Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 643246 |
| ensemblid | ENSG00000258102.5 |
| hgncid | 34390 |
| symbol | MAP1LC3B2 |
| name | microtubule associated protein 1 light chain 3 beta 2 |
| refseq_nuc | NM_001085481.3 |
| refseq_prot | NP_001078950.1 |
| ensembl_nuc | ENST00000556529.4 |
| ensembl_prot | ENSP00000450524.1 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 116559381 |
| end | 116576606 |
| strand | + |
| ver | v1.2 |
| region | chr12:116559381-116576606 |
| region5000 | chr12:116554381-116581606 |
| regionname0 | MAP1LC3B2_chr12_116559381_116576606 |
| regionname5000 | MAP1LC3B2_chr12_116554381_116581606 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 125 | 424 | 82 | 61 | 217 | 18 | 44 | 167 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | MPSEK others(120): Show |
chr12 | 116554381 | 116581606 |
| a0002 | 0/0 | 125 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | MPSEK others(120): Show |
chr12 | 116554381 | 116581606 |
| a0003 | 0/0 | 125 | 8 | 6 | 2 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | MPSEK others(120): Show |
chr12 | 116554381 | 116581606 |
| a0004 | 0/0 | 125 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | MPSEK others(120): Show |
chr12 | 116554381 | 116581606 |
| a0005 | 0/0 | 125 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | MPSEK others(120): Show |
chr12 | 116554381 | 116581606 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 375 | 420 | 82 | 60 | 214 | 18 | 44 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | ATGCC others(370): Show |
chr12 | 116554381 | 116581606 | ||
| a0001c0004 | 0/0 | 375 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | ATGCC others(370): Show |
chr12 | 116554381 | 116581606 | ||
| a0001c0005 | 0/0 | 375 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | ATGCC others(370): Show |
chr12 | 116554381 | 116581606 | ||
| a0001c0008 | 0/0 | 375 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | ATGCC others(370): Show |
chr12 | 116554381 | 116581606 | ||
| a0002c0002 | 0/0 | 375 | 12 | 11 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | ATGCC others(370): Show |
chr12 | 116554381 | 116581606 | ||
| a0003c0003 | 0/0 | 375 | 8 | 6 | 2 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | ATGCC others(370): Show |
chr12 | 116554381 | 116581606 | ||
| a0004c0006 | 0/0 | 375 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | ATGCC others(370): Show |
chr12 | 116554381 | 116581606 | ||
| a0005c0007 | 0/0 | 375 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | ATGCC others(370): Show |
chr12 | 116554381 | 116581606 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 818 | 92 | 6 | 4 | 71 | 5 | 6 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0002 | 0/0 | 819 | 72 | 0 | 16 | 38 | 7 | 11 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(814): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0003 | 0/0 | 817 | 70 | 1 | 16 | 53 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(812): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0004 | 0/0 | 818 | 29 | 9 | 2 | 15 | 0 | 3 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0005 | 0/0 | 818 | 23 | 10 | 5 | 0 | 4 | 4 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0006 | 0/0 | 818 | 15 | 2 | 1 | 12 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0007 | 1/0 | 818 | 14 | 10 | 1 | 0 | 1 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0008 | 0/0 | 819 | 14 | 0 | 3 | 5 | 0 | 6 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(814): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0009 | 0/0 | 818 | 11 | 4 | 4 | 0 | 1 | 2 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0010 | 0/1 | 818 | 11 | 2 | 3 | 1 | 0 | 4 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0011 | 0/0 | 817 | 4 | 0 | 0 | 4 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(812): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0012 | 0/0 | 816 | 9 | 2 | 0 | 6 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(811): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0013 | 0/0 | 818 | 9 | 9 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0014 | 0/0 | 818 | 7 | 2 | 2 | 0 | 0 | 3 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0015 | 0/0 | 818 | 6 | 1 | 1 | 1 | 0 | 3 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0016 | 0/0 | 817 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(812): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0017 | 0/0 | 816 | 5 | 5 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(811): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0018 | 0/0 | 816 | 4 | 4 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(811): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0019 | 0/0 | 817 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(812): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0020 | 0/0 | 817 | 3 | 0 | 0 | 3 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(812): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0021 | 0/0 | 818 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0022 | 0/0 | 818 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0023 | 0/0 | 816 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(811): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0024 | 0/0 | 816 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(811): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0025 | 0/0 | 818 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0026 | 0/0 | 818 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0027 | 0/0 | 818 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0028 | 0/0 | 816 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(811): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0029 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(812): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0030 | 0/0 | 817 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(812): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0031 | 0/0 | 816 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(811): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0032 | 0/0 | 818 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0033 | 0/0 | 817 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(812): Show |
chr12 | 116554381 | 116581606 |
| a0001c0001t0036 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | TCAAG others(814): Show |
chr12 | 116554381 | 116581606 |
| a0001c0004t0006 | 0/0 | 818 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0001c0005t0005 | 0/0 | 818 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0001c0008t0001 | 0/0 | 818 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0002c0002t0005 | 0/0 | 818 | 2 | 1 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0002c0002t0007 | 0/0 | 818 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0002c0002t0009 | 0/0 | 818 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0002c0002t0014 | 0/0 | 818 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0002c0002t0015 | 0/0 | 818 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0002c0002t0016 | 0/0 | 817 | 3 | 3 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(812): Show |
chr12 | 116554381 | 116581606 |
| a0002c0002t0034 | 0/0 | 818 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0002c0002t0035 | 0/0 | 818 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0003c0003t0011 | 0/0 | 817 | 6 | 6 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(812): Show |
chr12 | 116554381 | 116581606 |
| a0003c0003t0019 | 0/0 | 817 | 2 | 0 | 2 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(812): Show |
chr12 | 116554381 | 116581606 |
| a0004c0006t0010 | 0/0 | 818 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(813): Show |
chr12 | 116554381 | 116581606 |
| a0005c0007t0003 | 0/0 | 817 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | GCAAG others(812): Show |
chr12 | 116554381 | 116581606 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0001g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0004 | 0/0 | 4 | 0 | 1 | 1 | 2 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0390 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0393 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0394 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0395 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0396 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0002g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0001 | 0/0 | 9 | 0 | 1 | 8 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0003g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0004g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0005g0007 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0005g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0005g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0005g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0005g0361 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0005g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0005g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0005g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0005g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0006g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0006g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0006g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0006g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0006g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0007g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0007g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0007g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0007g0212 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0007g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0007g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0007g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0007g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0007g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0007g0387 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0008g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0008g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0008g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0008g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0008g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0008g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0008g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0008g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0008g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0008g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0008g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0008g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0008g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0008g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0009g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0009g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0009g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0009g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0009g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0009g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0009g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0009g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0009g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0009g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0009g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0010g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0010g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0010g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0010g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0010g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0010g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0010g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0010g0073 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0010g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0011g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0011g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0012g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0012g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0012g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0012g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0012g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0012g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0012g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0012g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0012g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0013g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0013g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0013g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0013g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0013g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0013g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0013g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0013g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0013g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0014g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0014g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0014g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0014g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0014g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0014g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0015g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0015g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0015g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0015g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0015g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0015g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0016g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0016g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0017g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0017g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0017g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0017g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0017g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0018g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0018g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0018g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0018g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0019g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0020g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0020g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0020g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0021g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0021g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0022g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0022g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0023g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0023g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0024g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0024g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0025g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0026g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0027g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0028g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0029g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0030g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0031g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0032g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0033g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0001t0036g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0004t0006g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0004t0006g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0005t0005g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0001c0008t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0002c0002t0005g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0002c0002t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0002c0002t0007g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0002c0002t0009g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0002c0002t0009g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0002c0002t0014g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0002c0002t0015g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0002c0002t0016g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0002c0002t0016g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0002c0002t0016g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0002c0002t0034g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0002c0002t0035g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0003c0003t0011g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0003c0003t0011g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0003c0003t0011g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0003c0003t0011g0401 