Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 252969 |
| ensemblid | ENSG00000154328.16 |
| hgncid | 18956 |
| symbol | NEIL2 |
| name | nei like DNA glycosylase 2 |
| refseq_nuc | NM_145043.4 |
| refseq_prot | NP_659480.1 |
| ensembl_nuc | ENST00000284503.7 |
| ensembl_prot | ENSP00000284503.6 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 11769710 |
| end | 11787345 |
| strand | + |
| ver | v1.2 |
| region | chr8:11769710-11787345 |
| region5000 | chr8:11764710-11792345 |
| regionname0 | NEIL2_chr8_11769710_11787345 |
| regionname5000 | NEIL2_chr8_11764710_11792345 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 332 | 356 | 79 | 83 | 134 | 14 | 44 | 100 | NEIL2_chr8_11764710_11792345 | NEIL2 | MPEGP others(327): Show |
chr8 | 11764710 | 11792345 |
| a0002 | 0/0 | 332 | 44 | 0 | 0 | 44 | 0 | 0 | 31 | NEIL2_chr8_11764710_11792345 | NEIL2 | MPEGP others(327): Show |
chr8 | 11764710 | 11792345 |
| a0003 | 0/0 | 332 | 24 | 13 | 0 | 11 | 0 | 0 | 11 | NEIL2_chr8_11764710_11792345 | NEIL2 | MPEGP others(327): Show |
chr8 | 11764710 | 11792345 |
| a0004 | 0/0 | 332 | 8 | 1 | 0 | 3 | 0 | 4 | 3 | NEIL2_chr8_11764710_11792345 | NEIL2 | MPEGP others(327): Show |
chr8 | 11764710 | 11792345 |
| a0005 | 0/0 | 332 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | NEIL2_chr8_11764710_11792345 | NEIL2 | MPEGP others(327): Show |
chr8 | 11764710 | 11792345 |
| a0006 | 0/0 | 332 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | NEIL2_chr8_11764710_11792345 | NEIL2 | MPEGP others(327): Show |
chr8 | 11764710 | 11792345 |
| a0007 | 0/0 | 332 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | MPEGP others(327): Show |
chr8 | 11764710 | 11792345 |
| a0008 | 0/0 | 45 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | MPEGP others(40): Show |
chr8 | 11764710 | 11792345 |
| a0009 | 0/0 | 332 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | MPEGP others(327): Show |
chr8 | 11764710 | 11792345 |
| a0010 | 0/0 | 332 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | MPEGP others(327): Show |
chr8 | 11764710 | 11792345 |
| a0011 | 0/0 | 332 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | MPEGP others(327): Show |
chr8 | 11764710 | 11792345 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 996 | 296 | 48 | 70 | 129 | 13 | 35 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 | ||
| a0001c0002 | 0/1 | 996 | 53 | 26 | 13 | 3 | 1 | 9 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 | ||
| a0001c0010 | 0/0 | 996 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 | ||
| a0001c0011 | 0/0 | 996 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 | ||
| a0001c0014 | 0/0 | 996 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 | ||
| a0001c0015 | 0/0 | 996 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 | ||
| a0001c0016 | 0/0 | 996 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 | ||
| a0001c0018 | 0/0 | 996 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 | ||
| a0002c0003 | 0/0 | 996 | 44 | 0 | 0 | 44 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 | ||
| a0003c0004 | 0/0 | 996 | 17 | 6 | 0 | 11 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 | ||
| a0003c0006 | 0/0 | 996 | 6 | 6 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 | ||
| a0003c0013 | 0/0 | 996 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 | ||
| a0004c0005 | 0/0 | 996 | 7 | 1 | 0 | 3 | 0 | 3 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 | ||
| a0004c0012 | 0/0 | 996 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 | ||
| a0005c0007 | 0/0 | 996 | 5 | 0 | 0 | 5 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 | ||
| a0006c0008 | 0/0 | 996 | 3 | 0 | 0 | 3 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 | ||
| a0007c0009 | 0/0 | 996 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 | ||
| a0008c0020 | 0/0 | 996 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 | ||
| a0009c0021 | 0/0 | 996 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 | ||
| a0010c0019 | 0/0 | 996 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 | ||
| a0011c0017 | 0/0 | 996 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | ATGCC others(991): Show |
chr8 | 11764710 | 11792345 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2701 | 96 | 1 | 13 | 68 | 1 | 13 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2696): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0002 | 0/0 | 2699 | 47 | 2 | 10 | 32 | 0 | 3 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0005 | 0/0 | 2699 | 23 | 0 | 8 | 7 | 0 | 8 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0006 | 0/0 | 2701 | 18 | 1 | 13 | 0 | 3 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2696): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0007 | 0/0 | 2701 | 14 | 14 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2696): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0009 | 0/0 | 2699 | 12 | 0 | 7 | 0 | 2 | 3 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0010 | 0/0 | 2701 | 12 | 1 | 7 | 0 | 3 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2696): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0011 | 0/0 | 2702 | 10 | 1 | 7 | 2 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2697): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0015 | 0/0 | 2699 | 6 | 6 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0016 | 0/0 | 2701 | 6 | 1 | 0 | 0 | 4 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2696): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0017 | 0/0 | 2699 | 5 | 0 | 0 | 5 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0019 | 1/0 | 2699 | 4 | 3 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0022 | 0/0 | 2701 | 4 | 4 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2696): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0024 | 0/0 | 2701 | 3 | 0 | 1 | 2 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2696): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0025 | 0/0 | 2702 | 3 | 0 | 0 | 2 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2697): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0026 | 0/0 | 2701 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2696): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0027 | 0/0 | 2699 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0028 | 0/0 | 2700 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2695): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0029 | 0/0 | 2700 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2695): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0032 | 0/0 | 2701 | 2 | 0 | 0 | 1 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2696): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0035 | 0/0 | 2698 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2693): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0037 | 0/0 | 2699 | 2 | 0 | 2 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0038 | 0/0 | 2698 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2693): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0039 | 0/0 | 2699 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0040 | 0/0 | 2699 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0041 | 0/0 | 2699 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0042 | 0/0 | 2702 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2697): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0045 | 0/0 | 2698 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2693): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0047 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2695): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0048 | 0/0 | 2701 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2696): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0049 | 0/0 | 2701 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2696): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0051 | 0/0 | 2699 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0053 | 0/0 | 2699 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0054 | 0/0 | 2699 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0056 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2695): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0057 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2695): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0058 | 0/0 | 2699 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0066 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2695): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0067 | 0/0 | 2701 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2696): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0068 | 0/0 | 2699 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0069 | 0/0 | 2699 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0001t0070 | 0/0 | 2699 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0002t0003 | 0/0 | 2699 | 2 | 0 | 0 | 1 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0002t0004 | 0/1 | 2699 | 28 | 8 | 11 | 1 | 1 | 6 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0002t0014 | 0/0 | 2699 | 6 | 6 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0002t0021 | 0/0 | 2699 | 4 | 4 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0002t0030 | 0/0 | 2699 | 2 | 0 | 1 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0002t0031 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2716): Show |
chr8 | 11764710 | 11792345 |
| a0001c0002t0036 | 0/0 | 2700 | 2 | 1 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2695): Show |
chr8 | 11764710 | 11792345 |
| a0001c0002t0052 | 0/0 | 2722 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2717): Show |
chr8 | 11764710 | 11792345 |
| a0001c0002t0059 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2695): Show |
chr8 | 11764710 | 11792345 |
| a0001c0002t0060 | 0/0 | 2699 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0002t0061 | 0/0 | 2698 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2693): Show |
chr8 | 11764710 | 11792345 |
| a0001c0002t0062 | 0/0 | 2699 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0002t0063 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2695): Show |
chr8 | 11764710 | 11792345 |
| a0001c0002t0064 | 0/0 | 2699 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0002t0065 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2695): Show |
chr8 | 11764710 | 11792345 |
| a0001c0010t0034 | 0/0 | 2699 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0011t0001 | 0/0 | 2701 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2696): Show |
chr8 | 11764710 | 11792345 |
| a0001c0014t0046 | 0/0 | 2699 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0001c0015t0007 | 0/0 | 2701 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2696): Show |
chr8 | 11764710 | 11792345 |
| a0001c0016t0007 | 0/0 | 2701 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2696): Show |
chr8 | 11764710 | 11792345 |
| a0001c0018t0031 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2716): Show |
chr8 | 11764710 | 11792345 |
| a0002c0003t0003 | 0/0 | 2699 | 27 | 0 | 0 | 27 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0002c0003t0008 | 0/0 | 2699 | 13 | 0 | 0 | 13 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0002c0003t0020 | 0/0 | 2700 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2695): Show |
chr8 | 11764710 | 11792345 |
| a0002c0003t0035 | 0/0 | 2698 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2693): Show |
chr8 | 11764710 | 11792345 |
| a0002c0003t0050 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2695): Show |
chr8 | 11764710 | 11792345 |
| a0003c0004t0003 | 0/0 | 2699 | 9 | 2 | 0 | 7 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0003c0004t0004 | 0/0 | 2699 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0003c0004t0018 | 0/0 | 2698 | 3 | 3 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2693): Show |
chr8 | 11764710 | 11792345 |
| a0003c0004t0020 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2695): Show |
chr8 | 11764710 | 11792345 |
| a0003c0004t0023 | 0/0 | 2699 | 3 | 0 | 0 | 3 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0003c0006t0012 | 0/0 | 2699 | 6 | 6 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0003c0013t0018 | 0/0 | 2698 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2693): Show |
chr8 | 11764710 | 11792345 |
| a0004c0005t0013 | 0/0 | 2700 | 5 | 1 | 0 | 1 | 0 | 3 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2695): Show |
chr8 | 11764710 | 11792345 |
| a0004c0005t0043 | 0/0 | 2701 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2696): Show |
chr8 | 11764710 | 11792345 |
| a0004c0005t0044 | 0/0 | 2701 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2696): Show |
chr8 | 11764710 | 11792345 |
| a0004c0012t0013 | 0/0 | 2700 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2695): Show |
chr8 | 11764710 | 11792345 |
| a0005c0007t0001 | 0/0 | 2701 | 5 | 0 | 0 | 5 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2696): Show |
chr8 | 11764710 | 11792345 |
| a0006c0008t0003 | 0/0 | 2699 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| a0006c0008t0020 | 0/0 | 2700 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2695): Show |
chr8 | 11764710 | 11792345 |
| a0007c0009t0033 | 0/0 | 2698 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2693): Show |
chr8 | 11764710 | 11792345 |
| a0008c0020t0006 | 0/0 | 2701 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2696): Show |
chr8 | 11764710 | 11792345 |
| a0009c0021t0018 | 0/0 | 2698 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2693): Show |
chr8 | 11764710 | 11792345 |
| a0010c0019t0055 | 0/0 | 2700 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2695): Show |
chr8 | 11764710 | 11792345 |
| a0011c0017t0004 | 0/0 | 2699 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | AAATC others(2694): Show |
chr8 | 11764710 | 11792345 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 23 | 0 | 2 | 17 | 0 | 4 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0009 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0011 | 0/0 | 7 | 0 | 2 | 4 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0015 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0003 | 0/0 | 11 | 1 | 1 | 9 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0004 | 0/0 | 7 | 0 | 5 | 2 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0019 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0021 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0005g0006 | 0/0 | 7 | 0 | 5 | 0 | 0 | 2 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0005g0027 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0005g0047 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0005g0053 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0005g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0006g0005 | 0/0 | 7 | 0 | 5 | 0 | 1 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0006g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0006g0054 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0006g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0006g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0006g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0007g0010 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0007g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0007g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0007g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0007g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0009g0006 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0009g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0009g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0009g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0009g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0009g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0009g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0009g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0009g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0009g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0010g0012 | 0/0 | 7 | 1 | 5 | 0 | 1 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0010g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0010g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0010g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0010g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0010g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0011g0002 | 0/0 | 8 | 1 | 6 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0011g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0011g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0015g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0015g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0015g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0015g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0015g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0016g0005 | 0/0 | 4 | 1 | 0 | 0 | 2 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0016g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0017g0004 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0019g0024 