Item | Value |
---|---|
geneid | 55758 |
ensemblid | ENSG00000117625.14 |
hgncid | 25594 |
symbol | RCOR3 |
name | REST corepressor 3 |
refseq_nuc | NM_001136223.3 |
refseq_prot | NP_001129695.1 |
ensembl_nuc | ENST00000419091.7 |
ensembl_prot | ENSP00000413929.2 |
mane_status | MANE Select |
chr | chr1 |
start | 211259366 |
end | 211316385 |
strand | + |
ver | v1.2 |
region | chr1:211259366-211316385 |
region5000 | chr1:211254366-211321385 |
regionname0 | RCOR3_chr1_211259366_211316385 |
regionname5000 | RCOR3_chr1_211254366_211321385 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1659 | 267 | 65 | 42 | 115 | 9 | 35 | RCOR3_chr1_211254366_211321385 | RCOR3 | ATGCC others(1654): Show |
chr1 | 211254366 | 211321385 | ||
a0001c0002 | 0/1 | 1659 | 44 | 7 | 12 | 18 | 1 | 5 | RCOR3_chr1_211254366_211321385 | RCOR3 | ATGCC others(1654): Show |
chr1 | 211254366 | 211321385 | ||
a0001c0003 | 0/0 | 1659 | 10 | 10 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | ATGCC others(1654): Show |
chr1 | 211254366 | 211321385 | ||
a0001c0004 | 0/0 | 1659 | 2 | 2 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | ATGCC others(1654): Show |
chr1 | 211254366 | 211321385 | ||
a0001c0005 | 0/0 | 1659 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | ATGCC others(1654): Show |
chr1 | 211254366 | 211321385 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4474 | 98 | 23 | 15 | 49 | 1 | 10 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4469): Show |
chr1 | 211254366 | 211321385 |
a0001c0001t0002 | 0/0 | 4473 | 104 | 11 | 20 | 54 | 5 | 14 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4468): Show |
chr1 | 211254366 | 211321385 |
a0001c0001t0003 | 0/0 | 4475 | 16 | 0 | 3 | 6 | 1 | 6 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4470): Show |
chr1 | 211254366 | 211321385 |
a0001c0001t0004 | 0/0 | 4474 | 13 | 12 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4469): Show |
chr1 | 211254366 | 211321385 |
a0001c0001t0005 | 1/0 | 4474 | 13 | 7 | 1 | 0 | 2 | 2 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4469): Show |
chr1 | 211254366 | 211321385 |
a0001c0001t0007 | 0/0 | 4474 | 5 | 5 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4469): Show |
chr1 | 211254366 | 211321385 |
a0001c0001t0008 | 0/0 | 4474 | 4 | 4 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4469): Show |
chr1 | 211254366 | 211321385 |
a0001c0001t0009 | 0/0 | 4476 | 3 | 0 | 0 | 0 | 0 | 3 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4471): Show |
chr1 | 211254366 | 211321385 |
a0001c0001t0010 | 0/0 | 4473 | 2 | 0 | 0 | 2 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4468): Show |
chr1 | 211254366 | 211321385 |
a0001c0001t0011 | 0/0 | 4474 | 2 | 2 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4469): Show |
chr1 | 211254366 | 211321385 |
a0001c0001t0012 | 0/0 | 4473 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4468): Show |
chr1 | 211254366 | 211321385 |
a0001c0001t0013 | 0/0 | 4473 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4468): Show |
chr1 | 211254366 | 211321385 |
a0001c0001t0014 | 0/0 | 4473 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4468): Show |
chr1 | 211254366 | 211321385 |
a0001c0001t0015 | 0/0 | 4474 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4469): Show |
chr1 | 211254366 | 211321385 |
a0001c0001t0016 | 0/0 | 4474 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4469): Show |
chr1 | 211254366 | 211321385 |
a0001c0001t0018 | 0/0 | 4474 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4469): Show |
chr1 | 211254366 | 211321385 |
a0001c0001t0019 | 0/0 | 4474 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4469): Show |
chr1 | 211254366 | 211321385 |
a0001c0002t0001 | 0/1 | 4474 | 37 | 6 | 8 | 18 | 0 | 4 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4469): Show |
chr1 | 211254366 | 211321385 |
a0001c0002t0006 | 0/0 | 4477 | 6 | 0 | 4 | 0 | 1 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4472): Show |
chr1 | 211254366 | 211321385 |
a0001c0002t0017 | 0/0 | 4474 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4469): Show |
chr1 | 211254366 | 211321385 |
a0001c0003t0001 | 0/0 | 4474 | 10 | 10 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4469): Show |
chr1 | 211254366 | 211321385 |
a0001c0004t0001 | 0/0 | 4474 | 2 | 2 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4469): Show |
chr1 | 211254366 | 211321385 |
a0001c0005t0001 | 0/0 | 4474 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | GTTGT others(4469): Show |
chr1 | 211254366 | 211321385 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0001 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0011 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0003g0003 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0004g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0005g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0005g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0005g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0005g0074 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0005g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0005g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0007g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0007g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0008g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0008g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0008g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0008g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0009g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0009g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0010g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0010g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0011g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0011g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0012g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0013g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0014g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0015g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0016g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0018g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0001t0019g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0086 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0006g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0006g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0006g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0006g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0006g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0006g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0002t0017g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0003t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0003t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0004t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0004t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
a0001c0005t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0153 | EUR | GBR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0003 | EUR | GBR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | CHS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | CHS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | CHS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG00597 | hp2 | a0001 | c0001 | t0012 | g0117 | EAS | CHS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0090 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG00673 | hp1 | a0001 | c0005 | t0001 | g0064 | EAS | CHS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | CHS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0232 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG00738 | hp2 | a0001 | c0002 | t0006 | g0135 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0021 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01069 | hp1 | a0001 | c0001 | t0013 | g0146 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0204 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0015 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01099 | hp1 | a0001 | c0002 | t0006 | g0126 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0091 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0293 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01167 | hp2 | a0001 | c0002 | t0006 | g0193 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0236 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01256 | hp1 | a0001 | c0001 | t0014 | g0152 | AMR | CLM | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0201 | AMR | CLM | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0207 | AMR | CLM | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | CLM | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | CLM | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0125 | EUR | IBS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01516 | hp2 | a0001 | c0001 | t0005 | g0006 | EUR | IBS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01517 | hp1 | a0001 | c0001 | t0005 | g0006 | EUR | IBS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0155 | EUR | IBS | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0197 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0093 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0140 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | KHV | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | KHV | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02055 | hp1 | a0001 | c0003 | t0001 | g0134 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02055 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | KHV | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0163 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0219 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CDX | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0256 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0205 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02293 | hp2 | a0001 | c0002 | t0006 | g0194 | AMR | PEL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0075 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0271 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0136 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02698 | hp1 | a0001 | c0002 | t0006 | g0199 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02717 | hp1 | a0001 | c0001 | t0007 | g0002 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0198 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02723 | hp1 | a0001 | c0003 | t0001 | g0132 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0027 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02809 | hp1 | a0001 | c0001 | t0008 | g0266 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02886 | hp2 | a0001 | c0003 | t0001 | g0211 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0269 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0077 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0270 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02922 | hp2 | a0001 | c0001 | t0008 | g0268 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02970 | hp2 | a0001 | c0001 | t0011 | g0080 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0218 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0196 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03041 | hp2 | a0001 | c0001 | t0008 | g0288 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03130 | hp1 | a0001 | c0004 | t0001 | g0290 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0208 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03139 | hp1 | a0001 | c0001 | t0007 | g0078 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0258 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03209 | hp1 | a0001 | c0001 | t0008 | g0267 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03209 | hp2 | a0001 | c0004 | t0001 | g0291 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03225 | hp2 | a0001 | c0002 | t0017 | g0128 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0206 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03453 | hp2 | a0001 | c0001 | t0018 | g0025 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0292 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0179 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0104 | SAS | STU | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03688 | hp2 | a0001 | c0001 | t0009 | g0228 | SAS | STU | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03710 | hp2 | a0001 | c0001 | t0005 | g0287 | SAS | PJL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03831 | hp1 | a0001 | c0001 | t0005 | g0253 | SAS | BEB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | BEB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | BEB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0285 | SAS | BEB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | BEB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0233 | SAS | BEB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | BEB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0240 | SAS | BEB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0230 | SAS | STU | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | STU | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0099 | SAS | BEB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0241 | SAS | BEB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG04204 | hp1 | a0001 | c0001 | t0009 | g0016 | SAS | STU | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | STU | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0234 | SAS | STU | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | STU | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18612 | hp1 | a0001 | c0002 | t0001 | g0215 | EAS | CHB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | CHB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | CHB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | YRI | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0130 | AFR | YRI | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18986 | hp2 | a0001 | c0001 | t0016 | g0231 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18995 | hp1 | a0001 | c0001 | t0010 | g0097 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18999 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19004 | hp2 | a0001 | c0001 | t0010 | g0103 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0142 | AFR | LWK | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19030 | hp2 | a0001 | c0001 | t0007 | g0002 | AFR | LWK | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | LWK | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19043 | hp2 | a0001 | c0001 | t0011 | g0079 | AFR | LWK | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0212 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19086 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19091 | hp1 | a0001 | c0001 | t0015 | g0176 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19091 | hp2 | a0001 | c0001 | t0019 | g0004 | EAS | JPT | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19240 | hp1 | a0001 | c0001 | t0007 | g0002 | AFR | YRI | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0076 | AFR | YRI | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0227 | EUR | TSI | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0259 | EUR | TSI | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0156 | EUR | TSI | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA20805 | hp2 | a0001 | c0002 | t0006 | g0210 | EUR | TSI | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA20905 | hp1 | a0001 | c0001 | t0009 | g0016 | SAS | GIH | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | GIH | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02109 | hp1 | a0001 | c0003 | t0001 | g0141 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG02559 | hp2 | a0001 | c0003 | t0001 | g0137 | AFR | ACB | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0255 | AFR | MSL | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | USA | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
HG06807 | hp2 | a0001 | c0003 | t0001 | g0129 | AFR | USA | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | USA | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0081 | AFR | USA | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0086 | REF | REF | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0074 | REF | REF | RCOR3_chr1_211254366_211321385 | RCOR3 | chr1 | 211254366 | 211321385 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:211259566 | C | T | 1 | a0001c0003 | 10 | HG02055.hp1 HG02109.hp1 HG02559.hp2 others(7): Show |
synonymous_variant | LOW | c.6C>T | p.Pro2Pro | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 1/12 | 201/4474 | 6/1662 | 2/553 | chr1 | 211259566 | |||
chr1:211278125 | T | C | 2 | a0001c0002 a0001c0003 |
53 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(50): Show |
synonymous_variant | LOW | c.525T>C | p.Asp175Asp | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/12 | 720/4474 | 525/1662 | 175/553 | chr1 | 211278125 | |||
chr1:211289306 | G | A | 1 | a0001c0004 | 2 | HG03130.hp1 HG03209.hp2 |
synonymous_variant | LOW | c.849G>A | p.Gln283Gln | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/12 | 1044/4474 | 849/1662 | 283/553 | chr1 | 211289306 | |||
chr1:211313702 | G | A | 1 | a0001c0005 | 1 | HG00673.hp1 | synonymous_variant | LOW | c.1596G>A | p.Thr532Thr | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 1791/4474 | 1596/1662 | 532/553 | chr1 | 211313702 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:211259456 | T | TCTC | 1 | a0001c0002t0006 | 6 | HG00738.hp2 HG01099.hp1 HG01167.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-90_-88dupCCT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 1/12 | 87 | INFO_REALIGN_3_PRIME | chr1 | 211259456 | |||||
chr1:211313952 | T | A | 1 | a0001c0001t0010 | 2 | NA18995.hp1 NA19004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*184T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 184 | chr1 | 211313952 | ||||||
chr1:211314005 | GT | G | 6 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0012 others(3): Show |
