004 | t0001 | g0072 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02896 | hp2 | a0004 | c0006 | t0002 | g0045 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02897 | hp1 | a0005 | c0005 | t0001 | g0056 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02897 | hp2 | a0004 | c0006 | t0002 | g0129 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02970 | hp1 | a0004 | c0006 | t0002 | g0130 | AFR | ESN | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0089 | AFR | MSL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | ESN | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03195 | hp1 | a0004 | c0006 | t0002 | g0046 | AFR | ESN | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03209 | hp1 | a0003 | c0004 | t0001 | g0011 | AFR | MSL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03209 | hp2 | a0005 | c0005 | t0001 | g0026 | AFR | MSL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03225 | hp2 | a0003 | c0004 | t0001 | g0011 | AFR | MSL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03453 | hp1 | a0003 | c0004 | t0001 | g0069 | AFR | MSL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03486 | hp2 | a0005 | c0015 | t0001 | g0055 | AFR | MSL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03490 | hp1 | a0004 | c0008 | t0001 | g0048 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03492 | hp1 | a0002 | c0003 | t0001 | g0004 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03492 | hp2 | a0004 | c0008 | t0001 | g0048 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03688 | hp1 | a0001 | c0007 | t0001 | g0013 | SAS | STU | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03704 | hp1 | a0001 | c0007 | t0001 | g0013 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03831 | hp2 | a0009 | c0013 | t0001 | g0001 | SAS | BEB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0076 | SAS | BEB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0053 | SAS | BEB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | STU | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG04228 | hp1 | a0002 | c0003 | t0001 | g0013 | SAS | STU | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18522 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | YRI | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18906 | hp2 | a0003 | c0004 | t0001 | g0070 | AFR | YRI | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18939 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18943 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18952 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18959 | hp2 | a0002 | c0003 | t0001 | g0111 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18965 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18966 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18967 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18967 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18977 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18980 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18986 | hp2 | a0002 | c0003 | t0001 | g0110 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18989 | hp2 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18999 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18999 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19006 | hp2 | a0002 | c0003 | t0001 | g0114 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19011 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19043 | hp2 | a0010 | c0009 | t0001 | g0081 | AFR | LWK | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19055 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19063 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19072 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19076 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19091 | hp1 | a0002 | c0003 | t0001 | g0004 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19240 | hp1 | a0005 | c0005 | t0001 | g0060 | AFR | YRI | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA20129 | hp1 | a0003 | c0004 | t0001 | g0170 | AFR | ASW | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA20129 | hp2 | a0005 | c0005 | t0001 | g0026 | AFR | ASW | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0007 | EUR | TSI | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | TSI | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | TSI | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA20905 | hp1 | a0002 | c0003 | t0001 | g0004 | SAS | GIH | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | GIH | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG01123 | hp2 | a0006 | c0012 | t0001 | g0001 | AMR | CLM | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG06807 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | USA | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | USA | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | USA | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0067 | REF | REF | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
homoSapiens | grch38p0 | a0003 | c0004 | t0001 | g0038 | REF | REF | ERICH2_chr2_170765378_170803977 | ERICH2 | chr2 | 170765378 | 170803977 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:170770709 | C | T | 1 | a0005 | 8 | HG00733.hp2 HG01261.hp2 HG02895.hp2 others(5): Show |
missense_variant | MODERATE | c.28C>T | p.Pro10Ser | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/10 | 332/1698 | 28/1311 | 10/436 | chr2 | 170770709 | |||
chr2:170770929 | G | T | 1 | a0008 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.248G>T | p.Trp83Leu | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/10 | 552/1698 | 248/1311 | 83/436 | chr2 | 170770929 | |||
chr2:170770974 | T | TGCCCCC | 1 | a0004 | 9 | HG01074.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
disruptive_inframe_insertion | MODERATE | c.309_314dupCCCGCC | p.Pro104_Pro105dup | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/10 | 619/1698 | 315/1311 | 105/436 | INFO_REALIGN_3_PRIME | chr2 | 170770974 | ||
chr2:170770974 | T | TGCCCCCG others(5): Show |
1 | a0009 | 1 | HG03831.hp2 | disruptive_inframe_insertion | MODERATE | c.303_314dupCCCGCCCC others(4): Show |
p.Pro102_Pro105dup | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/10 | 619/1698 | 315/1311 | 105/436 | INFO_REALIGN_3_PRIME | chr2 | 170770974 | ||
chr2:170771066 | G | T | 1 | a0006 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.385G>T | p.Val129Leu | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/10 | 689/1698 | 385/1311 | 129/436 | chr2 | 170771066 | |||
chr2:170771129 | G | A | 1 | a0002 | 18 | HG01168.hp1 HG01361.hp2 HG01516.hp2 others(15): Show |
missense_variant | MODERATE | c.448G>A | p.Ala150Thr | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/10 | 752/1698 | 448/1311 | 150/436 | chr2 | 170771129 | |||
chr2:170771166 | T | G | 9 | a0001 a0002 a0004 others(6): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
missense_variant | MODERATE | c.485T>G | p.Leu162Arg | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/10 | 789/1698 | 485/1311 | 162/436 | chr2 | 170771166 | |||
chr2:170782320 | G | A | 1 | a0010 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.799G>A | p.Glu267Lys | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 6/10 | 1103/1698 | 799/1311 | 267/436 | chr2 | 170782320 | |||
chr2:170798862 | G | A | 1 | a0004 | 6 | HG02647.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
missense_variant | MODERATE | c.1279G>A | p.Glu427Lys | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 10/10 | 1583/1698 | 1279/1311 | 427/436 | chr2 | 170798862 | |||
chr2:170798874 | G | A | 1 | a0007 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.1291G>A | p.Glu431Lys | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 10/10 | 1595/1698 | 1291/1311 | 431/436 | chr2 | 170798874 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:170770807 | G | C | 1 | a0005c0005 | 7 | HG00733.hp2 HG01261.hp2 HG02895.hp2 others(4): Show |
synonymous_variant | LOW | c.126G>C | p.Ala42Ala | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/10 | 430/1698 | 126/1311 | 42/436 | chr2 | 170770807 | |||
chr2:170771047 | C | G | 1 | a0001c0007 | 3 | HG02735.hp1 HG03688.hp1 HG03704.hp1 |
synonymous_variant | LOW | c.366C>G | p.Pro122Pro | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/10 | 670/1698 | 366/1311 | 122/436 | chr2 | 170771047 | |||
chr2:170782364 | A | G | 1 | a0001c0011 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.843A>G | p.Ser281Ser | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 6/10 | 1147/1698 | 843/1311 | 281/436 | chr2 | 170782364 | |||
chr2:170792892 | C | T | 3 | a0001c0002 a0006c0012 a0009c0013 |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
synonymous_variant | LOW | c.1086C>T | p.Tyr362Tyr | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/10 | 1390/1698 | 1086/1311 | 362/436 | chr2 | 170792892 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:170770437 | C | A | 1 | a0001c0002t0003 | 1 | NA18952.hp2 | 5_prime_UTR_variant | MODIFIER | c.-245C>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/10 | 245 | chr2 | 170770437 | ||||||
chr2:170798950 | T | A | 1 | a0004c0006t0002 | 6 | HG02647.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*56T>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 10/10 | 56 | chr2 | 170798950 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:170771267 | C | A | 2 | a0001c0002t0001g0053 a0001c0002t0001g0054 |
2 | HG02602.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.506+80C>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170771267 | |||||||
chr2:170771516 | C | G | 1 | a0003c0004t0001g0170 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.506+329C>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170771516 | |||||||
chr2:170771564 | GCC | G | 7 | a0005c0005t0001g0026 a0005c0005t0001g0056 a0005c0005t0001g0057 others(4): Show |
8 | HG00733.hp2 HG01261.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.506+379_506+380del others(2): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170771564 | ||||||