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0003c0003t0019g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0004c0006t0010g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| a0005c0007t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | GBR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0319 | EUR | GBR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0023 | EUR | GBR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | GBR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0330 | EUR | FIN | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0337 | EUR | FIN | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00323 | hp1 | a0001 | c0001 | t0005 | g0361 | EUR | FIN | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00323 | hp2 | a0001 | c0001 | t0009 | g0211 | EUR | FIN | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00408 | hp2 | a0001 | c0008 | t0001 | g0182 | EAS | CHS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0391 | EAS | CHS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00438 | hp2 | a0001 | c0001 | t0006 | g0048 | EAS | CHS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | CHS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CHS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00558 | hp1 | a0001 | c0001 | t0012 | g0274 | EAS | CHS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | CHS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0192 | EAS | CHS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0381 | EAS | CHS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | CHS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00609 | hp2 | a0001 | c0004 | t0006 | g0044 | EAS | CHS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00621 | hp1 | a0001 | c0001 | t0020 | g0084 | EAS | CHS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0386 | EAS | CHS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00639 | hp2 | a0001 | c0001 | t0008 | g0093 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0260 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0344 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | CHS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00735 | hp1 | a0001 | c0001 | t0010 | g0075 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00735 | hp2 | a0001 | c0005 | t0005 | g0258 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00738 | hp1 | a0001 | c0001 | t0014 | g0046 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0322 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG00741 | hp2 | a0001 | c0001 | t0033 | g0368 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01069 | hp1 | a0001 | c0001 | t0030 | g0011 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01071 | hp1 | a0001 | c0001 | t0014 | g0011 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0393 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0204 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0388 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01099 | hp1 | a0001 | c0001 | t0008 | g0062 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0106 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01106 | hp2 | a0001 | c0001 | t0009 | g0126 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0334 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0380 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01167 | hp2 | a0001 | c0001 | t0009 | g0109 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01168 | hp1 | a0003 | c0003 | t0019 | g0010 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0369 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01169 | hp1 | a0003 | c0003 | t0019 | g0010 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01169 | hp2 | a0001 | c0001 | t0009 | g0111 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01175 | hp1 | a0002 | c0002 | t0005 | g0155 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0360 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01192 | hp1 | a0001 | c0001 | t0010 | g0072 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0303 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01243 | hp1 | a0001 | c0001 | t0010 | g0028 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0135 | AMR | PUR | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | CLM | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0298 | AMR | CLM | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0026 | AMR | CLM | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01256 | hp2 | a0001 | c0001 | t0009 | g0110 | AMR | CLM | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0026 | AMR | CLM | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01358 | hp1 | a0001 | c0001 | t0008 | g0049 | AMR | CLM | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0383 | AMR | CLM | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | CLM | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01361 | hp2 | a0001 | c0001 | t0006 | g0079 | AMR | CLM | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0343 | AMR | CLM | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0146 | AMR | CLM | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0370 | EUR | IBS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0007 | EUR | IBS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0276 | EUR | IBS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | IBS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0007 | EUR | IBS | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0331 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01884 | hp2 | a0001 | c0001 | t0017 | g0304 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0186 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0316 | AMR | PEL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0382 | AMR | PEL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0147 | AMR | PEL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PEL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0293 | AMR | PEL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02004 | hp1 | a0001 | c0001 | t0015 | g0067 | AMR | PEL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0154 | AMR | PEL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02027 | hp1 | a0001 | c0001 | t0020 | g0082 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0326 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02055 | hp2 | a0002 | c0002 | t0016 | g0040 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0352 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0379 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0366 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0318 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02083 | hp1 | a0001 | c0001 | t0008 | g0085 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0317 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0183 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02135 | hp2 | a0001 | c0004 | t0006 | g0047 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0350 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02145 | hp2 | a0001 | c0001 | t0013 | g0263 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0215 | AMR | PEL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | PEL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0392 | EAS | CDX | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | CDX | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | CDX | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | CDX | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02257 | hp1 | a0002 | c0002 | t0005 | g0156 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0230 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0231 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PEL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02280 | hp1 | a0002 | c0002 | t0014 | g0032 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0104 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02451 | hp1 | a0001 | c0001 | t0021 | g0071 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02451 | hp2 | a0001 | c0001 | t0019 | g0070 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02572 | hp1 | a0004 | c0006 | t0010 | g0307 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02572 | hp2 | a0001 | c0001 | t0018 | g0076 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02602 | hp1 | a0001 | c0001 | t0005 | g0174 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0103 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0265 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02615 | hp2 | a0002 | c0002 | t0015 | g0042 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02622 | hp1 | a0001 | c0001 | t0018 | g0029 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02622 | hp2 | a0001 | c0001 | t0012 | g0291 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0289 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02630 | hp2 | a0001 | c0001 | t0017 | g0096 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02647 | hp1 | a0001 | c0001 | t0028 | g0068 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02647 | hp2 | a0001 | c0001 | t0013 | g0376 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02683 | hp1 | a0001 | c0001 | t0008 | g0069 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02683 | hp2 | a0001 | c0001 | t0015 | g0058 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0396 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0314 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02717 | hp2 | a0003 | c0003 | t0011 | g0008 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0189 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0402 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02735 | hp1 | a0001 | c0001 | t0008 | g0077 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0301 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02738 | hp2 | a0001 | c0001 | t0007 | g0210 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02809 | hp1 | a0001 | c0001 | t0025 | g0027 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02809 | hp2 | a0001 | c0001 | t0017 | g0015 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0333 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0222 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02886 | hp1 | a0003 | c0003 | t0011 | g0400 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0264 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02895 | hp1 | a0001 | c0001 | t0014 | g0013 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02895 | hp2 | a0002 | c0002 | t0035 | g0335 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0191 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02896 | hp2 | a0001 | c0001 | t0026 | g0198 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02897 | hp1 | a0001 | c0001 | t0014 | g0013 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0188 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02922 | hp1 | a0001 | c0001 | t0031 | g0015 | AFR | ESN | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02922 | hp2 | a0002 | c0002 | t0009 | g0358 | AFR | ESN | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0187 | AFR | ESN | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02965 | hp2 | a0001 | c0001 | t0032 | g0233 | AFR | ESN | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02970 | hp1 | a0001 | c0001 | t0023 | g0277 | AFR | ESN | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02970 | hp2 | a0003 | c0003 | t0011 | g0399 | AFR | ESN | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02976 | hp1 | a0001 | c0001 | t0016 | g0035 | AFR | ESN | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02976 | hp2 | a0001 | c0001 | t0012 | g0193 | AFR | ESN | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0022 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03017 | hp2 | a0001 | c0001 | t0005 | g0172 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03041 | hp1 | a0001 | c0001 | t0013 | g0190 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03041 | hp2 | a0001 | c0001 | t0024 | g0359 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0206 | AFR | MSL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03098 | hp2 | a0002 | c0002 | t0007 | g0136 | AFR | MSL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03130 | hp1 | a0001 | c0001 | t0009 | g0349 | AFR | ESN | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03130 | hp2 | a0001 | c0001 | t0013 | g0385 | AFR | ESN | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03139 | hp1 | a0003 | c0003 | t0011 | g0401 | AFR | ESN | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03139 | hp2 | a0002 | c0002 | t0009 | g0357 | AFR | ESN | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03195 | hp1 | a0002 | c0002 | t0034 | g0338 | AFR | ESN | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | ESN | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03209 | hp1 | a0001 | c0001 | t0023 | g0242 | AFR | MSL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03209 | hp2 | a0001 | c0001 | t0024 | g0205 | AFR | MSL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03225 | hp1 | a0001 | c0001 | t0009 | g0194 | AFR | MSL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0292 | AFR | MSL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03239 | hp1 | a0001 | c0001 | t0012 | g0355 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0378 | AFR | MSL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0257 | AFR | MSL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03486 | hp1 | a0001 | c0001 | t0025 | g0027 | AFR | MSL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0125 | AFR | MSL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03491 | hp1 | a0001 | c0001 | t0010 | g0014 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03491 | hp2 | a0001 | c0001 | t0008 | g0053 