Item | Value |
---|---|
geneid | 26155 |
ensemblid | ENSG00000188976.11 |
hgncid | 24517 |
symbol | NOC2L |
name | NOC2 like nucleolar associated transcriptional repressor |
refseq_nuc | NM_015658.4 |
refseq_prot | NP_056473.3 |
ensembl_nuc | ENST00000327044.7 |
ensembl_prot | ENSP00000317992.6 |
mane_status | MANE Select |
chr | chr1 |
start | 944203 |
end | 959256 |
strand | - |
ver | v1.2 |
region | chr1:944203-959256 |
region5000 | chr1:939203-964256 |
regionname0 | NOC2L_chr1_944203_959256 |
regionname5000 | NOC2L_chr1_939203_964256 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 749 | 375 | 86 | 73 | 163 | 14 | 38 | 120 | NOC2L_chr1_939203_964256 | NOC2L | MAAAG others(744): Show |
chr1 | 939203 | 964256 |
a0002 | 0/0 | 749 | 20 | 3 | 6 | 8 | 0 | 3 | 6 | NOC2L_chr1_939203_964256 | NOC2L | MAAAG others(744): Show |
chr1 | 939203 | 964256 |
a0003 | 0/0 | 749 | 9 | 0 | 3 | 0 | 2 | 4 | 0 | NOC2L_chr1_939203_964256 | NOC2L | MAAAG others(744): Show |
chr1 | 939203 | 964256 |
a0004 | 1/0 | 749 | 8 | 7 | 0 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | MAAAG others(744): Show |
chr1 | 939203 | 964256 |
a0005 | 0/0 | 749 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | NOC2L_chr1_939203_964256 | NOC2L | MAAAG others(744): Show |
chr1 | 939203 | 964256 |
a0006 | 0/0 | 749 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | MAAAG others(744): Show |
chr1 | 939203 | 964256 |
a0007 | 0/0 | 749 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | MAAAG others(744): Show |
chr1 | 939203 | 964256 |
a0008 | 0/0 | 749 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | MAAAG others(744): Show |
chr1 | 939203 | 964256 |
a0009 | 0/0 | 749 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | MAAAG others(744): Show |
chr1 | 939203 | 964256 |
a0010 | 0/0 | 749 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | MAAAG others(744): Show |
chr1 | 939203 | 964256 |
a0011 | 0/0 | 749 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | MAAAG others(744): Show |
chr1 | 939203 | 964256 |
a0012 | 0/0 | 749 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | MAAAG others(744): Show |
chr1 | 939203 | 964256 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2247 | 208 | 73 | 47 | 66 | 7 | 15 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0001c0002 | 0/1 | 2247 | 152 | 5 | 24 | 94 | 7 | 21 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0001c0006 | 0/0 | 2247 | 3 | 3 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0001c0008 | 0/0 | 2247 | 2 | 0 | 2 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0001c0011 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0001c0013 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0001c0014 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0001c0015 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0001c0018 | 0/0 | 2247 | 1 | 0 | 0 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0001c0019 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0001c0022 | 0/0 | 2247 | 1 | 0 | 0 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0001c0023 | 0/0 | 2247 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0001c0024 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0001c0025 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0002c0003 | 0/0 | 2247 | 20 | 3 | 6 | 8 | 0 | 3 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0003c0004 | 0/0 | 2247 | 9 | 0 | 3 | 0 | 2 | 4 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0004c0005 | 1/0 | 2247 | 8 | 7 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0005c0007 | 0/0 | 2247 | 3 | 0 | 0 | 0 | 0 | 3 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0006c0010 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0007c0016 | 0/0 | 2247 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0008c0020 | 0/0 | 2247 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0009c0009 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0010c0012 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0011c0021 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 | ||
a0012c0017 | 0/0 | 2247 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | ATGGC others(2242): Show |
chr1 | 939203 | 964256 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2757 | 144 | 57 | 37 | 29 | 7 | 14 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0001t0002 | 0/0 | 2751 | 52 | 5 | 9 | 37 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2746): Show |
chr1 | 939203 | 964256 |
a0001c0001t0004 | 0/0 | 2757 | 8 | 7 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0001t0006 | 0/0 | 2757 | 2 | 2 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0001t0008 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0001t0009 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0002t0001 | 0/1 | 2757 | 148 | 5 | 24 | 91 | 7 | 20 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0002t0005 | 0/0 | 2757 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0002t0007 | 0/0 | 2757 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0002t0010 | 0/0 | 2757 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0002t0011 | 0/0 | 2757 | 1 | 0 | 0 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0006t0001 | 0/0 | 2757 | 3 | 3 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0008t0004 | 0/0 | 2757 | 2 | 0 | 2 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0011t0004 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0013t0001 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0014t0001 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0015t0001 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0018t0001 | 0/0 | 2757 | 1 | 0 | 0 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0019t0001 | 0/0 | 2757 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0022t0001 | 0/0 | 2757 | 1 | 0 | 0 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0023t0004 | 0/0 | 2757 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0024t0001 | 0/0 | 2757 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0001c0025t0001 | 0/0 | 2757 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0002c0003t0003 | 0/0 | 2757 | 20 | 3 | 6 | 8 | 0 | 3 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0003c0004t0001 | 0/0 | 2757 | 7 | 0 | 1 | 0 | 2 | 4 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0003c0004t0005 | 0/0 | 2757 | 2 | 0 | 2 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0004c0005t0003 | 1/0 | 2757 | 8 | 7 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0005c0007t0001 | 0/0 | 2757 | 3 | 0 | 0 | 0 | 0 | 3 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0006c0010t0001 | 0/0 | 2757 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0007c0016t0001 | 0/0 | 2757 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0008c0020t0001 | 0/0 | 2757 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0009c0009t0001 | 0/0 | 2757 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0010c0012t0002 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2746): Show |
chr1 | 939203 | 964256 |
a0011c0021t0001 | 0/0 | 2757 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
a0012c0017t0001 | 0/0 | 2757 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | GCTTC others(2752): Show |
chr1 | 939203 | 964256 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 27 | 0 | 11 | 8 | 5 | 3 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0004 | 0/0 | 12 | 9 | 3 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0005 | 0/0 | 11 | 11 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0007 | 0/0 | 11 | 0 | 8 | 0 | 0 | 3 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0041 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0002g0002 | 0/0 | 30 | 2 | 8 | 19 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0002g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0004g0018 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0004g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0004g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0006g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0008g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0001t0009g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0001 | 0/0 | 70 | 0 | 11 | 46 | 3 | 10 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0006 | 0/0 | 11 | 0 | 1 | 8 | 0 | 2 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0009 | 0/0 | 6 | 1 | 2 | 0 | 2 | 1 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0011 | 0/0 | 5 | 2 | 1 | 0 | 1 | 1 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0015 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0028 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0007g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0010g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0002t0011g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0006t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0008t0004g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0011t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0013t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0014t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0015t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0018t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0019t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0022t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0023t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0024t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0001c0025t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0002c0003t0003g0008 | 0/0 | 6 | 1 | 2 | 3 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0002c0003t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0002c0003t0003g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0002c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0002c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0002c0003t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0002c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0002c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0002c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0002c0003t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0002c0003t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0002c0003t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0002c0003t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0003c0004t0001g0014 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0003c0004t0001g0029 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0003c0004t0005g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0004c0005t0003g0035 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0004c0005t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0004c0005t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0004c0005t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0004c0005t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0004c0005t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0005c0007t0001g0027 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0006c0010t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0007c0016t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0008c0020t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0009c0009t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0010c0012t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0011c0021t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