chr2:170771857 | T | C | 1 | a0001c0002t0001g0061 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.506+670T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170771857 | |||||||
chr2:170772280 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0062 |
9 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.506+1093T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170772280 | |||||||
chr2:170772553 | C | G | 50 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(47): Show |
105 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.506+1366C>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170772553 | |||||||
chr2:170772749 | G | T | 1 | a0001c0001t0001g0015 | 5 | HG00408.hp2 HG02040.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.506+1562G>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170772749 | |||||||
chr2:170772802 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.506+1615G>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170772802 | |||||||
chr2:170772932 | T | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0062 a0001c0001t0001g0064 others(2): Show |
12 | HG01891.hp1 HG02486.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.506+1745T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170772932 | |||||||
chr2:170772937 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0132 |
3 | HG02970.hp2 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.506+1750C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170772937 | |||||||
chr2:170773212 | T | A | 1 | a0005c0015t0001g0055 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.506+2025T>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170773212 | |||||||
chr2:170773526 | T | C | 1 | a0001c0002t0001g0007 | 8 | HG00733.hp1 HG01109.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.506+2339T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170773526 | |||||||
chr2:170773586 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.506+2399A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170773586 | |||||||
chr2:170773602 | C | T | 4 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(1): Show |
6 | HG02647.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.506+2415C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170773602 | |||||||
chr2:170773760 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.506+2573C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170773760 | |||||||
chr2:170773807 | C | T | 6 | a0005c0005t0001g0026 a0005c0005t0001g0056 a0005c0005t0001g0057 others(3): Show |
7 | HG00733.hp2 HG01261.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.506+2620C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170773807 | |||||||
chr2:170773974 | G | A | 1 | a0001c0002t0001g0068 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.506+2787G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170773974 | |||||||
chr2:170774010 | C | G | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(40): Show |
92 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.506+2823C>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170774010 | |||||||
chr2:170774121 | C | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(40): Show |
92 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.506+2934C>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170774121 | |||||||
chr2:170774562 | A | ATCT | 57 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(54): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.507-2583_507-2581d others(5): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170774562 | ||||||
chr2:170774564 | C | CTTCTTTT others(5): Show |
1 | a0008c0014t0001g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.507-2581_507-2580i others(14): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170774564 | ||||||
chr2:170774564 | C | CTTCTTTT others(6): Show |
4 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(1): Show |
6 | HG02647.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.507-2581_507-2580i others(15): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170774564 | ||||||
chr2:170774564 | CTTTT | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(34): Show |
83 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.507-2567_507-2564d others(6): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170774564 | ||||||
chr2:170774565 | T | TTC | 16 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0017 others(13): Show |
24 | HG00423.hp1 HG00733.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.507-2581_507-2580i others(4): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170774565 | ||||||
chr2:170774566 | T | TC | 58 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(55): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.507-2581_507-2580i others(3): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170774566 | |||||||
chr2:170774567 | T | C | 7 | a0001c0001t0001g0008 a0001c0002t0001g0001 a0001c0002t0001g0032 others(4): Show |
9 | HG01168.hp2 NA18522.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.507-2580T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170774567 | |||||||
chr2:170774570 | T | C | 1 | a0001c0001t0001g0044 | 2 | NA18954.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.507-2577T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170774570 | |||||||
chr2:170774571 | T | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(34): Show |
83 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.507-2576T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170774571 | |||||||
chr2:170774630 | C | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(112): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.507-2517C>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170774630 | |||||||
chr2:170774648 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.507-2499C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170774648 | |||||||
chr2:170774715 | A | G | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(113): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.507-2432A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170774715 | |||||||
chr2:170774733 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.507-2414G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170774733 | |||||||
chr2:170774748 | G | T | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(103): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.507-2399G>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170774748 | |||||||
chr2:170774796 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.507-2351C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170774796 | |||||||
chr2:170774856 | T | C | 1 | a0001c0002t0001g0075 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.507-2291T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170774856 | |||||||
chr2:170774923 | G | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(40): Show |
92 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.507-2224G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170774923 | |||||||
chr2:170775137 | C | CTAAATA | 168 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.507-2006_507-2005i others(8): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170775137 | ||||||
chr2:170775248 | T | C | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(40): Show |
92 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.507-1899T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170775248 | |||||||
chr2:170775270 | T | TA | 4 | a0001c0001t0001g0016 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
7 | HG00621.hp2 HG02922.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.507-1864dupA | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170775270 | ||||||
chr2:170775330 | G | T | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(40): Show |
92 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.507-1817G>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170775330 | |||||||
chr2:170775407 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.507-1740G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170775407 | |||||||
chr2:170775419 | G | A | 1 | a0001c0002t0001g0053 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.507-1728G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170775419 | |||||||
chr2:170775715 | C | T | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(110): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.507-1432C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170775715 | |||||||
chr2:170775771 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0102 a0001c0001t0001g0132 |
4 | HG02970.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.507-1376C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170775771 | |||||||
chr2:170775875 | C | CTT | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.507-1272_507-1271i others(4): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170775875 | |||||||
chr2:170775891 | C | T | 39 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0012 others(36): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.507-1256C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170775891 | |||||||
chr2:170775927 | T | C | 1 | a0004c0008t0001g0048 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.507-1220T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170775927 | |||||||
chr2:170775931 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0083 |
12 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.507-1216A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170775931 | |||||||
chr2:170776139 | C | A | 1 | a0001c0001t0001g0105 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.507-1008C>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170776139 | |||||||
chr2:170776139 | C | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(39): Show |
91 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.507-1008C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170776139 | |||||||