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03492 | hp1 | a0001 | c0001 | t0010 | g0014 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0227 | AFR | ESN | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03516 | hp2 | a0003 | c0003 | t0011 | g0008 | AFR | ESN | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03540 | hp2 | a0001 | c0001 | t0013 | g0098 | AFR | GWD | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03579 | hp1 | a0001 | c0001 | t0013 | g0262 | AFR | MSL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03579 | hp2 | a0001 | c0001 | t0015 | g0034 | AFR | MSL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0374 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03669 | hp2 | a0001 | c0001 | t0008 | g0059 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03704 | hp1 | a0001 | c0001 | t0010 | g0056 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03704 | hp2 | a0001 | c0001 | t0015 | g0041 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03710 | hp1 | a0001 | c0001 | t0008 | g0050 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | PJL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03831 | hp1 | a0001 | c0001 | t0010 | g0064 | SAS | BEB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03831 | hp2 | a0001 | c0001 | t0014 | g0054 | SAS | BEB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0299 | SAS | BEB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0390 | SAS | BEB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03942 | hp1 | a0001 | c0001 | t0009 | g0214 | SAS | BEB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03942 | hp2 | a0001 | c0001 | t0015 | g0052 | SAS | BEB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG04184 | hp1 | a0001 | c0001 | t0009 | g0372 | SAS | BEB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG04184 | hp2 | a0001 | c0001 | t0014 | g0045 | SAS | BEB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG04199 | hp1 | a0001 | c0001 | t0005 | g0363 | SAS | STU | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG04199 | hp2 | a0001 | c0001 | t0014 | g0051 | SAS | STU | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0022 | SAS | STU | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | STU | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0395 | SAS | STU | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG04228 | hp2 | a0001 | c0001 | t0008 | g0063 | SAS | STU | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0223 | AFR | YRI | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0241 | AFR | YRI | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18612 | hp1 | a0001 | c0001 | t0008 | g0087 | EAS | CHB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0254 | EAS | CHB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0354 | EAS | CHB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18747 | hp2 | a0001 | c0001 | t0006 | g0092 | EAS | CHB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18906 | hp1 | a0001 | c0001 | t0013 | g0118 | AFR | YRI | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | YRI | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18940 | hp2 | a0001 | c0001 | t0012 | g0235 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18942 | hp1 | a0001 | c0001 | t0008 | g0090 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18943 | hp2 | a0001 | c0001 | t0006 | g0095 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18944 | hp1 | a0001 | c0001 | t0008 | g0083 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0373 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0397 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0348 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0384 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18948 | hp2 | a0001 | c0001 | t0012 | g0329 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18956 | hp1 | a0001 | c0001 | t0010 | g0043 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18956 | hp2 | a0001 | c0001 | t0022 | g0055 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18957 | hp2 | a0001 | c0001 | t0012 | g0162 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0325 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18964 | hp1 | a0001 | c0001 | t0006 | g0080 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18965 | hp1 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0365 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18966 | hp1 | a0001 | c0001 | t0006 | g0088 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18968 | hp1 | a0001 | c0001 | t0006 | g0086 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0367 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0364 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18978 | hp2 | a0001 | c0001 | t0022 | g0061 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18979 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18979 | hp2 | a0001 | c0001 | t0036 | g0297 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18981 | hp1 | a0001 | c0001 | t0027 | g0078 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18982 | hp1 | a0001 | c0001 | t0006 | g0012 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18982 | hp2 | a0001 | c0001 | t0029 | g0060 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0375 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18986 | hp2 | a0001 | c0001 | t0008 | g0094 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18990 | hp1 | a0001 | c0001 | t0006 | g0065 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18992 | hp1 | a0001 | c0001 | t0011 | g0129 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18992 | hp2 | a0001 | c0001 | t0015 | g0091 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0332 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0398 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18999 | hp2 | a0001 | c0001 | t0012 | g0164 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0389 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19007 | hp1 | a0001 | c0001 | t0006 | g0089 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19009 | hp1 | a0001 | c0001 | t0012 | g0328 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0312 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0356 | AFR | LWK | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19030 | hp2 | a0001 | c0001 | t0021 | g0037 | AFR | LWK | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19043 | hp1 | a0001 | c0001 | t0018 | g0030 | AFR | LWK | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0251 | AFR | LWK | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19055 | hp2 | a0001 | c0001 | t0011 | g0005 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19060 | hp1 | a0001 | c0001 | t0006 | g0066 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0347 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19067 | hp1 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19070 | hp1 | a0005 | c0007 | t0003 | g0003 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19082 | hp1 | a0001 | c0001 | t0011 | g0005 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19083 | hp1 | a0001 | c0001 | t0020 | g0057 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19088 | hp2 | a0001 | c0001 | t0006 | g0081 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0033 | AFR | YRI | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA19240 | hp2 | a0001 | c0001 | t0013 | g0275 | AFR | YRI | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0377 | AFR | ASW | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | ASW | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0023 | EUR | TSI | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0336 | EUR | TSI | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0252 | EUR | TSI | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA20805 | hp2 | a0001 | c0001 | t0007 | g0387 | EUR | TSI | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0371 | SAS | GIH | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0394 | SAS | GIH | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0288 | AMR | CLM | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0121 | AMR | CLM | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02109 | hp2 | a0001 | c0001 | t0013 | g0099 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02486 | hp1 | a0001 | c0001 | t0016 | g0036 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02486 | hp2 | a0001 | c0001 | t0018 | g0031 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02559 | hp1 | a0002 | c0002 | t0016 | g0038 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG02559 | hp2 | a0001 | c0001 | t0017 | g0097 | AFR | ACB | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03471 | hp1 | a0001 | c0001 | t0017 | g0305 | AFR | MSL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG03471 | hp2 | a0003 | c0003 | t0011 | g0008 | AFR | MSL | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0074 | AFR | USA | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| HG06807 | hp2 | a0001 | c0001 | t0010 | g0009 | AFR | USA | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18955 | hp1 | a0001 | c0001 | t0011 | g0005 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA20300 | hp1 | a0002 | c0002 | t0016 | g0039 | AFR | USA | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0113 | AFR | USA | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | LWK | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0362 | AFR | LWK | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0010 | g0073 | REF | REF | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0212 | REF | REF | MAP1LC3B2_chr12_116554381_116581606 | MAP1LC3B2 | chr12 | 116554381 | 116581606 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:116575982 | G | A | 1 | a0004 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.40G>A | p.Glu14Lys | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 194/818 | 40/378 | 14/125 | chr12 | 116575982 | |||
| chr12:116576054 | T | C | 1 | a0005 | 1 | NA19070.hp1 | missense_variant | MODERATE | c.112T>C | p.Tyr38His | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 266/818 | 112/378 | 38/125 | chr12 | 116576054 | |||
| chr12:116576148 | G | A | 1 | a0003 | 8 | HG01168.hp1 HG01169.hp1 HG02717.hp2 others(5): Show |
missense_variant | MODERATE | c.206G>A | p.Arg69Lys | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 360/818 | 206/378 | 69/125 | chr12 | 116576148 | |||
| chr12:116576280 | G | A | 1 | a0002 | 12 | HG01175.hp1 HG02055.hp2 HG02257.hp1 others(9): Show |
missense_variant | MODERATE | c.338G>A | p.Cys113Tyr | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 492/818 | 338/378 | 113/125 | chr12 | 116576280 | |||
| chr12:116576292 | A | T | 1 | a0003 | 8 | HG01168.hp1 HG01169.hp1 HG02717.hp2 others(5): Show |
missense_variant | MODERATE | c.350A>T | p.Glu117Val | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 504/818 | 350/378 | 117/125 | chr12 | 116576292 | |||
| chr12:116576294 | A | G | 1 | a0002 | 12 | HG01175.hp1 HG02055.hp2 HG02257.hp1 others(9): Show |
missense_variant | MODERATE | c.352A>G | p.Thr118Ala | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 506/818 | 352/378 | 118/125 | chr12 | 116576294 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:116575951 | G | A | 1 | a0001c0005 | 1 | HG00735.hp2 | synonymous_variant | LOW | c.9G>A | p.Ser3Ser | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 163/818 | 9/378 | 3/125 | chr12 | 116575951 | |||
| chr12:116576017 | G | A | 1 | a0004c0006 | 1 | HG02572.hp1 | synonymous_variant | LOW | c.75G>A | p.Glu25Glu | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 229/818 | 75/378 | 25/125 | chr12 | 116576017 | |||
| chr12:116576077 | T | A | 1 | a0001c0004 | 2 | HG00609.hp2 HG02135.hp2 |
synonymous_variant | LOW | c.135T>A | p.Pro45Pro | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 289/818 | 135/378 | 45/125 | chr12 | 116576077 | |||
| chr12:116576248 | G | A | 1 | a0001c0008 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.306G>A | p.Glu102Glu | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 460/818 | 306/378 | 102/125 | chr12 | 116576248 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:116559381 | G | T | 1 | a0001c0001t0036 | 1 | NA18979.hp2 | 5_prime_UTR_variant | MODIFIER | c.-154G>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/2 | 16562 | chr12 | 116559381 | ||||||
| chr12:116559390 | G | A | 1 | a0001c0001t0026 | 1 | HG02896.hp2 | 5_prime_UTR_variant | MODIFIER | c.-145G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/2 | 16553 | chr12 | 116559390 | ||||||
| chr12:116559390 | G | C | 21 | a0001c0001t0006 a0001c0001t0008 a0001c0001t0010 others(18): Show |
80 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(77): Show |
5_prime_UTR_variant | MODIFIER | c.-145G>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/2 | 16553 | chr12 | 116559390 | ||||||
| chr12:116559421 | C | G | 2 | a0001c0001t0025 a0002c0002t0035 |
3 | HG02809.hp1 HG02895.hp2 HG03486.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-114C>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/2 | chr12 | 116559421 | |||||||
| chr12:116575871 | C | T | 7 | a0001c0001t0009 a0001c0001t0013 a0001c0001t0014 others(4): Show |
33 | HG00323.hp2 HG00738.hp1 HG01069.hp1 others(30): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-72C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | chr12 | 116575871 | |||||||
| chr12:116575895 | C | A | 1 | a0001c0001t0031 | 1 | HG02922.hp1 | 5_prime_UTR_variant | MODIFIER | c.-48C>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 48 | chr12 | 116575895 | ||||||
| chr12:116575899 | C | T | 2 | a0001c0001t0022 a0001c0001t0029 |
3 | NA18956.hp2 NA18978.hp2 NA18982.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-44C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | chr12 | 116575899 | |||||||
| chr12:116575922 | C | T | 2 | a0001c0001t0024 a0001c0001t0028 |
3 | HG02647.hp1 HG03041.hp2 HG03209.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-21C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | chr12 | 116575922 | |||||||
| chr12:116575923 | G | C | 1 | a0001c0001t0023 | 2 | HG02970.hp1 HG03209.hp1 |
5_prime_UTR_variant | MODIFIER | c.-20G>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 20 | chr12 | 116575923 | ||||||
| chr12:116575925 | G | C | 23 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(20): Show |
197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
5_prime_UTR_variant | MODIFIER | c.-18G>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 18 | chr12 | 116575925 | ||||||
| chr12:116576326 | G | GA | 12 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(9): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*12dupA | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 13 | INFO_REALIGN_3_PRIME | chr12 | 116576326 | |||||
| chr12:116576337 | T | C | 2 | a0001c0001t0013 a0001c0001t0025 |
11 | HG02109.hp2 HG02145.hp2 HG02647.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*17T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 17 | chr12 | 116576337 | ||||||
| chr12:116576369 | GA | G | 26 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(23): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
3_prime_UTR_variant | MODIFIER | c.*58delA | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 58 | INFO_REALIGN_3_PRIME | chr12 | 116576369 | |||||