a0012c0017t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0011 | EUR | GBR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0009 | EUR | GBR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | FIN | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0009 | EUR | FIN | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | FIN | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00438 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00438 | hp2 | a0006 | c0010 | t0001 | g0122 | EAS | CHS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00544 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00544 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00558 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00597 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | CHS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00621 | hp1 | a0001 | c0002 | t0010 | g0143 | EAS | CHS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00639 | hp1 | a0007 | c0016 | t0001 | g0148 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00642 | hp1 | a0002 | c0003 | t0003 | g0008 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00733 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00735 | hp2 | a0003 | c0004 | t0001 | g0014 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0018 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01070 | hp1 | a0002 | c0003 | t0003 | g0115 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0139 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01168 | hp1 | a0003 | c0004 | t0005 | g0048 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01169 | hp2 | a0003 | c0004 | t0005 | g0048 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0047 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0123 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0154 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01243 | hp1 | a0001 | c0008 | t0004 | g0032 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01255 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01256 | hp1 | a0002 | c0003 | t0003 | g0008 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0009 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01515 | hp1 | a0003 | c0004 | t0001 | g0014 | EUR | IBS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0049 | EUR | IBS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0028 | EUR | IBS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01517 | hp1 | a0003 | c0004 | t0001 | g0014 | EUR | IBS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | ACB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01934 | hp1 | a0008 | c0020 | t0001 | g0159 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0011 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0175 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01975 | hp2 | a0002 | c0003 | t0003 | g0081 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0047 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02056 | hp1 | a0001 | c0025 | t0001 | g0176 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02056 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02074 | hp1 | a0002 | c0003 | t0003 | g0034 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0165 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02129 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0161 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02145 | hp2 | a0001 | c0006 | t0001 | g0019 | AFR | ACB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02148 | hp1 | a0002 | c0003 | t0003 | g0036 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02155 | hp1 | a0002 | c0003 | t0003 | g0008 | EAS | CDX | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CDX | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02165 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | ACB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02258 | hp1 | a0001 | c0006 | t0001 | g0019 | AFR | ACB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02273 | hp1 | a0002 | c0003 | t0003 | g0075 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02523 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02572 | hp1 | a0004 | c0005 | t0003 | g0037 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0147 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02615 | hp1 | a0004 | c0005 | t0003 | g0082 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02615 | hp2 | a0004 | c0005 | t0003 | g0037 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02622 | hp1 | a0002 | c0003 | t0003 | g0079 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02622 | hp2 | a0001 | c0011 | t0004 | g0111 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02630 | hp2 | a0002 | c0003 | t0003 | g0080 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02683 | hp1 | a0005 | c0007 | t0001 | g0027 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02683 | hp2 | a0003 | c0004 | t0001 | g0029 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02735 | hp1 | a0001 | c0018 | t0001 | g0152 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02738 | hp1 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02738 | hp2 | a0001 | c0022 | t0001 | g0130 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02895 | hp2 | a0001 | c0006 | t0001 | g0019 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02922 | hp2 | a0001 | c0013 | t0001 | g0092 | AFR | ESN | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02965 | hp1 | a0001 | c0014 | t0001 | g0103 | AFR | ESN | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02965 | hp2 | a0002 | c0003 | t0003 | g0008 | AFR | ESN | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | ESN | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03017 | hp2 | a0005 | c0007 | t0001 | g0027 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03098 | hp2 | a0004 | c0005 | t0003 | g0083 | AFR | MSL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03130 | hp2 | a0001 | c0015 | t0001 | g0084 | AFR | ESN | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03209 | hp1 | a0004 | c0005 | t0003 | g0072 | AFR | MSL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0033 | AFR | MSL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03225 | hp1 | a0004 | c0005 | t0003 | g0074 | AFR | MSL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03239 | hp2 | a0001 | c0002 | t0001 | g0046 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | MSL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03490 | hp1 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03491 | hp1 | a0001 | c0002 | t0011 | g0150 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | MSL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03654 | hp2 | a0002 | c0003 | t0003 | g0070 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03669 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0125 | SAS | STU | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03704 | hp1 | a0003 | c0004 | t0001 | g0029 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03710 | hp1 | a0003 | c0004 | t0001 | g0014 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03710 | hp2 | a0002 | c0003 | t0003 | g0076 | SAS | PJL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03834 | hp2 | a0003 | c0004 | t0001 | g0029 | SAS | BEB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG04115 | hp1 | a0005 | c0007 | t0001 | g0027 | SAS | STU | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0006 | SAS | STU | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0144 | SAS | BEB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG04184 | hp2 | a0002 | c0003 | t0003 | g0077 | SAS | BEB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0046 | SAS | STU | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | STU | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | STU | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG04228 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | STU | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CHB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | CHB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0140 | EAS | CHB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18950 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18951 | hp2 | a0009 | c0009 | t0001 | g0121 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18959 | hp1 | a0002 | c0003 | t0003 | g0008 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18959 | hp2 | a0010 | c0012 | t0002 | g0056 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18962 | hp1 | a0002 | c0003 | t0003 | g0036 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18966 | hp1 | a0001 | c0002 | t0005 | g0151 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18971 | hp1 | a0001 | c0002 | t0007 | g0098 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18974 | hp2 | a0001 | c0024 | t0001 | g0173 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18977 | hp2 | a0002 | c0003 | t0003 | g0078 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18980 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18987 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18990 | hp2 | a0002 | c0003 | t0003 | g0008 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19000 | hp1 | a0002 | c0003 | t0003 | g0071 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19003 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19004 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19009 | hp1 | a0001 | c0019 | t0001 | g0128 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | LWK | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19043 | hp2 | a0001 | c0001 | t0009 | g0093 | AFR | LWK | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19054 | hp2 | a0011 | c0021 | t0001 | g0106 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19063 | hp1 | a0002 | c0003 | t0003 | g0034 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19070 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19077 | hp2 | a0012 | c0017 | t0001 | g0164 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19089 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19091 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19240 | hp1 | a0001 | c0023 | t0004 | g0068 | AFR | YRI | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0033 | AFR | YRI | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ASW | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0011 | AFR | ASW | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | TSI | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0049 | EUR | TSI | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | GIH | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | GIH | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG01123 | hp2 | a0001 | c0008 | t0004 | g0032 | AMR | CLM | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ACB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | ACB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03471 | hp1 | a0004 | c0005 | t0003 | g0035 | AFR | MSL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | MSL | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG06807 | hp1 | a0001 | c0001 | t0008 | g0169 | AFR | USA | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | USA | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | USA | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | LWK | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0117 | REF | REF | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
homoSapiens | grch38p0 | a0004 | c0005 | t0003 | g0035 | REF | REF | NOC2L_chr1_939203_964256 | NOC2L | chr1 | 939203 | 964256 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:945086 | T | C | 1 | a0005 | 3 | HG02683.hp1 HG03017.hp2 HG04115.hp1 |
missense_variant | MODERATE | c.2114A>G | p.Glu705Gly | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 18/19 | 2130/2757 | 2114/2250 | 705/749 | chr1 | 945086 | |||
chr1:945122 | C | T | 1 | a0007 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.2078G>A | p.Arg693Gln | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 18/19 | 2094/2757 | 2078/2250 | 693/749 | chr1 | 945122 | |||
chr1:945526 | G | A | 2 | a0009 a0012 |
2 | NA18951.hp2 NA19077.hp2 |
missense_variant | MODERATE | c.2045C>T | p.Ser682Leu | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 17/19 | 2061/2757 | 2045/2250 | 682/749 | chr1 | 945526 | |||
chr1:946538 | G | A | 1 | a0003 | 9 | HG00735.hp2 HG01168.hp1 HG01169.hp2 others(6): Show |
missense_variant | MODERATE | c.1667C>T | p.Ser556Leu | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 15/19 | 1683/2757 | 1667/2250 | 556/749 | chr1 | 946538 | |||
chr1:952049 | G | A | 1 | a0008 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.1282C>T | p.Leu428Phe | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/19 | 1298/2757 | 1282/2250 | 428/749 | chr1 | 952049 | |||
chr1:952587 | G | A | 1 | a0011 | 1 | NA19054.hp2 | missense_variant | MODERATE | c.1016C>T | p.Thr339Met | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 10/19 | 1032/2757 | 1016/2250 | 339/749 | chr1 | 952587 | |||
chr1:953279 | T | C | 10 | a0001 a0003 a0005 others(7): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
missense_variant | MODERATE | c.898A>G | p.Ile300Val | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 9/19 | 914/2757 | 898/2250 | 300/749 | chr1 | 953279 | |||
chr1:953858 | G | A | 1 | a0002 | 20 | HG00642.hp1 HG01070.hp1 HG01256.hp1 others(17): Show |
missense_variant | MODERATE | c.812C>T | p.Ala271Val | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 8/19 | 828/2757 | 812/2250 | 271/749 | chr1 | 953858 | |||
chr1:954041 | C | T | 1 | a0010 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.740G>A | p.Arg247His | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 7/19 | 756/2757 | 740/2250 | 247/749 | chr1 | 954041 | |||
chr1:957001 | C | T | 1 | a0006 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.379G>A | p.Ala127Thr | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 4/19 | 395/2757 | 379/2250 | 127/749 | chr1 | 957001 | |||
chr1:957268 | C | T | 1 | a0009 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.185G>A | p.Arg62His | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 3/19 | 201/2757 | 185/2250 | 62/749 | chr1 | 957268 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:945103 | A | G | 1 | a0001c0015 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.2097T>C | p.Asp699Asp | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 18/19 | 2113/2757 | 2097/2250 | 699/749 | chr1 | 945103 | |||
chr1:945573 | G | A | 1 | a0001c0018 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.1998C>T | p.Asp666Asp | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 17/19 | 2014/2757 | 1998/2250 | 666/749 | chr1 | 945573 | |||
chr1:946247 | G | A | 12 | a0001c0002 a0001c0018 a0001c0019 others(9): Show |
172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
synonymous_variant | LOW | c.1843C>T | p.Leu615Leu | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 16/19 | 1859/2757 | 1843/2250 | 615/749 | chr1 | 946247 | |||
chr1:948158 | C | T | 1 | a0001c0014 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.1632G>A | p.Pro544Pro | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/19 | 1648/2757 | 1632/2250 | 544/749 | chr1 | 948158 | |||
chr1:948200 | G | C | 1 | a0001c0019 | 1 | NA19009.hp1 | synonymous_variant | LOW | c.1590C>G | p.Thr530Thr | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/19 | 1606/2757 | 1590/2250 | 530/749 | chr1 | 948200 | |||
chr1:952091 | G | A | 1 | a0001c0008 | 2 | HG01123.hp2 HG01243.hp1 |
synonymous_variant | LOW | c.1240C>T | p.Leu414Leu | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/19 | 1256/2757 | 1240/2250 | 414/749 | chr1 | 952091 | |||
chr1:952421 | A | G | 23 | a0001c0001 a0001c0002 a0001c0006 others(20): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
synonymous_variant | LOW | c.1182T>C | p.Thr394Thr | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 10/19 | 1198/2757 | 1182/2250 | 394/749 | chr1 | 952421 | |||
chr1:953259 | T | C | 23 | a0001c0001 a0001c0002 a0001c0006 others(20): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
synonymous_variant | LOW | c.918A>G | p.Glu306Glu | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 9/19 | 934/2757 | 918/2250 | 306/749 | chr1 | 953259 | |||
chr1:953836 | G | A | 1 | a0001c0022 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.834C>T | p.Ser278Ser | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 8/19 | 850/2757 | 834/2250 | 278/749 | chr1 | 953836 | |||
chr1:953857 | C | T | 1 | a0001c0013 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.813G>A | p.Ala271Ala | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 8/19 | 829/2757 | 813/2250 | 271/749 | chr1 | 953857 | |||
chr1:954070 | C | A | 1 | a0001c0023 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.711G>T | p.Pro237Pro | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 7/19 | 727/2757 | 711/2250 | 237/749 | chr1 | 954070 | |||
chr1:956174 | C | T | 1 | a0001c0011 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.528G>A | p.Ala176Ala | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 5/19 | 544/2757 | 528/2250 | 176/749 | chr1 | 956174 | |||
chr1:957171 | C | T | 1 | a0001c0006 | 3 | HG02145.hp2 HG02258.hp1 HG02895.hp2 |
synonymous_variant | LOW | c.282G>A | p.Leu94Leu | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 3/19 | 298/2757 | 282/2250 | 94/749 | chr1 | 957171 | |||
chr1:957264 | T | C | 1 | a0001c0024 | 1 | NA18974.hp2 | synonymous_variant | LOW | c.189A>G | p.Lys63Lys | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 3/19 | 205/2757 | 189/2250 | 63/749 | chr1 | 957264 | |||
chr1:959057 | G | A | 1 | a0001c0025 | 1 | HG02056.hp1 | synonymous_variant | LOW | c.51C>T | p.Asp17Asp | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/19 | 67/2757 | 51/2250 | 17/749 | chr1 | 959057 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:944211 | A | G | 1 | a0001c0002t0011 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*483T>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 19/19 | 483 | chr1 | 944211 | ||||||
chr1:944215 | C | T | 1 | a0001c0002t0010 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*479G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 19/19 | 479 | chr1 | 944215 | ||||||
chr1:944238 | C | T | 1 | a0001c0001t0006 | 2 | HG03209.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*456G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 19/19 | 456 | chr1 | 944238 | ||||||
chr1:944293 | A | G | 1 | a0001c0001t0009 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*401T>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 19/19 | 401 | chr1 | 944293 | ||||||
chr1:944296 | G | A | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(26): Show |
381 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(378): Show |
3_prime_UTR_variant | MODIFIER | c.*398C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 19/19 | 398 | chr1 | 944296 | ||||||
chr1:944307 | T | C | 33 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(30): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
3_prime_UTR_variant | MODIFIER | c.*387A>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 19/19 | 387 | chr1 | 944307 | ||||||
chr1:944394 | G | T | 1 | a0001c0001t0008 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*300C>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 19/19 | 300 | chr1 | 944394 | ||||||
chr1:944409 | CCTGGAA | C | 2 | a0001c0001t0002 a0010c0012t0002 |
53 | HG00423.hp1 HG00609.hp2 HG01123.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*279_*284delTTCCAG | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 19/19 | 279 | chr1 | 944409 | ||||||
chr1:944413 | G | T | 1 | a0006c0010t0001 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*281C>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 19/19 | 281 | chr1 | 944413 | ||||||
chr1:944505 | C | T | 1 | a0001c0002t0007 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*189G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 19/19 | 189 | chr1 | 944505 | ||||||
chr1:944531 | G | A | 2 | a0001c0002t0005 a0003c0004t0005 |
3 | HG01168.hp1 HG01169.hp2 NA18966.hp1 |