chr2:170776143 | A | G | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(40): Show |
92 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.507-1004A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170776143 | |||||||
chr2:170776198 | T | C | 1 | a0001c0002t0001g0084 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.507-949T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170776198 | |||||||
chr2:170776320 | T | C | 4 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(1): Show |
6 | HG02647.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.507-827T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170776320 | |||||||
chr2:170776438 | T | C | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(40): Show |
92 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.507-709T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170776438 | |||||||
chr2:170776440 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.507-707C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170776440 | |||||||
chr2:170776488 | A | G | 63 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(60): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.507-659A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170776488 | |||||||
chr2:170776503 | G | A | 3 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0083 |
12 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.507-644G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170776503 | |||||||
chr2:170776516 | C | A | 73 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(70): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.507-631C>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170776516 | |||||||
chr2:170776737 | G | C | 1 | a0001c0002t0001g0085 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.507-410G>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170776737 | |||||||
chr2:170776755 | C | T | 7 | a0005c0005t0001g0026 a0005c0005t0001g0056 a0005c0005t0001g0057 others(4): Show |
8 | HG00733.hp2 HG01261.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.507-392C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170776755 | |||||||
chr2:170776755 | CAG | C | 6 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(3): Show |
9 | HG02258.hp1 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.507-388_507-387del others(2): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170776755 | ||||||
chr2:170776765 | CT | C | 48 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(45): Show |
99 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.507-369delT | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 170776765 | ||||||
chr2:170776801 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.507-346G>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170776801 | |||||||
chr2:170776811 | A | G | 7 | a0005c0005t0001g0026 a0005c0005t0001g0056 a0005c0005t0001g0057 others(4): Show |
8 | HG00733.hp2 HG01261.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.507-336A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170776811 | |||||||
chr2:170776928 | G | C | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(40): Show |
92 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.507-219G>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170776928 | |||||||
chr2:170777044 | A | G | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(40): Show |
92 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.507-103A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170777044 | |||||||
chr2:170777063 | C | A | 4 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(1): Show |
6 | HG02647.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.507-84C>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170777063 | |||||||
chr2:170777111 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.507-36T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 1/9 | chr2 | 170777111 | |||||||
chr2:170777187 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.537+10T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 2/9 | chr2 | 170777187 | |||||||
chr2:170777513 | G | A | 6 | a0005c0005t0001g0026 a0005c0005t0001g0056 a0005c0005t0001g0057 others(3): Show |
7 | HG00733.hp2 HG01261.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.586+88G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 3/9 | chr2 | 170777513 | |||||||
chr2:170777550 | A | G | 2 | a0001c0002t0001g0021 a0001c0002t0001g0101 |
4 | NA18945.hp2 NA18965.hp1 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-94A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 3/9 | chr2 | 170777550 | |||||||
chr2:170777594 | C | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(36): Show |
86 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.587-50C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 3/9 | chr2 | 170777594 | |||||||
chr2:170777837 | TA | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(113): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.623+158delA | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 4/9 | chr2 | 170777837 | |||||||
chr2:170777885 | C | T | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(40): Show |
92 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.623+205C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 4/9 | chr2 | 170777885 | |||||||
chr2:170777989 | G | C | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(40): Show |
92 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.623+309G>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 4/9 | chr2 | 170777989 | |||||||
chr2:170778007 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.623+327A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 4/9 | chr2 | 170778007 | |||||||
chr2:170778088 | G | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(40): Show |
92 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.623+408G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 4/9 | chr2 | 170778088 | |||||||
chr2:170778396 | T | C | 38 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(35): Show |
85 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.623+716T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 4/9 | chr2 | 170778396 | |||||||
chr2:170778658 | G | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(112): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.623+978G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 4/9 | chr2 | 170778658 | |||||||
chr2:170778673 | A | T | 1 | a0001c0001t0001g0128 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.623+993A>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 4/9 | chr2 | 170778673 | |||||||
chr2:170778828 | C | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0074 |
6 | HG01433.hp1 HG01928.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.624-965C>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 4/9 | chr2 | 170778828 | |||||||
chr2:170778865 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.624-928G>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 4/9 | chr2 | 170778865 | |||||||
chr2:170778883 | C | T | 73 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(70): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.624-910C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 4/9 | chr2 | 170778883 | |||||||
chr2:170778904 | G | A | 43 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(40): Show |
92 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.624-889G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 4/9 | chr2 | 170778904 | |||||||
chr2:170778975 | C | A | 73 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(70): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.624-818C>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 4/9 | chr2 | 170778975 | |||||||
chr2:170778984 | T | C | 73 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(70): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.624-809T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 4/9 | chr2 | 170778984 | |||||||
chr2:170779255 | G | A | 73 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(70): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.624-538G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 4/9 | chr2 | 170779255 | |||||||
chr2:170779257 | T | C | 1 | a0001c0001t0001g0138 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.624-536T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 4/9 | chr2 | 170779257 | |||||||
chr2:170779276 | T | C | 74 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(71): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.624-517T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 4/9 | chr2 | 170779276 | |||||||
chr2:170779389 | G | A | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(39): Show |
90 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.624-404G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 4/9 | chr2 | 170779389 | |||||||
chr2:170779559 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.624-234G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 4/9 | chr2 | 170779559 | |||||||
chr2:170779697 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.624-96T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 4/9 | chr2 | 170779697 | |||||||
chr2:170779913 | T | A | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 |
3 | HG02486.hp2 HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.719+25T>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | chr2 | 170779913 | |||||||
chr2:170779922 | G | A | 1 | a0001c0002t0001g0032 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.719+34G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | chr2 | 170779922 | |||||||
chr2:170779986 | C | T | 37 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(34): Show |
83 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.719+98C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | chr2 | 170779986 | |||||||
chr2:170780028 | G | A | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(39): Show |
90 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.719+140G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | chr2 | 170780028 | |||||||