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0019g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0022g0059 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0022g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0022g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0024g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0024g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0025g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0025g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0025g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0026g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0026g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0027g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0028g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0028g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0029g0066 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0032g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0032g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0035g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0037g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0038g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0039g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0040g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0041g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0042g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0045g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0047g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0048g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0049g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0051g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0053g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0054g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0056g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0057g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0058g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0066g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0067g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0068g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0069g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0001t0070g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0003g0057 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0004g0013 | 0/0 | 6 | 1 | 3 | 0 | 1 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0004g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0004g0065 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0004g0067 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0004g0068 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0004g0070 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0004g0202 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0004g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0014g0032 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0014g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0014g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0014g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0021g0069 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0021g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0021g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0030g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0030g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0031g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0036g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0036g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0052g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0059g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0060g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0061g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0062g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0063g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0064g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0002t0065g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0010t0034g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0010t0034g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0011t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0014t0046g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0015t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0016t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0001c0018t0031g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0002c0003t0003g0007 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0002c0003t0003g0008 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0002c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0002c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0002c0003t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0002c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0002c0003t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0002c0003t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0002c0003t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0002c0003t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0002c0003t0008g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0002c0003t0008g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0002c0003t0008g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0002c0003t0008g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0002c0003t0008g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0002c0003t0008g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0002c0003t0020g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0002c0003t0020g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0002c0003t0035g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0002c0003t0050g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0003c0004t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0003c0004t0003g0062 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0003c0004t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0003c0004t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0003c0004t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0003c0004t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0003c0004t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0003c0004t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0003c0004t0018g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0003c0004t0018g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0003c0004t0020g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0003c0004t0023g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0003c0004t0023g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0003c0004t0023g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0003c0006t0012g0022 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0003c0006t0012g0058 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0003c0013t0018g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0004c0005t0013g0023 | 0/0 | 4 | 1 | 0 | 0 | 0 | 3 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0004c0005t0013g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0004c0005t0043g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0004c0005t0044g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0004c0012t0013g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0005c0007t0001g0017 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0006c0008t0003g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0006c0008t0020g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0007c0009t0033g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0007c0009t0033g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0008c0020t0006g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0009c0021t0018g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0010c0019t0055g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| a0011c0017t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0016 | g0005 | EUR | GBR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00140 | hp2 | a0001 | c0001 | t0009 | g0006 | EUR | GBR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00280 | hp1 | a0001 | c0001 | t0016 | g0029 | EUR | FIN | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00280 | hp2 | a0001 | c0001 | t0006 | g0149 | EUR | FIN | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00323 | hp1 | a0001 | c0001 | t0010 | g0187 | EUR | FIN | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00323 | hp2 | a0001 | c0001 | t0010 | g0189 | EUR | FIN | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00408 | hp2 | a0001 | c0002 | t0030 | g0091 | EAS | CHS | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00423 | hp2 | a0001 | c0001 | t0026 | g0140 | EAS | CHS | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00438 | hp2 | a0002 | c0003 | t0003 | g0008 | EAS | CHS | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00544 | hp2 | a0001 | c0001 | t0005 | g0101 | EAS | CHS | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00558 | hp2 | a0002 | c0003 | t0008 | g0014 | EAS | CHS | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00621 | hp1 | a0001 | c0001 | t0038 | g0155 | EAS | CHS | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00621 | hp2 | a0002 | c0003 | t0008 | g0041 | EAS | CHS | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00639 | hp1 | a0001 | c0002 | t0004 | g0216 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00639 | hp2 | a0001 | c0002 | t0004 | g0013 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00642 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00642 | hp2 | a0001 | c0001 | t0006 | g0005 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00673 | hp1 | a0002 | c0003 | t0003 | g0008 | EAS | CHS | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00673 | hp2 | a0001 | c0001 | t0005 | g0114 | EAS | CHS | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00733 | hp1 | a0001 | c0001 | t0024 | g0038 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00735 | hp2 | a0001 | c0001 | t0006 | g0147 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00738 | hp2 | a0001 | c0002 | t0004 | g0013 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG00741 | hp2 | a0001 | c0001 | t0006 | g0146 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01070 | hp1 | a0001 | c0001 | t0006 | g0030 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0030 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01074 | hp2 | a0001 | c0001 | t0006 | g0055 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01081 | hp1 | a0001 | c0001 | t0010 | g0012 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01099 | hp2 | a0001 | c0001 | t0037 | g0049 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01106 | hp1 | a0001 | c0002 | t0004 | g0215 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01106 | hp2 | a0008 | c0020 | t0006 | g0029 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0150 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01109 | hp2 | a0001 | c0001 | t0037 | g0049 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01167 | hp1 | a0001 | c0001 | t0009 | g0109 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01167 | hp2 | a0001 | c0001 | t0049 | g0074 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01168 | hp1 | a0001 | c0001 | t0010 | g0012 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01169 | hp1 | a0001 | c0001 | t0010 | g0012 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01169 | hp2 | a0001 | c0001 | t0009 | g0108 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01175 | hp1 | a0001 | c0002 | t0004 | g0070 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01175 | hp2 | a0001 | c0001 | t0068 | g0030 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0055 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01243 | hp1 | a0001 | c0002 | t0004 | g0211 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01243 | hp2 | a0001 | c0001 | t0010 | g0012 | AMR | PUR | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01255 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01256 | hp1 | a0001 | c0001 | t0010 | g0186 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01256 | hp2 | a0001 | c0002 | t0004 | g0067 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01257 | hp1 | a0001 | c0001 | t0009 | g0111 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01257 | hp2 | a0001 | c0002 | t0004 | g0013 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01258 | hp1 | a0001 | c0001 | t0009 | g0112 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01258 | hp2 | a0001 | c0002 | t0004 | g0067 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01261 | hp1 | a0001 | c0001 | t0006 | g0054 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01346 | hp2 | a0001 | c0001 | t0009 | g0120 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01358 | hp1 | a0001 | c0002 | t0030 | g0122 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01361 | hp1 | a0001 | c0001 | t0005 | g0027 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01433 | hp2 | a0001 | c0001 | t0011 | g0002 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01496 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01496 | hp2 | a0001 | c0002 | t0004 | g0065 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01515 | hp1 | a0001 | c0001 | t0016 | g0029 | EUR | IBS | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01515 | hp2 | a0001 | c0001 | t0009 | g0100 | EUR | IBS | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01517 | hp1 | a0001 | c0002 | t0004 | g0013 | EUR | IBS | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01517 | hp2 | a0001 | c0001 | t0016 | g0005 | EUR | IBS | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0151 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01884 | hp2 | a0001 | c0001 | t0056 | g0164 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01891 | hp1 | a0001 | c0002 | t0004 | g0178 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01934 | hp1 | a0001 | c0002 | t0004 | g0070 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01934 | hp2 | a0001 | c0001 | t0011 | g0002 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0053 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01975 | hp1 | a0001 | c0001 | t0009 | g0102 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01978 | hp1 | a0001 | c0002 | t0061 | g0013 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01993 | hp2 | a0001 | c0001 | t0010 | g0188 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02004 | hp1 | a0001 | c0001 | t0010 | g0012 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02004 | hp2 | a0001 | c0001 | t0011 | g0002 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02015 | hp2 | a0002 | c0003 | t0020 | g0008 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02027 | hp1 | a0002 | c0003 | t0020 | g0061 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02027 | hp2 | a0001 | c0001 | t0042 | g0089 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02055 | hp1 | a0001 | c0002 | t0004 | g0213 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02055 | hp2 | a0001 | c0002 | t0063 | g0163 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02056 | hp1 | a0001 | c0001 | t0005 | g0131 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02056 | hp2 | a0006 | c0008 | t0003 | g0033 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02074 | hp1 | a0002 | c0003 | t0003 | g0061 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02129 | hp1 | a0001 | c0002 | t0003 | g0057 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02129 | hp2 | a0001 | c0011 | t0001 | g0121 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02132 | hp2 | a0002 | c0003 | t0008 | g0040 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02135 | hp1 | a0001 | c0001 | t0039 | g0016 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02145 | hp1 | a0001 | c0002 | t0036 | g0195 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02145 | hp2 | a0001 | c0018 | t0031 | g0031 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0084 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02155 | hp1 | a0002 | c0003 | t0003 | g0007 | EAS | CDX | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02155 | hp2 | a0002 | c0003 | t0008 | g0082 | EAS | CDX | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02165 | hp1 | a0001 | c0001 | t0026 | g0083 | EAS | CDX | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02257 | hp2 | a0001 | c0001 | t0011 | g0002 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02258 | hp1 | a0001 | c0001 | t0015 | g0124 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02258 | hp2 | a0003 | c0004 | t0004 | g0192 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02273 | hp1 | a0001 | c0001 | t0011 | g0002 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02280 | hp1 | a0001 | c0002 | t0059 | g0196 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02280 | hp2 | a0001 | c0001 | t0016 | g0005 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02293 | hp1 | a0001 | c0001 | t0011 | g0117 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02293 | hp2 | a0001 | c0001 | t0011 | g0002 