3_prime_UTR_variant | MODIFIER | c.*163C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 19/19 | 163 | chr1 | 944531 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:944858 | A | G | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.2144-58T>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 18/18 | chr1 | 944858 | |||||||
chr1:945010 | C | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(15): Show |
40 | HG00673.hp2 HG00741.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.2143+47G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 18/18 | chr1 | 945010 | |||||||
chr1:945024 | A | G | 1 | a0001c0002t0001g0149 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2143+33T>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 18/18 | chr1 | 945024 | |||||||
chr1:945259 | TC | T | 28 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0023 others(25): Show |
72 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.2054-114delG | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 17/18 | chr1 | 945259 | |||||||
chr1:945299 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2054-153A>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 17/18 | chr1 | 945299 | |||||||
chr1:945371 | A | G | 6 | a0001c0001t0001g0038 a0001c0001t0001g0073 a0001c0001t0001g0085 others(3): Show |
7 | HG01074.hp1 HG02976.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.2053+147T>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 17/18 | chr1 | 945371 | |||||||
chr1:945690 | G | A | 2 | a0001c0002t0001g0127 a0001c0002t0001g0147 |
2 | HG02602.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1918-37C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 16/18 | chr1 | 945690 | |||||||
chr1:945704 | G | A | 1 | a0001c0002t0001g0046 | 2 | HG03239.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.1918-51C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 16/18 | chr1 | 945704 | |||||||
chr1:945744 | GCCCCATG others(17): Show |
G | 1 | a0001c0001t0002g0067 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1918-115_1918-92de others(25): Show |
NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 16/18 | chr1 | 945744 | |||||||
chr1:945771 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0001g0104 |
2 | HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1918-118A>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 16/18 | chr1 | 945771 | |||||||
chr1:945917 | C | T | 1 | a0002c0003t0003g0077 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1917+256G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 16/18 | chr1 | 945917 | |||||||
chr1:945943 | G | A | 1 | a0001c0001t0002g0059 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1917+230C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 16/18 | chr1 | 945943 | |||||||
chr1:945997 | G | A | 18 | a0001c0001t0002g0002 a0001c0001t0002g0016 a0001c0001t0002g0017 others(15): Show |
51 | HG00423.hp1 HG00609.hp2 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.1917+176C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 16/18 | chr1 | 945997 | |||||||
chr1:946042 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1917+131C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 16/18 | chr1 | 946042 | |||||||
chr1:946126 | A | T | 1 | a0001c0001t0004g0031 | 2 | HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1917+47T>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 16/18 | chr1 | 946126 | |||||||
chr1:946132 | G | T | 1 | a0002c0003t0003g0070 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1917+41C>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 16/18 | chr1 | 946132 | |||||||
chr1:946307 | AG | A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0094 a0001c0001t0001g0096 others(1): Show |
4 | HG02559.hp1 HG02922.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1804-22delC | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 15/18 | chr1 | 946307 | |||||||
chr1:946354 | T | C | 6 | a0001c0001t0004g0018 a0001c0001t0004g0031 a0001c0001t0004g0042 others(3): Show |
11 | HG01069.hp1 HG01123.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1803+48A>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 15/18 | chr1 | 946354 | |||||||
chr1:946618 | A | G | 1 | a0001c0002t0001g0147 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1660-73T>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 946618 | |||||||
chr1:946624 | C | T | 1 | a0001c0001t0002g0016 | 3 | NA18995.hp1 NA19056.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1660-79G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 946624 | |||||||
chr1:946653 | G | A | 20 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0023 others(17): Show |
57 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1660-108C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 946653 | |||||||
chr1:946828 | C | T | 1 | a0001c0002t0001g0126 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1660-283G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 946828 | |||||||
chr1:946870 | C | A | 3 | a0001c0002t0001g0009 a0001c0002t0001g0123 a0001c0002t0001g0144 |
8 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.1660-325G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 946870 | |||||||
chr1:946888 | T | G | 1 | a0001c0001t0002g0060 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1660-343A>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 946888 | |||||||
chr1:947012 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0170 |
2 | HG01099.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1660-467C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947012 | |||||||
chr1:947187 | C | A | 1 | a0001c0001t0002g0061 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1660-642G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947187 | |||||||
chr1:947231 | C | T | 1 | a0001c0011t0004g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1660-686G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947231 | |||||||
chr1:947400 | C | CT | 3 | a0001c0001t0004g0018 a0001c0001t0004g0031 a0001c0008t0004g0032 |
7 | HG01069.hp1 HG01123.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1659+730dupA | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947400 | |||||||
chr1:947423 | A | G | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.1659+708T>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947423 | |||||||
chr1:947445 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1659+686G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947445 | |||||||
chr1:947451 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1659+680A>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947451 | |||||||
chr1:947516 | C | A | 1 | a0001c0001t0001g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1659+615G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947516 | |||||||
chr1:947588 | C | A | 1 | a0001c0001t0001g0057 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1659+543G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947588 | |||||||
chr1:947619 | A | G | 2 | a0001c0002t0001g0146 a0001c0002t0001g0156 |
2 | NA18965.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1659+512T>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947619 | |||||||
chr1:947628 | C | T | 6 | a0001c0001t0004g0018 a0001c0001t0004g0031 a0001c0001t0004g0042 others(3): Show |
11 | HG01069.hp1 HG01123.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1659+503G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947628 | |||||||
chr1:947636 | C | T | 1 | a0001c0002t0001g0125 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1659+495G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947636 | |||||||
chr1:947655 | A | G | 1 | a0001c0001t0001g0049 | 2 | HG01515.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1659+476T>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947655 | |||||||
chr1:947661 | C | G | 6 | a0001c0001t0004g0018 a0001c0001t0004g0031 a0001c0001t0004g0042 others(3): Show |
11 | HG01069.hp1 HG01123.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1659+470G>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947661 | |||||||
chr1:947680 | G | A | 1 | a0005c0007t0001g0027 | 3 | HG02683.hp1 HG03017.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1659+451C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947680 | |||||||
chr1:947683 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1659+448C>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947683 | |||||||
chr1:947692 | G | C | 1 | a0001c0001t0001g0057 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1659+439C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947692 | |||||||
chr1:947694 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1659+437G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947694 | |||||||
chr1:947696 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1659+435A>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947696 | |||||||
chr1:947711 | G | A | 2 | a0001c0002t0001g0011 a0001c0002t0001g0139 |
6 | HG00099.hp1 HG01106.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1659+420C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947711 | |||||||
chr1:947727 | G | C | 1 | a0002c0003t0003g0080 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1659+404C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947727 | |||||||
chr1:947811 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1659+320C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 947811 | |||||||
chr1:948039 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1659+92C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 948039 | |||||||
chr1:948083 | A | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0112 a0001c0001t0001g0113 |
4 | HG01109.hp1 HG02055.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1659+48T>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 14/18 | chr1 | 948083 | |||||||
chr1:948253 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1558-21G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 13/18 | chr1 | 948253 | |||||||
chr1:948319 | C | T | 6 | a0001c0001t0004g0018 a0001c0001t0004g0031 a0001c0001t0004g0042 others(3): Show |
11 | HG01069.hp1 HG01123.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1558-87G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 13/18 | chr1 | 948319 | |||||||
chr1:948711 | C | CACCCTGG others(34): Show |
145 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
375 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.1444-109_1444-108i others(43): Show |
NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 948711 | |||||||
chr1:948711 | C | CACCCTGG others(33): Show |
1 | a0001c0001t0002g0090 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1444-109_1444-108i others(42): Show |
NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 948711 | |||||||
chr1:948711 | C | G | 6 | a0001c0001t0004g0018 a0001c0001t0004g0031 a0001c0001t0004g0042 others(3): Show |
11 | HG01069.hp1 HG01123.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1444-108G>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 948711 | |||||||
chr1:948866 | G | A | 1 | a0002c0003t0003g0078 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1444-263C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 948866 | |||||||
chr1:948922 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1444-319G>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 948922 | |||||||
chr1:949014 | C | T | 1 | a0001c0001t0006g0033 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1444-411G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 949014 | |||||||
chr1:949022 | C | G | 4 | a0004c0005t0003g0037 a0004c0005t0003g0072 a0004c0005t0003g0082 others(1): Show |
5 | HG02572.hp1 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1444-419G>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 949022 | |||||||
chr1:949046 | A | AAACAGCA others(3): Show |
1 | a0001c0002t0001g0153 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1444-444_1444-443i others(12): Show |
NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 949046 | |||||||
chr1:949046 | A | AACAGCAA others(2): Show |
145 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
375 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(372): Show |
intron_variant | MODIFIER | c.1444-452_1444-444d others(11): Show |
NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 949046 | |||||||
chr1:949126 | G | C | 1 | a0001c0002t0001g0154 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1444-523C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 949126 | |||||||
chr1:949169 | CAGAG | C | 6 | a0001c0001t0004g0018 a0001c0001t0004g0031 a0001c0001t0004g0042 others(3): Show |
11 | HG01069.hp1 HG01123.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1444-570_1444-567d others(6): Show |
NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 949169 | |||||||
chr1:949171 | GAGAA | G | 60 | a0001c0001t0001g0045 a0001c0001t0001g0172 a0001c0002t0001g0001 others(57): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1444-572_1444-569d others(6): Show |
NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 949171 | |||||||
chr1:949255 | G | A | 3 | a0001c0001t0004g0018 a0001c0001t0004g0031 a0001c0008t0004g0032 |
7 | HG01069.hp1 HG01123.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1444-652C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 949255 | |||||||
chr1:949387 | G | A | 1 | a0001c0002t0001g0028 | 3 | HG01168.hp2 HG01516.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1444-784C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 949387 | |||||||
chr1:949435 | A | G | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.1444-832T>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 949435 | |||||||
chr1:949606 | T | C | 1 | a0001c0001t0001g0038 | 2 | HG02976.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1444-1003A>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 949606 | |||||||
chr1:949663 | T | C | 3 | a0001c0001t0004g0018 a0001c0001t0004g0031 a0001c0008t0004g0032 |
7 | HG01069.hp1 HG01123.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1444-1060A>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 949663 | |||||||
chr1:949775 | C | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0132 |
4 | NA18947.hp1 NA18987.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1444-1172G>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 949775 | |||||||
chr1:949793 | C | T | 1 | a0001c0001t0006g0033 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1444-1190G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 949793 | |||||||
chr1:949870 | C | T | 1 | a0001c0011t0004g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1443+1257G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 949870 | |||||||
chr1:949918 | G | A | 1 | a0001c0001t0002g0055 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1443+1209C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 949918 | |||||||
chr1:949955 | G | A | 4 | a0001c0002t0001g0015 a0001c0002t0001g0129 a0001c0002t0001g0145 others(1): Show |
7 | NA18953.hp1 NA18979.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.1443+1172C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 949955 | |||||||
chr1:950096 | G | A | 1 | a0001c0001t0002g0062 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1443+1031C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950096 | |||||||
chr1:950124 | G | A | 1 | a0001c0001t0002g0063 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1443+1003C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950124 | |||||||
chr1:950277 | G | A | 20 | a0001c0001t0001g0030 a0001c0001t0001g0057 a0001c0001t0002g0002 others(17): Show |
54 | HG00423.hp1 HG00609.hp2 HG01123.hp1 others(51): Show |
intron_variant | MODIFIER | c.1443+850C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950277 | |||||||
chr1:950285 | A | G | 1 | a0001c0001t0006g0033 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1443+842T>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950285 | |||||||
chr1:950296 | C | A | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.1443+831G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950296 | |||||||
chr1:950304 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1443+823A>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950304 | |||||||
chr1:950309 | G | A | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
398 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(395): Show |
intron_variant | MODIFIER | c.1443+818C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950309 | |||||||
chr1:950316 | G | A | 1 | a0001c0001t0002g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1443+811C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950316 | |||||||
chr1:950318 | C | T | 6 | a0001c0001t0004g0018 a0001c0001t0004g0031 a0001c0001t0004g0042 others(3): Show |
11 | HG01069.hp1 HG01123.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1443+809G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950318 | |||||||
chr1:950319 | A | G | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.1443+808T>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950319 | |||||||
chr1:950376 | C | T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0073 a0001c0001t0001g0085 others(2): Show |
6 | HG02976.hp2 HG03098.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1443+751G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950376 | |||||||
chr1:950413 | GCACAGGT others(21): Show |
G | 1 | a0001c0023t0004g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1443+686_1443+713d others(30): Show |
NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950413 | |||||||
chr1:950432 | G | T | 1 | a0003c0004t0005g0048 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1443+695C>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950432 | |||||||
chr1:950502 | GAC | G | 4 | a0001c0001t0001g0134 a0001c0001t0001g0168 a0002c0003t0003g0076 others(1): Show |
4 | HG00738.hp1 HG01192.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1443+623_1443+624d others(4): Show |
NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950502 | |||||||
chr1:950524 | C | T | 3 | a0001c0001t0004g0018 a0001c0001t0004g0031 a0001c0008t0004g0032 |
7 | HG01069.hp1 HG01123.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1443+603G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950524 | |||||||
chr1:950537 | G | A | 1 | a0001c0002t0001g0155 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1443+590C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950537 | |||||||
chr1:950542 | G | A | 5 | a0001c0001t0001g0038 a0001c0001t0001g0073 a0001c0001t0001g0085 others(2): Show |
6 | HG02976.hp2 HG03098.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1443+585C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950542 | |||||||
chr1:950565 | G | C | 22 | a0001c0001t0001g0030 a0001c0001t0001g0057 a0001c0001t0002g0002 others(19): Show |
56 | HG00423.hp1 HG00609.hp2 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.1443+562C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950565 | |||||||
chr1:950626 | T | C | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.1443+501A>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950626 | |||||||
chr1:950669 | ACAG | A | 124 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(121): Show |
320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.1443+455_1443+457d others(5): Show |
NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950669 | |||||||
chr1:950717 | T | C | 1 | a0004c0005t0003g0082 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1443+410A>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950717 | |||||||
chr1:950799 | CA | C | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.1443+327delT | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950799 | |||||||
chr1:950802 | TG | T | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.1443+324delC | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950802 | |||||||
chr1:950806 | C | CAG | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.1443+319_1443+320d others(4): Show |
NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950806 | |||||||
chr1:950826 | A | G | 6 | a0001c0001t0004g0018 a0001c0001t0004g0031 a0001c0001t0004g0042 others(3): Show |
11 | HG01069.hp1 HG01123.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1443+301T>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950826 | |||||||
chr1:950882 | T | C | 1 | a0001c0002t0001g0156 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1443+245A>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950882 | |||||||
chr1:950884 | C | A | 1 | a0001c0002t0001g0156 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1443+243G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950884 | |||||||
chr1:950930 | C | T | 1 | a0001c0002t0001g0145 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1443+197G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950930 | |||||||