| chr12:116576444 | C | A | 1 | a0001c0001t0032 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*124C>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 124 | chr12 | 116576444 | ||||||
| chr12:116576553 | C | A | 1 | a0001c0001t0027 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*233C>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 233 | chr12 | 116576553 | ||||||
| chr12:116576591 | T | TA | 3 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0036 |
87 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*264_*265insA | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 265 | INFO_REALIGN_3_PRIME | chr12 | 116576591 | |||||
| chr12:116576591 | TA | T | 12 | a0001c0001t0012 a0001c0001t0016 a0001c0001t0017 others(9): Show |
32 | HG00558.hp1 HG00741.hp2 HG01069.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*264delA | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 264 | INFO_REALIGN_3_PRIME | chr12 | 116576591 | |||||
| chr12:116576601 | A | G | 4 | a0001c0001t0003 a0001c0001t0020 a0002c0002t0034 others(1): Show |
75 | HG00597.hp2 HG00621.hp1 HG01071.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*281A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 2/2 | 281 | chr12 | 116576601 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:116559508 | T | A | 74 | a0001c0001t0006g0012 a0001c0001t0006g0033 a0001c0001t0006g0048 others(71): Show |
79 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.-102+75T>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116559508 | |||||||
| chr12:116559522 | T | C | 4 | a0001c0001t0017g0015 a0001c0001t0017g0096 a0001c0001t0017g0097 others(1): Show |
4 | HG02559.hp2 HG02630.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-102+89T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116559522 | |||||||
| chr12:116559771 | A | G | 5 | a0001c0001t0005g0402 a0003c0003t0011g0008 a0003c0003t0011g0399 others(2): Show |
7 | HG02717.hp2 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-102+338A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116559771 | |||||||
| chr12:116559920 | T | C | 1 | a0001c0001t0010g0028 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-102+487T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116559920 | |||||||
| chr12:116560068 | G | GA | 7 | a0001c0001t0006g0033 a0001c0001t0010g0009 a0001c0001t0018g0029 others(4): Show |
9 | HG01168.hp1 HG01169.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-102+645dupA | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560068 | ||||||
| chr12:116560119 | T | G | 1 | a0001c0001t0010g0028 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-102+686T>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560119 | |||||||
| chr12:116560163 | G | A | 2 | a0001c0001t0013g0098 a0001c0001t0013g0099 |
2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-102+730G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560163 | |||||||
| chr12:116560179 | T | A | 3 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0102 |
3 | HG03490.hp1 HG03492.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.-102+746T>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560179 | |||||||
| chr12:116560182 | G | C | 1 | a0001c0001t0005g0103 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-102+749G>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560182 | |||||||
| chr12:116560188 | C | CAATATAT others(3): Show |
1 | a0001c0001t0007g0104 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-102+755_-102+756i others(12): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560188 | |||||||
| chr12:116560188 | C | CCA | 3 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0003g0105 |
3 | HG03490.hp1 HG03492.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.-102+755_-102+756i others(4): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560188 | |||||||
| chr12:116560188 | C | CCATATAT others(29): Show |
1 | a0001c0001t0015g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-102+755_-102+756i others(38): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560188 | |||||||
| chr12:116560188 | CTA | C | 13 | a0001c0001t0001g0217 a0001c0001t0001g0221 a0001c0001t0001g0224 others(10): Show |
13 | HG00099.hp1 HG00423.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.-102+807_-102+808d others(4): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560188 | ||||||
| chr12:116560188 | CTATA | C | 11 | a0001c0001t0001g0232 a0001c0001t0002g0023 a0001c0001t0002g0228 others(8): Show |
13 | HG00140.hp1 HG01361.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-102+805_-102+808d others(6): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560188 | ||||||
| chr12:116560188 | CTATATA | C | 42 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(39): Show |
44 | HG00558.hp1 HG00609.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-102+803_-102+808d others(8): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560188 | ||||||
| chr12:116560188 | CTATATAT others(1): Show |
C | 31 | a0001c0001t0001g0276 a0001c0001t0001g0278 a0001c0001t0001g0279 others(28): Show |
31 | HG00438.hp1 HG00544.hp2 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.-102+801_-102+808d others(10): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560188 | ||||||
| chr12:116560188 | CTATATAT others(3): Show |
C | 30 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(27): Show |
31 | HG00099.hp2 HG00280.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.-102+799_-102+808d others(12): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560188 | ||||||
| chr12:116560188 | CTATATAT others(5): Show |
C | 21 | a0001c0001t0001g0340 a0001c0001t0001g0342 a0001c0001t0001g0345 others(18): Show |
23 | HG00642.hp2 HG01256.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.-102+797_-102+808d others(14): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560188 | ||||||
| chr12:116560188 | CTATATAT others(7): Show |
C | 21 | a0001c0001t0001g0362 a0001c0001t0001g0370 a0001c0001t0001g0371 others(18): Show |
21 | HG00323.hp1 HG00639.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-102+795_-102+808d others(16): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560188 | ||||||
| chr12:116560188 | CTATATAT others(9): Show |
C | 7 | a0001c0001t0001g0383 a0001c0001t0001g0384 a0001c0001t0002g0379 others(4): Show |
7 | HG00597.hp2 HG01167.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.-102+793_-102+808d others(18): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560188 | ||||||
| chr12:116560188 | CTATATAT others(11): Show |
C | 2 | a0001c0001t0003g0107 a0001c0001t0013g0385 |
2 | HG03130.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.-102+791_-102+808d others(20): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560188 | ||||||
| chr12:116560188 | CTATATAT others(13): Show |
C | 64 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0119 others(61): Show |
86 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(83): Show |
intron_variant | MODIFIER | c.-102+789_-102+808d others(22): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560188 | ||||||
| chr12:116560188 | CTATATAT others(15): Show |
C | 45 | a0001c0001t0001g0021 a0001c0001t0001g0160 a0001c0001t0001g0161 others(42): Show |
49 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.-102+787_-102+808d others(24): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560188 | ||||||
| chr12:116560188 | CTATATAT others(17): Show |
C | 2 | a0001c0001t0001g0391 a0001c0001t0002g0390 |
2 | HG00423.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-102+785_-102+808d others(26): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560188 | ||||||
| chr12:116560188 | CTATATAT others(19): Show |
C | 1 | a0001c0001t0002g0392 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-102+783_-102+808d others(28): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560188 | ||||||
| chr12:116560188 | CTATATAT others(23): Show |
C | 9 | a0001c0001t0002g0393 a0001c0001t0002g0394 a0001c0001t0006g0033 others(6): Show |
11 | HG01074.hp1 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.-102+779_-102+808d others(32): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560188 | ||||||
| chr12:116560188 | CTATATAT others(25): Show |
C | 2 | a0001c0001t0015g0041 a0002c0002t0015g0042 |
2 | HG02615.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-102+777_-102+808d others(34): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560188 | ||||||
| chr12:116560188 | CTATATAT others(27): Show |
C | 59 | a0001c0001t0002g0395 a0001c0001t0002g0396 a0001c0001t0002g0397 others(56): Show |
62 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.-102+775_-102+808d others(36): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560188 | ||||||
| chr12:116560188 | CTATATAT others(29): Show |
C | 2 | a0001c0001t0003g0398 a0001c0001t0006g0095 |
2 | NA18943.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.-102+773_-102+808d others(38): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560188 | ||||||
| chr12:116560189 | T | C | 8 | a0001c0001t0002g0102 a0001c0001t0010g0028 a0001c0001t0016g0035 others(5): Show |
8 | HG01243.hp1 HG02055.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-102+756T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560189 | |||||||
| chr12:116560191 | T | C | 1 | a0001c0001t0005g0106 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-102+758T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560191 | |||||||
| chr12:116560204 | A | ATATATAT others(25): Show |
1 | a0001c0001t0009g0211 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-102+792_-102+793i others(34): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560204 | ||||||
| chr12:116560211 | T | C | 3 | a0001c0001t0016g0035 a0001c0001t0016g0036 a0001c0001t0021g0037 |
3 | HG02486.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-102+778T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560211 | |||||||
| chr12:116560216 | A | G | 1 | a0001c0001t0015g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-102+783A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560216 | |||||||
| chr12:116560220 | A | G | 1 | a0001c0001t0015g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-102+787A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560220 | |||||||
| chr12:116560221 | T | C | 3 | a0001c0001t0002g0196 a0001c0001t0002g0197 a0001c0001t0003g0107 |
3 | HG00639.hp1 HG01081.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-102+788T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560221 | |||||||
| chr12:116560223 | T | C | 61 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0119 others(58): Show |
83 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.-102+790T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560223 | |||||||
| chr12:116560224 | A | ATATATAT others(11): Show |
1 | a0004c0006t0010g0307 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-102+798_-102+799i others(20): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560224 | ||||||
| chr12:116560225 | T | C | 44 | a0001c0001t0001g0021 a0001c0001t0001g0160 a0001c0001t0001g0161 others(41): Show |
48 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.-102+792T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560225 | |||||||
| chr12:116560226 | A | ATATATAT others(31): Show |
1 | a0001c0001t0016g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-102+808_-102+809i others(40): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560226 | ||||||
| chr12:116560226 | A | ATATATAT others(29): Show |
1 | a0001c0001t0016g0036 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-102+808_-102+809i others(38): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560226 | ||||||
| chr12:116560226 | A | ATATATAT others(27): Show |
1 | a0001c0001t0021g0037 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-102+808_-102+809i others(36): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560226 | ||||||
| chr12:116560226 | A | ATATATAT others(29): Show |
1 | a0001c0001t0010g0028 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-102+808_-102+809i others(38): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560226 | ||||||
| chr12:116560226 | A | G | 2 | a0001c0001t0013g0376 a0001c0001t0015g0034 |
2 | HG02647.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-102+793A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560226 | |||||||
| chr12:116560226 | ATATATAT others(9): Show |
A | 2 | a0001c0001t0002g0336 a0001c0001t0002g0337 |
2 | HG00280.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-102+797_-102+812d others(18): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560226 | ||||||
| chr12:116560228 | A | ATATATAT others(23): Show |
2 | a0002c0002t0016g0038 a0002c0002t0016g0039 |
2 | HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-102+808_-102+809i others(32): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560228 | ||||||
| chr12:116560228 | A | ATATATAT others(21): Show |
1 | a0002c0002t0016g0040 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-102+816_-102+817i others(30): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560228 | ||||||
| chr12:116560228 | A | G | 2 | a0001c0001t0001g0356 a0001c0001t0001g0377 |
2 | NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-102+795A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560228 | |||||||
| chr12:116560228 | ATATATAT others(7): Show |
A | 4 | a0001c0001t0001g0306 a0001c0001t0005g0007 a0001c0001t0017g0304 others(1): Show |
6 | HG01099.hp2 HG01516.hp1 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.-102+799_-102+812d others(16): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560228 | ||||||
| chr12:116560230 | A | G | 2 | a0001c0001t0005g0231 a0001c0001t0013g0376 |
2 | HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-102+797A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560230 | |||||||
| chr12:116560232 | A | G | 3 | a0001c0001t0001g0356 a0001c0001t0001g0377 a0001c0001t0009g0214 |
3 | HG03942.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-102+799A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560232 | |||||||
| chr12:116560233 | T | C | 1 | a0001c0001t0024g0205 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-102+800T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560233 | |||||||
| chr12:116560234 | A | G | 23 | a0001c0001t0001g0232 a0001c0001t0001g0290 a0001c0001t0001g0350 others(20): Show |
24 | HG00558.hp1 HG01074.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.-102+801A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560234 | |||||||
| chr12:116560236 | A | G | 3 | a0001c0001t0001g0356 a0001c0001t0001g0377 a0001c0001t0009g0214 |
3 | HG03942.hp1 NA19030.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-102+803A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560236 | |||||||
| chr12:116560238 | A | G | 186 | a0001c0001t0001g0021 a0001c0001t0001g0112 a0001c0001t0001g0117 others(183): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.-102+805A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560238 | |||||||
| chr12:116560239 | T | G | 1 | a0001c0001t0007g0210 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-102+806T>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560239 | |||||||
| chr12:116560240 | A | G | 1 | a0001c0001t0009g0214 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-102+807A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560240 | |||||||
| chr12:116560242 | G | A | 1 | a0001c0001t0009g0214 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-102+809G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560242 | |||||||