chr2:170780081 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.719+193G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | chr2 | 170780081 | |||||||
chr2:170780151 | ATAT | A | 5 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(2): Show |
7 | HG02258.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.719+268_719+270del others(3): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 170780151 | ||||||
chr2:170780340 | G | A | 37 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(34): Show |
83 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.719+452G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | chr2 | 170780340 | |||||||
chr2:170780634 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.719+746A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | chr2 | 170780634 | |||||||
chr2:170780777 | A | G | 1 | a0004c0006t0002g0130 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.719+889A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | chr2 | 170780777 | |||||||
chr2:170781350 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.720-891G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | chr2 | 170781350 | |||||||
chr2:170781366 | T | C | 1 | a0008c0014t0001g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.720-875T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | chr2 | 170781366 | |||||||
chr2:170781405 | G | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(39): Show |
90 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.720-836G>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | chr2 | 170781405 | |||||||
chr2:170781490 | C | T | 1 | a0001c0001t0001g0052 | 2 | HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.720-751C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | chr2 | 170781490 | |||||||
chr2:170781507 | G | A | 1 | a0003c0004t0001g0069 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.720-734G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | chr2 | 170781507 | |||||||
chr2:170781590 | G | A | 5 | a0001c0001t0001g0108 a0004c0006t0002g0045 a0004c0006t0002g0046 others(2): Show |
7 | HG02647.hp1 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.720-651G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | chr2 | 170781590 | |||||||
chr2:170781631 | T | TA | 7 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0074 others(4): Show |
11 | HG01261.hp2 HG01433.hp1 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.720-593dupA | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 170781631 | ||||||
chr2:170781631 | TA | T | 36 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(33): Show |
83 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.720-593delA | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 170781631 | ||||||
chr2:170781728 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.720-513A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | chr2 | 170781728 | |||||||
chr2:170781736 | T | TTTACTAA others(48): Show |
36 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(33): Show |
82 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.720-492_720-491ins others(55): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 170781736 | ||||||
chr2:170781736 | T | TTTACTAA others(48): Show |
1 | a0001c0001t0001g0125 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.720-497_720-496ins others(55): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 170781736 | ||||||
chr2:170781831 | T | A | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(39): Show |
90 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.720-410T>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | chr2 | 170781831 | |||||||
chr2:170781969 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.720-272T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | chr2 | 170781969 | |||||||
chr2:170782035 | C | T | 1 | a0008c0014t0001g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.720-206C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | chr2 | 170782035 | |||||||
chr2:170782122 | CTATT | C | 62 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(59): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.720-116_720-113del others(4): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr2 | 170782122 | ||||||
chr2:170782767 | T | A | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(39): Show |
90 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.868+378T>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 6/9 | chr2 | 170782767 | |||||||
chr2:170782838 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0078 a0004c0008t0001g0077 |
4 | HG01074.hp1 HG02055.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.868+449T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 6/9 | chr2 | 170782838 | |||||||
chr2:170782879 | G | C | 1 | a0001c0001t0001g0066 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.868+490G>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 6/9 | chr2 | 170782879 | |||||||
chr2:170782967 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.868+578A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 6/9 | chr2 | 170782967 | |||||||
chr2:170783036 | T | C | 50 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0018 others(47): Show |
138 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(135): Show |
intron_variant | MODIFIER | c.868+647T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 6/9 | chr2 | 170783036 | |||||||
chr2:170783055 | G | A | 1 | a0001c0002t0001g0087 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.868+666G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 6/9 | chr2 | 170783055 | |||||||
chr2:170783112 | T | A | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(113): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.868+723T>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 6/9 | chr2 | 170783112 | |||||||
chr2:170783131 | AAAAT | A | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(39): Show |
90 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.868+750_868+753del others(4): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 170783131 | ||||||
chr2:170783144 | A | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(39): Show |
90 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.868+755A>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 6/9 | chr2 | 170783144 | |||||||
chr2:170783145 | T | A | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(39): Show |
90 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.868+756T>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 6/9 | chr2 | 170783145 | |||||||
chr2:170783464 | G | T | 5 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(2): Show |
7 | HG02258.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.868+1075G>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 6/9 | chr2 | 170783464 | |||||||
chr2:170783506 | A | G | 1 | a0001c0002t0001g0100 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.868+1117A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 6/9 | chr2 | 170783506 | |||||||
chr2:170784088 | T | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0142 |
3 | NA18942.hp1 NA18995.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.869-558T>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 6/9 | chr2 | 170784088 | |||||||
chr2:170784109 | T | C | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG02080.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.869-537T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 6/9 | chr2 | 170784109 | |||||||
chr2:170784160 | A | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0051 a0001c0001t0001g0163 others(2): Show |
8 | HG00323.hp1 HG00639.hp2 HG00735.hp2 others(5): Show |
intron_variant | MODIFIER | c.869-486A>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 6/9 | chr2 | 170784160 | |||||||
chr2:170784224 | G | C | 52 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(49): Show |
105 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.869-422G>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 6/9 | chr2 | 170784224 | |||||||
chr2:170784343 | A | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(108): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.869-303A>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 6/9 | chr2 | 170784343 | |||||||
chr2:170784432 | T | C | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(108): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.869-214T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 6/9 | chr2 | 170784432 | |||||||
chr2:170785074 | G | A | 42 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(39): Show |
92 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.1056+241G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170785074 | |||||||
chr2:170785107 | G | A | 5 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(2): Show |
7 | HG02258.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1056+274G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170785107 | |||||||
chr2:170785196 | T | C | 37 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(34): Show |
85 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.1056+363T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170785196 | |||||||
chr2:170785481 | T | A | 1 | a0008c0014t0001g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1056+648T>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170785481 | |||||||
chr2:170785591 | GTTAT | G | 34 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(31): Show |
79 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1056+764_1056+767d others(6): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170785591 | ||||||
chr2:170785598 | A | T | 3 | a0001c0001t0001g0078 a0004c0008t0001g0077 a0005c0015t0001g0055 |
3 | HG01074.hp1 HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1056+765A>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170785598 | |||||||
