Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4077 |
| ensemblid | ENSG00000188554.15 |
| hgncid | 6746 |
| symbol | NBR1 |
| name | NBR1 autophagy cargo receptor |
| refseq_nuc | NM_005899.5 |
| refseq_prot | NP_005890.2 |
| ensembl_nuc | ENST00000590996.6 |
| ensembl_prot | ENSP00000466667.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 43171214 |
| end | 43211688 |
| strand | + |
| ver | v1.2 |
| region | chr17:43171214-43211688 |
| region5000 | chr17:43166214-43216688 |
| regionname0 | NBR1_chr17_43171214_43211688 |
| regionname5000 | NBR1_chr17_43166214_43216688 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 966 | 180 | 60 | 31 | 66 | 5 | 17 | 47 | NBR1_chr17_43166214_43216688 | NBR1 | MEPQV others(961): Show |
chr17 | 43166214 | 43216688 |
| a0002 | 0/1 | 966 | 117 | 18 | 24 | 52 | 5 | 17 | 36 | NBR1_chr17_43166214_43216688 | NBR1 | MEPQV others(961): Show |
chr17 | 43166214 | 43216688 |
| a0003 | 0/0 | 966 | 8 | 7 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | MEPQV others(961): Show |
chr17 | 43166214 | 43216688 |
| a0004 | 0/0 | 966 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | MEPQV others(961): Show |
chr17 | 43166214 | 43216688 |
| a0005 | 0/0 | 966 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | MEPQV others(961): Show |
chr17 | 43166214 | 43216688 |
| a0006 | 0/0 | 966 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | MEPQV others(961): Show |
chr17 | 43166214 | 43216688 |
| a0007 | 0/0 | 966 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | MEPQV others(961): Show |
chr17 | 43166214 | 43216688 |
| a0008 | 0/0 | 966 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | MEPQV others(961): Show |
chr17 | 43166214 | 43216688 |
| a0009 | 0/0 | 966 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | MEPQV others(961): Show |
chr17 | 43166214 | 43216688 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2898 | 179 | 60 | 30 | 66 | 5 | 17 | NBR1_chr17_43166214_43216688 | NBR1 | ATGGA others(2893): Show |
chr17 | 43166214 | 43216688 | ||
| a0001c0008 | 0/0 | 2898 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | ATGGA others(2893): Show |
chr17 | 43166214 | 43216688 | ||
| a0002c0002 | 0/1 | 2898 | 116 | 18 | 23 | 52 | 5 | 17 | NBR1_chr17_43166214_43216688 | NBR1 | ATGGA others(2893): Show |
chr17 | 43166214 | 43216688 | ||
| a0002c0009 | 0/0 | 2898 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | ATGGA others(2893): Show |
chr17 | 43166214 | 43216688 | ||
| a0003c0003 | 0/0 | 2898 | 8 | 7 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | ATGGA others(2893): Show |
chr17 | 43166214 | 43216688 | ||
| a0004c0004 | 0/0 | 2898 | 3 | 3 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | ATGGA others(2893): Show |
chr17 | 43166214 | 43216688 | ||
| a0005c0005 | 0/0 | 2898 | 2 | 0 | 0 | 2 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | ATGGA others(2893): Show |
chr17 | 43166214 | 43216688 | ||
| a0006c0007 | 0/0 | 2898 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | ATGGA others(2893): Show |
chr17 | 43166214 | 43216688 | ||
| a0007c0011 | 0/0 | 2898 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | ATGGA others(2893): Show |
chr17 | 43166214 | 43216688 | ||
| a0008c0006 | 0/0 | 2898 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | ATGGA others(2893): Show |
chr17 | 43166214 | 43216688 | ||
| a0009c0010 | 0/0 | 2898 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | ATGGA others(2893): Show |
chr17 | 43166214 | 43216688 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4613 | 148 | 35 | 29 | 66 | 5 | 12 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4608): Show |
chr17 | 43166214 | 43216688 |
| a0001c0001t0003 | 0/0 | 4614 | 20 | 18 | 0 | 0 | 0 | 2 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4609): Show |
chr17 | 43166214 | 43216688 |
| a0001c0001t0005 | 0/0 | 4613 | 2 | 0 | 0 | 0 | 0 | 2 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4608): Show |
chr17 | 43166214 | 43216688 |
| a0001c0001t0006 | 0/0 | 4614 | 2 | 2 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4609): Show |
chr17 | 43166214 | 43216688 |
| a0001c0001t0007 | 0/0 | 4613 | 2 | 2 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4608): Show |
chr17 | 43166214 | 43216688 |
| a0001c0001t0008 | 0/0 | 4613 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4608): Show |
chr17 | 43166214 | 43216688 |
| a0001c0001t0009 | 0/0 | 4613 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4608): Show |
chr17 | 43166214 | 43216688 |
| a0001c0001t0010 | 0/0 | 4613 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4608): Show |
chr17 | 43166214 | 43216688 |
| a0001c0001t0011 | 0/0 | 4613 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4608): Show |
chr17 | 43166214 | 43216688 |
| a0001c0001t0014 | 0/0 | 4613 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4608): Show |
chr17 | 43166214 | 43216688 |
| a0001c0008t0001 | 0/0 | 4613 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4608): Show |
chr17 | 43166214 | 43216688 |
| a0002c0002t0002 | 0/1 | 4613 | 115 | 18 | 23 | 51 | 5 | 17 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4608): Show |
chr17 | 43166214 | 43216688 |
| a0002c0002t0013 | 0/0 | 4613 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4608): Show |
chr17 | 43166214 | 43216688 |
| a0002c0009t0001 | 0/0 | 4613 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4608): Show |
chr17 | 43166214 | 43216688 |
| a0003c0003t0003 | 0/0 | 4614 | 8 | 7 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4609): Show |
chr17 | 43166214 | 43216688 |
| a0004c0004t0004 | 0/0 | 4613 | 3 | 3 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4608): Show |
chr17 | 43166214 | 43216688 |
| a0005c0005t0001 | 0/0 | 4613 | 2 | 0 | 0 | 2 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4608): Show |