chr1:950995 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1443+132C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 950995 | |||||||
chr1:951004 | G | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(17): Show |
42 | HG00673.hp2 HG00741.hp1 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1443+123C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 951004 | |||||||
chr1:951097 | G | A | 5 | a0001c0001t0004g0018 a0001c0001t0004g0031 a0001c0001t0004g0042 others(2): Show |
10 | HG01069.hp1 HG01123.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1443+30C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 951097 | |||||||
chr1:951112 | C | T | 5 | a0001c0001t0001g0038 a0001c0001t0001g0073 a0001c0001t0001g0085 others(2): Show |
6 | HG02976.hp2 HG03098.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1443+15G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 12/18 | chr1 | 951112 | |||||||
chr1:951329 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1332-91G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951329 | |||||||
chr1:951339 | C | G | 2 | a0001c0002t0001g0026 a0001c0002t0001g0124 |
4 | NA18974.hp1 NA18992.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.1332-101G>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951339 | |||||||
chr1:951387 | T | G | 1 | a0001c0002t0010g0143 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1332-149A>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951387 | |||||||
chr1:951408 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(100): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1332-170C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951408 | |||||||
chr1:951437 | C | CATTTT | 27 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(24): Show |
54 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(51): Show |
intron_variant | MODIFIER | c.1332-200_1332-199i others(7): Show |
NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951437 | |||||||
chr1:951437 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(100): Show |
277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.1332-199G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951437 | |||||||
chr1:951451 | G | GGGTCA | 4 | a0004c0005t0003g0037 a0004c0005t0003g0072 a0004c0005t0003g0082 others(1): Show |
5 | HG02572.hp1 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1332-218_1332-214d others(7): Show |
NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951451 | |||||||
chr1:951528 | C | A | 1 | a0001c0002t0001g0158 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1332-290G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951528 | |||||||
chr1:951642 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1331+358T>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951642 | |||||||
chr1:951660 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1331+340C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951660 | |||||||
chr1:951679 | G | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(17): Show |
42 | HG00673.hp2 HG00741.hp1 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1331+321C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951679 | |||||||
chr1:951714 | C | G | 5 | a0001c0001t0004g0018 a0001c0001t0004g0031 a0001c0001t0004g0042 others(2): Show |
10 | HG01069.hp1 HG01123.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1331+286G>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951714 | |||||||
chr1:951765 | A | T | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+235T>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951765 | |||||||
chr1:951766 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+234C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951766 | |||||||
chr1:951769 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+231C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951769 | |||||||
chr1:951771 | C | G | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+229G>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951771 | |||||||
chr1:951776 | C | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+224G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951776 | |||||||
chr1:951777 | C | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+223G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951777 | |||||||
chr1:951778 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+222C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951778 | |||||||
chr1:951781 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+219C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951781 | |||||||
chr1:951782 | T | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+218A>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951782 | |||||||
chr1:951782 | T | C | 6 | a0001c0001t0004g0018 a0001c0001t0004g0031 a0001c0001t0004g0042 others(3): Show |
11 | HG01069.hp1 HG01123.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1331+218A>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951782 | |||||||
chr1:951783 | T | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+217A>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951783 | |||||||
chr1:951784 | G | C | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+216C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951784 | |||||||
chr1:951785 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+215C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951785 | |||||||
chr1:951787 | G | C | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+213C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951787 | |||||||
chr1:951788 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+212C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951788 | |||||||
chr1:951790 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+210C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951790 | |||||||
chr1:951792 | T | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+208A>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951792 | |||||||
chr1:951796 | G | C | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+204C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951796 | |||||||
chr1:951797 | T | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+203A>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951797 | |||||||
chr1:951798 | C | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+202G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951798 | |||||||
chr1:951800 | C | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+200G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951800 | |||||||
chr1:951803 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+197C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951803 | |||||||
chr1:951804 | T | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+196A>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951804 | |||||||
chr1:951805 | G | C | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+195C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951805 | |||||||
chr1:951806 | C | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+194G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951806 | |||||||
chr1:951807 | C | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+193G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951807 | |||||||
chr1:951813 | G | T | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+187C>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951813 | |||||||
chr1:951814 | C | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+186G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951814 | |||||||
chr1:951816 | C | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+184G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951816 | |||||||
chr1:951817 | T | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+183A>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951817 | |||||||
chr1:951819 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+181C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951819 | |||||||
chr1:951821 | T | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+179A>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951821 | |||||||
chr1:951822 | C | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+178G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951822 | |||||||
chr1:951824 | C | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+176G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951824 | |||||||
chr1:951827 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+173C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951827 | |||||||
chr1:951832 | C | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+168G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951832 | |||||||
chr1:951834 | G | C | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+166C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951834 | |||||||
chr1:951836 | G | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+164C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951836 | |||||||
chr1:951837 | C | T | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+163G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951837 | |||||||
chr1:951839 | T | A | 1 | a0001c0001t0002g0065 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1331+161A>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951839 | |||||||
chr1:951885 | C | A | 1 | a0001c0002t0001g0047 | 2 | HG01175.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1331+115G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951885 | |||||||
chr1:951889 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1331+111C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 11/18 | chr1 | 951889 | |||||||
chr1:952157 | C | T | 5 | a0001c0001t0004g0018 a0001c0001t0004g0031 a0001c0001t0004g0042 others(2): Show |
10 | HG01069.hp1 HG01123.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1192-18G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 10/18 | chr1 | 952157 | |||||||
chr1:952180 | A | C | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.1192-41T>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 10/18 | chr1 | 952180 | |||||||
chr1:952197 | G | A | 2 | a0001c0002t0001g0025 a0001c0002t0001g0069 |
4 | NA18944.hp1 NA18977.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192-58C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 10/18 | chr1 | 952197 | |||||||
chr1:952271 | C | T | 2 | a0001c0002t0001g0123 a0001c0002t0001g0144 |
2 | HG01175.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1192-132G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 10/18 | chr1 | 952271 | |||||||