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02300 | hp1 | a0001 | c0001 | t0011 | g0002 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02451 | hp1 | a0001 | c0001 | t0015 | g0126 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02451 | hp2 | a0001 | c0002 | t0014 | g0032 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02523 | hp1 | a0002 | c0003 | t0003 | g0174 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02523 | hp2 | a0001 | c0001 | t0032 | g0175 | EAS | KHV | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02572 | hp1 | a0001 | c0002 | t0004 | g0194 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02572 | hp2 | a0001 | c0002 | t0004 | g0013 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02615 | hp1 | a0001 | c0001 | t0007 | g0145 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02615 | hp2 | a0001 | c0001 | t0022 | g0086 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02622 | hp2 | a0001 | c0002 | t0014 | g0064 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02630 | hp1 | a0001 | c0002 | t0004 | g0036 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02630 | hp2 | a0003 | c0004 | t0018 | g0035 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02698 | hp1 | a0001 | c0002 | t0004 | g0212 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0103 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0024 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02717 | hp2 | a0001 | c0001 | t0015 | g0125 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02723 | hp1 | a0001 | c0001 | t0010 | g0012 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02723 | hp2 | a0003 | c0006 | t0012 | g0022 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02735 | hp1 | a0001 | c0002 | t0003 | g0057 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02738 | hp1 | a0001 | c0001 | t0025 | g0038 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02738 | hp2 | a0004 | c0005 | t0013 | g0023 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02809 | hp1 | a0001 | c0001 | t0057 | g0160 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02809 | hp2 | a0001 | c0001 | t0019 | g0024 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02818 | hp1 | a0004 | c0005 | t0013 | g0023 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02818 | hp2 | a0001 | c0002 | t0004 | g0179 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02886 | hp1 | a0009 | c0021 | t0018 | g0035 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02895 | hp1 | a0001 | c0002 | t0014 | g0032 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02895 | hp2 | a0001 | c0001 | t0027 | g0003 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02896 | hp1 | a0003 | c0006 | t0012 | g0058 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02896 | hp2 | a0001 | c0001 | t0019 | g0024 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02897 | hp1 | a0001 | c0001 | t0027 | g0003 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02897 | hp2 | a0003 | c0006 | t0012 | g0058 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02922 | hp1 | a0001 | c0001 | t0015 | g0052 | AFR | ESN | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02922 | hp2 | a0001 | c0002 | t0014 | g0158 | AFR | ESN | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02965 | hp1 | a0003 | c0004 | t0003 | g0166 | AFR | ESN | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | ESN | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02970 | hp1 | a0001 | c0001 | t0007 | g0199 | AFR | ESN | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02970 | hp2 | a0001 | c0001 | t0035 | g0127 | AFR | ESN | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0020 | AFR | ESN | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02976 | hp2 | a0001 | c0016 | t0007 | g0184 | AFR | ESN | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03041 | hp2 | a0007 | c0009 | t0033 | g0162 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03098 | hp1 | a0003 | c0004 | t0018 | g0177 | AFR | MSL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | MSL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03130 | hp1 | a0001 | c0002 | t0065 | g0201 | AFR | ESN | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03130 | hp2 | a0001 | c0001 | t0067 | g0020 | AFR | ESN | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03139 | hp1 | a0001 | c0001 | t0015 | g0123 | AFR | ESN | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03139 | hp2 | a0001 | c0002 | t0021 | g0069 | AFR | ESN | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03195 | hp1 | a0003 | c0006 | t0012 | g0022 | AFR | ESN | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03195 | hp2 | a0001 | c0002 | t0021 | g0207 | AFR | ESN | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03209 | hp1 | a0007 | c0009 | t0033 | g0157 | AFR | MSL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03209 | hp2 | a0001 | c0001 | t0022 | g0059 | AFR | MSL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03225 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | MSL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03225 | hp2 | a0003 | c0013 | t0018 | g0180 | AFR | MSL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03239 | hp1 | a0001 | c0001 | t0009 | g0048 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03239 | hp2 | a0001 | c0002 | t0064 | g0200 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | MSL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03453 | hp2 | a0001 | c0001 | t0022 | g0059 | AFR | MSL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03486 | hp1 | a0001 | c0010 | t0034 | g0183 | AFR | MSL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03486 | hp2 | a0001 | c0001 | t0041 | g0072 | AFR | MSL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03490 | hp1 | a0001 | c0002 | t0004 | g0068 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03490 | hp2 | a0004 | c0005 | t0013 | g0023 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03491 | hp2 | a0001 | c0001 | t0016 | g0005 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03492 | hp2 | a0001 | c0002 | t0004 | g0068 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03516 | hp1 | a0010 | c0019 | t0055 | g0191 | AFR | ESN | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03516 | hp2 | a0001 | c0002 | t0052 | g0031 | AFR | ESN | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03540 | hp1 | a0001 | c0002 | t0060 | g0161 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03540 | hp2 | a0001 | c0002 | t0062 | g0064 | AFR | GWD | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03579 | hp1 | a0001 | c0001 | t0022 | g0085 | AFR | MSL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03579 | hp2 | a0001 | c0001 | t0051 | g0197 | AFR | MSL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03669 | hp1 | a0001 | c0002 | t0036 | g0206 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03669 | hp2 | a0001 | c0001 | t0009 | g0006 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03688 | hp1 | a0001 | c0002 | t0004 | g0013 | SAS | STU | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03688 | hp2 | a0001 | c0001 | t0005 | g0104 | SAS | STU | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03704 | hp1 | a0001 | c0001 | t0006 | g0005 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03704 | hp2 | a0001 | c0001 | t0009 | g0006 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03710 | hp1 | a0001 | c0001 | t0053 | g0063 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03831 | hp1 | a0001 | c0001 | t0005 | g0027 | SAS | BEB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | BEB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03834 | hp1 | a0004 | c0005 | t0013 | g0023 | SAS | BEB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03834 | hp2 | a0001 | c0002 | t0004 | g0214 | SAS | BEB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03927 | hp1 | a0001 | c0001 | t0032 | g0204 | SAS | BEB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03927 | hp2 | a0001 | c0001 | t0005 | g0048 | SAS | BEB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0134 | SAS | BEB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG04115 | hp1 | a0004 | c0012 | t0013 | g0210 | SAS | STU | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0141 | SAS | STU | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG04184 | hp1 | a0001 | c0001 | t0005 | g0047 | SAS | BEB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG04184 | hp2 | a0001 | c0001 | t0069 | g0148 | SAS | BEB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0130 | SAS | STU | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG04204 | hp1 | a0001 | c0001 | t0010 | g0063 | SAS | STU | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG04228 | hp1 | a0001 | c0002 | t0004 | g0203 | SAS | STU | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG04228 | hp2 | a0001 | c0001 | t0045 | g0027 | SAS | STU | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18522 | hp1 | a0001 | c0001 | t0058 | g0020 | AFR | YRI | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18522 | hp2 | a0011 | c0017 | t0004 | g0036 | AFR | YRI | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18612 | hp1 | a0001 | c0014 | t0046 | g0208 | EAS | CHB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18612 | hp2 | a0002 | c0003 | t0003 | g0008 | EAS | CHB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18747 | hp1 | a0002 | c0003 | t0003 | g0008 | EAS | CHB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | YRI | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18906 | hp2 | a0001 | c0002 | t0014 | g0159 | AFR | YRI | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18939 | hp2 | a0001 | c0001 | t0025 | g0079 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18941 | hp1 | a0002 | c0003 | t0003 | g0007 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18941 | hp2 | a0001 | c0001 | t0017 | g0004 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18943 | hp2 | a0002 | c0003 | t0008 | g0096 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18945 | hp1 | a0002 | c0003 | t0003 | g0007 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18951 | hp1 | a0001 | c0001 | t0048 | g0002 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18951 | hp2 | a0003 | c0004 | t0003 | g0034 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18954 | hp1 | a0002 | c0003 | t0003 | g0167 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18959 | hp2 | a0002 | c0003 | t0003 | g0007 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18960 | hp1 | a0002 | c0003 | t0003 | g0007 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18960 | hp2 | a0004 | c0005 | t0043 | g0081 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18961 | hp2 | a0001 | c0001 | t0028 | g0016 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18962 | hp1 | a0002 | c0003 | t0008 | g0014 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18964 | hp1 | a0002 | c0003 | t0003 | g0172 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18966 | hp1 | a0002 | c0003 | t0008 | g0041 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18968 | hp1 | a0003 | c0004 | t0023 | g0034 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18968 | hp2 | a0002 | c0003 | t0008 | g0014 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18970 | hp1 | a0001 | c0001 | t0005 | g0047 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18971 | hp2 | a0003 | c0004 | t0023 | g0060 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18973 | hp1 | a0001 | c0002 | t0004 | g0205 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18973 | hp2 | a0001 | c0001 | t0005 | g0143 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18974 | hp2 | a0002 | c0003 | t0003 | g0008 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18975 | hp1 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18975 | hp2 | a0002 | c0003 | t0003 | g0008 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18979 | hp2 | a0003 | c0004 | t0003 | g0176 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18982 | hp1 | a0001 | c0001 | t0028 | g0003 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18983 | hp2 | a0003 | c0004 | t0003 | g0173 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18984 | hp1 | a0002 | c0003 | t0003 | g0007 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18985 | hp2 | a0002 | c0003 | t0003 | g0007 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18986 | hp1 | a0002 | c0003 | t0003 | g0165 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18986 | hp2 | a0004 | c0005 | t0044 | g0182 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18988 | hp1 | a0002 | c0003 | t0008 | g0040 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18989 | hp2 | a0001 | c0001 | t0011 | g0028 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18994 | hp1 | a0001 | c0001 | t0025 | g0078 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18995 | hp1 | a0003 | c0004 | t0020 | g0060 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18997 | hp1 | a0002 | c0003 | t0003 | g0217 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18998 | hp2 | a0005 | c0007 | t0001 | g0017 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19000 | hp1 | a0001 | c0001 | t0047 | g0142 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19000 | hp2 | a0002 | c0003 | t0050 | g0014 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19001 | hp2 | a0002 | c0003 | t0035 | g0168 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19003 | hp2 | a0001 | c0001 | t0017 | g0004 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19005 | hp1 | a0003 | c0004 | t0003 | g0062 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19009 | hp1 | a0002 | c0003 | t0003 | g0170 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19009 | hp2 | a0002 | c0003 | t0008 | g0014 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19011 | hp1 | a0002 | c0003 | t0003 | g0008 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19011 | hp2 | a0004 | c0005 | t0013 | g0181 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19012 | hp2 | a0002 | c0003 | t0003 | g0007 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19030 | hp1 | a0003 | c0004 | t0003 | g0193 | AFR | LWK | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19030 | hp2 | a0001 | c0010 | t0034 | g0185 | AFR | LWK | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19043 | hp1 | a0001 | c0001 | t0070 | g0080 | AFR | LWK | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19043 | hp2 | a0001 | c0002 | t0004 | g0036 | AFR | LWK | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19054 | hp2 | a0002 | c0003 | t0003 | g0008 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19055 | hp1 | a0003 | c0004 | t0003 | g0034 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19056 | hp2 | a0002 | c0003 | t0003 | g0008 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19057 | hp2 | a0001 | c0001 | t0017 | g0004 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19058 | hp1 | a0001 | c0001 | t0017 | g0004 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19058 | hp2 | a0002 | c0003 | t0008 | g0014 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19060 | hp1 | a0001 | c0001 | t0024 | g0039 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19060 | hp2 | a0006 | c0008 | t0020 | g0033 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19063 | hp2 | a0005 | c0007 | t0001 | g0017 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19066 | hp1 | a0001 | c0001 | t0024 | g0039 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19066 | hp2 | a0005 | c0007 | t0001 | g0017 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19067 | hp2 | a0005 | c0007 | t0001 | g0017 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0053 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19070 | hp2 | a0002 | c0003 | t0008 | g0042 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19077 | hp2 | a0006 | c0008 | t0003 | g0033 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19079 | hp1 | a0002 | c0003 | t0003 | g0007 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19079 | hp2 | a0001 | c0001 | t0040 | g0139 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19082 | hp1 | a0003 | c0004 | t0023 | g0169 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19083 | hp1 | a0002 | c0003 | t0008 | g0042 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19084 | hp1 | a0001 | c0001 | t0017 | g0004 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19084 | hp2 | a0002 | c0003 | t0003 | g0007 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19085 | hp2 | a0005 | c0007 | t0001 | g0017 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19086 | hp2 | a0002 | c0003 | t0003 | g0218 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19088 | hp1 | a0003 | c0004 | t0003 | g0062 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19091 | hp1 | a0003 | c0004 | t0003 | g0171 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19240 | hp1 | a0001 | c0001 | t0029 | g0066 | AFR | YRI | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0144 | AFR | YRI | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA20129 | hp1 | a0001 | c0001 | t0015 | g0052 | AFR | ASW | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA20129 | hp2 | a0001 | c0002 | t0004 | g0065 | AFR | ASW | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA20752 | hp1 | a0001 | c0001 | t0010 | g0012 | EUR | TSI | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA20752 | hp2 | a0001 | c0001 | t0006 | g0005 | EUR | TSI | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | TSI | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0054 | EUR | TSI | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0006 | SAS | GIH | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | GIH | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG01123 | hp2 | a0001 | c0001 | t0009 | g0088 | AMR | CLM | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02109 | hp1 | a0001 | c0001 | t0019 | g0198 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02109 | hp2 | a0003 | c0006 | t0012 | g0022 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02486 | hp1 | a0001 | c0001 | t0066 | g0106 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02486 | hp2 | a0001 | c0002 | t0021 | g0209 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02559 | hp1 | a0001 | c0002 | t0014 | g0032 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG02559 | hp2 | a0001 | c0002 | t0021 | g0069 | AFR | ACB | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03471 | hp1 | a0001 | c0002 | t0031 | g0031 | AFR | MSL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG03471 | hp2 | a0001 | c0015 | t0007 | g0010 | AFR | MSL | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0010 | AFR | USA | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| HG06807 | hp2 | a0003 | c0006 | t0012 | g0022 | AFR | USA | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA20300 | hp1 | a0001 | c0001 | t0029 | g0066 | AFR | USA | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | USA | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA21309 | hp1 | a0001 | c0001 | t0054 | g0190 | AFR | LWK | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| NA21309 | hp2 | a0003 | c0004 | t0018 | g0035 | AFR | LWK | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0004 | g0202 | REF | REF | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0019 | g0024 | REF | REF | NEIL2_chr8_11764710_11792345 | NEIL2 | chr8 | 11764710 | 11792345 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:11771493 | C | T | 1 | a0009 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.46C>T | p.Pro16Ser | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/5 | 674/2699 | 46/999 | 16/332 | chr8 | 11771493 | |||
| chr8:11771583 | C | T | 1 | a0008 | 1 | HG01106.hp2 | stop_gained&splice_region_variant | HIGH | c.136C>T | p.Gln46* | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/5 | 764/2699 | 136/999 | 46/332 | chr8 | 11771583 | |||
| chr8:11779752 | T | C | 1 | a0007 | 2 | HG03041.hp2 HG03209.hp1 |
missense_variant | MODERATE | c.293T>C | p.Leu98Pro | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/5 | 921/2699 | 293/999 | 98/332 | chr8 | 11779752 | |||
| chr8:11779766 | C | T | 1 | a0003 | 6 | HG02109.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
missense_variant | MODERATE | c.307C>T | p.Arg103Trp | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/5 | 935/2699 | 307/999 | 103/332 | chr8 | 11779766 | |||
| chr8:11779767 | G | A | 3 | a0002 a0003 a0009 |
63 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(60): Show |
missense_variant | MODERATE | c.308G>A | p.Arg103Gln | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/5 | 936/2699 | 308/999 | 103/332 | chr8 | 11779767 | |||
| chr8:11779799 | G | T | 1 | a0010 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.340G>T | p.Asp114Tyr | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/5 | 968/2699 | 340/999 | 114/332 | chr8 | 11779799 | |||
| chr8:11779923 | G | T | 1 | a0011 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.464G>T | p.Arg155Met | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/5 | 1092/2699 | 464/999 | 155/332 | chr8 | 11779923 | |||
| chr8:11783298 | T | G | 1 | a0005 | 5 | NA18998.hp2 NA19063.hp2 NA19066.hp2 others(2): Show |
missense_variant | MODERATE | c.587T>G | p.Ile196Ser | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/5 | 1215/2699 | 587/999 | 196/332 | chr8 | 11783298 | |||
| chr8:11786044 | G | T | 2 | a0002 a0006 |
47 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(44): Show |
missense_variant | MODERATE | c.770G>T | p.Arg257Leu | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 1398/2699 | 770/999 | 257/332 | chr8 | 11786044 | |||
| chr8:11786184 | C | A | 1 | a0004 | 8 | HG02738.hp2 HG02818.hp1 HG03490.hp2 others(5): Show |
missense_variant | MODERATE | c.910C>A | p.Pro304Thr | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 1538/2699 | 910/999 | 304/332 | chr8 | 11786184 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:11771504 | T | G | 1 | a0001c0011 | 1 | HG02129.hp2 | synonymous_variant | LOW | c.57T>G | p.Gly19Gly | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/5 | 685/2699 | 57/999 | 19/332 | chr8 | 11771504 | |||
| chr8:11771513 | G | A | 1 | a0004c0012 | 1 | HG04115.hp1 | synonymous_variant | LOW | c.66G>A | p.Val22Val | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/5 | 694/2699 | 66/999 | 22/332 | chr8 | 11771513 | |||
| chr8:11779876 | C | A | 1 | a0001c0014 | 1 | NA18612.hp1 | synonymous_variant | LOW | c.417C>A | p.Gly139Gly | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/5 | 1045/2699 | 417/999 | 139/332 | chr8 | 11779876 | |||
| chr8:11779900 | C | T | 1 | a0001c0018 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.441C>T | p.Ser147Ser | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/5 | 1069/2699 | 441/999 | 147/332 | chr8 | 11779900 | |||
| chr8:11783275 | A | G | 5 | a0001c0002 a0001c0018 a0003c0006 others(2): Show |
62 | HG00408.hp2 HG00639.hp1 HG00639.hp2 others(59): Show |
synonymous_variant | LOW | c.564A>G | p.Pro188Pro | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/5 | 1192/2699 | 564/999 | 188/332 | chr8 | 11783275 | |||
| chr8:11783299 | C | T | 1 | a0010c0019 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.588C>T | p.Ile196Ile | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/5 | 1216/2699 | 588/999 | 196/332 | chr8 | 11783299 | |||
| chr8:11783344 | C | T | 2 | a0001c0010 a0001c0016 |
3 | HG02976.hp2 HG03486.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.633C>T | p.Gly211Gly | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/5 | 1261/2699 | 633/999 | 211/332 | chr8 | 11783344 | |||
| chr8:11786108 | C | T | 1 | a0003c0013 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.834C>T | p.Gly278Gly | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 1462/2699 | 834/999 | 278/332 | chr8 | 11786108 | |||
| chr8:11786222 | G | A | 2 | a0001c0010 a0001c0015 |
3 | HG03471.hp2 HG03486.hp1 NA19030.hp2 |
synonymous_variant | LOW | c.948G>A | p.Pro316Pro | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 1576/2699 | 948/999 | 316/332 | chr8 | 11786222 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:11769723 | C | T | 3 | a0001c0001t0024 a0001c0001t0025 a0001c0001t0070 |
7 | HG00733.hp1 HG02738.hp1 NA18939.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-615C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/5 | 1725 | chr8 | 11769723 | ||||||
| chr8:11769750 | A | G | 1 | a0001c0001t0037 | 2 | HG01099.hp2 HG01109.hp2 |
5_prime_UTR_variant | MODIFIER | c.-588A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/5 | 1698 | chr8 | 11769750 | ||||||
| chr8:11769752 | C | G | 5 | a0001c0001t0006 a0001c0001t0016 a0001c0001t0068 others(2): Show |
27 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-586C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/5 | 1696 | chr8 | 11769752 | ||||||
| chr8:11769804 | G | T | 1 | a0001c0001t0067 | 1 | HG03130.hp2 | 5_prime_UTR_variant | MODIFIER | c.-534G>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/5 | 1644 | chr8 | 11769804 | ||||||
| chr8:11769928 | C | G | 1 | a0001c0001t0037 | 2 | HG01099.hp2 HG01109.hp2 |
5_prime_UTR_variant | MODIFIER | c.-410C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/5 | 1520 | chr8 | 11769928 | ||||||
| chr8:11769945 | G | A | 9 | a0001c0001t0002 a0001c0001t0017 a0001c0001t0026 others(6): Show |
62 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(59): Show |
5_prime_UTR_variant | MODIFIER | c.-393G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/5 | 1503 | chr8 | 11769945 | ||||||
| chr8:11769962 | C | T | 1 | a0001c0001t0015 | 6 | HG02258.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-376C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/5 | 1486 | chr8 | 11769962 | ||||||
| chr8:11770078 | C | G | 2 | a0001c0001t0022 a0001c0001t0066 |
5 | HG02486.hp1 HG02615.hp2 HG03209.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-260C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/5 | chr8 | 11770078 | |||||||
| chr8:11770112 | G | C | 33 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(30): Show |
254 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(251): Show |
5_prime_UTR_variant | MODIFIER | c.-226G>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/5 | 1336 | chr8 | 11770112 | ||||||
| chr8:11770134 | A | G | 2 | a0001c0002t0021 a0001c0002t0065 |
5 | HG02486.hp2 HG02559.hp2 HG03130.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-204A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/5 | 1314 | chr8 | 11770134 | ||||||
| chr8:11770142 | T | TTCGAAGT others(15): Show |
3 | a0001c0002t0031 a0001c0002t0052 a0001c0018t0031 |
3 | HG02145.hp2 HG03471.hp1 HG03516.hp2 |
5_prime_UTR_variant | MODIFIER | c.-193_-172dupGAAGTC others(16): Show |
NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/5 | 1281 | INFO_REALIGN_3_PRIME | chr8 | 11770142 | |||||
| chr8:11770151 | C | A | 1 | a0001c0001t0051 | 1 | HG03579.hp2 | 5_prime_UTR_variant | MODIFIER | c.-187C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/5 | 1297 | chr8 | 11770151 | ||||||
| chr8:11770317 | A | C | 1 | a0001c0001t0040 | 1 | NA19079.hp2 | 5_prime_UTR_variant | MODIFIER | c.-21A>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/5 | 1131 | chr8 | 11770317 | ||||||
| chr8:11770326 | A | G | 1 | a0001c0001t0039 | 1 | HG02135.hp1 | 5_prime_UTR_variant | MODIFIER | c.-12A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/5 | 1122 | chr8 | 11770326 | ||||||
| chr8:11786294 | C | T | 24 | a0001c0001t0035 a0001c0002t0003 a0001c0002t0004 others(21): Show |
111 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*21C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 21 | chr8 | 11786294 | ||||||
| chr8:11786299 | C | T | 1 | a0001c0002t0064 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*26C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 26 | chr8 | 11786299 | ||||||
| chr8:11786306 | GC | G | 28 | a0001c0001t0035 a0001c0002t0003 a0001c0002t0004 others(25): Show |
117 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*34delC | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 34 | chr8 | 11786306 | ||||||
| chr8:11786406 | G | A | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(66): Show |
388 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(385): Show |
3_prime_UTR_variant | MODIFIER | c.*133G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 133 | chr8 | 11786406 | ||||||
| chr8:11786462 | C | G | 1 | a0001c0001t0048 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*189C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 189 | chr8 | 11786462 | ||||||
| chr8:11786463 | T | C | 1 | a0001c0001t0016 | 6 | HG00140.hp1 HG00280.hp1 HG01515.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*190T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 190 | chr8 | 11786463 | ||||||
| chr8:11786503 | C | T | 2 | a0001c0001t0056 a0001c0001t0057 |
2 | HG01884.hp2 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*230C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 230 | chr8 | 11786503 | ||||||
| chr8:11786551 | G | A | 1 | a0001c0001t0056 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*278G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 278 | chr8 | 11786551 | ||||||
| chr8:11786608 | T | C | 5 | a0001c0001t0007 a0001c0001t0058 a0001c0001t0067 others(2): Show |
18 | HG01891.hp2 HG02257.hp1 HG02615.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*335T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 335 | chr8 | 11786608 | ||||||
| chr8:11786628 | G | GCTT | 11 | a0001c0001t0001 a0001c0001t0022 a0001c0001t0024 others(8): Show |
117 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*355_*356insCTT | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 356 | chr8 | 11786628 | ||||||
| chr8:11786628 | G | GCTTT | 2 | a0001c0001t0011 a0001c0001t0025 |
13 | HG01433.hp2 HG01934.hp2 HG02004.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*355_*356insCTTT | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 356 | chr8 | 11786628 | ||||||
| chr8:11786628 | G | GT | 21 | a0001c0001t0028 a0001c0001t0047 a0001c0002t0003 others(18): Show |
107 | HG00408.hp2 HG00438.hp2 HG00558.hp2 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*371dupT | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 372 | INFO_REALIGN_3_PRIME | chr8 | 11786628 | |||||
| chr8:11786628 | G | GTT | 22 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0010 others(19): Show |
75 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*370_*371dupTT | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 372 | INFO_REALIGN_3_PRIME | chr8 | 11786628 | |||||
| chr8:11786650 | T | G | 1 | a0001c0001t0042 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*377T>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 377 | chr8 | 11786650 | ||||||
| chr8:11786760 | C | G | 1 | a0004c0005t0044 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*487C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 487 | chr8 | 11786760 | ||||||
| chr8:11786764 | A | C | 4 | a0001c0002t0014 a0001c0002t0060 a0001c0002t0062 others(1): Show |
9 | HG02055.hp2 HG02451.hp2 HG02559.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*491A>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 491 | chr8 | 11786764 | ||||||
| chr8:11786820 | T | C | 1 | a0001c0002t0062 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*547T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 547 | chr8 | 11786820 | ||||||
| chr8:11786892 | G | A | 1 | a0004c0005t0043 | 1 | NA18960.hp2 | 3_prime_UTR_variant | MODIFIER | c.*619G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 619 | chr8 | 11786892 | ||||||
| chr8:11787016 | AT | A | 22 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0022 others(19): Show |
145 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*756delT | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 756 | INFO_REALIGN_3_PRIME | chr8 | 11787016 | |||||
| chr8:11787138 | T | G | 57 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(54): Show |
349 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(346): Show |
3_prime_UTR_variant | MODIFIER | c.*865T>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 865 | chr8 | 11787138 | ||||||
| chr8:11787139 | C | A | 1 | a0001c0001t0017 | 5 | NA18941.hp2 NA19003.hp2 NA19057.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*866C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 866 | chr8 | 11787139 | ||||||
| chr8:11787139 | C | G | 56 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(53): Show |
344 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(341): Show |
3_prime_UTR_variant | MODIFIER | c.*866C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 866 | chr8 | 11787139 | ||||||
| chr8:11787180 | G | A | 2 | a0003c0006t0012 a0010c0019t0055 |
7 | HG02109.hp2 HG02723.hp2 HG02896.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*907G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 907 | chr8 | 11787180 | ||||||
| chr8:11787242 | A | G | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(25): Show |
232 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*969A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 969 | chr8 | 11787242 | ||||||
| chr8:11787245 | A | C | 1 | a0001c0014t0046 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*972A>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 972 | chr8 | 11787245 | ||||||
| chr8:11787261 | G | A | 1 | a0010c0019t0055 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*988G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 988 | chr8 | 11787261 | ||||||
| chr8:11787312 | C | T | 1 | a0001c0001t0009 | 12 | HG00140.hp2 HG01123.hp2 HG01167.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1039C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 5/5 | 1039 | chr8 | 11787312 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:11770359 | C | T | 2 | a0002c0003t0003g0217 a0002c0003t0003g0218 |
2 | NA18997.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-3+24C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/4 | chr8 | 11770359 | |||||||