| chr12:116560256 | A | G | 6 | a0001c0001t0004g0333 a0001c0001t0004g0334 a0001c0001t0013g0275 others(3): Show |
7 | HG01109.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-102+823A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560256 | |||||||
| chr12:116560466 | C | T | 1 | a0001c0001t0012g0274 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-102+1033C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560466 | |||||||
| chr12:116560489 | C | T | 1 | a0001c0001t0002g0394 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-102+1056C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560489 | |||||||
| chr12:116560733 | G | T | 1 | a0001c0001t0007g0227 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-102+1300G>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560733 | |||||||
| chr12:116560821 | T | TA | 312 | a0001c0001t0001g0021 a0001c0001t0001g0112 a0001c0001t0001g0117 others(309): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.-102+1401dupA | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116560821 | ||||||
| chr12:116560842 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-102+1409C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560842 | |||||||
| chr12:116560977 | C | G | 1 | a0001c0001t0003g0332 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-102+1544C>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116560977 | |||||||
| chr12:116561003 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-102+1570G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116561003 | |||||||
| chr12:116561207 | C | T | 1 | a0001c0001t0003g0157 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-102+1774C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116561207 | |||||||
| chr12:116561279 | T | TA | 30 | a0001c0001t0001g0232 a0001c0001t0001g0290 a0001c0001t0001g0350 others(27): Show |
31 | HG00558.hp1 HG01074.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.-102+1858dupA | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116561279 | ||||||
| chr12:116561592 | G | A | 3 | a0001c0001t0009g0109 a0001c0001t0009g0110 a0001c0001t0009g0111 |
3 | HG01167.hp2 HG01169.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.-102+2159G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116561592 | |||||||
| chr12:116561714 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-102+2281T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116561714 | |||||||
| chr12:116561737 | C | T | 6 | a0001c0001t0004g0333 a0001c0001t0004g0334 a0001c0001t0013g0275 others(3): Show |
7 | HG01109.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-102+2304C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116561737 | |||||||
| chr12:116561940 | T | A | 1 | a0001c0001t0003g0113 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-102+2507T>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116561940 | |||||||
| chr12:116562021 | CCAGT | C | 117 | a0001c0001t0001g0021 a0001c0001t0001g0160 a0001c0001t0001g0161 others(114): Show |
126 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.-102+2592_-102+259 others(8): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116562021 | ||||||
| chr12:116562055 | G | T | 24 | a0001c0001t0001g0232 a0001c0001t0001g0290 a0001c0001t0001g0350 others(21): Show |
25 | HG00558.hp1 HG01074.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.-102+2622G>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116562055 | |||||||
| chr12:116562056 | T | C | 217 | a0001c0001t0001g0021 a0001c0001t0001g0112 a0001c0001t0001g0117 others(214): Show |
252 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(249): Show |
intron_variant | MODIFIER | c.-102+2623T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116562056 | |||||||
| chr12:116562082 | A | C | 2 | a0001c0001t0023g0242 a0001c0001t0023g0277 |
2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-102+2649A>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116562082 | |||||||
| chr12:116562092 | G | A | 141 | a0001c0001t0001g0021 a0001c0001t0001g0160 a0001c0001t0001g0161 others(138): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.-102+2659G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116562092 | |||||||
| chr12:116562131 | C | T | 141 | a0001c0001t0001g0021 a0001c0001t0001g0160 a0001c0001t0001g0161 others(138): Show |
151 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.-102+2698C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116562131 | |||||||
| chr12:116562153 | G | A | 72 | a0001c0001t0002g0397 a0001c0001t0006g0012 a0001c0001t0006g0033 others(69): Show |
77 | HG00438.hp2 HG00609.hp2 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.-102+2720G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116562153 | |||||||
| chr12:116562184 | G | A | 3 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0116 |
3 | HG00558.hp2 HG00673.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.-102+2751G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116562184 | |||||||
| chr12:116562196 | C | T | 1 | a0001c0001t0003g0157 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-102+2763C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116562196 | |||||||
| chr12:116562227 | A | G | 231 | a0001c0001t0001g0021 a0001c0001t0001g0112 a0001c0001t0001g0117 others(228): Show |
267 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(264): Show |
intron_variant | MODIFIER | c.-102+2794A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116562227 | |||||||
| chr12:116562305 | C | T | 6 | a0001c0001t0001g0221 a0001c0001t0001g0259 a0001c0001t0001g0287 others(3): Show |
6 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(3): Show |
intron_variant | MODIFIER | c.-102+2872C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116562305 | |||||||
| chr12:116562315 | G | A | 2 | a0001c0001t0017g0304 a0001c0001t0017g0305 |
2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-102+2882G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116562315 | |||||||
| chr12:116562391 | G | A | 225 | a0001c0001t0001g0021 a0001c0001t0001g0112 a0001c0001t0001g0117 others(222): Show |
261 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(258): Show |
intron_variant | MODIFIER | c.-102+2958G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116562391 | |||||||
| chr12:116562539 | C | T | 13 | a0001c0001t0006g0081 a0001c0001t0006g0086 a0001c0001t0006g0088 others(10): Show |
13 | HG00621.hp1 HG02027.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.-102+3106C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116562539 | |||||||
| chr12:116562757 | C | T | 1 | a0001c0001t0004g0333 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-102+3324C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116562757 | |||||||
| chr12:116562760 | T | C | 7 | a0001c0001t0006g0033 a0001c0001t0010g0009 a0001c0001t0018g0029 others(4): Show |
9 | HG01168.hp1 HG01169.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-102+3327T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116562760 | |||||||
| chr12:116562770 | C | T | 6 | a0001c0001t0004g0333 a0001c0001t0004g0334 a0001c0001t0013g0275 others(3): Show |
7 | HG01109.hp2 HG02809.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-102+3337C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116562770 | |||||||
| chr12:116562950 | C | A | 114 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0119 others(111): Show |
141 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.-102+3517C>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116562950 | |||||||
| chr12:116563002 | T | C | 24 | a0001c0001t0001g0232 a0001c0001t0001g0290 a0001c0001t0001g0350 others(21): Show |
25 | HG00558.hp1 HG01074.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.-102+3569T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116563002 | |||||||
| chr12:116563002 | T | G | 1 | a0001c0001t0001g0117 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-102+3569T>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116563002 | |||||||
| chr12:116563008 | C | A | 2 | a0001c0001t0002g0158 a0001c0001t0002g0159 |
2 | NA18991.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.-102+3575C>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116563008 | |||||||
| chr12:116563025 | G | A | 2 | a0001c0001t0002g0360 a0001c0001t0005g0361 |
2 | HG00323.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-102+3592G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116563025 | |||||||
| chr12:116563044 | C | T | 1 | a0001c0001t0006g0092 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-102+3611C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116563044 | |||||||
| chr12:116563206 | A | G | 1 | a0001c0001t0003g0020 | 2 | HG02027.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-102+3773A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116563206 | |||||||
| chr12:116563222 | G | T | 1 | a0001c0001t0001g0306 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-102+3789G>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116563222 | |||||||
| chr12:116563295 | A | T | 1 | a0001c0001t0001g0117 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-102+3862A>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116563295 | |||||||
| chr12:116563320 | TG | T | 74 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0119 others(71): Show |
99 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(96): Show |
intron_variant | MODIFIER | c.-102+3888delG | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116563320 | |||||||
| chr12:116563388 | C | G | 84 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0119 others(81): Show |
109 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(106): Show |
intron_variant | MODIFIER | c.-102+3955C>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116563388 | |||||||
| chr12:116563540 | G | T | 138 | a0001c0001t0001g0021 a0001c0001t0001g0160 a0001c0001t0001g0161 others(135): Show |
148 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.-102+4107G>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116563540 | |||||||
| chr12:116563542 | T | A | 1 | a0001c0001t0003g0332 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-102+4109T>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116563542 | |||||||
| chr12:116563564 | A | G | 2 | a0001c0001t0009g0194 a0001c0001t0012g0193 |
2 | HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-102+4131A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116563564 | |||||||
| chr12:116563635 | A | G | 1 | a0001c0001t0002g0330 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-102+4202A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116563635 | |||||||
| chr12:116564202 | A | G | 4 | a0001c0001t0015g0034 a0001c0001t0016g0035 a0001c0001t0016g0036 others(1): Show |
4 | HG02486.hp1 HG02976.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-102+4769A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116564202 | |||||||
| chr12:116564225 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-102+4792T>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116564225 | |||||||
| chr12:116564295 | T | C | 1 | a0001c0001t0002g0293 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-102+4862T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116564295 | |||||||
| chr12:116564393 | A | AT | 80 | a0001c0001t0001g0112 a0001c0001t0001g0119 a0001c0001t0001g0122 others(77): Show |
105 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(102): Show |
intron_variant | MODIFIER | c.-102+4972dupT | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116564393 | ||||||
| chr12:116564588 | G | C | 41 | a0001c0001t0001g0021 a0001c0001t0001g0160 a0001c0001t0001g0161 others(38): Show |
45 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.-102+5155G>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116564588 | |||||||
| chr12:116564853 | G | A | 78 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0119 others(75): Show |
103 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(100): Show |
intron_variant | MODIFIER | c.-102+5420G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116564853 | |||||||
| chr12:116564943 | A | C | 1 | a0001c0001t0013g0262 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-102+5510A>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116564943 | |||||||
| chr12:116565071 | G | A | 41 | a0001c0001t0001g0021 a0001c0001t0001g0160 a0001c0001t0001g0161 others(38): Show |
45 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.-102+5638G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116565071 | |||||||
| chr12:116565117 | C | T | 1 | a0001c0001t0009g0372 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-102+5684C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116565117 | |||||||
| chr12:116565248 | T | G | 1 | a0001c0004t0006g0044 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-102+5815T>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116565248 | |||||||
| chr12:116565348 | C | T | 2 | a0002c0002t0005g0155 a0002c0002t0005g0156 |
2 | HG01175.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-102+5915C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116565348 | |||||||
| chr12:116565386 | C | T | 64 | a0001c0001t0001g0021 a0001c0001t0001g0160 a0001c0001t0001g0161 others(61): Show |
69 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.-102+5953C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116565386 | |||||||
| chr12:116565451 | C | G | 1 | a0001c0001t0006g0033 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-102+6018C>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116565451 | |||||||
| chr12:116565451 | C | T | 1 | a0001c0001t0004g0192 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-102+6018C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116565451 | |||||||
| chr12:116565605 | T | C | 1 | a0002c0002t0009g0357 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-102+6172T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116565605 | |||||||
| chr12:116565766 | C | T | 1 | a0001c0001t0027g0078 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-102+6333C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116565766 | |||||||
| chr12:116565937 | G | A | 10 | a0001c0001t0010g0028 a0001c0001t0015g0034 a0001c0001t0016g0035 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-102+6504G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116565937 | |||||||
| chr12:116565981 | G | A | 5 | a0001c0001t0004g0024 a0001c0001t0004g0204 a0001c0001t0004g0222 others(2): Show |
6 | HG01074.hp2 HG02109.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-102+6548G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116565981 | |||||||
| chr12:116566035 | C | T | 1 | a0001c0001t0002g0393 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-102+6602C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116566035 | |||||||
| chr12:116566159 | C | T | 1 | a0001c0001t0005g0257 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-102+6726C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116566159 | |||||||
| chr12:116566181 | G | C | 1 | a0001c0001t0012g0193 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-102+6748G>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116566181 | |||||||
| chr12:116566182 | G | C | 1 | a0001c0001t0013g0118 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-102+6749G>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116566182 | |||||||