110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*239delT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 239 | INFO_REALIGN_3_PRIME | chr1 | 211314005 | |||||
chr1:211314087 | T | C | 1 | a0001c0001t0004 | 13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*319T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 319 | chr1 | 211314087 | ||||||
chr1:211314173 | T | TA | 1 | a0001c0001t0009 | 3 | HG03688.hp2 HG04204.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*405_*406insA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 406 | chr1 | 211314173 | ||||||
chr1:211314212 | T | G | 1 | a0001c0001t0011 | 2 | HG02970.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*444T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 444 | chr1 | 211314212 | ||||||
chr1:211314259 | C | T | 1 | a0001c0001t0019 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*491C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 491 | chr1 | 211314259 | ||||||
chr1:211314261 | G | A | 1 | a0001c0001t0016 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*493G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 493 | chr1 | 211314261 | ||||||
chr1:211314334 | C | CT | 3 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0015 |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*576dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 577 | INFO_REALIGN_3_PRIME | chr1 | 211314334 | |||||
chr1:211314552 | T | G | 1 | a0001c0002t0017 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*784T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 784 | chr1 | 211314552 | ||||||
chr1:211314734 | A | G | 22 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(19): Show |
310 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(307): Show |
3_prime_UTR_variant | MODIFIER | c.*966A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 966 | chr1 | 211314734 | ||||||
chr1:211315196 | C | A | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(17): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
3_prime_UTR_variant | MODIFIER | c.*1428C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 1428 | chr1 | 211315196 | ||||||
chr1:211315376 | A | G | 1 | a0001c0001t0014 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1608A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 1608 | chr1 | 211315376 | ||||||
chr1:211315392 | A | G | 1 | a0001c0001t0018 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1624A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 1624 | chr1 | 211315392 | ||||||
chr1:211315427 | T | C | 1 | a0001c0001t0012 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1659T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 1659 | chr1 | 211315427 | ||||||
chr1:211315635 | G | A | 1 | a0001c0001t0008 | 4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1867G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 1867 | chr1 | 211315635 | ||||||
chr1:211315845 | T | G | 20 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(17): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
3_prime_UTR_variant | MODIFIER | c.*2077T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 2077 | chr1 | 211315845 | ||||||
chr1:211315861 | A | C | 1 | a0001c0001t0013 | 1 | HG01069.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2093A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 12/12 | 2093 | chr1 | 211315861 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:211259891 | C | A | 1 | a0001c0001t0001g0020 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.166+165C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 1/11 | chr1 | 211259891 | |||||||
chr1:211259924 | G | GC | 13 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(10): Show |
14 | HG00741.hp1 HG01192.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.167-175dupC | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 211259924 | ||||||
chr1:211260078 | T | A | 51 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(48): Show |
56 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.167-30T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 1/11 | chr1 | 211260078 | |||||||
chr1:211260268 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0018g0025 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.223+104T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260268 | |||||||
chr1:211260330 | C | T | 46 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(43): Show |
49 | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(46): Show |
intron_variant | MODIFIER | c.223+166C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260330 | |||||||
chr1:211260371 | C | G | 1 | a0001c0001t0001g0073 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.223+207C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260371 | |||||||
chr1:211260395 | G | T | 281 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(278): Show |
305 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.223+231G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260395 | |||||||
chr1:211260411 | G | A | 281 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(278): Show |
305 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(302): Show |
intron_variant | MODIFIER | c.223+247G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260411 | |||||||
chr1:211260481 | C | T | 1 | a0001c0001t0004g0293 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.223+317C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260481 | |||||||
chr1:211260616 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.223+452G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260616 | |||||||
chr1:211260631 | G | C | 1 | a0001c0002t0001g0083 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.223+467G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260631 | |||||||
chr1:211260640 | C | T | 1 | a0001c0001t0004g0292 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.223+476C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260640 | |||||||
chr1:211260692 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.223+528G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260692 | |||||||
chr1:211260699 | T | C | 1 | a0001c0001t0002g0084 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.223+535T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260699 | |||||||
chr1:211260751 | G | A | 1 | a0001c0001t0005g0253 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.223+587G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260751 | |||||||
chr1:211260754 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.223+590G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260754 | |||||||
chr1:211260922 | C | T | 1 | a0001c0001t0001g0023 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.223+758C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211260922 | |||||||
chr1:211261042 | C | T | 11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0243 others(8): Show |
11 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.223+878C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261042 | |||||||
chr1:211261124 | A | G | 1 | a0001c0001t0005g0081 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.223+960A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261124 | |||||||
chr1:211261135 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0018g0025 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.223+971G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261135 | |||||||
chr1:211261245 | G | T | 2 | a0001c0001t0011g0079 a0001c0001t0011g0080 |
2 | HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.223+1081G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261245 | |||||||
chr1:211261296 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.223+1132T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261296 | |||||||
chr1:211261341 | A | C | 11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0243 others(8): Show |
11 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.223+1177A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261341 | |||||||
chr1:211261350 | G | A | 48 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(45): Show |
52 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.223+1186G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261350 | |||||||
chr1:211261825 | G | T | 1 | a0001c0001t0002g0242 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.223+1661G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261825 | |||||||
chr1:211261919 | A | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | NA18959.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.223+1755A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261919 | |||||||
chr1:211261923 | C | CAAAAAAA | 33 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0032 others(30): Show |
35 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(32): Show |
intron_variant | MODIFIER | c.223+1771_223+1777d others(9): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211261923 | ||||||
chr1:211261923 | C | CAAAAAAA others(1): Show |
138 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(135): Show |
153 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.223+1770_223+1777d others(10): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211261923 | ||||||
chr1:211261923 | C | CAAAAAAA others(2): Show |
84 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0023 others(81): Show |
87 | HG00597.hp2 HG00642.hp1 HG00738.hp2 others(84): Show |
intron_variant | MODIFIER | c.223+1769_223+1777d others(11): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211261923 | ||||||
chr1:211261923 | C | CAAAAAAA others(3): Show |
3 | a0001c0001t0001g0022 a0001c0001t0001g0033 a0001c0002t0001g0087 |
3 | HG06807.hp1 NA18970.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.223+1768_223+1777d others(12): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211261923 | ||||||
chr1:211261923 | C | CAAAAAAA others(8): Show |
1 | a0001c0002t0001g0085 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.223+1763_223+1777d others(17): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211261923 | ||||||
chr1:211261931 | A | AAAAAAAC | 14 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(11): Show |
17 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.223+1773_223+1774i others(9): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211261931 | ||||||
chr1:211261978 | T | C | 99 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(96): Show |
110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.223+1814T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261978 | |||||||
chr1:211261997 | G | A | 51 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0027 others(48): Show |
53 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.223+1833G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211261997 | |||||||
chr1:211262005 | T | G | 1 | a0001c0001t0004g0257 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.223+1841T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262005 | |||||||
chr1:211262022 | A | T | 3 | a0001c0001t0002g0125 a0001c0001t0002g0191 a0001c0001t0002g0192 |
3 | HG01516.hp1 HG03239.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.223+1858A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262022 | |||||||
chr1:211262033 | C | CTT | 6 | a0001c0001t0001g0030 a0001c0001t0001g0244 a0001c0001t0001g0247 others(3): Show |
6 | HG01243.hp1 HG02922.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+1890_223+1891d others(4): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211262033 | ||||||
chr1:211262033 | C | CTTT | 45 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0031 others(42): Show |
51 | HG00099.hp2 HG00597.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.223+1889_223+1891d others(5): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211262033 | ||||||
chr1:211262033 | C | CTTTT | 94 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
100 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.223+1888_223+1891d others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211262033 | ||||||
chr1:211262033 | C | CTTTTT | 103 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0044 others(100): Show |
115 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.223+1887_223+1891d others(7): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211262033 | ||||||
chr1:211262033 | C | CTTTTTT | 28 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0264 others(25): Show |
28 | HG00597.hp2 HG01081.hp1 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.223+1886_223+1891d others(8): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211262033 | ||||||
chr1:211262130 | C | T | 2 | a0001c0001t0007g0002 a0001c0001t0007g0078 |
5 | HG02055.hp2 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+1966C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262130 | |||||||
chr1:211262145 | G | C | 26 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(23): Show |
27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.223+1981G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262145 | |||||||
chr1:211262152 | C | T | 51 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0027 others(48): Show |
53 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.223+1988C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262152 | |||||||
chr1:211262182 | C | T | 1 | a0001c0002t0001g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.223+2018C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262182 | |||||||
chr1:211262317 | G | A | 11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0243 others(8): Show |
11 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.223+2153G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262317 | |||||||
chr1:211262409 | G | T | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.223+2245G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262409 | |||||||
chr1:211262473 | CTG | C | 11 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0255 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.223+2314_223+2315d others(4): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211262473 | ||||||
chr1:211262663 | G | T | 1 | a0001c0001t0002g0124 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.223+2499G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262663 | |||||||
chr1:211262676 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.223+2512C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262676 | |||||||
chr1:211262722 | G | A | 2 | a0001c0001t0002g0149 a0001c0001t0002g0165 |
2 | HG01433.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.223+2558G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262722 | |||||||
chr1:211262815 | G | C | 1 | a0001c0002t0001g0133 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.223+2651G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262815 | |||||||
chr1:211262817 | C | T | 1 | a0001c0003t0001g0132 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.223+2653C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262817 | |||||||
chr1:211262822 | G | GT | 204 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0032 others(201): Show |
224 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.223+2671dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211262822 | ||||||
chr1:211262822 | G | GTT | 72 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(69): Show |
76 | HG00408.hp1 HG00558.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.223+2670_223+2671d others(4): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211262822 | ||||||
chr1:211262870 | C | CT | 11 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0255 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.223+2717dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211262870 | ||||||
chr1:211262870 | CT | C | 113 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(110): Show |
128 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.223+2717delT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211262870 | ||||||
chr1:211262938 | T | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(15): Show |
22 | HG00609.hp1 HG01099.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.223+2774T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211262938 | |||||||
chr1:211263016 | T | TC | 8 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0073 others(5): Show |
8 | HG01175.hp1 HG01261.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.223+2858dupC | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211263016 | ||||||
chr1:211263024 | G | C | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.223+2860G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263024 | |||||||
chr1:211263031 | C | T | 1 | a0001c0001t0004g0258 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.223+2867C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263031 | |||||||
chr1:211263039 | C | T | 1 | a0001c0002t0001g0219 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.223+2875C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263039 | |||||||
chr1:211263098 | C | T | 15 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0243 others(12): Show |
15 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.223+2934C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263098 | |||||||
chr1:211263141 | C | T | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.223+2977C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263141 | |||||||
chr1:211263277 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.223+3113G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263277 | |||||||
chr1:211263399 | T | A | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.223+3235T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263399 | |||||||
chr1:211263428 | AATTT | A | 73 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(70): Show |
84 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.223+3270_223+3273d others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211263428 | ||||||
chr1:211263432 | T | C | 78 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(75): Show |
81 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.223+3268T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263432 | |||||||