| chr8:11770583 | C | T | 1 | a0001c0002t0004g0216 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-3+248C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/4 | chr8 | 11770583 | |||||||
| chr8:11770620 | A | C | 22 | a0001c0001t0032g0204 a0001c0002t0004g0013 a0001c0002t0004g0067 others(19): Show |
31 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-3+285A>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/4 | chr8 | 11770620 | |||||||
| chr8:11770641 | G | A | 2 | a0001c0001t0002g0071 a0001c0001t0041g0072 |
2 | HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-3+306G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/4 | chr8 | 11770641 | |||||||
| chr8:11770653 | G | T | 21 | a0001c0001t0032g0204 a0001c0002t0004g0013 a0001c0002t0004g0068 others(18): Show |
29 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.-3+318G>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/4 | chr8 | 11770653 | |||||||
| chr8:11770663 | C | T | 10 | a0001c0002t0004g0013 a0001c0002t0004g0070 a0001c0002t0004g0211 others(7): Show |
16 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.-3+328C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/4 | chr8 | 11770663 | |||||||
| chr8:11770823 | C | G | 1 | a0001c0001t0029g0066 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-3+488C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/4 | chr8 | 11770823 | |||||||
| chr8:11770866 | T | A | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(192): Show |
369 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.-3+531T>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/4 | chr8 | 11770866 | |||||||
| chr8:11770947 | C | T | 1 | a0003c0006t0012g0022 | 4 | HG02109.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-499C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/4 | chr8 | 11770947 | |||||||
| chr8:11770962 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(117): Show |
241 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.-2-484C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/4 | chr8 | 11770962 | |||||||
| chr8:11771020 | GTGGGTCA others(3): Show |
G | 1 | a0001c0001t0002g0073 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-2-422_-2-413delGT others(8): Show |
NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr8 | 11771020 | ||||||
| chr8:11771140 | C | T | 22 | a0001c0001t0032g0204 a0001c0002t0004g0013 a0001c0002t0004g0065 others(19): Show |
32 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.-2-306C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/4 | chr8 | 11771140 | |||||||
| chr8:11771150 | T | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(84): Show |
177 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.-2-296T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/4 | chr8 | 11771150 | |||||||
| chr8:11771217 | G | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0001t0001g0075 others(3): Show |
9 | HG00735.hp1 HG01070.hp2 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-229G>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/4 | chr8 | 11771217 | |||||||
| chr8:11771250 | C | G | 29 | a0001c0001t0032g0175 a0002c0003t0003g0007 a0002c0003t0003g0008 others(26): Show |
50 | HG00438.hp2 HG00673.hp1 HG02015.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-196C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/4 | chr8 | 11771250 | |||||||
| chr8:11771366 | G | A | 6 | a0001c0010t0034g0183 a0001c0016t0007g0184 a0003c0013t0018g0180 others(3): Show |
9 | HG02738.hp2 HG02818.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-80G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/4 | chr8 | 11771366 | |||||||
| chr8:11771415 | G | A | 1 | a0001c0001t0015g0123 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-2-31G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 1/4 | chr8 | 11771415 | |||||||
| chr8:11771610 | T | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(177): Show |
346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.138+25T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11771610 | |||||||
| chr8:11771616 | C | G | 1 | a0001c0001t0029g0066 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.138+31C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11771616 | |||||||
| chr8:11771620 | C | G | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(75): Show |
167 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.138+35C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11771620 | |||||||
| chr8:11771630 | G | A | 1 | a0007c0009t0033g0157 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138+45G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11771630 | |||||||
| chr8:11771632 | G | A | 1 | a0003c0006t0012g0058 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.138+47G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11771632 | |||||||
| chr8:11771732 | G | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(172): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.138+147G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11771732 | |||||||
| chr8:11771763 | A | C | 1 | a0003c0006t0012g0058 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.138+178A>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11771763 | |||||||
| chr8:11771856 | G | T | 1 | a0001c0001t0029g0066 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.138+271G>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11771856 | |||||||
| chr8:11771858 | A | T | 22 | a0001c0001t0032g0204 a0001c0002t0004g0013 a0001c0002t0004g0065 others(19): Show |
32 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.138+273A>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11771858 | |||||||
| chr8:11771865 | G | A | 7 | a0001c0010t0034g0183 a0001c0016t0007g0184 a0003c0013t0018g0180 others(4): Show |
10 | HG02738.hp2 HG02818.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.138+280G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11771865 | |||||||
| chr8:11771932 | C | T | 1 | a0001c0001t0022g0059 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.138+347C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11771932 | |||||||
| chr8:11771941 | G | A | 2 | a0001c0010t0034g0185 a0002c0003t0003g0165 |
2 | NA18986.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.138+356G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11771941 | |||||||
| chr8:11771975 | C | T | 1 | a0001c0011t0001g0121 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.138+390C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11771975 | |||||||
| chr8:11772005 | C | T | 1 | a0001c0001t0002g0156 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.138+420C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772005 | |||||||
| chr8:11772018 | CATG | C | 6 | a0001c0001t0015g0052 a0001c0001t0015g0123 a0001c0001t0015g0124 others(3): Show |
8 | HG02258.hp1 HG02451.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.138+438_138+440del others(3): Show |
NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 11772018 | ||||||
| chr8:11772069 | G | C | 7 | a0001c0001t0010g0012 a0001c0001t0010g0063 a0001c0001t0010g0186 others(4): Show |
13 | HG00323.hp1 HG00323.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.138+484G>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772069 | |||||||
| chr8:11772104 | G | T | 1 | a0001c0001t0002g0056 | 2 | NA18957.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.138+519G>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772104 | |||||||
| chr8:11772128 | G | A | 22 | a0001c0001t0032g0204 a0001c0002t0004g0013 a0001c0002t0004g0065 others(19): Show |
32 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.138+543G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772128 | |||||||
| chr8:11772128 | G | C | 1 | a0003c0013t0018g0180 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.138+543G>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772128 | |||||||
| chr8:11772202 | C | CA | 72 | a0001c0001t0001g0128 a0001c0001t0010g0012 a0001c0001t0010g0063 others(69): Show |
113 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.138+625dupA | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 11772202 | ||||||
| chr8:11772273 | C | T | 1 | a0001c0001t0009g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.138+688C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772273 | |||||||
| chr8:11772276 | A | C | 5 | a0001c0001t0002g0021 a0001c0001t0002g0152 a0001c0001t0002g0153 others(2): Show |
8 | HG00621.hp1 HG03831.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.138+691A>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772276 | |||||||
| chr8:11772300 | C | G | 21 | a0001c0001t0006g0005 a0001c0001t0006g0030 a0001c0001t0006g0054 others(18): Show |
42 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.138+715C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772300 | |||||||
| chr8:11772301 | T | A | 7 | a0001c0001t0007g0010 a0001c0001t0007g0020 a0001c0001t0007g0144 others(4): Show |
15 | HG01891.hp2 HG02257.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.138+716T>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772301 | |||||||
| chr8:11772343 | A | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(119): Show |
241 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.138+758A>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772343 | |||||||
| chr8:11772401 | C | T | 1 | a0007c0009t0033g0157 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.138+816C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772401 | |||||||
| chr8:11772515 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.138+930C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772515 | |||||||
| chr8:11772551 | T | C | 35 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0016 others(32): Show |
67 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.138+966T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772551 | |||||||
| chr8:11772572 | A | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(120): Show |
242 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(239): Show |
intron_variant | MODIFIER | c.138+987A>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772572 | |||||||
| chr8:11772594 | C | G | 1 | a0001c0010t0034g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.138+1009C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772594 | |||||||
| chr8:11772644 | G | T | 3 | a0003c0004t0018g0035 a0003c0004t0018g0177 a0009c0021t0018g0035 |
4 | HG02630.hp2 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+1059G>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772644 | |||||||
| chr8:11772694 | C | T | 3 | a0001c0001t0007g0020 a0001c0001t0058g0020 a0001c0001t0067g0020 |
4 | HG01891.hp2 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+1109C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772694 | |||||||
| chr8:11772710 | C | T | 1 | a0003c0006t0012g0058 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.138+1125C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772710 | |||||||
| chr8:11772869 | C | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(13): Show |
43 | HG00673.hp2 HG01433.hp2 HG01934.hp2 others(40): Show |
intron_variant | MODIFIER | c.138+1284C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772869 | |||||||
| chr8:11772903 | A | G | 31 | a0001c0001t0001g0128 a0001c0001t0032g0175 a0002c0003t0003g0007 others(28): Show |
57 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.138+1318A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772903 | |||||||
| chr8:11772920 | C | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(79): Show |
166 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.138+1335C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772920 | |||||||
| chr8:11772941 | C | A | 1 | a0001c0001t0006g0054 | 2 | HG01261.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.138+1356C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11772941 | |||||||
| chr8:11773009 | C | A | 1 | a0003c0006t0012g0058 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.138+1424C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11773009 | |||||||
| chr8:11773017 | G | T | 1 | a0001c0001t0002g0141 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.138+1432G>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11773017 | |||||||
| chr8:11773268 | C | A | 1 | a0001c0010t0034g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.138+1683C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11773268 | |||||||
| chr8:11773350 | C | T | 5 | a0001c0001t0015g0052 a0001c0001t0015g0123 a0001c0001t0015g0124 others(2): Show |
6 | HG02258.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.138+1765C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11773350 | |||||||
| chr8:11773368 | C | G | 1 | a0001c0001t0041g0072 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.138+1783C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11773368 | |||||||
| chr8:11773406 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(111): Show |
229 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.138+1821C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11773406 | |||||||
| chr8:11773407 | G | A | 2 | a0001c0002t0014g0158 a0001c0002t0014g0159 |
2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.138+1822G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11773407 | |||||||
| chr8:11773560 | A | G | 3 | a0001c0001t0009g0111 a0001c0001t0009g0112 a0001c0001t0009g0120 |
3 | HG01257.hp1 HG01258.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.138+1975A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11773560 | |||||||
| chr8:11773644 | C | T | 1 | a0003c0004t0003g0176 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.138+2059C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11773644 | |||||||
| chr8:11773660 | T | C | 1 | a0001c0001t0057g0160 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.138+2075T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11773660 | |||||||
| chr8:11773668 | G | A | 1 | a0003c0006t0012g0022 | 4 | HG02109.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+2083G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11773668 | |||||||
| chr8:11773761 | T | C | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(241): Show |
438 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(435): Show |
intron_variant | MODIFIER | c.138+2176T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11773761 | |||||||
| chr8:11773836 | A | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0051 others(9): Show |
25 | HG00423.hp2 HG01433.hp2 HG01934.hp2 others(22): Show |
intron_variant | MODIFIER | c.138+2251A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11773836 | |||||||
| chr8:11773857 | C | G | 1 | a0001c0001t0001g0110 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.138+2272C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11773857 | |||||||
| chr8:11773995 | C | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(67): Show |
151 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.138+2410C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11773995 | |||||||
| chr8:11774042 | G | C | 24 | a0001c0001t0022g0059 a0001c0001t0029g0066 a0001c0001t0035g0127 others(21): Show |
34 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(31): Show |
intron_variant | MODIFIER | c.138+2457G>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11774042 | |||||||
| chr8:11774053 | A | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(118): Show |
238 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(235): Show |
intron_variant | MODIFIER | c.138+2468A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11774053 | |||||||
| chr8:11774124 | C | G | 9 | a0001c0001t0010g0012 a0001c0001t0010g0063 a0001c0001t0010g0186 others(6): Show |
15 | HG00323.hp1 HG00323.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.138+2539C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11774124 | |||||||
| chr8:11774222 | C | G | 36 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0016 others(33): Show |
68 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.138+2637C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11774222 | |||||||
| chr8:11774236 | A | G | 8 | a0001c0001t0010g0012 a0001c0001t0010g0063 a0001c0001t0010g0187 others(5): Show |
14 | HG00323.hp1 HG00323.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.138+2651A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11774236 | |||||||
| chr8:11774247 | C | T | 2 | a0001c0001t0006g0030 a0001c0001t0068g0030 |
3 | HG01070.hp1 HG01071.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.138+2662C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11774247 | |||||||
| chr8:11774248 | G | A | 2 | a0003c0004t0003g0193 a0003c0004t0004g0192 |
2 | HG02258.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.138+2663G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11774248 | |||||||
| chr8:11774252 | G | A | 1 | a0002c0003t0003g0167 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.138+2667G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11774252 | |||||||
| chr8:11774271 | A | G | 9 | a0001c0001t0010g0012 a0001c0001t0010g0063 a0001c0001t0010g0186 others(6): Show |
