Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9436 |
| ensemblid | ENSG00000096264.14 |
| hgncid | 6732 |
| symbol | NCR2 |
| name | natural cytotoxicity triggering receptor 2 |
| refseq_nuc | NM_004828.4 |
| refseq_prot | NP_004819.2 |
| ensembl_nuc | ENST00000373089.10 |
| ensembl_prot | ENSP00000362181.5 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 41335608 |
| end | 41350889 |
| strand | + |
| ver | v1.2 |
| region | chr6:41335608-41350889 |
| region5000 | chr6:41330608-41355889 |
| regionname0 | NCR2_chr6_41335608_41350889 |
| regionname5000 | NCR2_chr6_41330608_41355889 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 276 | 203 | 7 | 53 | 98 | 13 | 32 | 70 | NCR2_chr6_41330608_41355889 | NCR2 | MAWRA others(271): Show |
chr6 | 41330608 | 41355889 |
| a0002 | 1/1 | 276 | 90 | 41 | 11 | 26 | 0 | 10 | 19 | NCR2_chr6_41330608_41355889 | NCR2 | MAWRA others(271): Show |
chr6 | 41330608 | 41355889 |
| a0003 | 0/0 | 276 | 70 | 5 | 4 | 57 | 2 | 2 | 50 | NCR2_chr6_41330608_41355889 | NCR2 | MAWRA others(271): Show |
chr6 | 41330608 | 41355889 |
| a0004 | 0/0 | 276 | 22 | 20 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | MAWRA others(271): Show |
chr6 | 41330608 | 41355889 |
| a0005 | 0/0 | 276 | 12 | 4 | 4 | 0 | 2 | 2 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | MAWRA others(271): Show |
chr6 | 41330608 | 41355889 |
| a0006 | 0/0 | 276 | 11 | 7 | 0 | 2 | 1 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | MAWRA others(271): Show |
chr6 | 41330608 | 41355889 |
| a0007 | 0/0 | 276 | 8 | 4 | 2 | 2 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | MAWRA others(271): Show |
chr6 | 41330608 | 41355889 |
| a0008 | 0/0 | 276 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | MAWRA others(271): Show |
chr6 | 41330608 | 41355889 |
| a0009 | 0/0 | 276 | 5 | 1 | 1 | 2 | 0 | 1 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | MAWRA others(271): Show |
chr6 | 41330608 | 41355889 |
| a0010 | 0/0 | 276 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | NCR2_chr6_41330608_41355889 | NCR2 | MAWRA others(271): Show |
chr6 | 41330608 | 41355889 |
| a0011 | 0/0 | 276 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | MAWRA others(271): Show |
chr6 | 41330608 | 41355889 |
| a0012 | 0/0 | 276 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | MAWRA others(271): Show |
chr6 | 41330608 | 41355889 |
| a0013 | 0/0 | 276 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | MAWRA others(271): Show |
chr6 | 41330608 | 41355889 |
| a0014 | 0/0 | 276 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | MAWRA others(271): Show |
chr6 | 41330608 | 41355889 |
| a0015 | 0/0 | 276 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | MAWRA others(271): Show |
chr6 | 41330608 | 41355889 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 828 | 203 | 7 | 53 | 98 | 13 | 32 | NCR2_chr6_41330608_41355889 | NCR2 | ATGGC others(823): Show |
chr6 | 41330608 | 41355889 | ||
| a0002c0002 | 1/1 | 828 | 88 | 39 | 11 | 26 | 0 | 10 | NCR2_chr6_41330608_41355889 | NCR2 | ATGGC others(823): Show |
chr6 | 41330608 | 41355889 | ||
| a0002c0013 | 0/0 | 828 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | ATGGC others(823): Show |
chr6 | 41330608 | 41355889 | ||
| a0003c0003 | 0/0 | 828 | 69 | 5 | 4 | 56 | 2 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | ATGGC others(823): Show |
chr6 | 41330608 | 41355889 | ||
| a0003c0017 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | ATGGC others(823): Show |
chr6 | 41330608 | 41355889 | ||
| a0004c0004 | 0/0 | 828 | 22 | 20 | 2 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | ATGGC others(823): Show |
chr6 | 41330608 | 41355889 | ||
| a0005c0006 | 0/0 | 828 | 9 | 2 | 3 | 0 | 2 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | ATGGC others(823): Show |
chr6 | 41330608 | 41355889 | ||
| a0005c0011 | 0/0 | 828 | 3 | 2 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | ATGGC others(823): Show |
chr6 | 41330608 | 41355889 | ||
| a0006c0005 | 0/0 | 828 | 11 | 7 | 0 | 2 | 1 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | ATGGC others(823): Show |
chr6 | 41330608 | 41355889 | ||
| a0007c0007 | 0/0 | 828 | 8 | 4 | 2 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | ATGGC others(823): Show |
chr6 | 41330608 | 41355889 | ||
| a0008c0008 | 0/0 | 828 | 6 | 6 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | ATGGC others(823): Show |
chr6 | 41330608 | 41355889 | ||
| a0009c0009 | 0/0 | 828 | 5 | 1 | 1 | 2 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | ATGGC others(823): Show |
chr6 | 41330608 | 41355889 | ||
| a0010c0010 | 0/0 | 828 | 4 | 0 | 0 | 4 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | ATGGC others(823): Show |
chr6 | 41330608 | 41355889 | ||
| a0011c0018 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | ATGGC others(823): Show |
chr6 | 41330608 | 41355889 | ||
| a0011c0019 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | ATGGC others(823): Show |
chr6 | 41330608 | 41355889 | ||
| a0012c0012 | 0/0 | 828 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | ATGGC others(823): Show |
chr6 | 41330608 | 41355889 | ||
| a0013c0014 | 0/0 | 828 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | ATGGC others(823): Show |
chr6 | 41330608 | 41355889 | ||
| a0014c0016 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | ATGGC others(823): Show |
chr6 | 41330608 | 41355889 | ||
| a0015c0015 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | ATGGC others(823): Show |
chr6 | 41330608 | 41355889 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1125 | 201 | 7 | 53 | 98 | 12 | 31 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0001c0001t0004 | 0/0 | 1125 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0001c0001t0006 | 0/0 | 1125 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0002c0002t0002 | 1/1 | 1125 | 86 | 37 | 11 | 26 | 0 | 10 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0002c0002t0003 | 0/0 | 1125 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0002c0013t0002 | 0/0 | 1125 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0003c0003t0001 | 0/0 | 1125 | 68 | 5 | 4 | 55 | 2 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0003c0003t0005 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0003c0017t0001 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0004c0004t0001 | 0/0 | 1125 | 22 | 20 | 2 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0005c0006t0002 | 0/0 | 1125 | 9 | 2 | 3 | 0 | 2 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0005c0011t0002 | 0/0 | 1125 | 3 | 2 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0006c0005t0001 | 0/0 | 1125 | 11 | 7 | 0 | 2 | 1 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0007c0007t0001 | 0/0 | 1125 | 8 | 4 | 2 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0008c0008t0002 | 0/0 | 1125 | 6 | 6 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0009c0009t0001 | 0/0 | 1125 | 2 | 0 | 0 | 1 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0009c0009t0002 | 0/0 | 1125 | 3 | 1 | 1 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0010c0010t0001 | 0/0 | 1125 | 4 | 0 | 0 | 4 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0011c0018t0002 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0011c0019t0002 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0012c0012t0001 | 0/0 | 1125 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0013c0014t0001 | 0/0 | 1125 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0014c0016t0002 | 0/0 | 1125 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| a0015c0015t0001 | 0/0 | 1125 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | AGGCA others(1120): Show |
chr6 | 41330608 | 41355889 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 43 | 1 | 8 | 27 | 3 | 4 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0002 | 0/0 | 38 | 2 | 4 | 23 | 2 | 7 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0004 | 0/0 | 32 | 2 | 12 | 10 | 0 | 8 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0007 | 0/0 | 11 | 0 | 5 | 6 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0008 | 0/0 | 9 | 2 | 4 | 0 | 1 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0005 | 1/1 | 24 | 1 | 5 | 16 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0010 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0022 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0023 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0002t0003g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0002c0013t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0003 | 0/0 | 34 | 1 | 3 | 27 | 2 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0009 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0018 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0051 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0003t0005g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0003c0017t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0004c0004t0001g0006 | 0/0 | 11 | 11 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0004c0004t0001g0011 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0004c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0004c0004t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0004c0004t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0004c0004t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0004c0004t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0004c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0005c0006t0002g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0005c0006t0002g0039 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0005c0006t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0005c0006t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0005c0006t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0005c0006t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0005c0006t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0005c0011t0002g0025 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0006c0005t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0006c0005t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0006c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0006c0005t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0006c0005t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0006c0005t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0007c0007t0001g0012 