chr1:211263444 | C | CTG | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.223+3281_223+3282i others(4): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211263444 | ||||||
chr1:211263641 | T | C | 2 | a0001c0004t0001g0290 a0001c0004t0001g0291 |
2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.223+3477T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263641 | |||||||
chr1:211263820 | GT | G | 278 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(275): Show |
302 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.223+3666delT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211263820 | ||||||
chr1:211263826 | T | G | 2 | a0001c0001t0001g0273 a0001c0001t0002g0089 |
2 | HG01358.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.223+3662T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263826 | |||||||
chr1:211263855 | C | T | 1 | a0001c0001t0003g0241 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.223+3691C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211263855 | |||||||
chr1:211263956 | T | TACAG | 17 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0243 others(14): Show |
17 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.223+3793_223+3796d others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211263956 | ||||||
chr1:211264132 | T | C | 2 | a0001c0001t0003g0229 a0001c0001t0004g0255 |
2 | HG03471.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.223+3968T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211264132 | |||||||
chr1:211264214 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0018g0025 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.223+4050C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211264214 | |||||||
chr1:211264364 | G | A | 4 | a0001c0001t0008g0266 a0001c0001t0008g0267 a0001c0001t0008g0268 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+4200G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211264364 | |||||||
chr1:211264371 | A | G | 6 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0248 others(3): Show |
6 | HG02280.hp1 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+4207A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211264371 | |||||||
chr1:211264434 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.223+4270C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211264434 | |||||||
chr1:211264461 | C | T | 4 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0244 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+4297C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211264461 | |||||||
chr1:211264518 | C | CA | 78 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(75): Show |
81 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.223+4360dupA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211264518 | ||||||
chr1:211264838 | T | G | 4 | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0001g0052 others(1): Show |
4 | HG00558.hp1 NA18950.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+4674T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211264838 | |||||||
chr1:211264849 | T | C | 2 | a0001c0004t0001g0290 a0001c0004t0001g0291 |
2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.223+4685T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211264849 | |||||||
chr1:211264870 | G | T | 271 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(268): Show |
295 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.223+4706G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211264870 | |||||||
chr1:211265096 | C | T | 271 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(268): Show |
295 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.223+4932C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265096 | |||||||
chr1:211265139 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.223+4975G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265139 | |||||||
chr1:211265184 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0018g0025 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.223+5020T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265184 | |||||||
chr1:211265238 | T | A | 2 | a0001c0001t0003g0230 a0001c0001t0003g0240 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.223+5074T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265238 | |||||||
chr1:211265262 | TTAAATA | T | 11 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0255 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.223+5105_223+5110d others(8): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211265262 | ||||||
chr1:211265338 | T | G | 4 | a0001c0002t0006g0126 a0001c0002t0006g0135 a0001c0002t0006g0193 others(1): Show |
4 | HG00738.hp2 HG01099.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+5174T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265338 | |||||||
chr1:211265399 | A | G | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.223+5235A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265399 | |||||||
chr1:211265441 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.223+5277G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265441 | |||||||
chr1:211265444 | G | A | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.223+5280G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265444 | |||||||
chr1:211265545 | C | G | 11 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0255 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.223+5381C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265545 | |||||||
chr1:211265580 | G | A | 59 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(56): Show |
70 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.223+5416G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265580 | |||||||
chr1:211265602 | C | A | 48 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(45): Show |
52 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.223+5438C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265602 | |||||||
chr1:211265651 | G | A | 5 | a0001c0001t0003g0229 a0001c0001t0003g0237 a0001c0001t0003g0238 others(2): Show |
5 | HG00597.hp1 NA18747.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.223+5487G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265651 | |||||||
chr1:211265679 | A | G | 4 | a0001c0002t0006g0126 a0001c0002t0006g0135 a0001c0002t0006g0193 others(1): Show |
4 | HG00738.hp2 HG01099.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+5515A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265679 | |||||||
chr1:211265697 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0018g0025 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.223+5533G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265697 | |||||||
chr1:211265810 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.224-5422A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265810 | |||||||
chr1:211265827 | TA | T | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.224-5401delA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211265827 | ||||||
chr1:211265981 | G | C | 11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0243 others(8): Show |
11 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.224-5251G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211265981 | |||||||
chr1:211266020 | T | C | 1 | a0001c0002t0001g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.224-5212T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211266020 | |||||||
chr1:211266040 | G | T | 2 | a0001c0001t0001g0024 a0001c0001t0018g0025 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.224-5192G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211266040 | |||||||
chr1:211266108 | T | G | 4 | a0001c0001t0008g0266 a0001c0001t0008g0267 a0001c0001t0008g0268 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-5124T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211266108 | |||||||
chr1:211266185 | G | A | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.224-5047G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211266185 | |||||||
chr1:211266229 | A | G | 99 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(96): Show |
110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.224-5003A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211266229 | |||||||
chr1:211266475 | C | T | 271 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(268): Show |
295 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.224-4757C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211266475 | |||||||
chr1:211266503 | A | G | 2 | a0001c0004t0001g0290 a0001c0004t0001g0291 |
2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.224-4729A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211266503 | |||||||
chr1:211266537 | A | C | 1 | a0001c0001t0002g0182 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.224-4695A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211266537 | |||||||
chr1:211266745 | C | G | 11 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0255 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.224-4487C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211266745 | |||||||
chr1:211266841 | A | G | 1 | a0001c0002t0001g0140 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.224-4391A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211266841 | |||||||
chr1:211267047 | A | G | 1 | a0001c0001t0002g0155 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.224-4185A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211267047 | |||||||
chr1:211267120 | T | C | 1 | a0001c0002t0006g0193 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.224-4112T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211267120 | |||||||
chr1:211267277 | C | A | 1 | a0001c0001t0002g0094 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.224-3955C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211267277 | |||||||
chr1:211267501 | C | T | 1 | a0001c0001t0002g0181 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.224-3731C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211267501 | |||||||
chr1:211267692 | G | A | 271 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(268): Show |
295 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.224-3540G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211267692 | |||||||
chr1:211267739 | A | G | 3 | a0001c0001t0002g0147 a0001c0001t0002g0148 a0001c0001t0013g0146 |
3 | HG00741.hp2 HG01069.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.224-3493A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211267739 | |||||||
chr1:211267812 | C | T | 1 | a0001c0001t0018g0025 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.224-3420C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211267812 | |||||||
chr1:211267924 | A | T | 1 | a0001c0001t0011g0080 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.224-3308A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211267924 | |||||||
chr1:211268240 | G | A | 2 | a0001c0001t0002g0090 a0001c0001t0002g0156 |
2 | HG00642.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.224-2992G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268240 | |||||||
chr1:211268258 | A | G | 99 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(96): Show |
110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.224-2974A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268258 | |||||||
chr1:211268342 | A | G | 51 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0027 others(48): Show |
53 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.224-2890A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268342 | |||||||
chr1:211268355 | A | C | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.224-2877A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268355 | |||||||
chr1:211268369 | CT | C | 13 | a0001c0001t0001g0220 a0001c0001t0003g0003 a0001c0001t0003g0230 others(10): Show |
17 | HG00099.hp2 HG00738.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.224-2836delT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211268369 | ||||||
chr1:211268369 | CTTTT | C | 47 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(44): Show |
51 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.224-2839_224-2836d others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211268369 | ||||||
chr1:211268369 | CTTTTT | C | 25 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0031 others(22): Show |
25 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(22): Show |
intron_variant | MODIFIER | c.224-2840_224-2836d others(7): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211268369 | ||||||
chr1:211268369 | CTTTTTT | C | 176 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(173): Show |
192 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(189): Show |
intron_variant | MODIFIER | c.224-2841_224-2836d others(8): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211268369 | ||||||
chr1:211268390 | T | C | 65 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(62): Show |
69 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.224-2842T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268390 | |||||||
chr1:211268456 | C | G | 2 | a0001c0001t0002g0121 a0001c0001t0002g0188 |
2 | NA18978.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.224-2776C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268456 | |||||||
chr1:211268505 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.224-2727G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268505 | |||||||
chr1:211268540 | C | T | 99 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(96): Show |
110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.224-2692C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268540 | |||||||
chr1:211268605 | G | A | 1 | a0001c0002t0001g0219 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.224-2627G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268605 | |||||||
chr1:211268607 | C | T | 2 | a0001c0004t0001g0290 a0001c0004t0001g0291 |
2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.224-2625C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268607 | |||||||
chr1:211268626 | C | G | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.224-2606C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268626 | |||||||
chr1:211268744 | G | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0038 others(4): Show |
9 | HG01099.hp2 HG01192.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.224-2488G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268744 | |||||||
chr1:211268844 | A | G | 154 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(151): Show |
163 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(160): Show |
intron_variant | MODIFIER | c.224-2388A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268844 | |||||||
chr1:211268853 | TATAAC | T | 4 | a0001c0002t0006g0126 a0001c0002t0006g0135 a0001c0002t0006g0193 others(1): Show |
4 | HG00738.hp2 HG01099.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-2375_224-2371d others(7): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211268853 | ||||||
chr1:211268860 | TA | T | 11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0243 others(8): Show |
11 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.224-2371delA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211268860 | |||||||
chr1:211269139 | G | A | 26 | a0001c0001t0002g0084 a0001c0001t0002g0089 a0001c0001t0002g0090 others(23): Show |
26 | HG00642.hp1 HG01081.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.224-2093G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211269139 | |||||||
chr1:211269148 | G | GGT | 11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0243 others(8): Show |
11 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.224-2083_224-2082d others(4): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211269148 | ||||||
chr1:211269157 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0018g0025 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.224-2075C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211269157 | |||||||
chr1:211269207 | T | C | 5 | a0001c0001t0002g0082 a0001c0001t0002g0095 a0001c0001t0002g0096 others(2): Show |
5 | HG02080.hp1 NA18952.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-2025T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211269207 | |||||||
chr1:211269241 | A | G | 1 | a0001c0001t0009g0228 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.224-1991A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211269241 | |||||||
chr1:211269319 | C | T | 78 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(75): Show |
81 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.224-1913C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211269319 | |||||||
chr1:211269372 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.224-1860C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211269372 | |||||||
chr1:211269638 | T | C | 101 | a0001c0001t0001g0024 a0001c0001t0002g0001 a0001c0001t0002g0010 others(98): Show |
112 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.224-1594T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211269638 | |||||||
chr1:211269761 | CTAT | C | 11 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0255 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.224-1469_224-1467d others(5): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211269761 | ||||||
chr1:211269880 | C | CTACTAGC others(234): Show |
1 | a0001c0001t0002g0122 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.224-1348_224-1347i others(243): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211269880 | ||||||
chr1:211269937 | A | C | 1 | a0001c0001t0002g0156 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.224-1295A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211269937 | |||||||
chr1:211270066 | C | CT | 253 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(250): Show |
273 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(270): Show |
intron_variant | MODIFIER | c.224-1152dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211270066 | ||||||
chr1:211270131 | C | T | 1 | a0001c0002t0001g0209 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.224-1101C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211270131 | |||||||