| chr12:116566209 | T | C | 1 | a0001c0001t0001g0362 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-102+6776T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116566209 | |||||||
| chr12:116566371 | A | G | 1 | a0001c0001t0005g0378 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-102+6938A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116566371 | |||||||
| chr12:116566538 | G | GTTGTTTT others(1): Show |
22 | a0001c0001t0004g0333 a0001c0001t0004g0334 a0001c0001t0005g0378 others(19): Show |
23 | HG01109.hp2 HG01243.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.-102+7110_-102+711 others(12): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566538 | ||||||
| chr12:116566585 | G | A | 4 | a0003c0003t0011g0008 a0003c0003t0011g0399 a0003c0003t0011g0400 others(1): Show |
6 | HG02717.hp2 HG02886.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-102+7152G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116566585 | |||||||
| chr12:116566616 | T | TA | 75 | a0001c0001t0001g0171 a0001c0001t0001g0173 a0001c0001t0001g0176 others(72): Show |
81 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.-102+7206dupA | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566616 | ||||||
| chr12:116566616 | T | TAA | 70 | a0001c0001t0001g0021 a0001c0001t0001g0117 a0001c0001t0001g0142 others(67): Show |
89 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.-102+7205_-102+720 others(6): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566616 | ||||||
| chr12:116566616 | T | TAAA | 40 | a0001c0001t0001g0112 a0001c0001t0001g0130 a0001c0001t0001g0131 others(37): Show |
49 | HG00733.hp1 HG00735.hp1 HG01071.hp2 others(46): Show |
intron_variant | MODIFIER | c.-102+7204_-102+720 others(7): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566616 | ||||||
| chr12:116566616 | T | TAAAA | 48 | a0001c0001t0001g0119 a0001c0001t0001g0122 a0001c0001t0001g0124 others(45): Show |
49 | HG00621.hp1 HG00639.hp2 HG01069.hp1 others(46): Show |
intron_variant | MODIFIER | c.-102+7203_-102+720 others(8): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566616 | ||||||
| chr12:116566616 | T | TAAAAA | 8 | a0001c0001t0006g0048 a0001c0001t0006g0081 a0001c0001t0008g0094 others(5): Show |
8 | HG00438.hp2 HG00609.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-102+7202_-102+720 others(9): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566616 | ||||||
| chr12:116566616 | TA | T | 7 | a0001c0001t0001g0375 a0001c0001t0001g0384 a0001c0001t0002g0229 others(4): Show |
7 | HG01167.hp1 NA18948.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.-102+7206delA | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566616 | ||||||
| chr12:116566616 | TAA | T | 11 | a0001c0001t0004g0333 a0001c0001t0004g0334 a0001c0001t0005g0378 others(8): Show |
12 | HG01109.hp2 HG02809.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.-102+7205_-102+720 others(6): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566616 | ||||||
| chr12:116566616 | TAAAAAAA others(7): Show |
T | 10 | a0001c0001t0010g0028 a0001c0001t0015g0034 a0001c0001t0016g0035 others(7): Show |
10 | HG01243.hp1 HG02055.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-102+7193_-102+720 others(18): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566616 | ||||||
| chr12:116566651 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-102+7218G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116566651 | |||||||
| chr12:116566768 | C | G | 1 | a0001c0001t0002g0322 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-102+7335C>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116566768 | |||||||
| chr12:116566930 | C | CA | 31 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0296 others(28): Show |
33 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.-102+7538dupA | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566930 | ||||||
| chr12:116566930 | C | CAA | 42 | a0001c0001t0001g0217 a0001c0001t0001g0239 a0001c0001t0001g0240 others(39): Show |
42 | HG00438.hp1 HG00609.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-102+7537_-102+753 others(6): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566930 | ||||||
| chr12:116566930 | C | CAAA | 24 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0237 others(21): Show |
24 | HG00140.hp2 HG00621.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-102+7536_-102+753 others(7): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566930 | ||||||
| chr12:116566930 | C | CAAAA | 6 | a0001c0001t0001g0236 a0001c0001t0001g0259 a0001c0001t0001g0287 others(3): Show |
6 | HG00735.hp2 HG01069.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.-102+7535_-102+753 others(8): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566930 | ||||||
| chr12:116566930 | CA | C | 25 | a0001c0001t0001g0207 a0001c0001t0001g0302 a0001c0001t0001g0327 others(22): Show |
25 | HG00280.hp1 HG00733.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-102+7538delA | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566930 | ||||||
| chr12:116566930 | CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0004g0334 a0001c0001t0013g0275 |
2 | HG01109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-102+7529_-102+753 others(14): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566930 | ||||||
| chr12:116566930 | CAAAAAAA others(4): Show |
C | 13 | a0001c0001t0001g0161 a0001c0001t0002g0284 a0001c0001t0002g0337 others(10): Show |
14 | HG00280.hp2 HG02165.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.-102+7528_-102+753 others(15): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566930 | ||||||
| chr12:116566930 | CAAAAAAA others(5): Show |
C | 37 | a0001c0001t0001g0163 a0001c0001t0001g0171 a0001c0001t0001g0232 others(34): Show |
39 | HG00323.hp1 HG00558.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.-102+7527_-102+753 others(16): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566930 | ||||||
| chr12:116566930 | CAAAAAAA others(6): Show |
C | 87 | a0001c0001t0001g0021 a0001c0001t0001g0119 a0001c0001t0001g0160 others(84): Show |
95 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.-102+7526_-102+753 others(17): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566930 | ||||||
| chr12:116566930 | CAAAAAAA others(7): Show |
C | 23 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0169 others(20): Show |
23 | HG00639.hp2 HG01891.hp1 HG02004.hp1 others(20): Show |
intron_variant | MODIFIER | c.-102+7525_-102+753 others(18): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566930 | ||||||
| chr12:116566930 | CAAAAAAA others(8): Show |
C | 60 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0122 others(57): Show |
82 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(79): Show |
intron_variant | MODIFIER | c.-102+7524_-102+753 others(19): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566930 | ||||||
| chr12:116566930 | CAAAAAAA others(9): Show |
C | 6 | a0001c0001t0003g0107 a0001c0001t0003g0134 a0001c0001t0003g0154 others(3): Show |
6 | HG02004.hp2 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-102+7523_-102+753 others(20): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566930 | ||||||
| chr12:116566930 | CAAAAAAA others(10): Show |
C | 4 | a0001c0001t0002g0295 a0003c0003t0011g0008 a0003c0003t0011g0399 others(1): Show |
6 | HG02717.hp2 HG02970.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-102+7522_-102+753 others(21): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566930 | ||||||
| chr12:116566930 | CAAAAAAA others(12): Show |
C | 2 | a0001c0001t0010g0028 a0001c0001t0012g0328 |
2 | HG01243.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-102+7520_-102+753 others(23): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566930 | ||||||
| chr12:116566930 | CAAAAAAA others(13): Show |
C | 2 | a0001c0001t0005g0241 a0001c0001t0007g0025 |
3 | HG01891.hp2 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-102+7519_-102+753 others(24): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566930 | ||||||
| chr12:116566930 | CAAAAAAA others(19): Show |
C | 1 | a0001c0001t0013g0262 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-102+7513_-102+753 others(30): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566930 | ||||||
| chr12:116566930 | CAAAAAAA others(22): Show |
C | 1 | a0001c0001t0026g0198 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-102+7510_-102+753 others(33): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566930 | ||||||
| chr12:116566984 | A | AAACTGC | 4 | a0003c0003t0011g0008 a0003c0003t0011g0399 a0003c0003t0011g0400 others(1): Show |
6 | HG02717.hp2 HG02886.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-102+7553_-102+755 others(10): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116566984 | ||||||
| chr12:116567042 | C | T | 96 | a0001c0001t0001g0201 a0001c0001t0001g0217 a0001c0001t0001g0221 others(93): Show |
98 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(95): Show |
intron_variant | MODIFIER | c.-102+7609C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116567042 | |||||||
| chr12:116567102 | G | A | 3 | a0002c0002t0016g0038 a0002c0002t0016g0039 a0002c0002t0016g0040 |
3 | HG02055.hp2 HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-102+7669G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116567102 | |||||||
| chr12:116567122 | C | G | 13 | a0001c0001t0001g0117 a0001c0001t0001g0152 a0001c0001t0001g0202 others(10): Show |
17 | HG02165.hp1 NA18947.hp1 NA18954.hp2 others(14): Show |
intron_variant | MODIFIER | c.-102+7689C>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116567122 | |||||||
| chr12:116567194 | T | C | 15 | a0001c0001t0004g0024 a0001c0001t0004g0204 a0001c0001t0004g0206 others(12): Show |
16 | HG01074.hp2 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-102+7761T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116567194 | |||||||
| chr12:116567200 | T | C | 7 | a0001c0001t0006g0033 a0001c0001t0010g0009 a0001c0001t0018g0029 others(4): Show |
9 | HG01168.hp1 HG01169.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-102+7767T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116567200 | |||||||
| chr12:116567259 | G | T | 59 | a0001c0001t0001g0021 a0001c0001t0001g0119 a0001c0001t0001g0160 others(56): Show |
65 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.-102+7826G>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116567259 | |||||||
| chr12:116567267 | T | C | 50 | a0001c0001t0001g0324 a0001c0001t0002g0397 a0001c0001t0006g0066 others(47): Show |
51 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.-102+7834T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116567267 | |||||||
| chr12:116567448 | C | CT | 82 | a0001c0001t0001g0166 a0001c0001t0001g0185 a0001c0001t0001g0232 others(79): Show |
86 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.-102+8032dupT | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116567448 | ||||||
| chr12:116567448 | CT | C | 93 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0122 others(90): Show |
119 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(116): Show |
intron_variant | MODIFIER | c.-102+8032delT | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116567448 | ||||||
| chr12:116567514 | G | A | 1 | a0001c0001t0013g0385 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-102+8081G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116567514 | |||||||
| chr12:116567542 | G | A | 333 | a0001c0001t0001g0021 a0001c0001t0001g0112 a0001c0001t0001g0117 others(330): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.-102+8109G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116567542 | |||||||
| chr12:116567623 | C | A | 1 | a0001c0001t0015g0034 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-102+8190C>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116567623 | |||||||
| chr12:116567699 | G | A | 1 | a0001c0001t0013g0262 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-101-8143G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116567699 | |||||||
| chr12:116567759 | T | TA | 4 | a0001c0001t0010g0075 a0002c0002t0009g0357 a0002c0002t0009g0358 others(1): Show |
4 | HG00735.hp1 HG02280.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-101-8076dupA | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116567759 | ||||||
| chr12:116567765 | A | T | 1 | a0001c0001t0001g0207 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-101-8077A>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116567765 | |||||||
| chr12:116567767 | T | A | 122 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0217 others(119): Show |
128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.-101-8075T>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116567767 | |||||||
| chr12:116567769 | T | A | 3 | a0001c0001t0001g0350 a0001c0001t0001g0351 a0001c0001t0019g0070 |
3 | HG02145.hp1 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-101-8073T>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116567769 | |||||||
| chr12:116567775 | T | C | 2 | a0001c0001t0013g0190 a0002c0002t0034g0338 |
2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-101-8067T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116567775 | |||||||
| chr12:116567800 | G | A | 61 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0122 others(58): Show |
83 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.-101-8042G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116567800 | |||||||
| chr12:116567857 | C | A | 1 | a0001c0001t0010g0056 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-101-7985C>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116567857 | |||||||
| chr12:116567904 | T | C | 85 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0122 others(82): Show |
109 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(106): Show |
intron_variant | MODIFIER | c.-101-7938T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116567904 | |||||||
| chr12:116567953 | G | C | 1 | a0001c0001t0005g0186 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-101-7889G>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116567953 | |||||||
| chr12:116568040 | A | G | 84 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0122 others(81): Show |
108 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(105): Show |
intron_variant | MODIFIER | c.-101-7802A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116568040 | |||||||
| chr12:116568041 | G | C | 1 | a0001c0001t0002g0255 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-101-7801G>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116568041 | |||||||
| chr12:116568047 | A | G | 399 | a0001c0001t0001g0021 a0001c0001t0001g0112 a0001c0001t0001g0117 others(396): Show |
440 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(437): Show |
intron_variant | MODIFIER | c.-101-7795A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116568047 | |||||||
| chr12:116568128 | C | T | 1 | a0001c0001t0004g0183 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-101-7714C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116568128 | |||||||
| chr12:116568317 | G | A | 2 | a0001c0001t0001g0296 a0001c0001t0003g0381 |
2 | HG00597.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.-101-7525G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116568317 | |||||||
| chr12:116568472 | G | A | 11 | a0001c0001t0001g0232 a0001c0001t0001g0290 a0001c0001t0001g0350 others(8): Show |