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0007c0007t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0007c0007t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0007c0007t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0008c0008t0002g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0008c0008t0002g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0008c0008t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0008c0008t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0009c0009t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0009c0009t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0009c0009t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0009c0009t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0009c0009t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0010c0010t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0010c0010t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0011c0018t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0011c0019t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0012c0012t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0012c0012t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0013c0014t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0014c0016t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| a0015c0015t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | GBR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00140 | hp1 | a0005 | c0006 | t0002 | g0039 | EUR | GBR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00140 | hp2 | a0005 | c0006 | t0002 | g0071 | EUR | GBR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | FIN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00408 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00423 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00423 | hp2 | a0010 | c0010 | t0001 | g0019 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00438 | hp1 | a0006 | c0005 | t0001 | g0109 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00558 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00621 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00642 | hp1 | a0007 | c0007 | t0001 | g0095 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0151 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00735 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00738 | hp2 | a0005 | c0006 | t0002 | g0035 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00741 | hp1 | a0005 | c0011 | t0002 | g0025 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01081 | hp1 | a0009 | c0009 | t0002 | g0150 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01109 | hp1 | a0004 | c0004 | t0001 | g0057 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01168 | hp1 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01175 | hp2 | a0003 | c0003 | t0001 | g0003 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01192 | hp2 | a0005 | c0006 | t0002 | g0035 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0020 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01255 | hp1 | a0007 | c0007 | t0001 | g0012 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01261 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0022 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0073 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01496 | hp2 | a0003 | c0003 | t0001 | g0051 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0045 | EUR | IBS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01516 | hp2 | a0003 | c0003 | t0001 | g0003 | EUR | IBS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01517 | hp2 | a0003 | c0003 | t0001 | g0003 | EUR | IBS | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0015 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0022 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0075 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01934 | hp2 | a0004 | c0004 | t0001 | g0065 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0005 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02004 | hp1 | a0005 | c0006 | t0002 | g0074 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02004 | hp2 | a0013 | c0014 | t0001 | g0001 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02015 | hp1 | a0003 | c0003 | t0001 | g0055 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02015 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0092 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02055 | hp2 | a0002 | c0002 | t0003 | g0048 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02071 | hp2 | a0007 | c0007 | t0001 | g0122 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02129 | hp2 | a0006 | c0005 | t0001 | g0101 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02132 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02145 | hp1 | a0005 | c0011 | t0002 | g0025 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0034 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CDX | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | CDX | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02257 | hp1 | a0006 | c0005 | t0001 | g0016 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0086 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02258 | hp1 | a0002 | c0002 | t0002 | g0041 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02258 | hp2 | a0008 | c0008 | t0002 | g0043 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0077 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02280 | hp1 | a0002 | c0013 | t0002 | g0015 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0020 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0041 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02451 | hp2 | a0004 | c0004 | t0001 | g0006 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | KHV | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02572 | hp1 | a0008 | c0008 | t0002 | g0098 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02572 | hp2 | a0002 | c0002 | t0003 | g0048 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0040 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02615 | hp2 | a0003 | c0003 | t0001 | g0070 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02622 | hp1 | a0004 | c0004 | t0001 | g0006 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0021 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02630 | hp1 | a0004 | c0004 | t0001 | g0068 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0021 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0050 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0036 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02717 | hp1 | a0003 | c0003 | t0001 | g0153 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02723 | hp1 | a0006 | c0005 | t0001 | g0016 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02735 | hp2 | a0005 | c0006 | t0002 | g0090 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02809 | hp1 | a0004 | c0004 | t0001 | g0011 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0099 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02818 | hp2 | a0002 | c0002 | t0002 | g0034 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0081 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0015 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0050 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0003 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0015 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02922 | hp1 | a0007 | c0007 | t0001 | g0012 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02922 | hp2 | a0004 | c0004 | t0001 | g0006 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02965 | hp1 | a0008 | c0008 | t0002 | g0042 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0010 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02970 | hp1 | a0004 | c0004 | t0001 | g0006 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02970 | hp2 | a0004 | c0004 | t0001 | g0011 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0020 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03017 | hp1 | a0006 | c0005 | t0001 | g0108 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03041 | hp1 | a0004 | c0004 | t0001 | g0006 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0022 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03098 | hp1 | a0014 | c0016 | t0002 | g0149 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03098 | hp2 | a0004 | c0004 | t0001 | g0056 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03130 | hp2 | a0007 | c0007 | t0001 | g0012 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03139 | hp1 | a0005 | c0011 | t0002 | g0025 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03139 | hp2 | a0003 | c0003 | t0001 | g0051 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03195 | hp1 | a0006 | c0005 | t0001 | g0024 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03195 | hp2 | a0002 | c0013 | t0002 | g0015 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0021 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03209 | hp2 | a0004 | c0004 | t0001 | g0011 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03225 | hp1 | a0008 | c0008 | t0002 | g0042 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0037 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03453 | hp1 | a0002 | c0002 | t0002 | g0096 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03453 | hp2 | a0004 | c0004 | t0001 | g0011 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0082 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03486 | hp2 | a0003 | c0003 | t0001 | g0154 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03491 | hp1 | a0009 | c0009 | t0001 | g0094 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03516 | hp2 | a0008 | c0008 | t0002 | g0043 | AFR | ESN | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03540 | hp2 | a0004 | c0004 | t0001 | g0059 | AFR | GWD | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03579 | hp1 | a0006 | c0005 | t0001 | g0024 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03579 | hp2 | a0004 | c0004 | t0001 | g0006 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0087 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0036 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | STU | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03831 | hp2 | a0003 | c0003 | t0001 | g0018 | SAS | BEB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0023 | SAS | BEB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0023 | SAS | BEB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0091 | SAS | BEB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03942 | hp1 | a0003 | c0003 | t0001 | g0003 | SAS | BEB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0023 | SAS | STU | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG04115 | hp2 | a0001 | c0001 | t0006 | g0001 | SAS | STU | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0089 | SAS | STU | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0038 | SAS | STU | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0038 | SAS | STU | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG04228 | hp2 | a0005 | c0006 | t0002 | g0039 | SAS | STU | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0040 | AFR | YRI | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18522 | hp2 | a0006 | c0005 | t0001 | g0016 | AFR | YRI | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18906 | hp1 | a0004 | c0004 | t0001 | g0066 | AFR | YRI | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0097 | AFR | YRI | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18941 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18943 | hp1 | a0003 | c0003 | t0001 | g0064 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18944 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18946 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18946 | hp2 | a0003 | c0003 | t0001 | g0018 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18947 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18948 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18951 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18952 | hp1 | a0003 | c0003 | t0005 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18952 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18956 | hp1 | a0007 | c0007 | t0001 | g0125 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18959 | hp1 | a0012 | c0012 | t0001 | g0052 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18961 | hp2 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18963 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18964 | hp2 | a0003 | c0003 | t0001 | g0032 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18966 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18969 | hp2 | a0003 | c0003 | t0001 | g0033 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18973 | hp1 | a0003 | c0003 | t0001 | g0069 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18979 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18980 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18981 | hp2 | a0003 | c0003 | t0001 | g0060 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18985 | hp2 | a0003 | c0003 | t0001 | g0018 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18986 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18990 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18990 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18992 | hp2 | a0003 | c0017 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18993 | hp2 | a0003 | c0003 | t0001 | g0054 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18994 | hp1 | a0012 | c0012 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18995 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18999 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19000 | hp1 | a0009 | c0009 | t0001 | g0102 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19000 | hp2 | a0003 | c0003 | t0001 | g0031 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19001 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19002 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19004 | hp2 | a0015 | c0015 | t0001 | g0130 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19005 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19006 | hp1 | a0003 | c0003 | t0001 | g0030 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19006 | hp2 | a0009 | c0009 | t0002 | g0146 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19007 | hp1 | a0003 | c0003 | t0001 | g0061 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19010 | hp1 | a0003 | c0003 | t0001 | g0062 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19011 | hp1 | a0003 | c0003 | t0001 | g0033 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19030 | hp1 | a0009 | c0009 | t0002 | g0148 | AFR | LWK | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0147 | AFR | LWK | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19043 | hp1 | a0005 | c0006 | t0002 | g0093 | AFR | LWK | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19043 | hp2 | a0007 | c0007 | t0001 | g0012 | AFR | LWK | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19054 | hp1 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19056 | hp2 | a0003 | c0003 | t0001 | g0031 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19057 | hp1 | a0010 | c0010 | t0001 | g0058 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19060 | hp2 | a0003 | c0003 | t0001 | g0067 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19063 | hp2 | a0010 | c0010 | t0001 | g0019 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19064 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19065 | hp2 | a0010 | c0010 | t0001 | g0019 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19066 | hp1 | a0003 | c0003 | t0001 | g0030 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19066 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19067 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19070 | hp1 | a0003 | c0003 | t0001 | g0053 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19070 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19074 | hp2 | a0003 | c0003 | t0001 | g0063 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19076 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19078 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19081 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19082 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19088 | hp2 | a0003 | c0003 | t0001 | g0032 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19090 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19240 | hp1 | a0007 | c0007 | t0001 | g0012 | AFR | YRI | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA19240 | hp2 | a0004 | c0004 | t0001 | g0006 | AFR | YRI | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA20129 | hp1 | a0004 | c0004 | t0001 | g0006 | AFR | ASW | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | TSI | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | TSI | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA20805 | hp2 | a0006 | c0005 | t0001 | g0141 | EUR | TSI | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | GIH | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01123 | hp1 | a0002 | c0002 | t0002 | g0005 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02109 | hp1 | a0006 | c0005 | t0001 | g0024 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0037 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02486 | hp1 | a0004 | c0004 | t0001 | g0006 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02486 | hp2 | a0002 | c0002 | t0002 | g0088 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02559 | hp1 | a0004 | c0004 | t0001 | g0011 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG02559 | hp2 | a0011 | c0019 | t0002 | g0084 | AFR | ACB | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03471 | hp1 | a0008 | c0008 | t0002 | g0152 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG03471 | hp2 | a0004 | c0004 | t0001 | g0006 | AFR | MSL | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG06807 | hp1 | a0006 | c0005 | t0001 | g0016 | AFR | USA | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| HG06807 | hp2 | a0005 | c0006 | t0002 | g0083 | AFR | USA | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA20300 | hp2 | a0004 | c0004 | t0001 | g0006 | AFR | USA | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | LWK | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| NA21309 | hp2 | a0011 | c0018 | t0002 | g0085 | AFR | LWK | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0005 | REF | REF | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0002 | g0005 | REF | REF | NCR2_chr6_41330608_41355889 | NCR2 | chr6 | 41330608 | 41355889 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:41336093 | A | G | 1 | a0011 | 2 | HG02559.hp2 NA21309.hp2 |
missense_variant | MODERATE | c.59A>G | p.Gln20Arg | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/5 | 328/1125 | 59/831 | 20/276 | chr6 | 41336093 | |||
| chr6:41336125 | G | A | 1 | a0008 | 6 | HG02258.hp2 HG02572.hp1 HG02965.hp1 others(3): Show |
missense_variant | MODERATE | c.91G>A | p.Val31Met | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/5 | 360/1125 | 91/831 | 31/276 | chr6 | 41336125 | |||
| chr6:41336257 | A | G | 3 | a0003 a0004 a0010 |
96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
missense_variant | MODERATE | c.223A>G | p.Met75Val | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/5 | 492/1125 | 223/831 | 75/276 | chr6 | 41336257 | |||
| chr6:41336401 | G | A | 1 | a0013 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.367G>A | p.Val123Ile | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/5 | 636/1125 | 367/831 | 123/276 | chr6 | 41336401 | |||
| chr6:41341814 | T | C | 7 | a0001 a0006 a0007 others(4): Show |
230 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(227): Show |
missense_variant | MODERATE | c.415T>C | p.Ser139Pro | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 3/5 | 684/1125 | 415/831 | 139/276 | chr6 | 41341814 | |||
| chr6:41341887 | G | C | 1 | a0008 | 6 | HG02258.hp2 HG02572.hp1 HG02965.hp1 others(3): Show |
missense_variant | MODERATE | c.488G>C | p.Arg163Thr | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 3/5 | 757/1125 | 488/831 | 163/276 | chr6 | 41341887 | |||
| chr6:41342050 | C | T | 2 | a0012 a0015 |
3 | NA18959.hp1 NA18994.hp1 NA19004.hp2 |
missense_variant | MODERATE | c.545C>T | p.Thr182Met | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/5 | 814/1125 | 545/831 | 182/276 | chr6 | 41342050 | |||
| chr6:41342109 | G | A | 1 | a0014 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.604G>A | p.Val202Ile | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/5 | 873/1125 | 604/831 | 202/276 | chr6 | 41342109 | |||
| chr6:41350686 | T | A | 3 | a0003 a0007 a0009 |
83 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(80): Show |
missense_variant | MODERATE | c.653T>A | p.Ile218Lys | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 5/5 | 922/1125 | 653/831 | 218/276 | chr6 | 41350686 | |||