chr2:170785846 | A | G | 74 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(71): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.1056+1013A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170785846 | |||||||
chr2:170785876 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0074 |
6 | HG01433.hp1 HG01928.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1056+1043C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170785876 | |||||||
chr2:170785880 | TGTTGTGA others(7): Show |
T | 1 | a0001c0001t0001g0029 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1056+1050_1056+106 others(18): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170785880 | ||||||
chr2:170785927 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0145 |
2 | HG02738.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1056+1094G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170785927 | |||||||
chr2:170786128 | GC | G | 37 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(34): Show |
85 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.1056+1296delC | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170786128 | |||||||
chr2:170786139 | A | T | 4 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(1): Show |
6 | HG02647.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1056+1306A>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170786139 | |||||||
chr2:170786310 | A | G | 1 | a0001c0001t0001g0047 | 2 | HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1056+1477A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170786310 | |||||||
chr2:170786312 | AT | A | 34 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(31): Show |
79 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1056+1489delT | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170786312 | ||||||
chr2:170786382 | G | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0106 others(9): Show |
29 | HG00408.hp2 HG01168.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.1056+1549G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170786382 | |||||||
chr2:170786630 | C | T | 4 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(1): Show |
6 | HG02647.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1056+1797C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170786630 | |||||||
chr2:170786667 | A | G | 55 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0018 others(52): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.1056+1834A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170786667 | |||||||
chr2:170786735 | T | C | 2 | a0001c0001t0001g0050 a0001c0001t0001g0052 |
4 | HG00280.hp1 HG01261.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1056+1902T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170786735 | |||||||
chr2:170786801 | T | C | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(32): Show |
81 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1056+1968T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170786801 | |||||||
chr2:170786944 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1056+2111A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170786944 | |||||||
chr2:170786963 | G | C | 123 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1056+2130G>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170786963 | |||||||
chr2:170787031 | TTTTG | T | 44 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(41): Show |
95 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1056+2226_1056+222 others(8): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170787031 | ||||||
chr2:170787074 | G | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0074 |
6 | HG01433.hp1 HG01928.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1056+2241G>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170787074 | |||||||
chr2:170787207 | C | G | 4 | a0001c0002t0001g0012 a0001c0002t0001g0032 a0001c0002t0001g0076 others(1): Show |
9 | HG00099.hp2 HG00140.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1056+2374C>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170787207 | |||||||
chr2:170787241 | C | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0102 a0001c0001t0001g0132 |
4 | HG02970.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1056+2408C>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170787241 | |||||||
chr2:170787341 | TG | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1056+2509delG | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170787341 | |||||||
chr2:170787502 | G | T | 1 | a0008c0014t0001g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1056+2669G>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170787502 | |||||||
chr2:170787538 | T | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0106 others(9): Show |
29 | HG00408.hp2 HG01168.hp1 HG01361.hp2 others(26): Show |
intron_variant | MODIFIER | c.1056+2705T>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170787538 | |||||||
chr2:170787540 | A | G | 128 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1056+2707A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170787540 | |||||||
chr2:170787574 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0074 |
6 | HG01433.hp1 HG01928.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1056+2741C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170787574 | |||||||
chr2:170787685 | C | G | 6 | a0005c0005t0001g0026 a0005c0005t0001g0056 a0005c0005t0001g0057 others(3): Show |
7 | HG00733.hp2 HG01261.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1056+2852C>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170787685 | |||||||
chr2:170787896 | T | G | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.1056+3063T>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170787896 | |||||||
chr2:170787979 | A | G | 5 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(2): Show |
7 | HG02258.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1056+3146A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170787979 | |||||||
chr2:170788054 | T | G | 1 | a0003c0004t0001g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1056+3221T>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170788054 | |||||||
chr2:170788087 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1056+3254A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170788087 | |||||||
chr2:170788280 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0122 |
2 | HG00323.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1056+3447C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170788280 | |||||||
chr2:170788475 | T | TTTTTA | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.1056+3652_1056+365 others(9): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170788475 | ||||||
chr2:170788564 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1056+3731C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170788564 | |||||||
chr2:170788574 | C | T | 37 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(34): Show |
85 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.1056+3741C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170788574 | |||||||
chr2:170788578 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1056+3745T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170788578 | |||||||
chr2:170788597 | G | A | 5 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(2): Show |
7 | HG02258.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1056+3764G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170788597 | |||||||
chr2:170788933 | T | A | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.1057-3930T>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170788933 | |||||||
chr2:170788940 | CTTCT | C | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(162): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.1057-3904_1057-390 others(8): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170788940 | ||||||
chr2:170788959 | C | A | 41 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(38): Show |
90 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.1057-3904C>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170788959 | |||||||
chr2:170789030 | C | A | 6 | a0005c0005t0001g0026 a0005c0005t0001g0056 a0005c0005t0001g0057 others(3): Show |
7 | HG00733.hp2 HG01261.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1057-3833C>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170789030 | |||||||
chr2:170789127 | A | AT | 10 | a0001c0001t0001g0078 a0001c0002t0001g0086 a0001c0002t0001g0098 others(7): Show |
11 | HG00733.hp2 HG01074.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.1057-3720dupT | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170789127 | ||||||
chr2:170789127 | AT | A | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(32): Show |
80 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.1057-3720delT | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170789127 | ||||||
chr2:170789136 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1057-3727T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170789136 | |||||||
chr2:170789138 | T | C | 4 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(1): Show |
6 | HG02647.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057-3725T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170789138 | |||||||
chr2:170789155 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1057-3708G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170789155 | |||||||
chr2:170789180 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0001t0001g0082 |
6 | HG02451.hp1 HG02965.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057-3683G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170789180 | |||||||
chr2:170789208 | G | A | 5 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(2): Show |
7 | HG02258.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1057-3655G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170789208 | |||||||
chr2:170789271 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1057-3592T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170789271 | |||||||