chr1:952352 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1191+60C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 10/18 | chr1 | 952352 | |||||||
chr1:952654 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1003-54G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 9/18 | chr1 | 952654 | |||||||
chr1:952706 | C | G | 1 | a0001c0001t0001g0099 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1003-106G>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 9/18 | chr1 | 952706 | |||||||
chr1:952736 | C | A | 1 | a0001c0002t0001g0160 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1003-136G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 9/18 | chr1 | 952736 | |||||||
chr1:952824 | G | A | 1 | a0002c0003t0003g0079 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1003-224C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 9/18 | chr1 | 952824 | |||||||
chr1:952825 | G | A | 1 | a0003c0004t0001g0029 | 3 | HG02683.hp2 HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1003-225C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 9/18 | chr1 | 952825 | |||||||
chr1:952840 | G | A | 18 | a0001c0001t0002g0002 a0001c0001t0002g0016 a0001c0001t0002g0017 others(15): Show |
51 | HG00423.hp1 HG00609.hp2 HG01123.hp1 others(48): Show |
intron_variant | MODIFIER | c.1003-240C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 9/18 | chr1 | 952840 | |||||||
chr1:952859 | C | T | 6 | a0001c0001t0004g0018 a0001c0001t0004g0031 a0001c0001t0004g0042 others(3): Show |
11 | HG01069.hp1 HG01123.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.1003-259G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 9/18 | chr1 | 952859 | |||||||
chr1:952860 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1003-260C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 9/18 | chr1 | 952860 | |||||||
chr1:952914 | C | T | 1 | a0001c0001t0004g0114 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1002+261G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 9/18 | chr1 | 952914 | |||||||
chr1:952970 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1002+205C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 9/18 | chr1 | 952970 | |||||||
chr1:953062 | G | C | 1 | a0001c0006t0001g0019 | 3 | HG02145.hp2 HG02258.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1002+113C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 9/18 | chr1 | 953062 | |||||||
chr1:953107 | C | G | 1 | a0001c0001t0002g0066 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1002+68G>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 9/18 | chr1 | 953107 | |||||||
chr1:953108 | G | A | 1 | a0001c0002t0001g0161 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1002+67C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 9/18 | chr1 | 953108 | |||||||
chr1:953108 | G | C | 1 | a0001c0001t0002g0066 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1002+67C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 9/18 | chr1 | 953108 | |||||||
chr1:953111 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1002+64G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 9/18 | chr1 | 953111 | |||||||
chr1:953448 | T | C | 1 | a0002c0003t0003g0115 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.889-160A>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 8/18 | chr1 | 953448 | |||||||
chr1:953580 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.888+202C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 8/18 | chr1 | 953580 | |||||||
chr1:953751 | A | G | 22 | a0001c0001t0001g0030 a0001c0001t0001g0057 a0001c0001t0002g0002 others(19): Show |
56 | HG00423.hp1 HG00609.hp2 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.888+31T>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 8/18 | chr1 | 953751 | |||||||
chr1:953778 | G | C | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(150): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
splice_region_variant&intron_variant | LOW | c.888+4C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 8/18 | chr1 | 953778 | |||||||
chr1:953779 | A | C | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(150): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
splice_region_variant&intron_variant | LOW | c.888+3T>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 8/18 | chr1 | 953779 | |||||||
chr1:953906 | G | A | 1 | a0001c0001t0001g0020 | 3 | HG01243.hp2 HG02896.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.778-14C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 7/18 | chr1 | 953906 | |||||||
chr1:954092 | G | C | 2 | a0001c0001t0002g0065 a0001c0001t0002g0066 |
2 | NA18986.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.699-10C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954092 | |||||||
chr1:954133 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.699-51C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954133 | |||||||
chr1:954181 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.699-99C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954181 | |||||||
chr1:954218 | G | C | 1 | a0001c0023t0004g0068 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.699-136C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954218 | |||||||
chr1:954258 | G | C | 153 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(150): Show |
388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.699-176C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954258 | |||||||
chr1:954333 | C | A | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
386 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(383): Show |
intron_variant | MODIFIER | c.699-251G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954333 | |||||||
chr1:954334 | G | T | 1 | a0001c0001t0001g0107 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.699-252C>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954334 | |||||||
chr1:954335 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.699-253G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954335 | |||||||
chr1:954343 | G | A | 1 | a0001c0002t0001g0131 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.699-261C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954343 | |||||||
chr1:954496 | C | G | 1 | a0001c0001t0001g0040 | 2 | HG00741.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.699-414G>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954496 | |||||||
chr1:954626 | A | G | 4 | a0001c0002t0001g0025 a0001c0002t0001g0044 a0001c0002t0001g0069 others(1): Show |
7 | HG00621.hp1 NA18944.hp1 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.699-544T>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954626 | |||||||
chr1:954724 | G | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0023 others(22): Show |
68 | HG00323.hp2 HG00438.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.699-642C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954724 | |||||||
chr1:954726 | C | T | 1 | a0001c0002t0001g0142 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.699-644G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954726 | |||||||
chr1:954766 | G | A | 2 | a0001c0002t0001g0162 a0001c0023t0004g0068 |
2 | NA19070.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.699-684C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954766 | |||||||
chr1:954770 | T | C | 1 | a0002c0003t0003g0081 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.699-688A>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954770 | |||||||
chr1:954811 | G | T | 1 | a0001c0001t0001g0132 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.699-729C>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954811 | |||||||
chr1:954827 | G | GA | 8 | a0001c0001t0001g0022 a0001c0001t0001g0073 a0001c0001t0001g0107 others(5): Show |
10 | HG02155.hp2 HG03098.hp1 NA18980.hp1 others(7): Show |
intron_variant | MODIFIER | c.699-746dupT | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954827 | |||||||
chr1:954838 | A | C | 1 | a0001c0001t0002g0090 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.699-756T>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954838 | |||||||
chr1:954839 | C | A | 6 | a0001c0001t0001g0038 a0001c0001t0001g0073 a0001c0001t0001g0085 others(3): Show |
7 | HG02976.hp2 HG03098.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.699-757G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954839 | |||||||
chr1:954892 | G | C | 5 | a0001c0001t0004g0018 a0001c0001t0004g0031 a0001c0001t0004g0042 others(2): Show |
10 | HG01069.hp1 HG01123.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.699-810C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954892 | |||||||
chr1:954915 | G | C | 19 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(16): Show |
41 | HG00673.hp2 HG00741.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.699-833C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954915 | |||||||
chr1:954921 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.699-839C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 954921 | |||||||
chr1:955066 | C | T | 1 | a0001c0001t0006g0033 | 2 | HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.698+857G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 955066 | |||||||
chr1:955392 | C | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0109 a0001c0001t0001g0110 |
4 | HG02723.hp2 HG02809.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.698+531G>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 955392 | |||||||
chr1:955486 | G | A | 1 | a0001c0001t0001g0050 | 2 | HG03239.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.698+437C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 955486 | |||||||
chr1:955551 | G | A | 2 | a0001c0001t0001g0021 a0001c0002t0001g0165 |
4 | HG02083.hp1 HG02145.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.698+372C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 955551 | |||||||
chr1:955565 | A | T | 1 | a0001c0001t0002g0017 | 3 | NA18612.hp1 NA18983.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.698+358T>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 955565 | |||||||
chr1:955641 | G | A | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.698+282C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 955641 | |||||||
chr1:955669 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0101 |
6 | HG01358.hp1 HG01943.hp2 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.698+254G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 955669 | |||||||