| chr6:41350700 | A | G | 10 | a0001 a0003 a0004 others(7): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
missense_variant | MODERATE | c.667A>G | p.Met223Val | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 5/5 | 936/1125 | 667/831 | 223/276 | chr6 | 41350700 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:41342087 | G | A | 1 | a0003c0017 | 1 | NA18992.hp2 | synonymous_variant | LOW | c.582G>A | p.Val194Val | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/5 | 851/1125 | 582/831 | 194/276 | chr6 | 41342087 | |||
| chr6:41342093 | G | A | 1 | a0002c0013 | 2 | HG02280.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.588G>A | p.Val196Val | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/5 | 857/1125 | 588/831 | 196/276 | chr6 | 41342093 | |||
| chr6:41350840 | T | C | 1 | a0005c0011 | 3 | HG00741.hp1 HG02145.hp1 HG03139.hp1 |
synonymous_variant | LOW | c.807T>C | p.Asp269Asp | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 5/5 | 1076/1125 | 807/831 | 269/276 | chr6 | 41350840 | |||
| chr6:41350849 | T | C | 1 | a0011c0018 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.816T>C | p.Asp272Asp | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 5/5 | 1085/1125 | 816/831 | 272/276 | chr6 | 41350849 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:41335782 | G | A | 1 | a0001c0001t0004 | 1 | HG01515.hp2 | 5_prime_UTR_variant | MODIFIER | c.-95G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 1/5 | 95 | chr6 | 41335782 | ||||||
| chr6:41335833 | T | C | 1 | a0003c0003t0005 | 1 | NA18952.hp1 | 5_prime_UTR_variant | MODIFIER | c.-44T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 1/5 | 44 | chr6 | 41335833 | ||||||
| chr6:41335854 | T | C | 14 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(11): Show |
324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
5_prime_UTR_variant | MODIFIER | c.-23T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 1/5 | 23 | chr6 | 41335854 | ||||||
| chr6:41335854 | T | G | 1 | a0002c0002t0003 | 2 | HG02055.hp2 HG02572.hp2 |
5_prime_UTR_variant | MODIFIER | c.-23T>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 1/5 | 23 | chr6 | 41335854 | ||||||
| chr6:41335867 | A | C | 1 | a0001c0001t0006 | 1 | HG04115.hp2 | 5_prime_UTR_variant | MODIFIER | c.-10A>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 1/5 | 10 | chr6 | 41335867 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:41335994 | G | A | 1 | a0012c0012t0001g0052 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.52+66G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 1/4 | chr6 | 41335994 | |||||||
| chr6:41336046 | G | A | 30 | a0003c0003t0001g0003 a0003c0003t0001g0009 a0003c0003t0001g0018 others(27): Show |
92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.53-41G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 1/4 | chr6 | 41336046 | |||||||
| chr6:41336049 | C | T | 1 | a0001c0001t0001g0029 | 3 | NA18966.hp2 NA18973.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.53-38C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 1/4 | chr6 | 41336049 | |||||||
| chr6:41336067 | G | A | 30 | a0003c0003t0001g0003 a0003c0003t0001g0009 a0003c0003t0001g0018 others(27): Show |
92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.53-20G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 1/4 | chr6 | 41336067 | |||||||
| chr6:41336479 | G | A | 1 | a0002c0002t0002g0034 | 2 | HG02145.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.394+51G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41336479 | |||||||
| chr6:41336503 | C | T | 33 | a0003c0003t0001g0003 a0003c0003t0001g0009 a0003c0003t0001g0018 others(30): Show |
96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.394+75C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41336503 | |||||||
| chr6:41336505 | A | G | 1 | a0008c0008t0002g0152 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.394+77A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41336505 | |||||||
| chr6:41336529 | G | A | 1 | a0003c0003t0001g0053 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.394+101G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41336529 | |||||||
| chr6:41336885 | G | GA | 30 | a0003c0003t0001g0003 a0003c0003t0001g0009 a0003c0003t0001g0018 others(27): Show |
92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.394+465dupA | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 41336885 | ||||||
| chr6:41336953 | G | A | 33 | a0003c0003t0001g0003 a0003c0003t0001g0009 a0003c0003t0001g0018 others(30): Show |
96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.394+525G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41336953 | |||||||
| chr6:41336978 | T | C | 1 | a0003c0003t0001g0054 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.394+550T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41336978 | |||||||
| chr6:41337099 | C | G | 1 | a0002c0002t0002g0151 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.394+671C>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337099 | |||||||
| chr6:41337125 | T | C | 33 | a0003c0003t0001g0003 a0003c0003t0001g0009 a0003c0003t0001g0018 others(30): Show |
96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.394+697T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337125 | |||||||
| chr6:41337197 | A | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(148): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.394+769A>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337197 | |||||||
| chr6:41337231 | AG | A | 4 | a0002c0002t0002g0050 a0009c0009t0002g0148 a0009c0009t0002g0150 others(1): Show |
5 | HG01081.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+804delG | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337231 | |||||||
| chr6:41337264 | C | T | 7 | a0002c0002t0002g0014 a0002c0002t0002g0015 a0002c0002t0002g0049 others(4): Show |
15 | HG00621.hp1 HG00733.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.394+836C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337264 | |||||||
| chr6:41337337 | T | C | 33 | a0003c0003t0001g0003 a0003c0003t0001g0009 a0003c0003t0001g0018 others(30): Show |
96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.394+909T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337337 | |||||||
| chr6:41337351 | G | C | 1 | a0003c0003t0001g0055 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.394+923G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337351 | |||||||
| chr6:41337415 | G | A | 3 | a0003c0003t0001g0051 a0003c0003t0001g0153 a0003c0003t0001g0154 |
4 | HG01496.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.394+987G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337415 | |||||||
| chr6:41337434 | C | A | 1 | a0001c0001t0001g0079 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.394+1006C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337434 | |||||||
| chr6:41337447 | T | C | 33 | a0003c0003t0001g0003 a0003c0003t0001g0009 a0003c0003t0001g0018 others(30): Show |
96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.394+1019T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337447 | |||||||
| chr6:41337494 | C | T | 3 | a0003c0003t0001g0051 a0003c0003t0001g0153 a0003c0003t0001g0154 |
4 | HG01496.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.394+1066C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337494 | |||||||
| chr6:41337579 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.394+1151G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337579 | |||||||
| chr6:41337582 | A | G | 1 | a0002c0002t0003g0048 | 2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.394+1154A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337582 | |||||||
| chr6:41337631 | T | A | 2 | a0002c0002t0002g0081 a0002c0002t0002g0082 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.394+1203T>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337631 | |||||||
| chr6:41337669 | T | G | 1 | a0005c0006t0002g0071 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.394+1241T>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337669 | |||||||
| chr6:41337714 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.394+1286C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337714 | |||||||
| chr6:41337716 | G | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(64): Show |
211 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.394+1288G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41337716 | |||||||
| chr6:41338005 | T | C | 3 | a0001c0001t0001g0044 a0001c0001t0001g0100 a0006c0005t0001g0101 |
4 | HG02080.hp1 HG02129.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.394+1577T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338005 | |||||||
| chr6:41338121 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.394+1693C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338121 | |||||||
| chr6:41338222 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(115): Show |
341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.394+1794C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338222 | |||||||
| chr6:41338236 | A | T | 1 | a0005c0006t0002g0093 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.394+1808A>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338236 | |||||||
| chr6:41338238 | G | A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0026 others(19): Show |
64 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.394+1810G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338238 | |||||||
| chr6:41338265 | C | CA | 4 | a0002c0002t0002g0050 a0009c0009t0002g0148 a0009c0009t0002g0150 others(1): Show |
5 | HG01081.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+1839dupA | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 41338265 | ||||||
| chr6:41338270 | G | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0117 a0001c0001t0001g0118 |
13 | HG00735.hp2 HG01346.hp1 HG01928.hp2 others(10): Show |
intron_variant | MODIFIER | c.394+1842G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338270 | |||||||
| chr6:41338449 | A | T | 1 | a0003c0003t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.394+2021A>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338449 | |||||||
| chr6:41338451 | C | G | 2 | a0002c0002t0002g0041 a0002c0002t0002g0092 |
3 | HG02055.hp1 HG02258.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.394+2023C>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338451 | |||||||