chr1:211270211 | C | T | 1 | a0001c0001t0002g0093 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.224-1021C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211270211 | |||||||
chr1:211270212 | G | A | 1 | a0001c0002t0001g0195 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.224-1020G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211270212 | |||||||
chr1:211270298 | G | T | 2 | a0001c0001t0001g0024 a0001c0001t0018g0025 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.224-934G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211270298 | |||||||
chr1:211270317 | C | T | 1 | a0001c0002t0001g0127 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.224-915C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211270317 | |||||||
chr1:211270524 | A | G | 1 | a0001c0001t0008g0266 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.224-708A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211270524 | |||||||
chr1:211270548 | C | CA | 223 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0030 others(220): Show |
246 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(243): Show |
intron_variant | MODIFIER | c.224-672dupA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211270548 | ||||||
chr1:211270548 | C | CAA | 50 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(47): Show |
54 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.224-673_224-672dup others(2): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211270548 | ||||||
chr1:211270606 | A | G | 1 | a0001c0001t0001g0283 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.224-626A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211270606 | |||||||
chr1:211270689 | C | CT | 4 | a0001c0001t0008g0266 a0001c0001t0008g0267 a0001c0001t0008g0268 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-537dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211270689 | ||||||
chr1:211270777 | G | A | 1 | a0001c0001t0004g0269 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.224-455G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211270777 | |||||||
chr1:211270819 | TTGC | T | 273 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(270): Show |
300 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(297): Show |
intron_variant | MODIFIER | c.224-409_224-407del others(3): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 211270819 | ||||||
chr1:211271003 | T | C | 271 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(268): Show |
295 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.224-229T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211271003 | |||||||
chr1:211271040 | G | A | 78 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(75): Show |
81 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.224-192G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211271040 | |||||||
chr1:211271100 | G | A | 1 | a0001c0001t0002g0125 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.224-132G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211271100 | |||||||
chr1:211271109 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0018g0025 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.224-123G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211271109 | |||||||
chr1:211271135 | G | A | 1 | a0001c0001t0002g0158 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.224-97G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211271135 | |||||||
chr1:211271159 | C | G | 1 | a0001c0001t0005g0021 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.224-73C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 2/11 | chr1 | 211271159 | |||||||
chr1:211271376 | C | T | 4 | a0001c0002t0001g0085 a0001c0002t0001g0142 a0001c0002t0001g0207 others(1): Show |
4 | HG01257.hp2 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+67C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211271376 | |||||||
chr1:211271948 | G | A | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.301+639G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211271948 | |||||||
chr1:211272122 | G | A | 26 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(23): Show |
27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.301+813G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211272122 | |||||||
chr1:211272172 | C | G | 1 | a0001c0001t0002g0179 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.301+863C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211272172 | |||||||
chr1:211272463 | A | G | 51 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0027 others(48): Show |
53 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.301+1154A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211272463 | |||||||
chr1:211272612 | C | CT | 40 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0042 others(37): Show |
47 | HG00609.hp2 HG00673.hp1 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.301+1330dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 211272612 | ||||||
chr1:211272612 | C | CTT | 24 | a0001c0001t0001g0031 a0001c0001t0001g0144 a0001c0001t0001g0224 others(21): Show |
28 | HG00099.hp2 HG00597.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.301+1329_301+1330d others(4): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 211272612 | ||||||
chr1:211272612 | C | CTTT | 36 | a0001c0001t0001g0019 a0001c0001t0001g0254 a0001c0001t0001g0259 others(33): Show |
37 | HG01070.hp2 HG01884.hp1 HG02004.hp1 others(34): Show |
intron_variant | MODIFIER | c.301+1328_301+1330d others(5): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 211272612 | ||||||
chr1:211272612 | C | CTTTT | 33 | a0001c0001t0001g0032 a0001c0001t0001g0252 a0001c0001t0001g0263 others(30): Show |
33 | HG00642.hp1 HG01109.hp1 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.301+1327_301+1330d others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 211272612 | ||||||
chr1:211272612 | C | CTTTTT | 42 | a0001c0001t0001g0024 a0001c0001t0001g0264 a0001c0001t0001g0282 others(39): Show |
43 | HG00099.hp1 HG00738.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.301+1326_301+1330d others(7): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 211272612 | ||||||
chr1:211272612 | C | CTTTTTT | 53 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(50): Show |
64 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.301+1325_301+1330d others(8): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 211272612 | ||||||
chr1:211272612 | C | CTTTTTTT | 15 | a0001c0001t0002g0013 a0001c0001t0002g0029 a0001c0001t0002g0072 others(12): Show |
16 | HG00673.hp2 HG02523.hp1 HG02738.hp2 others(13): Show |
intron_variant | MODIFIER | c.301+1324_301+1330d others(9): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 211272612 | ||||||
chr1:211272654 | C | A | 1 | a0001c0002t0017g0128 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.301+1345C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211272654 | |||||||
chr1:211272683 | G | A | 2 | a0001c0001t0007g0002 a0001c0001t0007g0078 |
5 | HG02055.hp2 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+1374G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211272683 | |||||||
chr1:211272771 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0018g0025 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.302-1439G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211272771 | |||||||
chr1:211272864 | G | A | 26 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(23): Show |
27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.302-1346G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211272864 | |||||||
chr1:211273096 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.302-1114G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211273096 | |||||||
chr1:211273370 | G | A | 73 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(70): Show |
77 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.302-840G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211273370 | |||||||
chr1:211273612 | A | G | 11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0243 others(8): Show |
11 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.302-598A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211273612 | |||||||
chr1:211273635 | C | T | 11 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0255 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.302-575C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211273635 | |||||||
chr1:211274058 | C | G | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.302-152C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211274058 | |||||||
chr1:211274060 | C | G | 6 | a0001c0001t0002g0012 a0001c0001t0002g0101 a0001c0001t0002g0116 others(3): Show |
7 | HG00597.hp2 HG00733.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.302-150C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211274060 | |||||||
chr1:211274093 | CT | C | 271 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(268): Show |
295 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.302-107delT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 211274093 | ||||||
chr1:211274155 | C | G | 2 | a0001c0001t0005g0005 a0001c0001t0005g0077 |
4 | HG02486.hp2 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-55C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 3/11 | chr1 | 211274155 | |||||||
chr1:211274283 | G | A | 99 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(96): Show |
110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.354+21G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 4/11 | chr1 | 211274283 | |||||||
chr1:211274778 | A | G | 2 | a0001c0001t0003g0230 a0001c0001t0003g0240 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.354+516A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 4/11 | chr1 | 211274778 | |||||||
chr1:211275479 | C | CA | 4 | a0001c0001t0008g0266 a0001c0001t0008g0267 a0001c0001t0008g0268 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.355-777dupA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 211275479 | ||||||
chr1:211275521 | A | G | 2 | a0001c0001t0002g0119 a0001c0001t0012g0117 |
2 | HG00597.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.355-736A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 4/11 | chr1 | 211275521 | |||||||
chr1:211275529 | T | C | 13 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(10): Show |
14 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.355-728T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 4/11 | chr1 | 211275529 | |||||||
chr1:211275805 | A | ATTAC | 11 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0255 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.355-452_355-451ins others(4): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 4/11 | chr1 | 211275805 | |||||||
chr1:211276109 | A | G | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.355-148A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 4/11 | chr1 | 211276109 | |||||||
chr1:211276655 | A | G | 1 | a0001c0001t0002g0177 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.516+237A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211276655 | |||||||
chr1:211276815 | C | G | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.516+397C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211276815 | |||||||
chr1:211276831 | T | A | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.516+413T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211276831 | |||||||
chr1:211276852 | C | T | 1 | a0001c0001t0003g0234 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.516+434C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211276852 | |||||||
chr1:211276958 | C | T | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.516+540C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211276958 | |||||||
chr1:211277005 | G | GA | 10 | a0001c0001t0001g0261 a0001c0001t0001g0263 a0001c0001t0001g0264 others(7): Show |
10 | HG03491.hp2 HG03834.hp2 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.516+589dupA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 211277005 | ||||||
chr1:211277013 | G | T | 26 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(23): Show |
27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.516+595G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211277013 | |||||||
chr1:211277022 | G | T | 1 | a0001c0001t0004g0269 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.516+604G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211277022 | |||||||
chr1:211277073 | G | A | 6 | a0001c0002t0006g0126 a0001c0002t0006g0135 a0001c0002t0006g0193 others(3): Show |
6 | HG00738.hp2 HG01099.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.516+655G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211277073 | |||||||
chr1:211277085 | C | CA | 18 | a0001c0001t0001g0044 a0001c0001t0002g0158 a0001c0001t0003g0003 others(15): Show |
22 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.516+678dupA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 211277085 | ||||||
chr1:211277089 | A | G | 2 | a0001c0001t0007g0002 a0001c0001t0007g0078 |
5 | HG02055.hp2 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.516+671A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211277089 | |||||||
chr1:211277169 | C | CT | 15 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0243 others(12): Show |
15 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.516+761dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 211277169 | ||||||
chr1:211277173 | T | C | 1 | a0001c0001t0002g0150 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.516+755T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211277173 | |||||||
chr1:211277716 | A | T | 1 | a0001c0001t0004g0270 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.517-401A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211277716 | |||||||
chr1:211277920 | T | G | 1 | a0001c0003t0001g0129 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.517-197T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | chr1 | 211277920 | |||||||
chr1:211278051 | TATC | T | 78 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(75): Show |
81 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.517-61_517-59delTC others(1): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 211278051 | ||||||
chr1:211278516 | G | T | 4 | a0001c0001t0002g0012 a0001c0001t0002g0101 a0001c0001t0002g0116 others(1): Show |
5 | HG00733.hp2 HG01358.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.641+275G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | chr1 | 211278516 | |||||||
chr1:211278672 | A | G | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.641+431A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | chr1 | 211278672 | |||||||
chr1:211278714 | G | A | 99 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(96): Show |
110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.641+473G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | chr1 | 211278714 | |||||||
chr1:211278788 | TAA | T | 17 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0243 others(14): Show |
17 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.642-447_642-446del others(2): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 211278788 | ||||||
chr1:211278871 | A | G | 1 | a0001c0002t0001g0087 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.642-367A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | chr1 | 211278871 | |||||||
chr1:211278900 | G | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(53): Show |
60 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.642-338G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | chr1 | 211278900 | |||||||
chr1:211279004 | T | G | 1 | a0001c0002t0001g0200 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.642-234T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | chr1 | 211279004 | |||||||
chr1:211279048 | G | C | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.642-190G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | chr1 | 211279048 | |||||||
chr1:211279102 | G | A | 56 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(53): Show |
60 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.642-136G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | chr1 | 211279102 | |||||||
chr1:211279187 | TA | T | 281 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(278): Show |
311 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(308): Show |
intron_variant | MODIFIER | c.642-36delA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 211279187 | ||||||
chr1:211279187 | TAA | T | 7 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0067 others(4): Show |
7 | HG02717.hp2 HG02886.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.642-37_642-36delAA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 211279187 | ||||||
chr1:211279336 | G | A | 99 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(96): Show |
110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.720+20G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211279336 | |||||||
chr1:211279386 | G | A | 99 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(96): Show |
110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.720+70G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211279386 | |||||||
chr1:211279408 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.720+92G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211279408 | |||||||
chr1:211279503 | A | G | 78 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(75): Show |
81 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.720+187A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211279503 | |||||||
chr1:211279796 | G | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(20): Show |
27 | HG00609.hp1 HG01099.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.720+480G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211279796 | |||||||
chr1:211279884 | G | C | 11 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0255 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.720+568G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211279884 | |||||||
chr1:211280466 | A | G | 1 | a0001c0002t0001g0197 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.720+1150A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211280466 | |||||||