chr2:170789275 | C | G | 1 | a0001c0001t0001g0027 | 2 | HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1057-3588C>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170789275 | |||||||
chr2:170789340 | A | G | 2 | a0001c0002t0001g0036 a0001c0002t0001g0097 |
3 | HG02056.hp2 NA18967.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1057-3523A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170789340 | |||||||
chr2:170789376 | T | A | 1 | a0001c0002t0001g0089 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1057-3487T>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170789376 | |||||||
chr2:170789389 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1057-3474A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170789389 | |||||||
chr2:170789453 | A | G | 124 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1057-3410A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170789453 | |||||||
chr2:170789664 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1057-3199C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170789664 | |||||||
chr2:170789752 | T | C | 1 | a0005c0005t0001g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1057-3111T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170789752 | |||||||
chr2:170789769 | A | G | 4 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(1): Show |
6 | HG02647.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057-3094A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170789769 | |||||||
chr2:170789842 | G | T | 1 | a0003c0004t0001g0070 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1057-3021G>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170789842 | |||||||
chr2:170789910 | TA | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0135 a0001c0001t0001g0158 others(3): Show |
16 | HG00673.hp1 HG02135.hp2 NA18939.hp2 others(13): Show |
intron_variant | MODIFIER | c.1057-2951delA | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170789910 | ||||||
chr2:170790157 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1057-2706C>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170790157 | |||||||
chr2:170790221 | C | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1057-2642C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170790221 | |||||||
chr2:170790228 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0074 |
6 | HG01433.hp1 HG01928.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1057-2635G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170790228 | |||||||
chr2:170790282 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1057-2581G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170790282 | |||||||
chr2:170790299 | G | A | 1 | a0008c0014t0001g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1057-2564G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170790299 | |||||||
chr2:170790764 | A | T | 1 | a0002c0003t0001g0113 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1057-2099A>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170790764 | |||||||
chr2:170790770 | C | T | 4 | a0001c0001t0001g0140 a0001c0001t0001g0145 a0001c0001t0001g0156 others(1): Show |
4 | HG01123.hp1 HG02738.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1057-2093C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170790770 | |||||||
chr2:170790803 | C | CA | 5 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0126 others(2): Show |
8 | HG01123.hp1 HG01928.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.1057-2043dupA | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170790803 | ||||||
chr2:170790803 | C | CAA | 4 | a0001c0001t0001g0074 a0004c0006t0002g0045 a0004c0006t0002g0046 others(1): Show |
6 | HG01433.hp1 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1057-2044_1057-204 others(6): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170790803 | ||||||
chr2:170790803 | CA | C | 6 | a0001c0001t0001g0065 a0001c0001t0001g0120 a0001c0001t0001g0142 others(3): Show |
6 | HG01069.hp2 HG02735.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1057-2043delA | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170790803 | ||||||
chr2:170790891 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1057-1972T>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170790891 | |||||||
chr2:170790982 | A | G | 1 | a0001c0002t0001g0096 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1057-1881A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170790982 | |||||||
chr2:170791064 | G | T | 6 | a0005c0005t0001g0026 a0005c0005t0001g0056 a0005c0005t0001g0057 others(3): Show |
7 | HG00733.hp2 HG01261.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1057-1799G>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170791064 | |||||||
chr2:170791142 | TTAACC | T | 1 | a0001c0001t0001g0020 | 3 | HG02818.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1057-1718_1057-171 others(9): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170791142 | ||||||
chr2:170791201 | A | C | 2 | a0001c0001t0001g0078 a0004c0008t0001g0077 |
2 | HG01074.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.1057-1662A>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170791201 | |||||||
chr2:170791213 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1057-1650A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170791213 | |||||||
chr2:170791315 | G | T | 4 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(1): Show |
6 | HG02647.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057-1548G>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170791315 | |||||||
chr2:170791390 | G | A | 1 | a0003c0004t0001g0071 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1057-1473G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170791390 | |||||||
chr2:170791527 | T | TAAAAAAA others(1): Show |
64 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
129 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.1057-1330_1057-132 others(12): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170791527 | ||||||
chr2:170791527 | T | TAAAAAAA others(2): Show |
52 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(49): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.1057-1331_1057-132 others(13): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170791527 | ||||||
chr2:170791527 | T | TAAAAAAA others(3): Show |
11 | a0001c0001t0001g0043 a0001c0001t0001g0079 a0001c0001t0001g0138 others(8): Show |
14 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1057-1332_1057-132 others(14): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170791527 | ||||||
chr2:170791533 | A | AAAAAAAA others(1): Show |
34 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(31): Show |
79 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1057-1323_1057-132 others(12): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170791533 | ||||||
chr2:170791551 | G | A | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.1057-1312G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170791551 | |||||||
chr2:170791563 | G | A | 5 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(2): Show |
7 | HG02258.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1057-1300G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170791563 | |||||||
chr2:170791607 | G | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.1057-1256G>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170791607 | |||||||
chr2:170791638 | C | T | 2 | a0001c0002t0001g0095 a0001c0002t0001g0099 |
2 | NA18939.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1057-1225C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170791638 | |||||||
chr2:170791647 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1057-1216G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170791647 | |||||||
chr2:170791703 | TAAATA | T | 5 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(2): Show |
7 | HG02258.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1057-1146_1057-114 others(9): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170791703 | ||||||
chr2:170791707 | TAAAATAA others(4): Show |
T | 40 | a0001c0001t0001g0039 a0001c0002t0001g0001 a0001c0002t0001g0007 others(37): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.1057-1141_1057-113 others(15): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170791707 | ||||||
chr2:170791764 | T | A | 8 | a0001c0001t0001g0078 a0004c0008t0001g0077 a0005c0005t0001g0026 others(5): Show |
9 | HG00733.hp2 HG01074.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.1057-1099T>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170791764 | |||||||
chr2:170792077 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0028 |
5 | HG01928.hp1 HG01943.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1057-786A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170792077 | |||||||
chr2:170792407 | AAAT | A | 3 | a0004c0006t0002g0045 a0004c0006t0002g0129 a0004c0006t0002g0130 |
4 | HG02647.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1057-450_1057-448d others(5): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170792407 | ||||||
chr2:170792474 | A | G | 168 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.1057-389A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170792474 | |||||||
chr2:170792500 | A | G | 2 | a0001c0001t0001g0042 a0001c0001t0001g0107 |
3 | HG02027.hp2 HG02165.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.1057-363A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170792500 | |||||||
chr2:170792519 | A | C | 1 | a0001c0001t0001g0119 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1057-344A>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | chr2 | 170792519 | |||||||
chr2:170792549 | TTAAAA | T | 4 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(1): Show |
6 | HG02647.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057-309_1057-305d others(7): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 170792549 | ||||||
chr2:170793134 | G | A | 61 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(58): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.1114+214G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170793134 | |||||||