| chr6:41338552 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.394+2124A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338552 | |||||||
| chr6:41338792 | G | A | 1 | a0007c0007t0001g0012 | 5 | HG01255.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.394+2364G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338792 | |||||||
| chr6:41338886 | T | C | 1 | a0002c0002t0002g0072 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.394+2458T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338886 | |||||||
| chr6:41338957 | G | A | 33 | a0003c0003t0001g0003 a0003c0003t0001g0009 a0003c0003t0001g0018 others(30): Show |
96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.394+2529G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41338957 | |||||||
| chr6:41339101 | G | A | 1 | a0005c0006t0002g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.394+2673G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339101 | |||||||
| chr6:41339147 | C | A | 3 | a0003c0003t0001g0051 a0003c0003t0001g0153 a0003c0003t0001g0154 |
4 | HG01496.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.395-2647C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339147 | |||||||
| chr6:41339169 | C | T | 4 | a0002c0002t0002g0050 a0009c0009t0002g0148 a0009c0009t0002g0150 others(1): Show |
5 | HG01081.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.395-2625C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339169 | |||||||
| chr6:41339186 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(70): Show |
228 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.395-2608G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339186 | |||||||
| chr6:41339207 | G | A | 2 | a0003c0003t0001g0030 a0003c0003t0001g0031 |
4 | NA19000.hp2 NA19006.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.395-2587G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339207 | |||||||
| chr6:41339220 | C | A | 3 | a0003c0003t0001g0051 a0003c0003t0001g0153 a0003c0003t0001g0154 |
4 | HG01496.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.395-2574C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339220 | |||||||
| chr6:41339223 | G | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(69): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.395-2571G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339223 | |||||||
| chr6:41339250 | T | C | 33 | a0003c0003t0001g0003 a0003c0003t0001g0009 a0003c0003t0001g0018 others(30): Show |
96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.395-2544T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339250 | |||||||
| chr6:41339305 | G | A | 33 | a0003c0003t0001g0003 a0003c0003t0001g0009 a0003c0003t0001g0018 others(30): Show |
96 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.395-2489G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339305 | |||||||
| chr6:41339360 | A | G | 1 | a0002c0002t0002g0078 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.395-2434A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339360 | |||||||
| chr6:41339523 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.395-2271T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339523 | |||||||
| chr6:41339533 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.395-2261C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339533 | |||||||
| chr6:41339546 | G | A | 2 | a0001c0001t0001g0119 a0003c0003t0001g0018 |
4 | HG03831.hp2 NA18946.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.395-2248G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339546 | |||||||
| chr6:41339739 | G | T | 1 | a0007c0007t0001g0095 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.395-2055G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339739 | |||||||
| chr6:41339773 | T | C | 30 | a0003c0003t0001g0003 a0003c0003t0001g0009 a0003c0003t0001g0018 others(27): Show |
92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.395-2021T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339773 | |||||||
| chr6:41339856 | A | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0017 others(9): Show |
56 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.395-1938A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41339856 | |||||||
| chr6:41340130 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.395-1664T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41340130 | |||||||
| chr6:41340147 | C | CTTTA | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(59): Show |
204 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.395-1620_395-1617d others(6): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 41340147 | ||||||
| chr6:41340147 | C | CTTTATTT others(1): Show |
31 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0047 others(28): Show |
91 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.395-1624_395-1617d others(10): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 41340147 | ||||||
| chr6:41340147 | C | CTTTATTT others(5): Show |
10 | a0002c0002t0002g0096 a0002c0002t0002g0097 a0003c0003t0001g0009 others(7): Show |
18 | HG00621.hp2 HG01934.hp2 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.395-1628_395-1617d others(14): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 41340147 | ||||||
| chr6:41340147 | C | CTTTATTT others(9): Show |
17 | a0002c0002t0002g0034 a0002c0002t0002g0036 a0002c0002t0002g0086 others(14): Show |
24 | HG02109.hp1 HG02145.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.395-1632_395-1617d others(18): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 41340147 | ||||||
| chr6:41340147 | C | CTTTATTT others(13): Show |
15 | a0001c0001t0001g0029 a0002c0002t0002g0010 a0002c0002t0002g0021 others(12): Show |
33 | HG00741.hp1 HG01081.hp1 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.395-1636_395-1617d others(22): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 41340147 | ||||||
| chr6:41340147 | C | CTTTATTT others(17): Show |
7 | a0002c0002t0002g0022 a0002c0002t0002g0023 a0002c0002t0002g0040 others(4): Show |
14 | HG00140.hp1 HG01361.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.395-1640_395-1617d others(26): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr6 | 41340147 | ||||||
| chr6:41340225 | G | A | 30 | a0003c0003t0001g0003 a0003c0003t0001g0009 a0003c0003t0001g0018 others(27): Show |
92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.395-1569G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41340225 | |||||||
| chr6:41340351 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(69): Show |
227 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.395-1443G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41340351 | |||||||
| chr6:41340414 | G | A | 4 | a0002c0002t0002g0037 a0002c0002t0002g0041 a0002c0002t0002g0092 others(1): Show |
6 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.395-1380G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41340414 | |||||||
| chr6:41340425 | C | G | 37 | a0002c0002t0002g0050 a0003c0003t0001g0003 a0003c0003t0001g0009 others(34): Show |
101 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.395-1369C>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41340425 | |||||||
| chr6:41340427 | G | T | 1 | a0003c0003t0001g0064 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.395-1367G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41340427 | |||||||
| chr6:41340430 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.395-1364G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41340430 | |||||||
| chr6:41340491 | C | T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(66): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.395-1303C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41340491 | |||||||
| chr6:41340667 | C | T | 7 | a0002c0002t0002g0050 a0003c0003t0001g0051 a0003c0003t0001g0153 others(4): Show |
9 | HG01081.hp1 HG01496.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.395-1127C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41340667 | |||||||
| chr6:41341130 | C | T | 4 | a0002c0002t0002g0050 a0009c0009t0002g0148 a0009c0009t0002g0150 others(1): Show |
5 | HG01081.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.395-664C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41341130 | |||||||
| chr6:41341153 | C | T | 7 | a0002c0002t0002g0050 a0003c0003t0001g0051 a0003c0003t0001g0153 others(4): Show |
9 | HG01081.hp1 HG01496.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.395-641C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41341153 | |||||||
| chr6:41341615 | G | A | 31 | a0003c0003t0001g0003 a0003c0003t0001g0009 a0003c0003t0001g0018 others(28): Show |
93 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.395-179G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41341615 | |||||||
| chr6:41341710 | C | A | 3 | a0001c0001t0001g0029 a0006c0005t0001g0016 a0006c0005t0001g0024 |
10 | HG02109.hp1 HG02257.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.395-84C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41341710 | |||||||
| chr6:41341782 | C | T | 1 | a0001c0001t0001g0028 | 3 | HG00609.hp2 HG02165.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.395-12C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 2/4 | chr6 | 41341782 | |||||||
| chr6:41341947 | C | T | 1 | a0005c0006t0002g0093 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.530+18C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 3/4 | chr6 | 41341947 | |||||||
| chr6:41341960 | G | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(75): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.530+31G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 3/4 | chr6 | 41341960 | |||||||
| chr6:41342293 | T | C | 13 | a0002c0002t0002g0010 a0002c0002t0002g0021 a0002c0002t0002g0022 others(10): Show |
28 | HG00140.hp1 HG01361.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.644+144T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41342293 | |||||||
| chr6:41342483 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG00639.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.644+334C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41342483 | |||||||
| chr6:41342524 | T | C | 1 | a0004c0004t0001g0065 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.644+375T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41342524 | |||||||
| chr6:41342581 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.644+432C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41342581 | |||||||