chr1:211280563 | A | G | 4 | a0001c0001t0008g0266 a0001c0001t0008g0267 a0001c0001t0008g0268 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+1247A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211280563 | |||||||
chr1:211280572 | C | G | 1 | a0001c0001t0002g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.720+1256C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211280572 | |||||||
chr1:211280591 | C | G | 2 | a0001c0001t0002g0149 a0001c0001t0002g0165 |
2 | HG01433.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.720+1275C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211280591 | |||||||
chr1:211280639 | A | G | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.720+1323A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211280639 | |||||||
chr1:211280653 | A | G | 1 | a0001c0001t0002g0105 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.720+1337A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211280653 | |||||||
chr1:211280706 | G | A | 1 | a0001c0001t0005g0006 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.720+1390G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211280706 | |||||||
chr1:211280971 | C | T | 1 | a0001c0001t0004g0257 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.720+1655C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211280971 | |||||||
chr1:211280984 | C | CA | 18 | a0001c0001t0002g0028 a0001c0001t0002g0153 a0001c0001t0002g0181 others(15): Show |
20 | HG00099.hp1 HG01081.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.720+1685dupA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211280984 | ||||||
chr1:211280984 | C | CAA | 91 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(88): Show |
102 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.720+1684_720+1685d others(4): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211280984 | ||||||
chr1:211280984 | CA | C | 69 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(66): Show |
80 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.720+1685delA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211280984 | ||||||
chr1:211281001 | AG | A | 27 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(24): Show |
28 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.720+1687delG | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211281001 | ||||||
chr1:211281034 | C | T | 8 | a0001c0001t0004g0017 a0001c0001t0004g0255 a0001c0001t0004g0256 others(5): Show |
9 | HG01109.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.720+1718C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211281034 | |||||||
chr1:211281331 | G | C | 2 | a0001c0004t0001g0290 a0001c0004t0001g0291 |
2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.720+2015G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211281331 | |||||||
chr1:211281560 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0018g0025 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.720+2244G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211281560 | |||||||
chr1:211281673 | A | G | 1 | a0001c0001t0003g0238 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.720+2357A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211281673 | |||||||
chr1:211282017 | G | A | 2 | a0001c0001t0002g0185 a0001c0001t0002g0190 |
2 | HG01081.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.720+2701G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211282017 | |||||||
chr1:211282286 | CA | C | 48 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(45): Show |
52 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.720+2972delA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211282286 | ||||||
chr1:211282454 | A | G | 4 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0244 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.720+3138A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211282454 | |||||||
chr1:211282503 | G | GT | 11 | a0001c0001t0001g0023 a0001c0001t0001g0044 a0001c0001t0001g0055 others(8): Show |
12 | HG00642.hp1 HG00741.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.720+3203dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211282503 | ||||||
chr1:211282589 | C | A | 99 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(96): Show |
110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.720+3273C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211282589 | |||||||
chr1:211282660 | G | A | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.720+3344G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211282660 | |||||||
chr1:211282943 | T | C | 1 | a0001c0002t0017g0128 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.720+3627T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211282943 | |||||||
chr1:211283119 | T | C | 1 | a0001c0001t0005g0253 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.720+3803T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211283119 | |||||||
chr1:211283263 | G | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0244 others(2): Show |
5 | HG01243.hp1 HG02257.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+3947G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211283263 | |||||||
chr1:211283604 | A | G | 1 | a0001c0002t0001g0195 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.720+4288A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211283604 | |||||||
chr1:211283637 | C | T | 4 | a0001c0001t0005g0006 a0001c0001t0005g0021 a0001c0001t0005g0253 others(1): Show |
5 | HG00741.hp1 HG01516.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+4321C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211283637 | |||||||
chr1:211283638 | G | A | 1 | a0001c0001t0002g0169 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.720+4322G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211283638 | |||||||
chr1:211283690 | G | A | 8 | a0001c0001t0001g0144 a0001c0001t0001g0220 a0001c0001t0001g0221 others(5): Show |
8 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.720+4374G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211283690 | |||||||
chr1:211283741 | T | C | 114 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0243 others(111): Show |
125 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(122): Show |
intron_variant | MODIFIER | c.720+4425T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211283741 | |||||||
chr1:211283785 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.720+4469A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211283785 | |||||||
chr1:211283812 | A | AT | 78 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(75): Show |
81 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.720+4510dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211283812 | ||||||
chr1:211283916 | C | T | 11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0243 others(8): Show |
11 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.720+4600C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211283916 | |||||||
chr1:211284064 | A | T | 1 | a0001c0001t0001g0284 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.720+4748A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211284064 | |||||||
chr1:211284210 | C | T | 4 | a0001c0001t0008g0266 a0001c0001t0008g0267 a0001c0001t0008g0268 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+4894C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211284210 | |||||||
chr1:211284376 | G | A | 26 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(23): Show |
27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.721-4802G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211284376 | |||||||
chr1:211284479 | G | C | 27 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(24): Show |
28 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.721-4699G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211284479 | |||||||
chr1:211284502 | C | CTTTA | 123 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(120): Show |
137 | HG00408.hp2 HG00558.hp2 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.721-4654_721-4651d others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211284502 | ||||||
chr1:211284502 | C | CTTTATTT others(1): Show |
16 | a0001c0001t0001g0024 a0001c0001t0001g0053 a0001c0001t0001g0056 others(13): Show |
16 | HG00558.hp1 HG00642.hp1 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.721-4658_721-4651d others(10): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211284502 | ||||||
chr1:211284502 | C | CTTTATTT others(5): Show |
1 | a0001c0001t0002g0092 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.721-4662_721-4651d others(14): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211284502 | ||||||
chr1:211284520 | TTATTTAT others(1): Show |
T | 80 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(77): Show |
83 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(80): Show |
intron_variant | MODIFIER | c.721-4650_721-4643d others(10): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211284520 | ||||||
chr1:211284524 | TTATG | T | 17 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(14): Show |
21 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.721-4650_721-4647d others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211284524 | ||||||
chr1:211284528 | G | T | 183 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(180): Show |
199 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.721-4650G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211284528 | |||||||
chr1:211284548 | G | A | 1 | a0001c0003t0001g0134 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.721-4630G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211284548 | |||||||
chr1:211284574 | GT | G | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-4603delT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211284574 | |||||||
chr1:211284794 | T | C | 109 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(106): Show |
115 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.721-4384T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211284794 | |||||||
chr1:211285058 | T | C | 2 | a0001c0001t0002g0088 a0001c0001t0002g0151 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.721-4120T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211285058 | |||||||
chr1:211285154 | C | G | 1 | a0001c0001t0002g0072 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.721-4024C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211285154 | |||||||
chr1:211285196 | T | A | 1 | a0001c0001t0001g0044 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.721-3982T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211285196 | |||||||
chr1:211285297 | A | C | 1 | a0001c0001t0001g0043 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.721-3881A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211285297 | |||||||
chr1:211285465 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.721-3713G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211285465 | |||||||
chr1:211285839 | G | A | 1 | a0001c0001t0003g0235 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.721-3339G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211285839 | |||||||
chr1:211285892 | T | C | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.721-3286T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211285892 | |||||||
chr1:211286032 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.721-3146C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286032 | |||||||
chr1:211286215 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.721-2963C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286215 | |||||||
chr1:211286312 | CT | C | 271 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(268): Show |
295 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.721-2851delT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 211286312 | ||||||
chr1:211286338 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.721-2840C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286338 | |||||||
chr1:211286368 | C | T | 2 | a0001c0001t0002g0182 a0001c0001t0015g0176 |
2 | NA19070.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.721-2810C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286368 | |||||||
chr1:211286452 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.721-2726C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286452 | |||||||
chr1:211286523 | G | A | 2 | a0001c0004t0001g0290 a0001c0004t0001g0291 |
2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.721-2655G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286523 | |||||||
chr1:211286549 | C | T | 2 | a0001c0001t0007g0002 a0001c0001t0007g0078 |
5 | HG02055.hp2 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-2629C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286549 | |||||||
chr1:211286610 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0018g0025 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.721-2568A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286610 | |||||||
chr1:211286625 | T | C | 4 | a0001c0001t0008g0266 a0001c0001t0008g0267 a0001c0001t0008g0268 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-2553T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286625 | |||||||
chr1:211286687 | G | A | 2 | a0001c0001t0002g0121 a0001c0001t0002g0188 |
2 | NA18978.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.721-2491G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286687 | |||||||
chr1:211286820 | A | G | 4 | a0001c0001t0002g0091 a0001c0001t0002g0093 a0001c0001t0002g0109 others(1): Show |
4 | HG01109.hp1 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.721-2358A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286820 | |||||||
chr1:211286924 | C | G | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-2254C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211286924 | |||||||
chr1:211287255 | T | C | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-1923T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211287255 | |||||||
chr1:211287487 | A | G | 2 | a0001c0002t0006g0199 a0001c0002t0006g0210 |
2 | HG02698.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.721-1691A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211287487 | |||||||
chr1:211287490 | A | G | 2 | a0001c0001t0003g0230 a0001c0001t0003g0240 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.721-1688A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211287490 | |||||||
chr1:211287538 | G | A | 2 | a0001c0001t0007g0002 a0001c0001t0007g0078 |
5 | HG02055.hp2 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-1640G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211287538 | |||||||
chr1:211287552 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.721-1626G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211287552 | |||||||
chr1:211287659 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0018g0025 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.721-1519T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211287659 | |||||||
chr1:211287750 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.721-1428G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211287750 | |||||||
chr1:211287832 | C | A | 5 | a0001c0002t0001g0015 a0001c0002t0001g0027 a0001c0002t0001g0127 others(2): Show |
6 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.721-1346C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211287832 | |||||||
chr1:211287885 | C | T | 1 | a0001c0001t0002g0158 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.721-1293C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211287885 | |||||||
chr1:211288008 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.721-1170G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288008 | |||||||
chr1:211288166 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.721-1012C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288166 | |||||||
chr1:211288218 | A | T | 51 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0027 others(48): Show |
53 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.721-960A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288218 | |||||||
chr1:211288312 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0067 |
2 | NA18977.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.721-866A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288312 | |||||||
chr1:211288348 | C | T | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.721-830C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288348 | |||||||
chr1:211288390 | G | A | 51 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0027 others(48): Show |
53 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.721-788G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288390 | |||||||
chr1:211288463 | C | A | 1 | a0001c0001t0002g0098 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.721-715C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288463 | |||||||
chr1:211288496 | T | C | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.721-682T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288496 | |||||||
chr1:211288513 | A | AAATT | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.721-665_721-664ins others(4): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288513 | |||||||
chr1:211288519 | A | G | 100 | a0001c0001t0001g0023 a0001c0001t0002g0001 a0001c0001t0002g0010 others(97): Show |
111 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.721-659A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288519 | |||||||
chr1:211288637 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0018g0025 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.721-541A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288637 | |||||||
chr1:211288685 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.721-493T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288685 | |||||||
chr1:211288727 | C | G | 1 | a0001c0001t0016g0231 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.721-451C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288727 | |||||||
chr1:211288775 | G | A | 271 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(268): Show |