15 | HG00323.hp1 HG00323.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.138+2686A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11774271 | |||||||
| chr8:11774294 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0115 |
3 | NA18980.hp1 NA18984.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.138+2709G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11774294 | |||||||
| chr8:11774313 | TG | T | 35 | a0001c0001t0001g0128 a0002c0003t0003g0007 a0002c0003t0003g0008 others(32): Show |
63 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.138+2729delG | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11774313 | |||||||
| chr8:11774362 | G | A | 7 | a0001c0001t0010g0012 a0001c0001t0010g0063 a0001c0001t0010g0186 others(4): Show |
13 | HG00323.hp1 HG00323.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.138+2777G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11774362 | |||||||
| chr8:11774395 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.138+2810C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11774395 | |||||||
| chr8:11774397 | A | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(188): Show |
349 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(346): Show |
intron_variant | MODIFIER | c.138+2812A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11774397 | |||||||
| chr8:11774463 | G | C | 1 | a0001c0001t0001g0087 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.138+2878G>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11774463 | |||||||
| chr8:11774523 | C | A | 9 | a0001c0001t0010g0012 a0001c0001t0010g0063 a0001c0001t0010g0186 others(6): Show |
15 | HG00323.hp1 HG00323.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.138+2938C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11774523 | |||||||
| chr8:11774770 | C | A | 14 | a0001c0001t0006g0005 a0001c0001t0006g0030 a0001c0001t0006g0054 others(11): Show |
27 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.138+3185C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11774770 | |||||||
| chr8:11774770 | C | G | 8 | a0001c0001t0006g0151 a0001c0001t0007g0010 a0001c0001t0007g0020 others(5): Show |
16 | HG01884.hp1 HG01891.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.138+3185C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11774770 | |||||||
| chr8:11774846 | C | G | 4 | a0001c0001t0015g0052 a0001c0001t0015g0123 a0001c0001t0015g0125 others(1): Show |
5 | HG02451.hp1 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.138+3261C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11774846 | |||||||
| chr8:11775019 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(149): Show |
295 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(292): Show |
intron_variant | MODIFIER | c.138+3434A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11775019 | |||||||
| chr8:11775072 | T | C | 7 | a0001c0001t0007g0010 a0001c0001t0007g0020 a0001c0001t0007g0144 others(4): Show |
15 | HG01891.hp2 HG02257.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.138+3487T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11775072 | |||||||
| chr8:11775241 | C | T | 2 | a0001c0001t0009g0108 a0001c0001t0009g0109 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.138+3656C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11775241 | |||||||
| chr8:11775318 | AAGC | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(112): Show |
230 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(227): Show |
intron_variant | MODIFIER | c.138+3740_138+3742d others(5): Show |
NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 11775318 | ||||||
| chr8:11775327 | C | T | 2 | a0001c0002t0021g0069 a0001c0002t0021g0207 |
3 | HG02559.hp2 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.138+3742C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11775327 | |||||||
| chr8:11775589 | C | T | 1 | a0005c0007t0001g0017 | 5 | NA18998.hp2 NA19063.hp2 NA19066.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+4004C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11775589 | |||||||
| chr8:11775592 | C | A | 4 | a0003c0013t0018g0180 a0004c0005t0013g0023 a0004c0005t0013g0181 others(1): Show |
7 | HG02738.hp2 HG02818.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-4006C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11775592 | |||||||
| chr8:11775653 | C | T | 1 | a0010c0019t0055g0191 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.139-3945C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11775653 | |||||||
| chr8:11775679 | A | G | 43 | a0001c0001t0022g0059 a0001c0001t0032g0204 a0001c0001t0054g0190 others(40): Show |
62 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.139-3919A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11775679 | |||||||
| chr8:11775801 | A | G | 36 | a0001c0010t0034g0183 a0001c0016t0007g0184 a0002c0003t0003g0007 others(33): Show |
64 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.139-3797A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11775801 | |||||||
| chr8:11775853 | A | G | 1 | a0001c0001t0029g0066 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.139-3745A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11775853 | |||||||
| chr8:11775934 | G | A | 36 | a0001c0010t0034g0183 a0001c0016t0007g0184 a0002c0003t0003g0007 others(33): Show |
64 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.139-3664G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11775934 | |||||||
| chr8:11775949 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.139-3649C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11775949 | |||||||
| chr8:11775998 | C | T | 4 | a0003c0013t0018g0180 a0004c0005t0013g0023 a0004c0005t0013g0181 others(1): Show |
7 | HG02738.hp2 HG02818.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-3600C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11775998 | |||||||
| chr8:11776037 | A | G | 36 | a0001c0010t0034g0183 a0001c0016t0007g0184 a0002c0003t0003g0007 others(33): Show |
64 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.139-3561A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11776037 | |||||||
| chr8:11776075 | A | T | 1 | a0001c0001t0025g0079 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.139-3523A>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11776075 | |||||||
| chr8:11776098 | T | G | 2 | a0001c0002t0004g0216 a0001c0002t0030g0122 |
2 | HG00639.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.139-3500T>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11776098 | |||||||
| chr8:11776329 | C | T | 1 | a0001c0002t0004g0215 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.139-3269C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11776329 | |||||||
| chr8:11776340 | C | G | 2 | a0001c0002t0004g0068 a0001c0002t0036g0206 |
3 | HG03490.hp1 HG03492.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.139-3258C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11776340 | |||||||
| chr8:11776348 | G | A | 1 | a0001c0001t0006g0146 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.139-3250G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11776348 | |||||||
| chr8:11776455 | C | T | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(232): Show |
426 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(423): Show |
intron_variant | MODIFIER | c.139-3143C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11776455 | |||||||
| chr8:11776457 | C | T | 1 | a0001c0001t0005g0107 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.139-3141C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11776457 | |||||||
| chr8:11776464 | T | C | 1 | a0001c0002t0064g0200 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.139-3134T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11776464 | |||||||
| chr8:11776555 | A | G | 5 | a0001c0001t0015g0052 a0001c0001t0015g0123 a0001c0001t0015g0124 others(2): Show |
6 | HG02258.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-3043A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11776555 | |||||||
| chr8:11776685 | T | A | 22 | a0001c0001t0006g0005 a0001c0001t0006g0030 a0001c0001t0006g0054 others(19): Show |
43 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.139-2913T>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11776685 | |||||||
| chr8:11776720 | C | T | 1 | a0003c0004t0003g0176 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.139-2878C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11776720 | |||||||
| chr8:11776793 | C | G | 10 | a0001c0001t0022g0059 a0001c0001t0054g0190 a0001c0002t0014g0032 others(7): Show |
13 | HG02055.hp2 HG02451.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.139-2805C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11776793 | |||||||
| chr8:11776861 | G | A | 1 | a0001c0002t0021g0207 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.139-2737G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11776861 | |||||||
| chr8:11776933 | G | C | 1 | a0001c0001t0032g0175 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.139-2665G>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11776933 | |||||||
| chr8:11776953 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.139-2645G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11776953 | |||||||
| chr8:11776995 | A | G | 36 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0016 others(33): Show |
69 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.139-2603A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11776995 | |||||||
| chr8:11777012 | C | T | 38 | a0001c0010t0034g0183 a0001c0016t0007g0184 a0002c0003t0003g0007 others(35): Show |
66 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.139-2586C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777012 | |||||||
| chr8:11777062 | C | G | 2 | a0004c0005t0013g0181 a0004c0005t0044g0182 |
2 | NA18986.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.139-2536C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777062 | |||||||
| chr8:11777090 | C | T | 35 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0016 others(32): Show |
67 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.139-2508C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777090 | |||||||
| chr8:11777152 | C | G | 1 | a0001c0001t0037g0049 | 2 | HG01099.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.139-2446C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777152 | |||||||
| chr8:11777162 | C | CT | 22 | a0001c0001t0006g0005 a0001c0001t0006g0030 a0001c0001t0006g0054 others(19): Show |
43 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.139-2426dupT | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 11777162 | ||||||
| chr8:11777162 | CT | C | 7 | a0001c0001t0015g0052 a0001c0001t0015g0123 a0001c0001t0015g0124 others(4): Show |
9 | HG02258.hp1 HG02451.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.139-2426delT | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 11777162 | ||||||
| chr8:11777231 | A | C | 37 | a0001c0001t0001g0118 a0001c0001t0002g0003 a0001c0001t0002g0004 others(34): Show |
69 | HG00408.hp1 HG00609.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.139-2367A>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777231 | |||||||
| chr8:11777254 | A | G | 3 | a0004c0005t0013g0023 a0004c0005t0013g0181 a0004c0005t0044g0182 |
6 | HG02738.hp2 HG02818.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-2344A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777254 | |||||||
| chr8:11777273 | A | C | 1 | a0001c0001t0035g0127 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.139-2325A>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777273 | |||||||
| chr8:11777300 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(80): Show |
168 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.139-2298A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777300 | |||||||
| chr8:11777309 | T | G | 1 | a0001c0002t0014g0158 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.139-2289T>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777309 | |||||||
| chr8:11777356 | A | G | 2 | a0001c0001t0015g0125 a0001c0001t0015g0126 |
2 | HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.139-2242A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777356 | |||||||
| chr8:11777358 | C | T | 3 | a0004c0005t0013g0023 a0004c0005t0013g0181 a0004c0005t0044g0182 |
6 | HG02738.hp2 HG02818.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-2240C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777358 | |||||||
| chr8:11777385 | A | T | 1 | a0001c0001t0057g0160 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.139-2213A>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777385 | |||||||
| chr8:11777404 | C | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(237): Show |
431 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(428): Show |
intron_variant | MODIFIER | c.139-2194C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777404 | |||||||
| chr8:11777577 | T | A | 3 | a0004c0005t0013g0023 a0004c0005t0013g0181 a0004c0005t0044g0182 |
6 | HG02738.hp2 HG02818.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.139-2021T>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777577 | |||||||
| chr8:11777671 | A | T | 1 | a0001c0001t0056g0164 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.139-1927A>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777671 | |||||||
| chr8:11777686 | C | A | 2 | a0004c0005t0013g0023 a0004c0005t0013g0181 |
5 | HG02738.hp2 HG02818.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-1912C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777686 | |||||||
| chr8:11777691 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.139-1907A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777691 | |||||||
| chr8:11777803 | C | G | 1 | a0007c0009t0033g0157 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.139-1795C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777803 | |||||||
| chr8:11777858 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.139-1740A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777858 | |||||||
| chr8:11777875 | C | T | 1 | a0001c0001t0015g0126 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.139-1723C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777875 | |||||||
| chr8:11777882 | C | A | 1 | a0010c0019t0055g0191 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.139-1716C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777882 | |||||||
| chr8:11777935 | G | C | 2 | a0001c0001t0010g0063 a0001c0001t0053g0063 |
2 | HG03710.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.139-1663G>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777935 | |||||||
| chr8:11777958 | C | A | 1 | a0001c0002t0059g0196 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.139-1640C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11777958 | |||||||
| chr8:11778060 | T | C | 77 | a0001c0001t0006g0005 a0001c0001t0006g0030 a0001c0001t0006g0054 others(74): Show |
124 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.139-1538T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11778060 | |||||||
| chr8:11778095 | C | A | 1 | a0003c0004t0004g0192 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.139-1503C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11778095 | |||||||
| chr8:11778107 | A | G | 16 | a0001c0001t0006g0005 a0001c0001t0006g0030 a0001c0001t0006g0054 others(13): Show |
29 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.139-1491A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11778107 | |||||||
| chr8:11778257 | A | G | 1 | a0001c0001t0070g0080 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.139-1341A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11778257 | |||||||
| chr8:11778290 | G | GTTTTTTT | 7 | a0001c0001t0009g0088 a0001c0001t0010g0012 a0001c0001t0010g0063 others(4): Show |
13 | HG00323.hp2 HG01081.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.139-1294_139-1288d others(9): Show |
NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 11778290 | ||||||
| chr8:11778290 | GT | G | 8 | a0001c0001t0002g0021 a0001c0001t0002g0153 a0001c0001t0002g0154 others(5): Show |
11 | HG01358.hp1 HG03239.hp1 HG03688.hp2 others(8): Show |
intron_variant | MODIFIER | c.139-1288delT | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 11778290 | ||||||
| chr8:11778290 | GTT | G | 71 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0037 others(68): Show |
121 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.139-1289_139-1288d others(4): Show |
NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 11778290 | ||||||
| chr8:11778290 | GTTT | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(143): Show |
281 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.139-1290_139-1288d others(5): Show |
NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 11778290 | ||||||
| chr8:11778290 | GTTTT | G | 7 | a0001c0001t0015g0124 a0001c0001t0024g0038 a0001c0001t0025g0038 others(4): Show |
7 | HG00733.hp1 HG02258.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.139-1291_139-1288d others(6): Show |
NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 11778290 | ||||||