| chr6:41342704 | G | A | 1 | a0004c0004t0001g0056 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.644+555G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41342704 | |||||||
| chr6:41342767 | GA | G | 1 | a0005c0011t0002g0025 | 3 | HG00741.hp1 HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.644+624delA | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 41342767 | ||||||
| chr6:41342791 | T | TG | 5 | a0001c0001t0001g0027 a0001c0001t0001g0114 a0001c0001t0001g0119 others(2): Show |
7 | HG00323.hp1 HG00733.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.644+643dupG | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 41342791 | ||||||
| chr6:41342967 | C | T | 8 | a0002c0002t0002g0023 a0002c0002t0002g0036 a0002c0002t0002g0038 others(5): Show |
12 | HG02698.hp2 HG02735.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.644+818C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41342967 | |||||||
| chr6:41343037 | T | C | 4 | a0002c0002t0002g0050 a0009c0009t0002g0148 a0009c0009t0002g0150 others(1): Show |
5 | HG01081.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.644+888T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343037 | |||||||
| chr6:41343132 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.644+983A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343132 | |||||||
| chr6:41343140 | T | C | 1 | a0009c0009t0001g0094 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.644+991T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343140 | |||||||
| chr6:41343167 | C | T | 4 | a0002c0002t0002g0010 a0002c0002t0002g0040 a0002c0002t0002g0086 others(1): Show |
11 | HG02257.hp2 HG02486.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.644+1018C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343167 | |||||||
| chr6:41343599 | T | C | 3 | a0002c0002t0002g0014 a0002c0002t0002g0049 a0009c0009t0002g0146 |
8 | HG00621.hp1 NA18950.hp1 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.644+1450T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343599 | |||||||
| chr6:41343625 | G | T | 3 | a0003c0003t0001g0051 a0003c0003t0001g0153 a0003c0003t0001g0154 |
4 | HG01496.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.644+1476G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343625 | |||||||
| chr6:41343629 | A | G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.644+1480A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343629 | |||||||
| chr6:41343648 | G | A | 8 | a0002c0002t0002g0023 a0002c0002t0002g0036 a0002c0002t0002g0038 others(5): Show |
12 | HG02698.hp2 HG02735.hp2 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.644+1499G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343648 | |||||||
| chr6:41343685 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0004g0045 |
2 | HG01081.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.644+1536T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343685 | |||||||
| chr6:41343807 | CT | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(74): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.644+1660delT | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 41343807 | ||||||
| chr6:41343822 | G | C | 34 | a0001c0001t0001g0029 a0002c0002t0002g0096 a0002c0002t0002g0097 others(31): Show |
93 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.644+1673G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343822 | |||||||
| chr6:41343897 | T | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(125): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.644+1748T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343897 | |||||||
| chr6:41343900 | A | G | 77 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(74): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.644+1751A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343900 | |||||||
| chr6:41343918 | G | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(80): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.644+1769G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343918 | |||||||
| chr6:41343939 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.644+1790A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41343939 | |||||||
| chr6:41343965 | TCTCC | T | 4 | a0002c0002t0002g0050 a0009c0009t0002g0148 a0009c0009t0002g0150 others(1): Show |
5 | HG01081.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.644+1820_644+1823d others(6): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 41343965 | ||||||
| chr6:41344083 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(121): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.644+1934A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344083 | |||||||
| chr6:41344106 | G | A | 1 | a0002c0002t0002g0072 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.644+1957G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344106 | |||||||
| chr6:41344154 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(81): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.644+2005T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344154 | |||||||
| chr6:41344240 | C | T | 5 | a0002c0002t0002g0050 a0002c0002t0002g0096 a0009c0009t0002g0148 others(2): Show |
6 | HG01081.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.644+2091C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344240 | |||||||
| chr6:41344484 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.644+2335G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344484 | |||||||
| chr6:41344508 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0079 |
5 | NA18939.hp2 NA18956.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.644+2359C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344508 | |||||||
| chr6:41344525 | C | T | 10 | a0002c0002t0002g0010 a0002c0002t0002g0021 a0002c0002t0002g0022 others(7): Show |
24 | HG01361.hp2 HG01884.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.644+2376C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344525 | |||||||
| chr6:41344554 | A | T | 4 | a0002c0002t0002g0050 a0002c0002t0002g0096 a0009c0009t0002g0148 others(1): Show |
5 | HG01081.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.644+2405A>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344554 | |||||||
| chr6:41344664 | T | C | 4 | a0008c0008t0002g0042 a0008c0008t0002g0043 a0008c0008t0002g0098 others(1): Show |
6 | HG02258.hp2 HG02572.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.644+2515T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344664 | |||||||
| chr6:41344681 | G | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(112): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.644+2532G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344681 | |||||||
| chr6:41344716 | T | C | 3 | a0003c0003t0001g0051 a0003c0003t0001g0153 a0003c0003t0001g0154 |
4 | HG01496.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.644+2567T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344716 | |||||||
| chr6:41344794 | C | T | 4 | a0001c0001t0001g0029 a0006c0005t0001g0016 a0006c0005t0001g0024 others(1): Show |
11 | HG02109.hp1 HG02257.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.644+2645C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344794 | |||||||
| chr6:41344796 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.644+2647C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344796 | |||||||
| chr6:41344802 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.644+2653G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344802 | |||||||
| chr6:41344838 | G | C | 1 | a0001c0001t0001g0046 | 2 | HG01993.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.644+2689G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344838 | |||||||
| chr6:41344983 | G | A | 1 | a0004c0004t0001g0059 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.644+2834G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344983 | |||||||
| chr6:41344998 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.644+2849G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41344998 | |||||||
| chr6:41345118 | A | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0134 |
4 | HG00323.hp1 HG00733.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.644+2969A>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345118 | |||||||
| chr6:41345244 | C | G | 1 | a0005c0006t0002g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.644+3095C>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345244 | |||||||
| chr6:41345322 | C | A | 1 | a0002c0002t0002g0073 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.644+3173C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345322 | |||||||
| chr6:41345427 | G | A | 1 | a0005c0011t0002g0025 | 3 | HG00741.hp1 HG02145.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.644+3278G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345427 | |||||||
| chr6:41345427 | G | C | 3 | a0003c0003t0001g0051 a0003c0003t0001g0153 a0003c0003t0001g0154 |
4 | HG01496.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.644+3278G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345427 | |||||||
| chr6:41345509 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.644+3360C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345509 | |||||||
| chr6:41345572 | C | T | 2 | a0005c0011t0002g0025 a0009c0009t0001g0094 |
4 | HG00741.hp1 HG02145.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.644+3423C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345572 | |||||||
| chr6:41345589 | C | G | 7 | a0001c0001t0001g0029 a0003c0003t0001g0051 a0003c0003t0001g0153 others(4): Show |
15 | HG01496.hp2 HG02109.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.644+3440C>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345589 | |||||||
| chr6:41345627 | G | A | 4 | a0002c0002t0002g0050 a0002c0002t0002g0096 a0009c0009t0002g0148 others(1): Show |
5 | HG01081.hp1 HG02647.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.644+3478G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345627 | |||||||
| chr6:41345635 | T | C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0080 others(9): Show |
32 | HG00099.hp1 HG01069.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.644+3486T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345635 | |||||||
| chr6:41345648 | T | C | 25 | a0003c0003t0001g0003 a0003c0003t0001g0009 a0003c0003t0001g0018 others(22): Show |
75 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.644+3499T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345648 | |||||||