chr1:955679 | C | T | 62 | a0001c0001t0001g0045 a0001c0001t0001g0172 a0001c0002t0001g0001 others(59): Show |
175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.698+244G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 955679 | |||||||
chr1:955718 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.698+205C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 955718 | |||||||
chr1:955743 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.698+180A>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 955743 | |||||||
chr1:955810 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.698+113T>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 955810 | |||||||
chr1:955897 | C | T | 2 | a0001c0001t0002g0054 a0001c0001t0002g0055 |
2 | HG02523.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.698+26G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 955897 | |||||||
chr1:955898 | C | T | 1 | a0001c0002t0001g0141 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.698+25G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 6/18 | chr1 | 955898 | |||||||
chr1:956021 | G | A | 1 | a0001c0008t0004g0032 | 2 | HG01123.hp2 HG01243.hp1 |
splice_region_variant&intron_variant | LOW | c.608-8C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 5/18 | chr1 | 956021 | |||||||
chr1:956044 | G | C | 1 | a0001c0001t0002g0090 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.608-31C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 5/18 | chr1 | 956044 | |||||||
chr1:956063 | C | T | 1 | a0001c0002t0001g0140 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.607+32G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 5/18 | chr1 | 956063 | |||||||
chr1:956240 | C | A | 1 | a0003c0004t0005g0048 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.487-25G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 4/18 | chr1 | 956240 | |||||||
chr1:956279 | G | A | 3 | a0001c0001t0001g0138 a0004c0005t0003g0072 a0004c0005t0003g0083 |
3 | HG03098.hp2 HG03209.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.487-64C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 4/18 | chr1 | 956279 | |||||||
chr1:956507 | G | GA | 3 | a0001c0001t0001g0119 a0002c0003t0003g0036 a0004c0005t0003g0072 |
4 | HG02148.hp1 HG03209.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-293dupT | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 4/18 | chr1 | 956507 | |||||||
chr1:956509 | A | G | 1 | a0001c0001t0001g0043 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.487-294T>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 4/18 | chr1 | 956509 | |||||||
chr1:956518 | T | C | 6 | a0001c0001t0001g0038 a0001c0001t0001g0073 a0001c0001t0001g0085 others(3): Show |
7 | HG01074.hp1 HG02976.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.487-303A>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 4/18 | chr1 | 956518 | |||||||
chr1:956565 | A | G | 63 | a0001c0001t0001g0045 a0001c0001t0001g0172 a0001c0001t0002g0166 others(60): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.486+329T>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 4/18 | chr1 | 956565 | |||||||
chr1:956632 | C | T | 14 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0021 others(11): Show |
29 | HG01099.hp1 HG01243.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.486+262G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 4/18 | chr1 | 956632 | |||||||
chr1:956696 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.486+198G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 4/18 | chr1 | 956696 | |||||||
chr1:956715 | C | T | 6 | a0001c0001t0004g0018 a0001c0001t0004g0031 a0001c0001t0004g0042 others(3): Show |
11 | HG01069.hp1 HG01123.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.486+179G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 4/18 | chr1 | 956715 | |||||||
chr1:956761 | C | T | 1 | a0001c0015t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.486+133G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 4/18 | chr1 | 956761 | |||||||
chr1:956816 | C | G | 1 | a0001c0002t0001g0139 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.486+78G>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 4/18 | chr1 | 956816 | |||||||
chr1:956846 | C | T | 1 | a0001c0001t0002g0016 | 3 | NA18995.hp1 NA19056.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.486+48G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 4/18 | chr1 | 956846 | |||||||
chr1:957080 | G | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(17): Show |
44 | HG00673.hp2 HG00741.hp1 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.354+19C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 3/18 | chr1 | 957080 | |||||||
chr1:957091 | G | A | 6 | a0001c0001t0001g0038 a0001c0001t0001g0073 a0001c0001t0001g0085 others(3): Show |
7 | HG01074.hp1 HG02976.hp2 HG03098.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.354+8C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 3/18 | chr1 | 957091 | |||||||
chr1:957294 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.180-21C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 957294 | |||||||
chr1:957341 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.180-68C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 957341 | |||||||
chr1:957344 | C | T | 1 | a0001c0015t0001g0084 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.180-71G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 957344 | |||||||
chr1:957365 | G | A | 155 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(152): Show |
391 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.180-92C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 957365 | |||||||
chr1:957396 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.180-123C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 957396 | |||||||
chr1:957400 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.180-127G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 957400 | |||||||
chr1:957493 | C | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0091 |
5 | HG01884.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.180-220G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 957493 | |||||||
chr1:957548 | C | G | 1 | a0001c0001t0001g0091 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.180-275G>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 957548 | |||||||
chr1:957814 | G | C | 1 | a0001c0002t0001g0051 | 2 | HG01069.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.180-541C>G | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 957814 | |||||||
chr1:957900 | G | A | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
398 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(395): Show |
intron_variant | MODIFIER | c.180-627C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 957900 | |||||||
chr1:958061 | C | CT | 32 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0043 others(29): Show |
72 | HG00323.hp2 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.180-789dupA | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 958061 | |||||||
chr1:958061 | C | CTT | 4 | a0001c0001t0001g0023 a0001c0001t0001g0118 a0001c0001t0001g0119 others(1): Show |
6 | HG01074.hp1 HG01928.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.180-790_180-789dup others(2): Show |
NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 958061 | |||||||
chr1:958081 | TC | T | 46 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0013 others(43): Show |
100 | HG00423.hp1 HG00621.hp1 HG00673.hp2 others(97): Show |
intron_variant | MODIFIER | c.180-809delG | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 958081 | |||||||
chr1:958082 | C | T | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.180-809G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 958082 | |||||||
chr1:958084 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.180-811G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 958084 | |||||||
chr1:958161 | C | A | 1 | a0001c0011t0004g0111 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.179+768G>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 958161 | |||||||
chr1:958193 | C | T | 1 | a0001c0001t0002g0053 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.179+736G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 958193 | |||||||
chr1:958214 | G | A | 1 | a0001c0002t0001g0175 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.179+715C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 958214 | |||||||
chr1:958235 | A | G | 19 | a0001c0001t0001g0030 a0001c0001t0001g0057 a0001c0001t0002g0002 others(16): Show |
53 | HG00423.hp1 HG00609.hp2 HG01123.hp1 others(50): Show |
intron_variant | MODIFIER | c.179+694T>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 958235 | |||||||
chr1:958251 | A | G | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(149): Show |
387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
intron_variant | MODIFIER | c.179+678T>C | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 958251 | |||||||
chr1:958339 | G | A | 125 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(122): Show |
320 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.179+590C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 958339 | |||||||
chr1:958502 | G | A | 3 | a0001c0001t0001g0041 a0001c0001t0001g0112 a0001c0001t0001g0113 |
4 | HG01109.hp1 HG02055.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.179+427C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 958502 | |||||||
chr1:958602 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.179+327G>A | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 958602 | |||||||
chr1:958790 | G | A | 2 | a0001c0001t0004g0042 a0001c0001t0004g0114 |
3 | HG01891.hp2 HG02647.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.179+139C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 2/18 | chr1 | 958790 | |||||||
chr1:959139 | G | A | 1 | a0002c0003t0003g0115 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.27-58C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 1/18 | chr1 | 959139 | |||||||
chr1:959185 | G | A | 1 | a0001c0002t0001g0177 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.26+30C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 1/18 | chr1 | 959185 | |||||||
chr1:959193 | G | A | 85 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0023 others(82): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.26+22C>T | NOC2L | ENSG00000188976.11 | transcript | ENST00000327044.7 | protein_coding | 1/18 | chr1 | 959193 |