11 | HG00558.hp1 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.-101-7370G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116568472 | |||||||
| chr12:116568570 | A | G | 2 | a0001c0001t0023g0242 a0001c0001t0023g0277 |
2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-101-7272A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116568570 | |||||||
| chr12:116568835 | T | C | 1 | a0002c0002t0014g0032 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-101-7007T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116568835 | |||||||
| chr12:116568868 | C | CT | 215 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0217 others(212): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.-101-6960dupT | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116568868 | ||||||
| chr12:116568868 | C | CTT | 74 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0122 others(71): Show |
97 | HG00544.hp1 HG00558.hp2 HG00673.hp1 others(94): Show |
intron_variant | MODIFIER | c.-101-6961_-101-696 others(6): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116568868 | ||||||
| chr12:116568892 | T | TCTCA | 291 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0122 others(288): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-101-6947_-101-694 others(8): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116568892 | ||||||
| chr12:116568930 | A | G | 26 | a0001c0001t0004g0137 a0001c0001t0005g0378 a0001c0001t0006g0033 others(23): Show |
28 | HG01106.hp2 HG01167.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.-101-6912A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116568930 | |||||||
| chr12:116569009 | A | G | 344 | a0001c0001t0001g0021 a0001c0001t0001g0112 a0001c0001t0001g0117 others(341): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.-101-6833A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116569009 | |||||||
| chr12:116569015 | A | T | 291 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0122 others(288): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.-101-6827A>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116569015 | |||||||
| chr12:116569083 | C | T | 3 | a0002c0002t0016g0038 a0002c0002t0016g0039 a0002c0002t0016g0040 |
3 | HG02055.hp2 HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-101-6759C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116569083 | |||||||
| chr12:116569105 | G | A | 216 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0122 others(213): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.-101-6737G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116569105 | |||||||
| chr12:116569110 | C | T | 1 | a0001c0001t0026g0198 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-101-6732C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116569110 | |||||||
| chr12:116569153 | C | T | 4 | a0001c0001t0006g0081 a0001c0001t0006g0088 a0001c0001t0006g0089 others(1): Show |
4 | NA18942.hp1 NA18966.hp1 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.-101-6689C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116569153 | |||||||
| chr12:116569157 | C | T | 14 | a0001c0001t0001g0217 a0001c0001t0001g0236 a0001c0001t0001g0237 others(11): Show |
14 | HG00621.hp2 NA18948.hp1 NA18952.hp1 others(11): Show |
intron_variant | MODIFIER | c.-101-6685C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116569157 | |||||||
| chr12:116569172 | C | G | 74 | a0001c0001t0001g0324 a0001c0001t0004g0137 a0001c0001t0005g0378 others(71): Show |
77 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.-101-6670C>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116569172 | |||||||
| chr12:116569327 | G | A | 3 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0191 |
3 | HG02723.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-101-6515G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116569327 | |||||||
| chr12:116569419 | C | A | 9 | a0001c0001t0004g0137 a0001c0001t0007g0125 a0001c0001t0007g0135 others(6): Show |
9 | HG01106.hp2 HG01167.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-101-6423C>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116569419 | |||||||
| chr12:116569469 | G | A | 46 | a0001c0001t0001g0021 a0001c0001t0001g0119 a0001c0001t0001g0160 others(43): Show |
51 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.-101-6373G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116569469 | |||||||
| chr12:116569571 | T | C | 161 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0122 others(158): Show |
188 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(185): Show |
intron_variant | MODIFIER | c.-101-6271T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116569571 | |||||||
| chr12:116569692 | A | G | 1 | a0001c0001t0007g0187 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-101-6150A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116569692 | |||||||
| chr12:116569709 | C | A | 1 | a0001c0001t0005g0186 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-101-6133C>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116569709 | |||||||
| chr12:116569791 | C | T | 1 | a0001c0001t0024g0205 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-101-6051C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116569791 | |||||||
| chr12:116569814 | G | A | 4 | a0001c0001t0005g0188 a0001c0001t0005g0189 a0001c0001t0005g0191 others(1): Show |
4 | HG02723.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-101-6028G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116569814 | |||||||
| chr12:116569851 | C | T | 3 | a0002c0002t0009g0357 a0002c0002t0009g0358 a0002c0002t0014g0032 |
3 | HG02280.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-101-5991C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116569851 | |||||||
| chr12:116569879 | A | C | 110 | a0001c0001t0001g0021 a0001c0001t0001g0119 a0001c0001t0001g0160 others(107): Show |
118 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-101-5963A>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116569879 | |||||||
| chr12:116570008 | C | T | 4 | a0001c0001t0005g0378 a0002c0002t0009g0357 a0002c0002t0009g0358 others(1): Show |
4 | HG02280.hp1 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-101-5834C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116570008 | |||||||
| chr12:116570010 | C | T | 1 | a0001c0001t0003g0170 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-101-5832C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116570010 | |||||||
| chr12:116570271 | C | T | 1 | a0001c0001t0008g0053 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-101-5571C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116570271 | |||||||
| chr12:116570346 | C | T | 2 | a0001c0001t0025g0027 a0002c0002t0035g0335 |
3 | HG02809.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-101-5496C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116570346 | |||||||
| chr12:116570371 | G | A | 2 | a0001c0001t0002g0284 a0001c0001t0015g0091 |
2 | HG02165.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.-101-5471G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116570371 | |||||||
| chr12:116570480 | G | T | 3 | a0001c0001t0010g0028 a0002c0002t0005g0155 a0002c0002t0005g0156 |
3 | HG01175.hp1 HG01243.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-101-5362G>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116570480 | |||||||
| chr12:116570518 | A | G | 109 | a0001c0001t0001g0124 a0001c0001t0001g0133 a0001c0001t0001g0148 others(106): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(110): Show |
intron_variant | MODIFIER | c.-101-5324A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116570518 | |||||||
| chr12:116570564 | G | T | 50 | a0001c0001t0001g0021 a0001c0001t0001g0132 a0001c0001t0001g0160 others(47): Show |
52 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.-101-5278G>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116570564 | |||||||
| chr12:116570667 | T | C | 1 | a0001c0001t0005g0257 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-101-5175T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116570667 | |||||||
| chr12:116570669 | T | C | 1 | a0001c0001t0005g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-101-5173T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116570669 | |||||||
| chr12:116570670 | G | A | 1 | a0001c0001t0005g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-101-5172G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116570670 | |||||||
| chr12:116570780 | C | G | 121 | a0001c0001t0001g0117 a0001c0001t0001g0145 a0001c0001t0001g0152 others(118): Show |
124 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.-101-5062C>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116570780 | |||||||
| chr12:116571005 | C | A | 6 | a0001c0001t0005g0007 a0001c0001t0005g0103 a0001c0001t0005g0172 others(3): Show |
8 | HG01099.hp2 HG01168.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.-101-4837C>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116571005 | |||||||
| chr12:116571010 | T | A | 7 | a0001c0001t0001g0319 a0001c0001t0005g0007 a0001c0001t0005g0103 others(4): Show |
9 | HG00099.hp2 HG01099.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.-101-4832T>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116571010 | |||||||
| chr12:116571121 | C | T | 3 | a0001c0001t0007g0104 a0001c0001t0007g0292 a0001c0001t0010g0009 |
4 | HG02280.hp2 HG03195.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-101-4721C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116571121 | |||||||
| chr12:116571131 | A | G | 1 | a0001c0001t0010g0028 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-101-4711A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116571131 | |||||||
| chr12:116571446 | G | A | 1 | a0001c0001t0004g0247 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-101-4396G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116571446 | |||||||
| chr12:116571458 | C | CT | 72 | a0001c0001t0001g0119 a0001c0001t0001g0130 a0001c0001t0001g0131 others(69): Show |
84 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.-101-4344dupT | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571458 | ||||||
| chr12:116571458 | C | CTT | 61 | a0001c0001t0001g0021 a0001c0001t0001g0112 a0001c0001t0001g0117 others(58): Show |
68 | HG00408.hp2 HG00621.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.-101-4345_-101-434 others(6): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571458 | ||||||
| chr12:116571458 | C | CTTT | 28 | a0001c0001t0001g0145 a0001c0001t0001g0169 a0001c0001t0001g0224 others(25): Show |
29 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.-101-4346_-101-434 others(7): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571458 | ||||||
| chr12:116571458 | C | CTTTT | 6 | a0001c0001t0003g0019 a0001c0001t0003g0123 a0001c0001t0003g0157 others(3): Show |
7 | HG00438.hp2 HG01192.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.-101-4347_-101-434 others(8): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571458 | ||||||
| chr12:116571458 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0032g0233 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-101-4353_-101-434 others(14): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571458 | ||||||
| chr12:116571458 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0009g0349 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-101-4358_-101-434 others(19): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571458 | ||||||
| chr12:116571458 | CT | C | 6 | a0001c0001t0003g0105 a0001c0001t0004g0299 a0001c0001t0007g0025 others(3): Show |
7 | HG01891.hp2 HG02572.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.-101-4344delT | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571458 | ||||||
| chr12:116571458 | CTT | C | 11 | a0001c0001t0007g0187 a0001c0001t0011g0129 a0001c0001t0012g0164 others(8): Show |
11 | HG02451.hp2 HG02559.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-101-4345_-101-434 others(6): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571458 | ||||||
| chr12:116571458 | CTTT | C | 10 | a0001c0001t0007g0104 a0001c0001t0007g0292 a0001c0001t0011g0005 others(7): Show |
12 | HG00558.hp1 HG01884.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-101-4346_-101-434 others(7): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571458 | ||||||
| chr12:116571458 | CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0009g0194 a0001c0001t0009g0326 a0001c0001t0009g0331 |
3 | HG01884.hp1 HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-101-4353_-101-434 others(14): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571458 | ||||||
| chr12:116571458 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0202 a0001c0001t0001g0256 a0001c0001t0001g0383 others(1): Show |
4 | HG00741.hp2 HG01358.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.-101-4354_-101-434 others(15): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571458 | ||||||
| chr12:116571458 | CTTTTTTT others(5): Show |
C | 8 | a0001c0001t0001g0221 a0001c0001t0001g0259 a0001c0001t0001g0276 others(5): Show |
8 | HG00099.hp1 HG01069.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.-101-4355_-101-434 others(16): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571458 | ||||||
| chr12:116571458 | CTTTTTTT others(6): Show |
C | 14 | a0001c0001t0001g0176 a0001c0001t0002g0100 a0001c0001t0002g0101 others(11): Show |
14 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-101-4356_-101-434 others(17): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571458 | ||||||
| chr12:116571458 | CTTTTTTT others(7): Show |
C | 33 | a0001c0001t0001g0163 a0001c0001t0001g0171 a0001c0001t0001g0173 others(30): Show |
33 | HG00735.hp2 HG01106.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.-101-4357_-101-434 others(18): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571458 | ||||||
| chr12:116571458 | CTTTTTTT others(8): Show |
C | 88 | a0001c0001t0001g0285 a0001c0001t0002g0004 a0001c0001t0002g0016 others(85): Show |
98 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.-101-4358_-101-434 others(19): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571458 | ||||||
| chr12:116571458 | CTTTTTTT others(9): Show |
C | 13 | a0001c0001t0002g0158 a0001c0001t0002g0298 a0001c0001t0004g0024 others(10): Show |
14 | HG01074.hp2 HG01109.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.-101-4359_-101-434 others(20): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571458 | ||||||
| chr12:116571458 | CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0004g0230 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-101-4360_-101-434 others(21): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571458 | ||||||
| chr12:116571458 | CTTTTTTT others(11): Show |
C | 5 | a0001c0001t0002g0269 a0001c0001t0002g0300 a0001c0001t0004g0318 others(2): Show |
5 | HG02040.hp1 HG02080.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.-101-4361_-101-434 others(22): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571458 | ||||||
| chr12:116571458 | CTTTTTTT others(13): Show |
C | 3 | a0001c0001t0007g0125 a0001c0001t0007g0135 a0001c0001t0010g0009 |
4 | HG01243.hp2 HG03195.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-101-4363_-101-434 others(24): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571458 | ||||||
| chr12:116571458 | CTTTTTTT others(21): Show |
C | 1 | a0001c0001t0004g0317 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-101-4371_-101-434 others(32): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571458 | ||||||