| chr6:41345728 | T | A | 1 | a0003c0003t0001g0060 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.644+3579T>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345728 | |||||||
| chr6:41345738 | T | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(109): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.644+3589T>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345738 | |||||||
| chr6:41345752 | T | C | 1 | a0003c0003t0001g0053 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.644+3603T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345752 | |||||||
| chr6:41345770 | G | A | 2 | a0005c0011t0002g0025 a0009c0009t0001g0094 |
4 | HG00741.hp1 HG02145.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.644+3621G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345770 | |||||||
| chr6:41345796 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.644+3647C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345796 | |||||||
| chr6:41345861 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.644+3712C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345861 | |||||||
| chr6:41345892 | G | A | 4 | a0001c0001t0001g0115 a0003c0003t0001g0051 a0003c0003t0001g0153 others(1): Show |
5 | HG00639.hp1 HG01496.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.644+3743G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345892 | |||||||
| chr6:41345899 | A | G | 3 | a0003c0003t0001g0051 a0003c0003t0001g0153 a0003c0003t0001g0154 |
4 | HG01496.hp2 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.644+3750A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345899 | |||||||
| chr6:41345922 | C | T | 1 | a0014c0016t0002g0149 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.644+3773C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345922 | |||||||
| chr6:41345953 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.644+3804C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345953 | |||||||
| chr6:41345971 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(115): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.644+3822A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41345971 | |||||||
| chr6:41346026 | C | T | 1 | a0003c0003t0001g0033 | 2 | NA18969.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.644+3877C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346026 | |||||||
| chr6:41346098 | G | A | 1 | a0004c0004t0001g0057 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.644+3949G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346098 | |||||||
| chr6:41346112 | A | G | 1 | a0003c0003t0001g0070 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.644+3963A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346112 | |||||||
| chr6:41346133 | T | A | 1 | a0001c0001t0001g0105 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.644+3984T>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346133 | |||||||
| chr6:41346160 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(149): Show |
406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.644+4011G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346160 | |||||||
| chr6:41346183 | A | G | 8 | a0002c0002t0002g0050 a0002c0002t0002g0096 a0003c0003t0001g0051 others(5): Show |
12 | HG00741.hp1 HG01081.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.644+4034A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346183 | |||||||
| chr6:41346249 | C | T | 1 | a0001c0001t0001g0026 | 3 | HG01168.hp2 HG01169.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.644+4100C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346249 | |||||||
| chr6:41346263 | G | C | 8 | a0002c0002t0002g0050 a0002c0002t0002g0096 a0003c0003t0001g0051 others(5): Show |
12 | HG00741.hp1 HG01081.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.644+4114G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346263 | |||||||
| chr6:41346272 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.644+4123T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346272 | |||||||
| chr6:41346274 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.644+4125C>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346274 | |||||||
| chr6:41346286 | G | A | 1 | a0002c0002t0002g0096 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.644+4137G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346286 | |||||||
| chr6:41346289 | C | T | 7 | a0002c0002t0002g0050 a0002c0002t0002g0096 a0003c0003t0001g0051 others(4): Show |
9 | HG01081.hp1 HG01496.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.644+4140C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346289 | |||||||
| chr6:41346309 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.644+4160C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346309 | |||||||
| chr6:41346376 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.644+4227G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346376 | |||||||
| chr6:41346429 | A | G | 4 | a0008c0008t0002g0042 a0008c0008t0002g0043 a0008c0008t0002g0098 others(1): Show |
6 | HG02258.hp2 HG02572.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.645-4249A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346429 | |||||||
| chr6:41346445 | G | A | 1 | a0003c0003t0001g0061 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.645-4233G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346445 | |||||||
| chr6:41346501 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.645-4177C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346501 | |||||||
| chr6:41346568 | G | A | 1 | a0011c0019t0002g0084 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.645-4110G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346568 | |||||||
| chr6:41346597 | T | G | 11 | a0001c0001t0001g0029 a0002c0002t0002g0050 a0002c0002t0002g0096 others(8): Show |
20 | HG01081.hp1 HG01496.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.645-4081T>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346597 | |||||||
| chr6:41346671 | G | A | 1 | a0003c0003t0001g0062 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.645-4007G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346671 | |||||||
| chr6:41346677 | T | G | 8 | a0002c0002t0002g0050 a0002c0002t0002g0088 a0002c0002t0002g0096 others(5): Show |
10 | HG01081.hp1 HG01496.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.645-4001T>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346677 | |||||||
| chr6:41346828 | A | AGAGG | 9 | a0001c0001t0001g0029 a0001c0001t0001g0129 a0002c0002t0002g0036 others(6): Show |
16 | HG02071.hp1 HG02559.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.645-3827_645-3824d others(6): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 41346828 | ||||||
| chr6:41346828 | A | AGAGGGAG others(1): Show |
1 | a0006c0005t0001g0024 | 3 | HG02109.hp1 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.645-3831_645-3824d others(10): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 41346828 | ||||||
| chr6:41346828 | AGAGG | A | 10 | a0001c0001t0001g0123 a0002c0002t0002g0082 a0003c0003t0001g0051 others(7): Show |
15 | HG00642.hp1 HG00673.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.645-3827_645-3824d others(6): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 41346828 | ||||||
| chr6:41346844 | G | A | 1 | a0002c0002t0002g0049 | 2 | NA18950.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.645-3834G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41346844 | |||||||
| chr6:41347086 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.645-3592G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347086 | |||||||
| chr6:41347107 | T | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(139): Show |
385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.645-3571T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347107 | |||||||
| chr6:41347169 | C | T | 11 | a0002c0002t0002g0034 a0002c0002t0002g0037 a0002c0002t0002g0041 others(8): Show |
18 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.645-3509C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347169 | |||||||
| chr6:41347217 | A | C | 2 | a0010c0010t0001g0019 a0010c0010t0001g0058 |
4 | HG00423.hp2 NA19057.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.645-3461A>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347217 | |||||||
| chr6:41347220 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(114): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.645-3458G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347220 | |||||||
| chr6:41347246 | A | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0080 others(10): Show |
25 | HG00099.hp1 HG00741.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.645-3432A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347246 | |||||||
| chr6:41347272 | G | T | 8 | a0003c0003t0001g0051 a0003c0003t0001g0153 a0003c0003t0001g0154 others(5): Show |
13 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.645-3406G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347272 | |||||||
| chr6:41347474 | T | C | 24 | a0003c0003t0001g0003 a0003c0003t0001g0009 a0003c0003t0001g0018 others(21): Show |
70 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.645-3204T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347474 | |||||||
| chr6:41347498 | G | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(111): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.645-3180G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347498 | |||||||
| chr6:41347572 | C | T | 1 | a0009c0009t0001g0094 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.645-3106C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347572 | |||||||
| chr6:41347614 | G | C | 1 | a0006c0005t0001g0024 | 3 | HG02109.hp1 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.645-3064G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347614 | |||||||
| chr6:41347732 | G | C | 1 | a0002c0002t0002g0147 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.645-2946G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347732 | |||||||
| chr6:41347734 | G | T | 1 | a0003c0003t0001g0032 | 2 | NA18964.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.645-2944G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347734 | |||||||
| chr6:41347735 | G | T | 1 | a0003c0003t0001g0032 | 2 | NA18964.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.645-2943G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347735 | |||||||
| chr6:41347860 | G | A | 6 | a0001c0001t0001g0126 a0003c0003t0001g0051 a0003c0003t0001g0154 others(3): Show |