295 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.721-403G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288775 | |||||||
chr1:211288778 | C | A | 271 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(268): Show |
295 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.721-400C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288778 | |||||||
chr1:211288883 | A | G | 2 | a0001c0002t0006g0199 a0001c0002t0006g0210 |
2 | HG02698.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.721-295A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211288883 | |||||||
chr1:211289088 | G | T | 11 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0255 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.721-90G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 7/11 | chr1 | 211289088 | |||||||
chr1:211289562 | G | C | 1 | a0001c0001t0002g0094 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.939+166G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211289562 | |||||||
chr1:211289628 | C | A | 1 | a0001c0001t0002g0084 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.939+232C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211289628 | |||||||
chr1:211289714 | A | G | 11 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0255 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.939+318A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211289714 | |||||||
chr1:211289765 | GGTT | G | 49 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(46): Show |
53 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.939+375_939+377del others(3): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211289765 | ||||||
chr1:211289822 | A | G | 2 | a0001c0004t0001g0290 a0001c0004t0001g0291 |
2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.939+426A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211289822 | |||||||
chr1:211289950 | C | A | 1 | a0001c0001t0001g0265 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.939+554C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211289950 | |||||||
chr1:211289982 | A | G | 11 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0255 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.939+586A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211289982 | |||||||
chr1:211290070 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0001g0225 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.939+674G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211290070 | |||||||
chr1:211290363 | G | A | 47 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(44): Show |
51 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.939+967G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211290363 | |||||||
chr1:211290393 | A | C | 1 | a0001c0001t0002g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.939+997A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211290393 | |||||||
chr1:211290473 | C | T | 26 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(23): Show |
27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.939+1077C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211290473 | |||||||
chr1:211290487 | G | C | 1 | a0001c0001t0002g0106 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.939+1091G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211290487 | |||||||
chr1:211290561 | A | T | 2 | a0001c0001t0002g0119 a0001c0001t0012g0117 |
2 | HG00597.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.939+1165A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211290561 | |||||||
chr1:211290672 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0263 |
2 | NA18941.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.939+1276G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211290672 | |||||||
chr1:211290773 | C | T | 78 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(75): Show |
81 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(78): Show |
intron_variant | MODIFIER | c.939+1377C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211290773 | |||||||
chr1:211290972 | G | GT | 55 | a0001c0001t0001g0024 a0001c0001t0001g0246 a0001c0001t0002g0108 others(52): Show |
57 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(54): Show |
intron_variant | MODIFIER | c.939+1586dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211290972 | ||||||
chr1:211291714 | ACATAGGC | A | 55 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(52): Show |
59 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.939+2321_939+2327d others(9): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211291714 | ||||||
chr1:211291737 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.939+2341T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211291737 | |||||||
chr1:211291789 | C | T | 5 | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0001g0052 others(2): Show |
5 | HG00558.hp1 HG02132.hp2 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.939+2393C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211291789 | |||||||
chr1:211291968 | A | T | 55 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(52): Show |
59 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.939+2572A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211291968 | |||||||
chr1:211292057 | G | T | 1 | a0001c0001t0001g0060 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.939+2661G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211292057 | |||||||
chr1:211292192 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.939+2796T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211292192 | |||||||
chr1:211292208 | T | C | 6 | a0001c0002t0006g0126 a0001c0002t0006g0135 a0001c0002t0006g0193 others(3): Show |
6 | HG00738.hp2 HG01099.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.939+2812T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211292208 | |||||||
chr1:211292237 | G | A | 26 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(23): Show |
27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.939+2841G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211292237 | |||||||
chr1:211292275 | A | G | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.939+2879A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211292275 | |||||||
chr1:211292281 | G | A | 100 | a0001c0001t0001g0023 a0001c0001t0002g0001 a0001c0001t0002g0010 others(97): Show |
111 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.939+2885G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211292281 | |||||||
chr1:211292303 | C | T | 1 | a0001c0003t0001g0132 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.939+2907C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211292303 | |||||||
chr1:211292620 | T | A | 100 | a0001c0001t0001g0023 a0001c0001t0002g0001 a0001c0001t0002g0010 others(97): Show |
111 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.940-3056T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211292620 | |||||||
chr1:211292785 | G | A | 1 | a0001c0003t0001g0141 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.940-2891G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211292785 | |||||||
chr1:211292921 | TA | T | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.940-2751delA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211292921 | ||||||
chr1:211293017 | G | T | 1 | a0001c0001t0001g0252 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.940-2659G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293017 | |||||||
chr1:211293033 | G | A | 11 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0255 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.940-2643G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293033 | |||||||
chr1:211293086 | A | AAAAT | 120 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(117): Show |
135 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.940-2559_940-2556d others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211293086 | ||||||
chr1:211293086 | A | AAAATAAA others(1): Show |
51 | a0001c0001t0001g0022 a0001c0001t0001g0034 a0001c0001t0001g0060 others(48): Show |
51 | HG00642.hp1 HG00738.hp2 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.940-2563_940-2556d others(10): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211293086 | ||||||
chr1:211293086 | A | AAAATAAA others(5): Show |
65 | a0001c0001t0001g0019 a0001c0001t0001g0031 a0001c0001t0001g0144 others(62): Show |
68 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.940-2567_940-2556d others(14): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211293086 | ||||||
chr1:211293086 | A | AAAATAAA others(9): Show |
17 | a0001c0001t0001g0030 a0001c0001t0001g0221 a0001c0001t0001g0244 others(14): Show |
19 | HG00733.hp1 HG01070.hp1 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.940-2571_940-2556d others(18): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211293086 | ||||||
chr1:211293086 | AAAATAAA others(5): Show |
A | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.940-2567_940-2556d others(14): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211293086 | ||||||
chr1:211293118 | T | TAAATAAA others(10): Show |
3 | a0001c0001t0001g0032 a0001c0001t0001g0259 a0001c0001t0001g0265 |
3 | HG01192.hp1 HG04115.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.940-2556_940-2555i others(19): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211293118 | ||||||
chr1:211293386 | C | T | 2 | a0001c0001t0001g0053 a0001c0001t0001g0263 |
2 | HG00558.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.940-2290C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293386 | |||||||
chr1:211293419 | A | G | 281 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(278): Show |
308 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(305): Show |
intron_variant | MODIFIER | c.940-2257A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293419 | |||||||
chr1:211293444 | A | G | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.940-2232A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293444 | |||||||
chr1:211293561 | C | A | 1 | a0001c0001t0001g0243 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.940-2115C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293561 | |||||||
chr1:211293644 | G | A | 100 | a0001c0001t0001g0023 a0001c0001t0002g0001 a0001c0001t0002g0010 others(97): Show |
111 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.940-2032G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293644 | |||||||
chr1:211293739 | A | G | 3 | a0001c0001t0002g0164 a0001c0001t0002g0184 a0001c0001t0002g0242 |
3 | NA18980.hp2 NA19078.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.940-1937A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293739 | |||||||
chr1:211293801 | T | G | 1 | a0001c0001t0002g0170 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.940-1875T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293801 | |||||||
chr1:211293933 | A | G | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.940-1743A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293933 | |||||||
chr1:211293968 | G | A | 1 | a0001c0002t0001g0027 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.940-1708G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293968 | |||||||
chr1:211293994 | T | C | 1 | a0001c0002t0001g0195 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.940-1682T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211293994 | |||||||
chr1:211294145 | T | G | 4 | a0001c0001t0008g0266 a0001c0001t0008g0267 a0001c0001t0008g0268 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.940-1531T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294145 | |||||||
chr1:211294260 | T | C | 2 | a0001c0001t0001g0281 a0001c0001t0001g0286 |
2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.940-1416T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294260 | |||||||
chr1:211294312 | T | C | 281 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(278): Show |
308 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(305): Show |
intron_variant | MODIFIER | c.940-1364T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294312 | |||||||
chr1:211294367 | G | T | 1 | a0001c0001t0001g0282 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.940-1309G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294367 | |||||||
chr1:211294510 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.940-1166C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294510 | |||||||
chr1:211294567 | GACTTTTC others(35): Show |
G | 1 | a0001c0001t0001g0066 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.940-1108_940-1067d others(44): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294567 | |||||||
chr1:211294586 | C | CT | 108 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): Show |
115 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.940-1069dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211294586 | ||||||
chr1:211294586 | CT | C | 145 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0030 others(142): Show |
164 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.940-1069delT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211294586 | ||||||
chr1:211294590 | T | C | 12 | a0001c0001t0002g0100 a0001c0001t0004g0017 a0001c0001t0004g0018 others(9): Show |
14 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.940-1086T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294590 | |||||||
chr1:211294618 | C | T | 11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0243 others(8): Show |
11 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.940-1058C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294618 | |||||||
chr1:211294624 | G | C | 281 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(278): Show |
308 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(305): Show |
intron_variant | MODIFIER | c.940-1052G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294624 | |||||||
chr1:211294628 | C | T | 108 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(105): Show |
114 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.940-1048C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294628 | |||||||
chr1:211294676 | A | G | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.940-1000A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294676 | |||||||
chr1:211294691 | G | A | 3 | a0001c0001t0002g0028 a0001c0001t0002g0149 a0001c0001t0002g0165 |
3 | HG01433.hp1 HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.940-985G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294691 | |||||||
chr1:211294832 | G | A | 2 | a0001c0001t0003g0230 a0001c0001t0003g0240 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.940-844G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211294832 | |||||||
chr1:211295002 | T | C | 1 | a0001c0002t0001g0213 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.940-674T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211295002 | |||||||
chr1:211295041 | C | A | 1 | a0001c0002t0001g0214 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.940-635C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211295041 | |||||||
chr1:211295042 | T | C | 1 | a0001c0001t0002g0165 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.940-634T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211295042 | |||||||
chr1:211295066 | T | TG | 16 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0031 others(13): Show |
16 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.940-610_940-609ins others(1): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211295066 | |||||||
chr1:211295066 | T | TTG | 119 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(116): Show |
127 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.940-609_940-608ins others(2): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211295066 | ||||||
chr1:211295066 | T | TTTG | 126 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0034 others(123): Show |
141 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.940-609_940-608ins others(3): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211295066 | ||||||
chr1:211295066 | T | TTTTG | 14 | a0001c0001t0001g0024 a0001c0001t0001g0282 a0001c0001t0001g0284 others(11): Show |
15 | HG00642.hp1 HG00741.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.940-609_940-608ins others(4): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 211295066 | ||||||
chr1:211295431 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.940-245A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211295431 | |||||||
chr1:211295468 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.940-208G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211295468 | |||||||
chr1:211295512 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.940-164A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211295512 | |||||||
chr1:211295616 | G | A | 1 | a0001c0002t0001g0201 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.940-60G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 8/11 | chr1 | 211295616 | |||||||
chr1:211295906 | A | G | 2 | a0001c0002t0001g0085 a0001c0002t0001g0208 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1017+153A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211295906 | |||||||
chr1:211296155 | A | C | 26 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(23): Show |
27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.1017+402A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211296155 | |||||||
chr1:211296155 | A | T | 1 | a0001c0001t0001g0254 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1017+402A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211296155 | |||||||
chr1:211296208 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1017+455T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211296208 | |||||||
chr1:211296338 | TA | T | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.1017+587delA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 211296338 | ||||||
chr1:211296746 | A | C | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.1017+993A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211296746 | |||||||
chr1:211296847 | T | C | 1 | a0001c0004t0001g0291 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1017+1094T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211296847 | |||||||