| chr12:116571503 | C | T | 2 | a0001c0001t0001g0278 a0001c0001t0001g0283 |
2 | HG00438.hp1 HG00544.hp2 |
intron_variant | MODIFIER | c.-101-4339C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116571503 | |||||||
| chr12:116571552 | C | G | 7 | a0001c0001t0013g0262 a0001c0001t0013g0376 a0001c0001t0024g0205 others(4): Show |
8 | HG02647.hp1 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-101-4290C>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116571552 | |||||||
| chr12:116571566 | C | G | 2 | a0001c0001t0007g0125 a0001c0001t0007g0135 |
2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-101-4276C>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116571566 | |||||||
| chr12:116571573 | C | T | 2 | a0002c0002t0005g0155 a0002c0002t0005g0156 |
2 | HG01175.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-101-4269C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116571573 | |||||||
| chr12:116571702 | C | G | 26 | a0001c0001t0004g0024 a0001c0001t0004g0137 a0001c0001t0004g0204 others(23): Show |
30 | HG01074.hp2 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.-101-4140C>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116571702 | |||||||
| chr12:116571711 | A | G | 212 | a0001c0001t0001g0374 a0001c0001t0002g0004 a0001c0001t0002g0016 others(209): Show |
229 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.-101-4131A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116571711 | |||||||
| chr12:116571717 | G | A | 1 | a0001c0001t0003g0107 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-101-4125G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116571717 | |||||||
| chr12:116571723 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0152 |
2 | NA18970.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.-101-4119C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116571723 | |||||||
| chr12:116571759 | A | G | 212 | a0001c0001t0001g0374 a0001c0001t0002g0004 a0001c0001t0002g0016 others(209): Show |
229 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.-101-4083A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116571759 | |||||||
| chr12:116571830 | C | T | 101 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0023 others(98): Show |
106 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-101-4012C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116571830 | |||||||
| chr12:116571876 | G | T | 3 | a0001c0001t0024g0205 a0001c0001t0024g0359 a0001c0001t0028g0068 |
3 | HG02647.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-101-3966G>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116571876 | |||||||
| chr12:116571892 | G | GT | 6 | a0001c0001t0001g0279 a0001c0001t0001g0310 a0001c0001t0008g0090 others(3): Show |
6 | HG02647.hp1 HG03041.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-101-3939dupT | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571892 | ||||||
| chr12:116571911 | A | T | 1 | a0003c0003t0011g0401 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-101-3931A>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116571911 | |||||||
| chr12:116571965 | C | CA | 190 | a0001c0001t0001g0130 a0001c0001t0001g0310 a0001c0001t0002g0004 others(187): Show |
219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.-101-3866dupA | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116571965 | ||||||
| chr12:116571975 | A | C | 8 | a0001c0001t0009g0214 a0001c0001t0009g0372 a0001c0001t0014g0011 others(5): Show |
8 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-101-3867A>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116571975 | |||||||
| chr12:116572025 | G | A | 212 | a0001c0001t0001g0374 a0001c0001t0002g0004 a0001c0001t0002g0016 others(209): Show |
229 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.-101-3817G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116572025 | |||||||
| chr12:116572027 | G | A | 77 | a0001c0001t0001g0374 a0001c0001t0004g0022 a0001c0001t0004g0183 others(74): Show |
85 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.-101-3815G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116572027 | |||||||
| chr12:116572129 | C | A | 1 | a0002c0002t0034g0338 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-101-3713C>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116572129 | |||||||
| chr12:116572187 | C | T | 1 | a0001c0001t0007g0210 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-101-3655C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116572187 | |||||||
| chr12:116572316 | T | C | 11 | a0001c0001t0013g0098 a0001c0001t0013g0099 a0001c0001t0013g0118 others(8): Show |
12 | HG02109.hp2 HG02145.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.-101-3526T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116572316 | |||||||
| chr12:116572369 | C | CT | 21 | a0001c0001t0001g0250 a0001c0001t0001g0310 a0001c0001t0001g0324 others(18): Show |
22 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.-101-3460dupT | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116572369 | ||||||
| chr12:116572369 | C | CTT | 12 | a0001c0001t0005g0172 a0001c0001t0013g0098 a0001c0001t0013g0099 others(9): Show |
13 | HG02109.hp2 HG02145.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.-101-3461_-101-346 others(6): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116572369 | ||||||
| chr12:116572369 | C | CTTT | 46 | a0001c0001t0001g0374 a0001c0001t0001g0391 a0001c0001t0004g0022 others(43): Show |
51 | HG00423.hp2 HG00597.hp1 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.-101-3462_-101-346 others(7): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116572369 | ||||||
| chr12:116572369 | C | CTTTT | 22 | a0001c0001t0009g0211 a0001c0001t0011g0005 a0001c0001t0011g0129 others(19): Show |
24 | HG00323.hp2 HG00558.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.-101-3463_-101-346 others(8): Show |
MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116572369 | ||||||
| chr12:116572369 | CT | C | 186 | a0001c0001t0001g0117 a0001c0001t0001g0130 a0001c0001t0001g0152 others(183): Show |
215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.-101-3460delT | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116572369 | ||||||
| chr12:116572607 | G | T | 1 | a0001c0001t0010g0009 | 2 | HG03195.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-101-3235G>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116572607 | |||||||
| chr12:116572619 | C | T | 3 | a0002c0002t0009g0357 a0002c0002t0009g0358 a0002c0002t0014g0032 |
3 | HG02280.hp1 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-101-3223C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116572619 | |||||||
| chr12:116572653 | G | A | 103 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0023 others(100): Show |
108 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-101-3189G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116572653 | |||||||
| chr12:116572775 | A | C | 15 | a0001c0001t0004g0024 a0001c0001t0004g0137 a0001c0001t0004g0204 others(12): Show |
16 | HG01074.hp2 HG01109.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-101-3067A>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116572775 | |||||||
| chr12:116572789 | A | G | 103 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0023 others(100): Show |
108 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-101-3053A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116572789 | |||||||
| chr12:116572799 | C | G | 90 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0023 others(87): Show |
95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.-101-3043C>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116572799 | |||||||
| chr12:116572856 | G | A | 22 | a0001c0001t0004g0024 a0001c0001t0004g0137 a0001c0001t0004g0204 others(19): Show |
23 | HG01074.hp2 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.-101-2986G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116572856 | |||||||
| chr12:116572962 | G | C | 3 | a0002c0002t0016g0038 a0002c0002t0016g0039 a0002c0002t0016g0040 |
3 | HG02055.hp2 HG02559.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-101-2880G>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116572962 | |||||||
| chr12:116573001 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-101-2841C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116573001 | |||||||
| chr12:116573190 | C | T | 3 | a0001c0001t0009g0109 a0001c0001t0009g0110 a0001c0001t0009g0111 |
3 | HG01167.hp2 HG01169.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.-101-2652C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116573190 | |||||||
| chr12:116573201 | G | A | 22 | a0001c0001t0004g0024 a0001c0001t0004g0137 a0001c0001t0004g0204 others(19): Show |
23 | HG01074.hp2 HG01109.hp2 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.-101-2641G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116573201 | |||||||
| chr12:116573319 | G | A | 85 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0023 others(82): Show |
90 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.-101-2523G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116573319 | |||||||
| chr12:116573333 | A | G | 19 | a0001c0001t0004g0024 a0001c0001t0004g0137 a0001c0001t0004g0204 others(16): Show |
20 | HG01074.hp2 HG01109.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.-101-2509A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116573333 | |||||||
| chr12:116573504 | C | G | 1 | a0001c0001t0001g0374 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-101-2338C>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116573504 | |||||||
| chr12:116573630 | C | T | 103 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0023 others(100): Show |
108 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-101-2212C>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116573630 | |||||||
| chr12:116573658 | A | G | 4 | a0002c0002t0005g0155 a0002c0002t0005g0156 a0002c0002t0015g0042 others(1): Show |
4 | HG01175.hp1 HG02257.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.-101-2184A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116573658 | |||||||
| chr12:116573947 | G | A | 1 | a0001c0001t0005g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-101-1895G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116573947 | |||||||
| chr12:116574036 | G | A | 2 | a0001c0001t0005g0251 a0001c0001t0015g0034 |
2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-101-1806G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116574036 | |||||||
| chr12:116574248 | T | TA | 198 | a0001c0001t0001g0374 a0001c0001t0001g0391 a0001c0001t0002g0004 others(195): Show |
214 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.-101-1583dupA | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116574248 | ||||||
| chr12:116574517 | G | A | 1 | a0001c0001t0015g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-101-1325G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116574517 | |||||||
| chr12:116574655 | G | GA | 12 | a0001c0001t0001g0250 a0001c0001t0009g0349 a0001c0001t0013g0098 others(9): Show |
14 | HG02109.hp2 HG02145.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.-101-1176dupA | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116574655 | ||||||
| chr12:116574655 | GA | G | 161 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0023 others(158): Show |
185 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.-101-1176delA | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116574655 | ||||||
| chr12:116574659 | A | G | 1 | a0001c0001t0005g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-101-1183A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116574659 | |||||||
| chr12:116574730 | G | A | 205 | a0001c0001t0001g0374 a0001c0001t0002g0004 a0001c0001t0002g0016 others(202): Show |
219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.-101-1112G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116574730 | |||||||
| chr12:116574747 | G | T | 3 | a0001c0001t0024g0205 a0001c0001t0024g0359 a0001c0001t0028g0068 |
3 | HG02647.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-101-1095G>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116574747 | |||||||
| chr12:116574757 | T | A | 2 | a0001c0001t0007g0125 a0001c0001t0007g0135 |
2 | HG01243.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-101-1085T>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116574757 | |||||||
| chr12:116574819 | G | T | 3 | a0001c0001t0024g0205 a0001c0001t0024g0359 a0001c0001t0028g0068 |
3 | HG02647.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-101-1023G>T | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116574819 | |||||||
| chr12:116574996 | G | A | 90 | a0001c0001t0002g0004 a0001c0001t0002g0016 a0001c0001t0002g0023 others(87): Show |
95 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.-101-846G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116574996 | |||||||
| chr12:116575095 | A | G | 97 | a0001c0001t0001g0374 a0001c0001t0004g0022 a0001c0001t0004g0024 others(94): Show |
106 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.-101-747A>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116575095 | |||||||
| chr12:116575121 | G | A | 1 | a0001c0001t0007g0210 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-101-721G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116575121 | |||||||
| chr12:116575137 | G | A | 10 | a0001c0001t0013g0098 a0001c0001t0013g0099 a0001c0001t0013g0118 others(7): Show |
11 | HG02109.hp2 HG02145.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-101-705G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116575137 | |||||||
| chr12:116575180 | C | CA | 29 | a0001c0001t0001g0250 a0001c0001t0002g0102 a0001c0001t0002g0336 others(26): Show |
32 | HG00280.hp2 HG00735.hp2 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.-101-646dupA | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | INFO_REALIGN_3_PRIME | chr12 | 116575180 | ||||||
| chr12:116575366 | G | A | 2 | a0001c0001t0007g0314 a0001c0001t0010g0028 |
2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-101-476G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116575366 | |||||||
| chr12:116575385 | G | C | 140 | a0001c0001t0001g0374 a0001c0001t0002g0004 a0001c0001t0002g0016 others(137): Show |
148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.-101-457G>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116575385 | |||||||
| chr12:116575390 | T | C | 37 | a0001c0001t0001g0374 a0001c0001t0004g0022 a0001c0001t0004g0183 others(34): Show |
40 | HG00323.hp2 HG00597.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.-101-452T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116575390 | |||||||
| chr12:116575545 | G | A | 166 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(163): Show |
175 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.-101-297G>A | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116575545 | |||||||
| chr12:116575596 | T | C | 100 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0238 others(97): Show |
105 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.-101-246T>C | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116575596 | |||||||
| chr12:116575645 | C | G | 1 | a0001c0001t0009g0214 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-101-197C>G | MAP1LC3B2 | ENSG00000258102.5 | transcript | ENST00000556529.4 | protein_coding | 1/1 | chr12 | 116575645 |