7 | HG01081.hp1 HG01496.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.645-2818G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347860 | |||||||
| chr6:41347981 | G | A | 1 | a0002c0002t0002g0076 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.645-2697G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41347981 | |||||||
| chr6:41348034 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(105): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.645-2644G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348034 | |||||||
| chr6:41348158 | T | C | 2 | a0006c0005t0001g0024 a0014c0016t0002g0149 |
4 | HG02109.hp1 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.645-2520T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348158 | |||||||
| chr6:41348225 | G | T | 1 | a0005c0006t0002g0039 | 2 | HG00140.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.645-2453G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348225 | |||||||
| chr6:41348252 | C | T | 1 | a0002c0002t0002g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.645-2426C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348252 | |||||||
| chr6:41348433 | T | C | 2 | a0003c0003t0001g0153 a0007c0007t0001g0095 |
2 | HG00642.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.645-2245T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348433 | |||||||
| chr6:41348465 | C | CA | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
306 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(303): Show |
intron_variant | MODIFIER | c.645-2203dupA | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 41348465 | ||||||
| chr6:41348473 | A | AC | 12 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0080 others(9): Show |
24 | HG00099.hp1 HG00741.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.645-2205_645-2204i others(3): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348473 | |||||||
| chr6:41348512 | A | C | 8 | a0003c0003t0001g0051 a0003c0003t0001g0153 a0003c0003t0001g0154 others(5): Show |
13 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.645-2166A>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348512 | |||||||
| chr6:41348659 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(111): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.645-2019G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348659 | |||||||
| chr6:41348794 | G | T | 1 | a0001c0001t0001g0128 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.645-1884G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348794 | |||||||
| chr6:41348816 | G | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0080 others(8): Show |
23 | HG00099.hp1 HG00741.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.645-1862G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348816 | |||||||
| chr6:41348941 | G | T | 1 | a0002c0002t0002g0034 | 2 | HG02145.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.645-1737G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348941 | |||||||
| chr6:41348952 | C | A | 7 | a0003c0003t0001g0051 a0003c0003t0001g0153 a0003c0003t0001g0154 others(4): Show |
12 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.645-1726C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348952 | |||||||
| chr6:41348962 | C | T | 8 | a0003c0003t0001g0051 a0003c0003t0001g0153 a0003c0003t0001g0154 others(5): Show |
13 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.645-1716C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41348962 | |||||||
| chr6:41349005 | T | C | 7 | a0003c0003t0001g0051 a0003c0003t0001g0153 a0003c0003t0001g0154 others(4): Show |
12 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.645-1673T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349005 | |||||||
| chr6:41349026 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(111): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.645-1652C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349026 | |||||||
| chr6:41349075 | T | TTTTTA | 8 | a0003c0003t0001g0051 a0003c0003t0001g0153 a0003c0003t0001g0154 others(5): Show |
13 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.645-1602_645-1598d others(7): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr6 | 41349075 | ||||||
| chr6:41349114 | T | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(78): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.645-1564T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349114 | |||||||
| chr6:41349135 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.645-1543T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349135 | |||||||
| chr6:41349197 | C | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(111): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.645-1481C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349197 | |||||||
| chr6:41349514 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.645-1164C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349514 | |||||||
| chr6:41349540 | G | C | 1 | a0001c0001t0001g0107 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.645-1138G>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349540 | |||||||
| chr6:41349553 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.645-1125A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349553 | |||||||
| chr6:41349586 | TC | T | 1 | a0006c0005t0001g0024 | 3 | HG02109.hp1 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.645-1091delC | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349586 | |||||||
| chr6:41349689 | C | G | 8 | a0003c0003t0001g0051 a0003c0003t0001g0153 a0003c0003t0001g0154 others(5): Show |
13 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.645-989C>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349689 | |||||||
| chr6:41349697 | C | T | 7 | a0003c0003t0001g0051 a0003c0003t0001g0153 a0003c0003t0001g0154 others(4): Show |
12 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.645-981C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349697 | |||||||
| chr6:41349698 | C | A | 8 | a0003c0003t0001g0051 a0003c0003t0001g0153 a0003c0003t0001g0154 others(5): Show |
13 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.645-980C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349698 | |||||||
| chr6:41349803 | C | T | 4 | a0006c0005t0001g0016 a0009c0009t0001g0094 a0011c0018t0002g0085 others(1): Show |
7 | HG02257.hp1 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.645-875C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349803 | |||||||
| chr6:41349972 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-706G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349972 | |||||||
| chr6:41349973 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-705C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349973 | |||||||
| chr6:41349975 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-703C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349975 | |||||||
| chr6:41349977 | T | A | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-701T>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349977 | |||||||
| chr6:41349978 | T | G | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-700T>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349978 | |||||||
| chr6:41349979 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-699C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349979 | |||||||
| chr6:41349983 | AGTTTGCC others(121): Show |
A | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-694_645-567del | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41349983 | |||||||
| chr6:41350026 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.645-652A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350026 | |||||||
| chr6:41350066 | C | T | 4 | a0008c0008t0002g0042 a0008c0008t0002g0043 a0008c0008t0002g0098 others(1): Show |
6 | HG02258.hp2 HG02572.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.645-612C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350066 | |||||||
| chr6:41350112 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-566C>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350112 | |||||||
| chr6:41350115 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-563C>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350115 | |||||||
| chr6:41350116 | T | A | 1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-562T>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350116 | |||||||
| chr6:41350121 | G | T | 4 | a0008c0008t0002g0042 a0008c0008t0002g0043 a0008c0008t0002g0098 others(1): Show |
6 | HG02258.hp2 HG02572.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.645-557G>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350121 | |||||||
| chr6:41350122 | A | AGAAAAAA others(122): Show |
1 | a0001c0001t0001g0145 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645-556_645-555ins others(129): Show |
NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350122 | |||||||
| chr6:41350180 | C | T | 1 | a0003c0003t0001g0063 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.645-498C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350180 | |||||||
| chr6:41350191 | C | T | 1 | a0009c0009t0001g0094 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.645-487C>T | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350191 | |||||||
| chr6:41350256 | G | A | 1 | a0010c0010t0001g0058 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.645-422G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350256 | |||||||
| chr6:41350319 | G | A | 4 | a0008c0008t0002g0042 a0008c0008t0002g0043 a0008c0008t0002g0098 others(1): Show |
6 | HG02258.hp2 HG02572.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.645-359G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350319 | |||||||
| chr6:41350363 | A | G | 8 | a0003c0003t0001g0051 a0003c0003t0001g0153 a0003c0003t0001g0154 others(5): Show |
13 | HG00642.hp1 HG01081.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.645-315A>G | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350363 | |||||||
| chr6:41350445 | G | A | 1 | a0005c0006t0002g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.645-233G>A | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350445 | |||||||
| chr6:41350519 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(111): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.645-159T>C | NCR2 | ENSG00000096264.14 | transcript | ENST00000373089.10 | protein_coding | 4/4 | chr6 | 41350519 |