chr1:211297152 | A | G | 2 | a0001c0002t0001g0139 a0001c0002t0001g0200 |
2 | NA18939.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1017+1399A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211297152 | |||||||
chr1:211297175 | G | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0244 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017+1422G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211297175 | |||||||
chr1:211297296 | A | C | 1 | a0001c0001t0002g0089 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1017+1543A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211297296 | |||||||
chr1:211297385 | C | G | 40 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(37): Show |
43 | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.1017+1632C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211297385 | |||||||
chr1:211297391 | G | A | 1 | a0001c0001t0002g0105 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1017+1638G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211297391 | |||||||
chr1:211297485 | C | T | 27 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(24): Show |
28 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.1017+1732C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211297485 | |||||||
chr1:211297494 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1017+1741G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211297494 | |||||||
chr1:211297516 | G | A | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.1017+1763G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211297516 | |||||||
chr1:211298163 | A | T | 6 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0248 others(3): Show |
6 | HG02280.hp1 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1017+2410A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211298163 | |||||||
chr1:211298256 | G | A | 2 | a0001c0001t0004g0018 a0001c0001t0004g0271 |
3 | HG01884.hp2 HG02615.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1017+2503G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211298256 | |||||||
chr1:211298331 | AAG | A | 4 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0244 others(1): Show |
4 | HG01243.hp1 HG02257.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1017+2581_1017+258 others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 211298331 | ||||||
chr1:211298354 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0018g0025 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1017+2601A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211298354 | |||||||
chr1:211298778 | G | A | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1017+3025G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211298778 | |||||||
chr1:211299001 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1017+3248C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211299001 | |||||||
chr1:211299044 | G | A | 1 | a0001c0002t0006g0210 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1017+3291G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211299044 | |||||||
chr1:211299067 | A | G | 1 | a0001c0001t0004g0270 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1017+3314A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211299067 | |||||||
chr1:211299087 | AGTACAGA others(5): Show |
A | 1 | a0001c0001t0001g0023 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1017+3338_1017+334 others(16): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 211299087 | ||||||
chr1:211299201 | G | A | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.1017+3448G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211299201 | |||||||
chr1:211299206 | T | C | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1017+3453T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211299206 | |||||||
chr1:211299389 | G | A | 1 | a0001c0001t0002g0090 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1017+3636G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211299389 | |||||||
chr1:211299440 | G | A | 1 | a0001c0002t0001g0195 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1017+3687G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211299440 | |||||||
chr1:211299637 | CG | C | 26 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(23): Show |
27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.1017+3888delG | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 211299637 | ||||||
chr1:211299663 | G | A | 1 | a0001c0001t0002g0026 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1017+3910G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211299663 | |||||||
chr1:211299794 | G | A | 7 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(4): Show |
8 | HG00609.hp1 HG02083.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.1017+4041G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211299794 | |||||||
chr1:211299865 | T | G | 11 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0255 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1017+4112T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211299865 | |||||||
chr1:211300039 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1018-4044C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300039 | |||||||
chr1:211300071 | C | CT | 106 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0035 others(103): Show |
118 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.1018-3994dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 211300071 | ||||||
chr1:211300071 | C | CTT | 23 | a0001c0001t0001g0265 a0001c0001t0002g0026 a0001c0001t0002g0082 others(20): Show |
27 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.1018-3995_1018-399 others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 211300071 | ||||||
chr1:211300071 | CT | C | 3 | a0001c0001t0007g0002 a0001c0001t0007g0078 a0001c0002t0001g0204 |
6 | HG01070.hp1 HG02055.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1018-3994delT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 211300071 | ||||||
chr1:211300075 | T | C | 2 | a0001c0001t0001g0281 a0001c0001t0001g0286 |
2 | HG02630.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1018-4008T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300075 | |||||||
chr1:211300362 | G | A | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.1018-3721G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300362 | |||||||
chr1:211300398 | C | G | 1 | a0001c0001t0002g0105 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1018-3685C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300398 | |||||||
chr1:211300402 | T | C | 2 | a0001c0001t0007g0002 a0001c0001t0007g0078 |
5 | HG02055.hp2 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1018-3681T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300402 | |||||||
chr1:211300406 | G | C | 1 | a0001c0001t0002g0156 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1018-3677G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300406 | |||||||
chr1:211300507 | T | G | 1 | a0001c0001t0001g0250 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1018-3576T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300507 | |||||||
chr1:211300799 | A | G | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.1018-3284A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300799 | |||||||
chr1:211300906 | A | G | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
302 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(299): Show |
intron_variant | MODIFIER | c.1018-3177A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300906 | |||||||
chr1:211300908 | G | A | 99 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(96): Show |
110 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.1018-3175G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300908 | |||||||
chr1:211300913 | C | CGT | 5 | a0001c0001t0001g0031 a0001c0001t0002g0090 a0001c0001t0002g0185 others(2): Show |
5 | HG00642.hp1 HG01081.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1018-3168_1018-316 others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 211300913 | ||||||
chr1:211300917 | C | T | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.1018-3166C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300917 | |||||||
chr1:211300979 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1018-3104C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211300979 | |||||||
chr1:211301106 | A | T | 4 | a0001c0001t0001g0024 a0001c0001t0002g0099 a0001c0001t0002g0227 others(1): Show |
4 | HG03195.hp1 HG03453.hp2 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1018-2977A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211301106 | |||||||
chr1:211301161 | T | C | 2 | a0001c0001t0002g0185 a0001c0001t0002g0190 |
2 | HG01081.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.1018-2922T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211301161 | |||||||
chr1:211301381 | G | A | 1 | a0001c0001t0002g0089 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1018-2702G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211301381 | |||||||
chr1:211301413 | T | G | 1 | a0001c0001t0001g0252 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1018-2670T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211301413 | |||||||
chr1:211301521 | G | A | 11 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0255 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1018-2562G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211301521 | |||||||
chr1:211301552 | T | C | 1 | a0001c0001t0010g0103 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1018-2531T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211301552 | |||||||
chr1:211301700 | G | A | 26 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(23): Show |
27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.1018-2383G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211301700 | |||||||
chr1:211301903 | T | C | 1 | a0001c0001t0002g0125 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1018-2180T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211301903 | |||||||
chr1:211301991 | A | C | 27 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(24): Show |
28 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.1018-2092A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211301991 | |||||||
chr1:211302043 | T | A | 11 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0255 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1018-2040T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211302043 | |||||||
chr1:211302094 | A | G | 2 | a0001c0002t0001g0138 a0001c0002t0001g0214 |
2 | NA19060.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1018-1989A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211302094 | |||||||
chr1:211302192 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1018-1891T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211302192 | |||||||
chr1:211302461 | A | G | 56 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(53): Show |
60 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1018-1622A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211302461 | |||||||
chr1:211302584 | C | T | 2 | a0001c0001t0001g0245 a0001c0002t0001g0131 |
2 | HG02559.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1018-1499C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211302584 | |||||||
chr1:211302679 | C | T | 11 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0255 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1018-1404C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211302679 | |||||||
chr1:211302911 | C | A | 2 | a0001c0001t0001g0024 a0001c0001t0018g0025 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1018-1172C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211302911 | |||||||
chr1:211303081 | C | G | 138 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(135): Show |
145 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.1018-1002C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211303081 | |||||||
chr1:211303147 | C | T | 56 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(53): Show |
60 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1018-936C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211303147 | |||||||
chr1:211303625 | GA | G | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.1018-451delA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr1 | 211303625 | ||||||
chr1:211303721 | T | C | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.1018-362T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211303721 | |||||||
chr1:211303730 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1018-353G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211303730 | |||||||
chr1:211303895 | A | G | 1 | a0001c0002t0001g0197 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1018-188A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211303895 | |||||||
chr1:211304057 | T | G | 4 | a0001c0001t0002g0091 a0001c0001t0002g0093 a0001c0001t0002g0109 others(1): Show |
4 | HG01109.hp1 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1018-26T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 9/11 | chr1 | 211304057 | |||||||
chr1:211304400 | C | T | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.1075+260C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211304400 | |||||||
chr1:211304679 | C | T | 4 | a0001c0002t0006g0126 a0001c0002t0006g0135 a0001c0002t0006g0193 others(1): Show |
4 | HG00738.hp2 HG01099.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+539C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211304679 | |||||||
chr1:211304708 | C | A | 281 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(278): Show |
308 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(305): Show |
intron_variant | MODIFIER | c.1075+568C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211304708 | |||||||
chr1:211304857 | A | G | 4 | a0001c0001t0008g0266 a0001c0001t0008g0267 a0001c0001t0008g0268 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+717A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211304857 | |||||||
chr1:211304981 | T | C | 4 | a0001c0001t0002g0091 a0001c0001t0002g0093 a0001c0001t0002g0109 others(1): Show |
4 | HG01109.hp1 HG01891.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+841T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211304981 | |||||||
chr1:211305116 | G | A | 2 | a0001c0001t0002g0099 a0001c0001t0002g0227 |
2 | HG04184.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1075+976G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211305116 | |||||||
chr1:211305232 | A | G | 1 | a0001c0001t0002g0174 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1075+1092A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211305232 | |||||||
chr1:211305233 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1075+1093T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211305233 | |||||||
chr1:211305788 | G | A | 1 | a0001c0001t0004g0257 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1075+1648G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211305788 | |||||||
chr1:211305809 | A | C | 1 | a0001c0001t0001g0279 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1075+1669A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211305809 | |||||||
chr1:211305914 | G | C | 1 | a0001c0001t0001g0254 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1075+1774G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211305914 | |||||||
chr1:211305989 | G | A | 17 | a0001c0001t0002g0179 a0001c0001t0003g0003 a0001c0001t0003g0229 others(14): Show |
21 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.1075+1849G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211305989 | |||||||
chr1:211306209 | C | G | 1 | a0001c0001t0002g0098 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1075+2069C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211306209 | |||||||
chr1:211306211 | G | C | 63 | a0001c0001t0001g0261 a0001c0001t0001g0263 a0001c0001t0001g0264 others(60): Show |
65 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.1075+2071G>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211306211 | |||||||
chr1:211306233 | T | A | 113 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0243 others(110): Show |
124 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.1075+2093T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211306233 | |||||||
chr1:211306484 | A | G | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.1075+2344A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211306484 | |||||||
chr1:211306842 | G | T | 1 | a0001c0001t0002g0100 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1075+2702G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211306842 | |||||||
chr1:211307074 | T | C | 3 | a0001c0001t0001g0264 a0001c0001t0001g0275 a0001c0001t0001g0289 |
3 | NA18956.hp1 NA18969.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1075+2934T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211307074 | |||||||
chr1:211307142 | T | G | 1 | a0001c0001t0002g0192 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1075+3002T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211307142 | |||||||
chr1:211307241 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1075+3101C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211307241 | |||||||
chr1:211307296 | C | T | 2 | a0001c0004t0001g0290 a0001c0004t0001g0291 |
2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1075+3156C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211307296 | |||||||
chr1:211307486 | AAAAAGAA others(3): Show |
A | 1 | a0001c0001t0001g0024 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1075+3361_1075+337 others(14): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211307486 | ||||||
chr1:211307490 | A | AAGAATTT others(6): Show |
10 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0255 others(7): Show |
12 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1075+3350_1075+335 others(17): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211307490 | |||||||
chr1:211307490 | A | AGAATTTA others(5): Show |
267 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(264): Show |