chr17 | 43166214 | 43216688 |
| a0006c0007t0001 | 0/0 | 4613 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4608): Show |
chr17 | 43166214 | 43216688 |
| a0007c0011t0012 | 0/0 | 4613 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4608): Show |
chr17 | 43166214 | 43216688 |
| a0008c0006t0002 | 0/0 | 4613 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4608): Show |
chr17 | 43166214 | 43216688 |
| a0009c0010t0001 | 0/0 | 4613 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | AGATT others(4608): Show |
chr17 | 43166214 | 43216688 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0004 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0003g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0008g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0010g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0011g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0001t0014g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0001c0008t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0006 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0009 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0106 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0002t0013g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0002c0009t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0003c0003t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0003c0003t0003g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0003c0003t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0003c0003t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0003c0003t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0003c0003t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0004c0004t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0004c0004t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0004c0004t0004g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0005c0005t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0005c0005t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0006c0007t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0007c0011t0012g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0008c0006t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| a0009c0010t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0002 | g0103 | EUR | GBR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0242 | EUR | GBR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0191 | EUR | GBR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0027 | EUR | GBR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00280 | hp1 | a0002 | c0002 | t0002 | g0115 | EUR | FIN | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0020 | EUR | FIN | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | CHS | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | CHS | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | CHS | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0056 | EAS | CHS | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00558 | hp2 | a0005 | c0005 | t0001 | g0222 | EAS | CHS | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00597 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | CHS | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | CHS | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0017 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG00741 | hp2 | a0002 | c0002 | t0002 | g0104 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01074 | hp2 | a0001 | c0008 | t0001 | g0248 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0100 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0063 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0072 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01109 | hp1 | a0003 | c0003 | t0003 | g0026 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0101 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01169 | hp1 | a0001 | c0001 | t0014 | g0238 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0090 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01243 | hp2 | a0002 | c0009 | t0001 | g0135 | AMR | PUR | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0066 | AMR | CLM | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0006 | AMR | CLM | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0055 | AMR | CLM | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0096 | AMR | CLM | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0064 | EUR | IBS | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | IBS | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01891 | hp1 | a0003 | c0003 | t0003 | g0026 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0078 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0079 | AMR | PEL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0006 | AMR | PEL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0051 | AMR | PEL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0059 | AMR | PEL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PEL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0047 | AMR | PEL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | KHV | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0108 | EAS | KHV | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | KHV | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0164 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0007 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0107 | EAS | KHV | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02074 | hp2 | a0002 | c0002 | t0002 | g0049 | EAS | KHV | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02145 | hp2 | a0006 | c0007 | t0001 | g0123 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CDX | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | CDX | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | CDX | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CDX | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | PEL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02280 | hp1 | a0003 | c0003 | t0003 | g0147 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0080 | AMR | PEL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0169 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | KHV | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0132 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0067 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02615 | hp2 | a0004 | c0004 | t0004 | g0120 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02622 | hp2 | a0003 | c0003 | t0003 | g0016 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0009 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02630 | hp2 | a0003 | c0003 | t0003 | g0016 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0065 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0082 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0048 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0021 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0058 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0091 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0160 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0137 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0008 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0008 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0159 | AFR | ESN | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | ESN | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | ESN | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0166 | AFR | ESN | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0077 | AFR | ESN | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03017 | hp1 | a0002 | c0002 | t0002 | g0006 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0097 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0138 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03098 | hp2 | a0003 | c0003 | t0003 | g0150 | AFR | MSL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0095 | AFR | ESN | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | ESN | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0131 | AFR | ESN | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03209 | hp1 | a0001 | c0001 | t0010 | g0154 | AFR | MSL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03225 | hp1 | a0007 | c0011 | t0012 | g0122 | AFR | MSL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | MSL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0062 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0162 | AFR | MSL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0155 | AFR | MSL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0024 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0198 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0024 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0216 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | ESN | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0007 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | MSL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0054 | AFR | MSL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0009 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03688 | hp1 | a0001 | c0001 | t0011 | g0190 | SAS | STU | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03688 | hp2 | a0002 | c0002 | t0002 | g0017 | SAS | STU | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0020 | SAS | PJL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0068 | SAS | BEB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | STU | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0257 | SAS | STU | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0260 | SAS | STU | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0085 | SAS | STU | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18522 | hp1 | a0003 | c0003 | t0003 | g0158 | AFR | YRI | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18522 | hp2 | a0004 | c0004 | t0004 | g0119 | AFR | YRI | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | YRI | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18939 | hp2 | a0005 | c0005 | t0001 | g0224 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18940 | hp1 | a0008 | c0006 | t0002 | g0089 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18987 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0023 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19004 | hp2 | a0002 | c0002 | t0013 | g0010 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0038 | AFR | LWK | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | LWK | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19060 | hp1 | a0009 | c0010 | t0001 | g0252 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0019 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19080 | hp2 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19081 | hp2 | a0002 | c0002 | t0002 | g0092 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19086 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | YRI | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0007 | AFR | YRI | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA20129 | hp1 | a0004 | c0004 | t0004 | g0121 | AFR | ASW | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ASW | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0102 | EUR | TSI | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0042 | SAS | GIH | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0098 | SAS | GIH | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0045 | AMR | CLM | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0247 