| chr8:11778395 | C | T | 37 | a0002c0003t0003g0007 a0002c0003t0003g0008 a0002c0003t0003g0061 others(34): Show |
65 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.139-1203C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11778395 | |||||||
| chr8:11778418 | G | A | 8 | a0001c0001t0009g0088 a0001c0001t0010g0012 a0001c0001t0010g0063 others(5): Show |
14 | HG00323.hp1 HG00323.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-1180G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11778418 | |||||||
| chr8:11778437 | T | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(80): Show |
181 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.139-1161T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11778437 | |||||||
| chr8:11778508 | G | A | 8 | a0001c0001t0009g0088 a0001c0001t0010g0012 a0001c0001t0010g0063 others(5): Show |
14 | HG00323.hp1 HG00323.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-1090G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11778508 | |||||||
| chr8:11778541 | A | G | 1 | a0001c0001t0006g0055 | 2 | HG01074.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.139-1057A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11778541 | |||||||
| chr8:11778674 | A | G | 54 | a0001c0001t0009g0088 a0001c0001t0010g0012 a0001c0001t0010g0063 others(51): Show |
89 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.139-924A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11778674 | |||||||
| chr8:11778709 | TG | T | 7 | a0001c0001t0007g0010 a0001c0001t0007g0020 a0001c0001t0007g0144 others(4): Show |
15 | HG01891.hp2 HG02257.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.139-886delG | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 11778709 | ||||||
| chr8:11778943 | G | GA | 58 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(55): Show |
123 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.139-633dupA | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 11778943 | ||||||
| chr8:11778943 | G | GAA | 69 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0050 others(66): Show |
120 | HG00280.hp2 HG00438.hp2 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.139-634_139-633dup others(2): Show |
NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 11778943 | ||||||
| chr8:11778943 | G | GAAA | 35 | a0001c0001t0006g0005 a0001c0001t0006g0030 a0001c0001t0006g0054 others(32): Show |
57 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.139-635_139-633dup others(3): Show |
NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 11778943 | ||||||
| chr8:11778943 | G | GAAAAA | 4 | a0001c0001t0002g0021 a0001c0001t0002g0071 a0001c0001t0002g0138 others(1): Show |
7 | HG03453.hp1 HG03486.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.139-637_139-633dup others(5): Show |
NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 11778943 | ||||||
| chr8:11778943 | G | GAAAAAA | 48 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0043 others(45): Show |
91 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.139-638_139-633dup others(6): Show |
NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 11778943 | ||||||
| chr8:11778943 | G | GAAAAAAA | 19 | a0001c0001t0001g0037 a0001c0001t0001g0097 a0001c0001t0002g0016 others(16): Show |
28 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.139-639_139-633dup others(7): Show |
NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 11778943 | ||||||
| chr8:11778967 | A | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(238): Show |
435 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(432): Show |
intron_variant | MODIFIER | c.139-631A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11778967 | |||||||
| chr8:11778998 | A | G | 34 | a0002c0003t0003g0007 a0002c0003t0003g0008 a0002c0003t0003g0061 others(31): Show |
61 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.139-600A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11778998 | |||||||
| chr8:11779156 | A | AG | 16 | a0001c0001t0001g0090 a0001c0001t0002g0132 a0001c0001t0006g0147 others(13): Show |
17 | HG00621.hp2 HG00735.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.139-437dupG | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr8 | 11779156 | ||||||
| chr8:11779225 | C | T | 2 | a0004c0005t0013g0023 a0004c0005t0013g0181 |
5 | HG02738.hp2 HG02818.hp1 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-373C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11779225 | |||||||
| chr8:11779317 | T | G | 1 | a0001c0001t0011g0117 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.139-281T>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11779317 | |||||||
| chr8:11779323 | C | T | 3 | a0001c0002t0031g0031 a0001c0002t0052g0031 a0001c0018t0031g0031 |
3 | HG02145.hp2 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.139-275C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11779323 | |||||||
| chr8:11779353 | T | C | 69 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0037 others(66): Show |
120 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.139-245T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11779353 | |||||||
| chr8:11779361 | T | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(241): Show |
438 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(435): Show |
intron_variant | MODIFIER | c.139-237T>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11779361 | |||||||
| chr8:11779375 | T | G | 34 | a0001c0001t0009g0100 a0001c0001t0032g0204 a0001c0001t0057g0160 others(31): Show |
50 | HG00639.hp1 HG00639.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.139-223T>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11779375 | |||||||
| chr8:11779385 | C | T | 1 | a0001c0001t0005g0103 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.139-213C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11779385 | |||||||
| chr8:11779393 | C | A | 8 | a0001c0001t0009g0088 a0001c0001t0010g0012 a0001c0001t0010g0063 others(5): Show |
14 | HG00323.hp1 HG00323.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-205C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11779393 | |||||||
| chr8:11779401 | C | T | 1 | a0001c0001t0005g0047 | 2 | HG04184.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.139-197C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11779401 | |||||||
| chr8:11779413 | A | G | 8 | a0001c0001t0009g0088 a0001c0001t0010g0012 a0001c0001t0010g0063 others(5): Show |
14 | HG00323.hp1 HG00323.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-185A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11779413 | |||||||
| chr8:11779424 | C | T | 8 | a0001c0001t0009g0088 a0001c0001t0010g0012 a0001c0001t0010g0063 others(5): Show |
14 | HG00323.hp1 HG00323.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-174C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11779424 | |||||||
| chr8:11779442 | G | A | 2 | a0001c0002t0004g0178 a0001c0002t0004g0179 |
2 | HG01891.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.139-156G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11779442 | |||||||
| chr8:11779489 | C | T | 8 | a0001c0001t0009g0088 a0001c0001t0010g0012 a0001c0001t0010g0063 others(5): Show |
14 | HG00323.hp1 HG00323.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.139-109C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11779489 | |||||||
| chr8:11779493 | C | T | 36 | a0002c0003t0003g0007 a0002c0003t0003g0008 a0002c0003t0003g0061 others(33): Show |
63 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.139-105C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11779493 | |||||||
| chr8:11779553 | C | G | 1 | a0001c0001t0010g0189 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.139-45C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 2/4 | chr8 | 11779553 | |||||||
| chr8:11780130 | C | G | 2 | a0001c0002t0004g0178 a0001c0002t0004g0179 |
2 | HG01891.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.491+180C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11780130 | |||||||
| chr8:11780134 | A | C | 38 | a0001c0001t0056g0164 a0001c0001t0057g0160 a0002c0003t0003g0007 others(35): Show |
65 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.491+184A>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11780134 | |||||||
| chr8:11780358 | T | A | 1 | a0001c0001t0001g0015 | 6 | NA18950.hp2 NA18952.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.491+408T>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11780358 | |||||||
| chr8:11780437 | G | A | 2 | a0001c0001t0056g0164 a0001c0001t0057g0160 |
2 | HG01884.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.491+487G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11780437 | |||||||
| chr8:11780443 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0095 |
2 | NA19005.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.491+493C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11780443 | |||||||
| chr8:11780522 | G | A | 1 | a0010c0019t0055g0191 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.491+572G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11780522 | |||||||
| chr8:11780523 | G | T | 1 | a0010c0019t0055g0191 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.491+573G>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11780523 | |||||||
| chr8:11780567 | C | T | 1 | a0001c0002t0004g0205 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.491+617C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11780567 | |||||||
| chr8:11780625 | G | A | 1 | a0001c0011t0001g0121 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.491+675G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11780625 | |||||||
| chr8:11780691 | A | G | 1 | a0001c0001t0002g0137 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.491+741A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11780691 | |||||||
| chr8:11780735 | A | G | 38 | a0001c0010t0034g0183 a0001c0016t0007g0184 a0002c0003t0003g0007 others(35): Show |
65 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.491+785A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11780735 | |||||||
| chr8:11780760 | T | C | 1 | a0001c0001t0019g0198 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.491+810T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11780760 | |||||||
| chr8:11780852 | T | G | 8 | a0001c0001t0009g0088 a0001c0001t0010g0012 a0001c0001t0010g0063 others(5): Show |
14 | HG00323.hp1 HG00323.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.491+902T>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11780852 | |||||||
| chr8:11780961 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.491+1011G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11780961 | |||||||
| chr8:11780967 | C | A | 2 | a0001c0001t0056g0164 a0001c0001t0057g0160 |
2 | HG01884.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.491+1017C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11780967 | |||||||
| chr8:11781088 | C | T | 1 | a0010c0019t0055g0191 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.491+1138C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781088 | |||||||
| chr8:11781127 | C | G | 6 | a0001c0001t0005g0053 a0001c0001t0005g0131 a0001c0001t0005g0143 others(3): Show |
8 | HG01943.hp2 HG02056.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.491+1177C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781127 | |||||||
| chr8:11781173 | TTG | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(85): Show |
172 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.491+1228_491+1229d others(4): Show |
NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 11781173 | ||||||
| chr8:11781276 | A | G | 3 | a0003c0004t0018g0035 a0003c0004t0018g0177 a0009c0021t0018g0035 |
4 | HG02630.hp2 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.491+1326A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781276 | |||||||
| chr8:11781314 | C | T | 8 | a0001c0001t0009g0088 a0001c0001t0010g0012 a0001c0001t0010g0063 others(5): Show |
14 | HG00323.hp1 HG00323.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.491+1364C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781314 | |||||||
| chr8:11781369 | C | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(53): Show |
128 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.491+1419C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781369 | |||||||
| chr8:11781473 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.491+1523T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781473 | |||||||
| chr8:11781476 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(238): Show |
435 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(432): Show |
intron_variant | MODIFIER | c.491+1526C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781476 | |||||||
| chr8:11781479 | T | C | 31 | a0002c0003t0003g0007 a0002c0003t0003g0008 a0002c0003t0003g0061 others(28): Show |
58 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.491+1529T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781479 | |||||||
| chr8:11781551 | G | T | 2 | a0001c0002t0004g0178 a0001c0002t0004g0179 |
2 | HG01891.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.491+1601G>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781551 | |||||||
| chr8:11781604 | T | C | 26 | a0001c0001t0001g0044 a0001c0001t0002g0004 a0001c0001t0002g0019 others(23): Show |
45 | HG00544.hp2 HG00621.hp1 HG01346.hp1 others(42): Show |
intron_variant | MODIFIER | c.492-1599T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781604 | |||||||
| chr8:11781719 | A | G | 1 | a0003c0006t0012g0058 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.492-1484A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781719 | |||||||
| chr8:11781745 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1458T>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781745 | |||||||
| chr8:11781747 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1456T>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781747 | |||||||
| chr8:11781748 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1455T>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781748 | |||||||
| chr8:11781750 | GTCTTTGA others(60): Show |
G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1452_492-1386d others(69): Show |
NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781750 | |||||||
| chr8:11781770 | T | C | 1 | a0001c0001t0006g0005 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.492-1433T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781770 | |||||||
| chr8:11781821 | A | T | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1382A>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781821 | |||||||
| chr8:11781824 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1379C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781824 | |||||||
| chr8:11781827 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1376A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781827 | |||||||
| chr8:11781829 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1374A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781829 | |||||||
| chr8:11781830 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1373C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781830 | |||||||
| chr8:11781831 | A | T | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1372A>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781831 | |||||||
| chr8:11781834 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1369A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781834 | |||||||
| chr8:11781841 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1362C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781841 | |||||||
| chr8:11781845 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1358A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781845 | |||||||
| chr8:11781847 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1356C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781847 | |||||||
| chr8:11781848 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1355C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781848 | |||||||
| chr8:11781849 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1354C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781849 | |||||||
| chr8:11781850 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1353A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781850 | |||||||
| chr8:11781851 | G | GGGTGGGG others(70): Show |
1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1351_492-1350i others(79): Show |
NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 11781851 | ||||||
| chr8:11781853 | A | T | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1350A>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781853 | |||||||
| chr8:11781856 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1347A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781856 | |||||||
| chr8:11781857 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1346A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781857 | |||||||
| chr8:11781859 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1344A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781859 | |||||||