289 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.1075+3360_1075+336 others(16): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211307490 | ||||||
chr1:211307529 | A | T | 1 | a0001c0001t0002g0156 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1075+3389A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211307529 | |||||||
chr1:211307562 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1075+3422T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211307562 | |||||||
chr1:211307783 | A | T | 1 | a0001c0002t0001g0195 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1075+3643A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211307783 | |||||||
chr1:211307791 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1075+3651C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211307791 | |||||||
chr1:211308001 | C | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0058 others(1): Show |
4 | NA18990.hp1 NA19002.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.1075+3861C>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308001 | |||||||
chr1:211308015 | AAGAT | A | 26 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(23): Show |
27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.1075+3879_1075+388 others(8): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308015 | ||||||
chr1:211308182 | A | AGACACCA others(27): Show |
1 | a0001c0001t0003g0238 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1075+4044_1075+407 others(38): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308182 | ||||||
chr1:211308187 | C | T | 6 | a0001c0001t0002g0106 a0001c0001t0002g0111 a0001c0001t0002g0112 others(3): Show |
6 | HG00558.hp2 HG04228.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1075+4047C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308187 | |||||||
chr1:211308332 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1075+4192T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308332 | |||||||
chr1:211308498 | T | C | 11 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0255 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1076-4222T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308498 | |||||||
chr1:211308636 | T | C | 17 | a0001c0001t0002g0179 a0001c0001t0003g0003 a0001c0001t0003g0229 others(14): Show |
21 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.1076-4084T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308636 | |||||||
chr1:211308660 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1076-4060T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308660 | |||||||
chr1:211308662 | TTTTTTTT others(4): Show |
T | 29 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(26): Show |
30 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(27): Show |
intron_variant | MODIFIER | c.1076-4036_1076-402 others(15): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308662 | ||||||
chr1:211308663 | TTTTTTTT others(3): Show |
T | 4 | a0001c0001t0004g0256 a0001c0001t0004g0270 a0001c0001t0004g0271 others(1): Show |
4 | HG02257.hp2 HG02615.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1076-4047_1076-403 others(14): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308663 | ||||||
chr1:211308664 | TTTTTTTT others(2): Show |
T | 7 | a0001c0001t0001g0024 a0001c0001t0004g0017 a0001c0001t0004g0018 others(4): Show |
9 | HG01884.hp2 HG02451.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1076-4047_1076-403 others(13): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308664 | ||||||
chr1:211308665 | TTTTTTTT others(12): Show |
T | 1 | a0001c0001t0001g0245 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1076-4047_1076-402 others(23): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308665 | ||||||
chr1:211308670 | TTTGTTTT others(7): Show |
T | 1 | a0001c0001t0002g0001 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1076-4047_1076-403 others(18): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308670 | ||||||
chr1:211308671 | TTGTTTTT others(6): Show |
T | 57 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(54): Show |
63 | HG00099.hp1 HG00408.hp2 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.1076-4047_1076-403 others(17): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308671 | ||||||
chr1:211308672 | TGTTTTTT others(5): Show |
T | 42 | a0001c0001t0002g0001 a0001c0001t0002g0011 a0001c0001t0002g0012 others(39): Show |
43 | HG00558.hp2 HG00597.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1076-4047_1076-403 others(16): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308672 | |||||||
chr1:211308673 | G | GT | 9 | a0001c0001t0001g0254 a0001c0001t0003g0003 a0001c0001t0003g0229 others(6): Show |
11 | HG00099.hp2 HG00738.hp1 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.1076-4037dupT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308673 | ||||||
chr1:211308673 | G | GTT | 9 | a0001c0001t0002g0179 a0001c0001t0003g0003 a0001c0001t0003g0234 others(6): Show |
9 | HG00597.hp1 HG02165.hp2 HG03492.hp1 others(6): Show |
intron_variant | MODIFIER | c.1076-4038_1076-403 others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308673 | ||||||
chr1:211308673 | G | T | 9 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0244 others(6): Show |
9 | HG01243.hp1 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1076-4047G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308673 | |||||||
chr1:211308674 | TTTTTTTT others(3): Show |
T | 2 | a0001c0002t0001g0140 a0001c0002t0001g0219 |
2 | HG01928.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1076-4036_1076-402 others(14): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308674 | ||||||
chr1:211308680 | T | G | 1 | a0001c0001t0008g0266 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1076-4040T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308680 | |||||||
chr1:211308681 | T | G | 3 | a0001c0001t0008g0267 a0001c0001t0008g0268 a0001c0001t0008g0288 |
3 | HG02922.hp2 HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1076-4039T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308681 | |||||||
chr1:211308683 | T | TTG | 44 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0027 others(41): Show |
46 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.1076-4037_1076-403 others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308683 | |||||||
chr1:211308684 | G | T | 151 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(148): Show |
163 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(160): Show |
intron_variant | MODIFIER | c.1076-4036G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308684 | |||||||
chr1:211308687 | T | TG | 54 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(51): Show |
58 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.1076-4033_1076-403 others(5): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308687 | |||||||
chr1:211308692 | T | G | 2 | a0001c0001t0001g0243 a0001c0001t0001g0249 |
2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1076-4028T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308692 | |||||||
chr1:211308694 | T | G | 2 | a0001c0001t0001g0243 a0001c0001t0001g0249 |
2 | HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1076-4026T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308694 | |||||||
chr1:211308694 | T | TG | 5 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0251 others(2): Show |
5 | HG02280.hp1 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1076-4026_1076-402 others(5): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308694 | |||||||
chr1:211308695 | T | G | 1 | a0001c0002t0001g0140 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1076-4025T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308695 | |||||||
chr1:211308696 | T | G | 5 | a0001c0001t0001g0243 a0001c0001t0001g0246 a0001c0001t0001g0248 others(2): Show |
5 | HG02280.hp1 HG02970.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1076-4024T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308696 | |||||||
chr1:211308698 | T | G | 8 | a0001c0001t0001g0030 a0001c0001t0001g0243 a0001c0001t0001g0244 others(5): Show |
8 | HG01243.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1076-4022T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308698 | |||||||
chr1:211308698 | T | TTTTTTTT others(7): Show |
1 | a0001c0001t0001g0250 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1076-4021_1076-402 others(18): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308698 | ||||||
chr1:211308716 | AT | A | 277 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(274): Show |
301 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(298): Show |
intron_variant | MODIFIER | c.1076-3991delT | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211308716 | ||||||
chr1:211308717 | T | C | 2 | a0001c0001t0002g0167 a0001c0001t0002g0173 |
2 | NA18982.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1076-4003T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308717 | |||||||
chr1:211308718 | T | C | 96 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(93): Show |
107 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.1076-4002T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308718 | |||||||
chr1:211308768 | G | A | 11 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0255 others(8): Show |
13 | HG01109.hp2 HG01884.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1076-3952G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308768 | |||||||
chr1:211308769 | TG | T | 98 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(95): Show |
109 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.1076-3950delG | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308769 | |||||||
chr1:211308952 | T | A | 17 | a0001c0001t0002g0179 a0001c0001t0003g0003 a0001c0001t0003g0229 others(14): Show |
21 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.1076-3768T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308952 | |||||||
chr1:211308955 | G | A | 1 | a0001c0001t0002g0178 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1076-3765G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308955 | |||||||
chr1:211308971 | T | C | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.1076-3749T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211308971 | |||||||
chr1:211309086 | T | TA | 32 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0059 others(29): Show |
37 | HG01070.hp1 HG01070.hp2 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1076-3614dupA | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211309086 | ||||||
chr1:211309086 | T | TAA | 134 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): Show |
145 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(142): Show |
intron_variant | MODIFIER | c.1076-3615_1076-361 others(6): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211309086 | ||||||
chr1:211309086 | T | TAAA | 105 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(102): Show |
116 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.1076-3616_1076-361 others(7): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211309086 | ||||||
chr1:211309227 | T | C | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1076-3493T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309227 | |||||||
chr1:211309277 | A | G | 26 | a0001c0001t0001g0019 a0001c0001t0001g0032 a0001c0001t0001g0252 others(23): Show |
27 | HG01070.hp2 HG01192.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.1076-3443A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309277 | |||||||
chr1:211309404 | ATGACTTA others(6): Show |
A | 1 | a0001c0001t0003g0238 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1076-3314_1076-330 others(17): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 211309404 | ||||||
chr1:211309444 | C | T | 1 | a0001c0001t0003g0238 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1076-3276C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309444 | |||||||
chr1:211309457 | A | C | 1 | a0001c0001t0003g0238 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1076-3263A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309457 | |||||||
chr1:211309458 | T | A | 1 | a0001c0001t0003g0238 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1076-3262T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309458 | |||||||
chr1:211309459 | A | G | 1 | a0001c0001t0003g0238 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1076-3261A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309459 | |||||||
chr1:211309461 | G | A | 1 | a0001c0001t0003g0238 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1076-3259G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309461 | |||||||
chr1:211309468 | T | G | 1 | a0001c0001t0003g0238 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1076-3252T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309468 | |||||||
chr1:211309470 | TGCCAGCA others(4): Show |
T | 1 | a0001c0001t0003g0238 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1076-3249_1076-323 others(15): Show |
RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309470 | |||||||
chr1:211309482 | A | T | 1 | a0001c0001t0003g0238 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1076-3238A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309482 | |||||||
chr1:211309563 | C | G | 98 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(95): Show |
109 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.1076-3157C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309563 | |||||||
chr1:211309744 | G | T | 1 | a0001c0001t0001g0024 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1076-2976G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309744 | |||||||
chr1:211309845 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0244 a0001c0001t0001g0247 |
3 | HG01243.hp1 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1076-2875G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309845 | |||||||
chr1:211309915 | A | T | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.1076-2805A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309915 | |||||||
chr1:211309966 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1076-2754C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309966 | |||||||
chr1:211309978 | T | C | 279 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.1076-2742T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211309978 | |||||||
chr1:211310026 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1076-2694C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211310026 | |||||||
chr1:211310310 | G | T | 16 | a0001c0001t0003g0003 a0001c0001t0003g0229 a0001c0001t0003g0230 others(13): Show |
20 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.1076-2410G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211310310 | |||||||
chr1:211310516 | G | T | 4 | a0001c0001t0008g0266 a0001c0001t0008g0267 a0001c0001t0008g0268 others(1): Show |
4 | HG02809.hp1 HG02922.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1076-2204G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211310516 | |||||||
chr1:211310608 | C | G | 1 | a0001c0001t0003g0235 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1076-2112C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211310608 | |||||||
chr1:211310629 | C | G | 1 | a0001c0001t0001g0250 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1076-2091C>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211310629 | |||||||
chr1:211310672 | A | G | 2 | a0001c0001t0002g0111 a0001c0001t0002g0112 |
2 | NA18990.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1076-2048A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211310672 | |||||||
chr1:211310758 | A | T | 53 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0027 others(50): Show |
55 | HG00733.hp1 HG00738.hp2 HG01070.hp1 others(52): Show |
intron_variant | MODIFIER | c.1076-1962A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211310758 | |||||||
chr1:211310918 | T | A | 6 | a0001c0001t0004g0017 a0001c0001t0004g0255 a0001c0001t0004g0256 others(3): Show |
7 | HG01109.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1076-1802T>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211310918 | |||||||
chr1:211311718 | A | T | 109 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(106): Show |
115 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.1076-1002A>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211311718 | |||||||
chr1:211311770 | A | G | 1 | a0001c0001t0003g0233 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1076-950A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211311770 | |||||||
chr1:211311851 | A | G | 1 | a0001c0001t0005g0081 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1076-869A>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211311851 | |||||||
chr1:211311885 | A | C | 2 | a0001c0001t0001g0024 a0001c0001t0018g0025 |
2 | HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1076-835A>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211311885 | |||||||
chr1:211312159 | T | G | 1 | a0001c0001t0002g0107 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1076-561T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211312159 | |||||||
chr1:211312183 | G | T | 1 | a0001c0001t0001g0254 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1076-537G>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211312183 | |||||||
chr1:211312195 | T | G | 1 | a0001c0001t0002g0178 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1076-525T>G | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211312195 | |||||||
chr1:211312529 | G | A | 1 | a0001c0001t0004g0257 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1076-191G>A | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 10/11 | chr1 | 211312529 | |||||||
chr1:211313236 | C | T | 1 | a0001c0001t0004g0257 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1318-188C>T | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 11/11 | chr1 | 211313236 | |||||||
chr1:211313365 | T | C | 1 | a0001c0001t0003g0232 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1318-59T>C | RCOR3 | ENSG00000117625.14 | transcript | ENST00000419091.7 | protein_coding | 11/11 | chr1 | 211313365 |