chr2:170793323 | A | G | 1 | a0004c0008t0001g0077 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1114+403A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170793323 | |||||||
chr2:170793324 | TAGTC | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0062 |
9 | HG01891.hp1 HG02559.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1114+411_1114+414d others(6): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 170793324 | ||||||
chr2:170793326 | G | A | 1 | a0002c0003t0001g0113 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1114+406G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170793326 | |||||||
chr2:170793386 | T | C | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(32): Show |
81 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1114+466T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170793386 | |||||||
chr2:170793529 | A | T | 6 | a0005c0005t0001g0026 a0005c0005t0001g0056 a0005c0005t0001g0057 others(3): Show |
7 | HG00733.hp2 HG01261.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1114+609A>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170793529 | |||||||
chr2:170794003 | T | C | 1 | a0001c0001t0001g0019 | 3 | HG03195.hp2 HG03486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1114+1083T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170794003 | |||||||
chr2:170794057 | CCTTT | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0001c0002t0001g0084 |
6 | HG02965.hp1 HG03195.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1114+1151_1114+115 others(8): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 170794057 | ||||||
chr2:170794096 | CCTTT | C | 5 | a0005c0005t0001g0026 a0005c0005t0001g0056 a0005c0005t0001g0057 others(2): Show |
6 | HG00733.hp2 HG01261.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1114+1185_1114+118 others(8): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 170794096 | ||||||
chr2:170794105 | C | CT | 49 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(46): Show |
94 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.1114+1206dupT | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 170794105 | ||||||
chr2:170794105 | C | CTT | 54 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0015 others(51): Show |
131 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1114+1205_1114+120 others(6): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 170794105 | ||||||
chr2:170794105 | C | CTTT | 7 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0102 others(4): Show |
10 | HG01891.hp1 HG02257.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1114+1204_1114+120 others(7): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 170794105 | ||||||
chr2:170794105 | CT | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(47): Show |
102 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1114+1206delT | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 170794105 | ||||||
chr2:170794105 | CTTTTT | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0083 others(2): Show |
16 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.1114+1202_1114+120 others(9): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 170794105 | ||||||
chr2:170794257 | C | G | 1 | a0001c0001t0001g0025 | 3 | HG00639.hp2 HG00735.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1114+1337C>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170794257 | |||||||
chr2:170794327 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0062 a0001c0001t0001g0064 others(3): Show |
13 | HG01891.hp1 HG02486.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1114+1407C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170794327 | |||||||
chr2:170794498 | T | C | 2 | a0001c0002t0001g0091 a0001c0002t0001g0096 |
2 | HG02135.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1114+1578T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170794498 | |||||||
chr2:170794522 | A | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0083 |
12 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1114+1602A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170794522 | |||||||
chr2:170794601 | T | C | 38 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(35): Show |
87 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.1114+1681T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170794601 | |||||||
chr2:170794742 | TA | T | 4 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(1): Show |
6 | HG02647.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1114+1825delA | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 170794742 | ||||||
chr2:170794963 | C | A | 38 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(35): Show |
87 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.1114+2043C>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170794963 | |||||||
chr2:170795045 | A | G | 1 | a0001c0001t0001g0050 | 2 | HG00280.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1114+2125A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170795045 | |||||||
chr2:170795063 | C | T | 58 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(55): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.1114+2143C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170795063 | |||||||
chr2:170795346 | G | A | 5 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(2): Show |
7 | HG02258.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1114+2426G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170795346 | |||||||
chr2:170795370 | C | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1114+2450C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170795370 | |||||||
chr2:170795450 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1114+2530G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170795450 | |||||||
chr2:170795494 | C | T | 34 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(31): Show |
79 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1115-2547C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170795494 | |||||||
chr2:170795501 | C | T | 1 | a0003c0004t0001g0071 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1115-2540C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170795501 | |||||||
chr2:170795587 | T | A | 1 | a0004c0008t0001g0048 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1115-2454T>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170795587 | |||||||
chr2:170795606 | C | A | 1 | a0001c0001t0001g0080 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1115-2435C>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170795606 | |||||||
chr2:170795855 | G | A | 117 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1115-2186G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170795855 | |||||||
chr2:170795891 | G | A | 38 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(35): Show |
87 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.1115-2150G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170795891 | |||||||
chr2:170796098 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0078 a0004c0008t0001g0077 |
4 | HG01074.hp1 HG02055.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1115-1943T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796098 | |||||||
chr2:170796237 | T | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0074 |
6 | HG01433.hp1 HG01928.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1115-1804T>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796237 | |||||||
chr2:170796239 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0074 |
6 | HG01433.hp1 HG01928.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1115-1802C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796239 | |||||||
chr2:170796264 | C | T | 1 | a0001c0001t0001g0022 | 3 | HG00735.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1115-1777C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796264 | |||||||
chr2:170796410 | ATC | A | 52 | a0001c0001t0001g0009 a0001c0001t0001g0018 a0001c0001t0001g0043 others(49): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.1115-1617_1115-161 others(6): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 170796410 | ||||||
chr2:170796422 | C | CTT | 7 | a0001c0001t0001g0151 a0005c0005t0001g0026 a0005c0005t0001g0056 others(4): Show |
8 | HG00733.hp2 HG01261.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1115-1618_1115-161 others(6): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 170796422 | ||||||
chr2:170796423 | T | TTTG | 4 | a0001c0001t0001g0017 a0001c0001t0001g0074 a0001c0001t0001g0152 others(1): Show |
6 | HG00741.hp1 HG01433.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.1115-1618_1115-161 others(7): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796423 | |||||||
chr2:170796423 | TC | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0120 |
6 | NA18946.hp2 NA18950.hp2 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.1115-1617delC | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796423 | |||||||
chr2:170796424 | C | G | 7 | a0001c0001t0001g0151 a0005c0005t0001g0026 a0005c0005t0001g0056 others(4): Show |
8 | HG00733.hp2 HG01261.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1115-1617C>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796424 | |||||||
chr2:170796424 | C | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(102): Show |
226 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.1115-1617C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796424 | |||||||
chr2:170796425 | T | TG | 8 | a0001c0001t0001g0024 a0001c0001t0001g0118 a0001c0001t0001g0149 others(5): Show |
13 | HG01074.hp2 HG01168.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.1115-1616_1115-161 others(5): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796425 | |||||||
chr2:170796426 | T | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
205 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.1115-1615T>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796426 | |||||||