| chr8:11781861 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1342A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781861 | |||||||
| chr8:11781862 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1341C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781862 | |||||||
| chr8:11781864 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1339A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781864 | |||||||
| chr8:11781866 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1337C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781866 | |||||||
| chr8:11781867 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1336C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781867 | |||||||
| chr8:11781868 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1335T>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781868 | |||||||
| chr8:11781872 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1331C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781872 | |||||||
| chr8:11781873 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1330A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781873 | |||||||
| chr8:11781874 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1329A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781874 | |||||||
| chr8:11781875 | C | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1328C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781875 | |||||||
| chr8:11781876 | A | T | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1327A>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781876 | |||||||
| chr8:11781878 | A | T | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1325A>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781878 | |||||||
| chr8:11781880 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1323T>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781880 | |||||||
| chr8:11781882 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1321A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781882 | |||||||
| chr8:11781883 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1320A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781883 | |||||||
| chr8:11781885 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1318A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781885 | |||||||
| chr8:11781886 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1317C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781886 | |||||||
| chr8:11781888 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1315C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781888 | |||||||
| chr8:11781889 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1314T>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781889 | |||||||
| chr8:11781890 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.492-1313G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781890 | |||||||
| chr8:11781902 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.492-1301A>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781902 | |||||||
| chr8:11781920 | C | T | 15 | a0002c0003t0003g0008 a0002c0003t0003g0061 a0002c0003t0003g0174 others(12): Show |
30 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.492-1283C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781920 | |||||||
| chr8:11781927 | G | T | 1 | a0001c0001t0026g0140 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.492-1276G>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11781927 | |||||||
| chr8:11782037 | C | A | 1 | a0001c0001t0002g0136 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.492-1166C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11782037 | |||||||
| chr8:11782097 | A | G | 8 | a0001c0001t0009g0088 a0001c0001t0010g0012 a0001c0001t0010g0063 others(5): Show |
14 | HG00323.hp1 HG00323.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.492-1106A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11782097 | |||||||
| chr8:11782102 | T | C | 5 | a0001c0001t0015g0052 a0001c0001t0015g0123 a0001c0001t0015g0124 others(2): Show |
6 | HG02258.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.492-1101T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11782102 | |||||||
| chr8:11782209 | C | T | 1 | a0001c0001t0029g0066 | 2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.492-994C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11782209 | |||||||
| chr8:11782269 | C | CA | 3 | a0001c0010t0034g0183 a0001c0010t0034g0185 a0001c0016t0007g0184 |
3 | HG02976.hp2 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.492-929dupA | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 11782269 | ||||||
| chr8:11782317 | C | T | 1 | a0001c0001t0040g0139 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.492-886C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11782317 | |||||||
| chr8:11782387 | T | C | 45 | a0001c0001t0009g0088 a0001c0001t0010g0012 a0001c0001t0010g0063 others(42): Show |
79 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.492-816T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11782387 | |||||||
| chr8:11782396 | G | T | 1 | a0001c0001t0002g0135 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.492-807G>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11782396 | |||||||
| chr8:11782482 | C | T | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(51): Show |
125 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.492-721C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11782482 | |||||||
| chr8:11782493 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.492-710C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11782493 | |||||||
| chr8:11782527 | T | G | 2 | a0001c0010t0034g0183 a0001c0016t0007g0184 |
2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.492-676T>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11782527 | |||||||
| chr8:11782673 | G | A | 37 | a0002c0003t0003g0007 a0002c0003t0003g0008 a0002c0003t0003g0061 others(34): Show |
65 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.492-530G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11782673 | |||||||
| chr8:11782677 | C | T | 1 | a0001c0001t0001g0045 | 2 | NA18957.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.492-526C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11782677 | |||||||
| chr8:11782687 | T | G | 38 | a0002c0003t0003g0007 a0002c0003t0003g0008 a0002c0003t0003g0061 others(35): Show |
66 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.492-516T>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11782687 | |||||||
| chr8:11782722 | T | C | 1 | a0002c0003t0008g0042 | 2 | NA19070.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.492-481T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11782722 | |||||||
| chr8:11782743 | C | T | 1 | a0010c0019t0055g0191 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.492-460C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11782743 | |||||||
| chr8:11782763 | ACTACGTT others(120): Show |
A | 37 | a0002c0003t0003g0007 a0002c0003t0003g0008 a0002c0003t0003g0061 others(34): Show |
65 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.492-436_492-310del | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 11782763 | ||||||
| chr8:11782767 | C | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(201): Show |
370 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.492-436C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11782767 | |||||||
| chr8:11782829 | G | A | 1 | a0001c0001t0009g0048 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.492-374G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11782829 | |||||||
| chr8:11782837 | TGTAACGA others(253): Show |
T | 1 | a0001c0001t0022g0085 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.492-331_492-72del | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr8 | 11782837 | ||||||
| chr8:11782914 | G | A | 2 | a0003c0006t0012g0022 a0003c0006t0012g0058 |
6 | HG02109.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.492-289G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11782914 | |||||||
| chr8:11782920 | T | C | 1 | a0003c0013t0018g0180 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.492-283T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11782920 | |||||||
| chr8:11783102 | C | T | 20 | a0001c0001t0006g0005 a0001c0001t0006g0030 a0001c0001t0006g0054 others(17): Show |
41 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.492-101C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11783102 | |||||||
| chr8:11783153 | G | C | 28 | a0002c0003t0003g0007 a0002c0003t0003g0008 a0002c0003t0003g0061 others(25): Show |
54 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.492-50G>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11783153 | |||||||
| chr8:11783195 | C | T | 1 | a0003c0006t0012g0022 | 4 | HG02109.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.492-8C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 3/4 | chr8 | 11783195 | |||||||
| chr8:11783547 | C | A | 5 | a0001c0001t0015g0052 a0001c0001t0015g0123 a0001c0001t0015g0124 others(2): Show |
6 | HG02258.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.688+148C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11783547 | |||||||
| chr8:11783693 | C | G | 1 | a0001c0002t0064g0200 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.688+294C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11783693 | |||||||
| chr8:11783727 | C | T | 5 | a0001c0001t0015g0052 a0001c0001t0015g0123 a0001c0001t0015g0124 others(2): Show |
6 | HG02258.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.688+328C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11783727 | |||||||
| chr8:11783803 | C | T | 1 | a0001c0001t0035g0127 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.688+404C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11783803 | |||||||
| chr8:11783804 | G | A | 1 | a0001c0001t0002g0056 | 2 | NA18957.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.688+405G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11783804 | |||||||
| chr8:11783815 | G | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(70): Show |
148 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.688+416G>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11783815 | |||||||
| chr8:11783898 | C | T | 29 | a0001c0002t0003g0057 a0001c0002t0004g0013 a0001c0002t0004g0036 others(26): Show |
41 | HG00408.hp2 HG00639.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.688+499C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11783898 | |||||||
| chr8:11783920 | C | T | 1 | a0003c0004t0003g0171 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.688+521C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11783920 | |||||||
| chr8:11784048 | C | CA | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(104): Show |
208 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.688+650dupA | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 11784048 | ||||||
| chr8:11784055 | G | A | 1 | a0001c0001t0001g0116 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.688+656G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11784055 | |||||||
| chr8:11784144 | C | T | 4 | a0001c0001t0005g0053 a0001c0001t0005g0131 a0001c0001t0005g0143 others(1): Show |
5 | HG01943.hp2 HG02056.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.688+745C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11784144 | |||||||
| chr8:11784228 | T | C | 1 | a0001c0001t0069g0148 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.688+829T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11784228 | |||||||
| chr8:11784231 | G | T | 2 | a0007c0009t0033g0157 a0007c0009t0033g0162 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.688+832G>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11784231 | |||||||
| chr8:11784315 | T | A | 38 | a0002c0003t0003g0007 a0002c0003t0003g0008 a0002c0003t0003g0061 others(35): Show |
66 | HG00438.hp2 HG00558.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.688+916T>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11784315 | |||||||
| chr8:11784362 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(135): Show |
267 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.688+963T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11784362 | |||||||
| chr8:11784487 | T | C | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(238): Show |
435 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(432): Show |
intron_variant | MODIFIER | c.688+1088T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11784487 | |||||||
| chr8:11784578 | C | G | 5 | a0001c0001t0029g0066 a0001c0001t0056g0164 a0001c0001t0057g0160 others(2): Show |
6 | HG01884.hp2 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.688+1179C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11784578 | |||||||
| chr8:11784663 | T | C | 2 | a0007c0009t0033g0157 a0007c0009t0033g0162 |
2 | HG03041.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.688+1264T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11784663 | |||||||
| chr8:11784698 | A | G | 4 | a0003c0004t0003g0171 a0004c0005t0013g0023 a0004c0005t0013g0181 others(1): Show |
7 | HG02738.hp2 HG02818.hp1 HG03490.hp2 others(4): Show |
intron_variant | MODIFIER | c.689-1265A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11784698 | |||||||
| chr8:11784818 | G | A | 1 | a0003c0004t0004g0192 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.689-1145G>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11784818 | |||||||
| chr8:11785036 | T | C | 70 | a0001c0001t0001g0043 a0001c0001t0002g0003 a0001c0001t0002g0004 others(67): Show |
116 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.689-927T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11785036 | |||||||
| chr8:11785070 | C | G | 4 | a0001c0001t0009g0102 a0001c0001t0009g0111 a0001c0001t0009g0112 others(1): Show |
4 | HG01257.hp1 HG01258.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.689-893C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11785070 | |||||||
| chr8:11785135 | G | T | 5 | a0001c0001t0015g0052 a0001c0001t0015g0123 a0001c0001t0015g0124 others(2): Show |
6 | HG02258.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.689-828G>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11785135 | |||||||
| chr8:11785205 | A | AT | 5 | a0001c0001t0010g0012 a0001c0001t0010g0186 a0001c0001t0010g0187 others(2): Show |
11 | HG00323.hp1 HG00323.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.689-750dupT | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr8 | 11785205 | ||||||
| chr8:11785206 | T | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(94): Show |
197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.689-757T>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11785206 | |||||||
| chr8:11785264 | C | T | 1 | a0001c0010t0034g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.689-699C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11785264 | |||||||
| chr8:11785361 | A | G | 166 | a0001c0001t0001g0043 a0001c0001t0001g0076 a0001c0001t0002g0003 others(163): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.689-602A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11785361 | |||||||
| chr8:11785422 | C | A | 1 | a0001c0001t0056g0164 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.689-541C>A | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11785422 | |||||||
| chr8:11785508 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.689-455C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11785508 | |||||||
| chr8:11785610 | C | G | 1 | a0001c0001t0069g0148 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.689-353C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11785610 | |||||||
| chr8:11785689 | A | G | 1 | a0001c0001t0001g0115 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.689-274A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11785689 | |||||||
| chr8:11785717 | T | C | 1 | a0001c0001t0007g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.689-246T>C | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11785717 | |||||||
| chr8:11785769 | A | G | 1 | a0001c0001t0057g0160 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.689-194A>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11785769 | |||||||
| chr8:11785784 | T | G | 1 | a0001c0001t0002g0134 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.689-179T>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11785784 | |||||||
| chr8:11785926 | C | G | 1 | a0001c0010t0034g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.689-37C>G | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11785926 | |||||||
| chr8:11785949 | C | T | 1 | a0001c0010t0034g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.689-14C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11785949 | |||||||
| chr8:11785950 | C | T | 66 | a0001c0001t0001g0018 a0001c0001t0001g0099 a0001c0001t0032g0175 others(63): Show |
108 | HG00408.hp2 HG00438.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.689-13C>T | NEIL2 | ENSG00000154328.16 | transcript | ENST00000284503.7 | protein_coding | 4/4 | chr8 | 11785950 |