chr2:170796427 | T | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0120 |
6 | NA18946.hp2 NA18950.hp2 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.1115-1614T>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796427 | |||||||
chr2:170796428 | G | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(111): Show |
240 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.1115-1613G>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796428 | |||||||
chr2:170796431 | TTTTTTTT others(2): Show |
T | 42 | a0001c0001t0001g0009 a0001c0001t0001g0043 a0001c0001t0001g0079 others(39): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(115): Show |
intron_variant | MODIFIER | c.1115-1601_1115-159 others(13): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 170796431 | ||||||
chr2:170796432 | TTTTTTTT others(1): Show |
T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0063 a0001c0001t0001g0080 others(3): Show |
9 | HG01884.hp2 HG02258.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1115-1601_1115-159 others(12): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 170796432 | ||||||
chr2:170796437 | T | G | 8 | a0001c0001t0001g0151 a0005c0005t0001g0026 a0005c0005t0001g0056 others(5): Show |
9 | HG00733.hp2 HG01261.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1115-1604T>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796437 | |||||||
chr2:170796437 | T | TG | 4 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(1): Show |
6 | HG02647.hp1 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1115-1604_1115-160 others(5): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796437 | |||||||
chr2:170796440 | G | GAT | 5 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(2): Show |
7 | HG02258.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1115-1601_1115-160 others(6): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796440 | |||||||
chr2:170796440 | G | GGTTT | 2 | a0001c0001t0001g0006 a0001c0001t0001g0062 |
8 | HG01891.hp1 HG02559.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1115-1601_1115-160 others(8): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796440 | |||||||
chr2:170796440 | G | GTTT | 60 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(57): Show |
120 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.1115-1590_1115-158 others(7): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 170796440 | ||||||
chr2:170796440 | G | GTTTT | 9 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(6): Show |
11 | HG00323.hp1 HG00738.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.1115-1591_1115-158 others(8): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 170796440 | ||||||
chr2:170796440 | G | T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0074 others(9): Show |
16 | HG00733.hp2 HG00741.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.1115-1601G>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796440 | |||||||
chr2:170796452 | T | TTC | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(32): Show |
81 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1115-1588_1115-158 others(6): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 170796452 | ||||||
chr2:170796462 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0117 |
3 | HG01070.hp1 HG03017.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1115-1579G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796462 | |||||||
chr2:170796498 | C | T | 1 | a0001c0002t0001g0087 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1115-1543C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796498 | |||||||
chr2:170796529 | A | G | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.1115-1512A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796529 | |||||||
chr2:170796540 | ATCC | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0125 a0001c0011t0001g0124 |
4 | HG01891.hp2 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1115-1496_1115-149 others(7): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 170796540 | ||||||
chr2:170796583 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1115-1458G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796583 | |||||||
chr2:170796592 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1115-1449C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796592 | |||||||
chr2:170796652 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG03654.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1115-1389G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796652 | |||||||
chr2:170796732 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0074 |
6 | HG01433.hp1 HG01928.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1115-1309C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796732 | |||||||
chr2:170796745 | G | A | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.1115-1296G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170796745 | |||||||
chr2:170797097 | A | C | 1 | a0002c0003t0001g0110 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1115-944A>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170797097 | |||||||
chr2:170797246 | AAAAC | A | 5 | a0004c0006t0002g0045 a0004c0006t0002g0046 a0004c0006t0002g0129 others(2): Show |
7 | HG02258.hp1 HG02647.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1115-783_1115-780d others(6): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 170797246 | ||||||
chr2:170797300 | T | A | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1115-741T>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170797300 | |||||||
chr2:170797433 | C | T | 1 | a0005c0005t0001g0060 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1115-608C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170797433 | |||||||
chr2:170797480 | T | G | 1 | a0001c0001t0001g0041 | 2 | NA18982.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1115-561T>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170797480 | |||||||
chr2:170797530 | T | G | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.1115-511T>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170797530 | |||||||
chr2:170797598 | G | C | 1 | a0003c0004t0001g0069 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1115-443G>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170797598 | |||||||
chr2:170797608 | G | A | 1 | a0002c0003t0001g0113 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1115-433G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170797608 | |||||||
chr2:170797699 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0102 a0001c0001t0001g0132 |
4 | HG02970.hp2 HG02976.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1115-342C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170797699 | |||||||
chr2:170797762 | A | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0148 a0001c0001t0001g0150 others(1): Show |
5 | HG00738.hp2 HG01255.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.1115-279A>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170797762 | |||||||
chr2:170797795 | GA | G | 5 | a0003c0004t0001g0072 a0004c0006t0002g0045 a0004c0006t0002g0046 others(2): Show |
7 | HG02647.hp1 HG02809.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1115-227delA | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 170797795 | ||||||
chr2:170797795 | GAAAA | G | 3 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0083 |
12 | HG01884.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1115-230_1115-227d others(6): Show |
ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 170797795 | ||||||
chr2:170797796 | A | G | 1 | a0001c0001t0001g0029 | 2 | HG02055.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1115-245A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170797796 | |||||||
chr2:170797807 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0030 a0005c0015t0001g0055 |
6 | HG02965.hp1 HG03195.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1115-234A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170797807 | |||||||
chr2:170797811 | A | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(117): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1115-230A>G | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170797811 | |||||||
chr2:170798002 | G | A | 1 | a0001c0002t0001g0087 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1115-39G>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170798002 | |||||||
chr2:170798040 | G | T | 1 | a0001c0002t0001g0094 | 1 | HG00558.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1115-1G>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 8/9 | chr2 | 170798040 | |||||||
chr2:170798153 | A | C | 123 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1186+41A>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 9/9 | chr2 | 170798153 | |||||||
chr2:170798183 | C | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0028 a0001c0001t0001g0074 |
6 | HG01433.hp1 HG01928.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.1186+71C>A | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 9/9 | chr2 | 170798183 | |||||||
chr2:170798263 | G | C | 123 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1186+151G>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 9/9 | chr2 | 170798263 | |||||||
chr2:170798316 | C | T | 2 | a0001c0001t0001g0019 a0001c0001t0001g0030 |
5 | HG02965.hp1 HG03195.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1186+204C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 9/9 | chr2 | 170798316 | |||||||
chr2:170798511 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1187-259C>T | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 9/9 | chr2 | 170798511 | |||||||
chr2:170798633 | T | C | 1 | a0001c0002t0001g0093 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1187-137T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 9/9 | chr2 | 170798633 | |||||||
chr2:170798741 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1187-29T>C | ERICH2 | ENSG00000204334.8 | transcript | ENST00000697325.1 | protein_coding | 9/9 | chr2 | 170798741 |