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0168 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02559 | hp1 | a0003 | c0003 | t0003 | g0146 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0163 | AFR | USA | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0037 | AFR | USA | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18955 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0249 | AFR | USA | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | USA | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0259 | AFR | LWK | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0106 | REF | REF | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0157 | REF | REF | NBR1_chr17_43166214_43216688 | NBR1 | chr17 | 43166214 | 43216688 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:43186377 | C | T | 1 | a0005 | 2 | HG00558.hp2 NA18939.hp2 |
missense_variant | MODERATE | c.335C>T | p.Ala112Val | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/21 | 433/4613 | 335/2901 | 112/966 | chr17 | 43186377 | |||
| chr17:43189718 | T | C | 1 | a0007 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.611T>C | p.Leu204Ser | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 8/21 | 709/4613 | 611/2901 | 204/966 | chr17 | 43189718 | |||
| chr17:43190748 | C | T | 1 | a0009 | 1 | NA19060.hp1 | missense_variant | MODERATE | c.835C>T | p.Arg279Cys | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 9/21 | 933/4613 | 835/2901 | 279/966 | chr17 | 43190748 | |||
| chr17:43191443 | G | A | 1 | a0003 | 8 | HG01109.hp1 HG01891.hp1 HG02280.hp1 others(5): Show |
missense_variant | MODERATE | c.935G>A | p.Arg312His | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 10/21 | 1033/4613 | 935/2901 | 312/966 | chr17 | 43191443 | |||
| chr17:43195031 | C | A | 1 | a0008 | 1 | NA18940.hp1 | missense_variant | MODERATE | c.1742C>A | p.Thr581Asn | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/21 | 1840/4613 | 1742/2901 | 581/966 | chr17 | 43195031 | |||
| chr17:43196507 | C | T | 1 | a0006 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.1777C>T | p.Pro593Ser | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 15/21 | 1875/4613 | 1777/2901 | 593/966 | chr17 | 43196507 | |||
| chr17:43196947 | A | G | 1 | a0004 | 3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.1867A>G | p.Met623Val | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/21 | 1965/4613 | 1867/2901 | 623/966 | chr17 | 43196947 | |||
| chr17:43209907 | A | G | 1 | a0004 | 3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.2734A>G | p.Ile912Val | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 21/21 | 2832/4613 | 2734/2901 | 912/966 | chr17 | 43209907 | |||
| chr17:43209941 | A | G | 4 | a0002 a0004 a0007 others(1): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
missense_variant | MODERATE | c.2768A>G | p.His923Arg | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 21/21 | 2866/4613 | 2768/2901 | 923/966 | chr17 | 43209941 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:43189608 | C | T | 2 | a0004c0004 a0007c0011 |
4 | HG02615.hp2 HG03225.hp1 NA18522.hp2 others(1): Show |
synonymous_variant | LOW | c.501C>T | p.Asn167Asn | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 8/21 | 599/4613 | 501/2901 | 167/966 | chr17 | 43189608 | |||
| chr17:43191498 | C | T | 1 | a0002c0009 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.990C>T | p.His330His | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 10/21 | 1088/4613 | 990/2901 | 330/966 | chr17 | 43191498 | |||
| chr17:43193386 | A | G | 1 | a0001c0008 | 1 | HG01074.hp2 | synonymous_variant | LOW | c.1272A>G | p.Thr424Thr | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 12/21 | 1370/4613 | 1272/2901 | 424/966 | chr17 | 43193386 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:43171258 | C | G | 1 | a0001c0001t0007 | 2 | HG02572.hp2 HG03195.hp2 |
5_prime_UTR_variant | MODIFIER | c.-54C>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/21 | 4542 | chr17 | 43171258 | ||||||
| chr17:43171273 | C | G | 1 | a0001c0001t0014 | 1 | HG01169.hp1 | 5_prime_UTR_variant | MODIFIER | c.-39C>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/21 | 4527 | chr17 | 43171273 | ||||||
| chr17:43210194 | G | A | 1 | a0004c0004t0004 | 3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*120G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 21/21 | 120 | chr17 | 43210194 | ||||||
| chr17:43210253 | C | G | 5 | a0002c0002t0002 a0002c0002t0013 a0004c0004t0004 others(2): Show |
120 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*179C>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 21/21 | 179 | chr17 | 43210253 | ||||||
| chr17:43210346 | C | T | 1 | a0002c0002t0013 | 1 | NA19004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*272C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 21/21 | 272 | chr17 | 43210346 | ||||||
| chr17:43210469 | C | T | 1 | a0001c0001t0011 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*395C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 21/21 | 395 | chr17 | 43210469 | ||||||
| chr17:43210474 | G | A | 2 | a0001c0001t0008 a0001c0001t0009 |
2 | HG02922.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*400G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 21/21 | 400 | chr17 | 43210474 | ||||||
| chr17:43210525 | C | T | 1 | a0001c0001t0006 | 2 | HG02451.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*451C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 21/21 | 451 | chr17 | 43210525 | ||||||
| chr17:43210702 | C | T | 3 | a0002c0002t0002 a0002c0002t0013 a0008c0006t0002 |
116 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*628C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 21/21 | 628 | chr17 | 43210702 | ||||||
| chr17:43210718 | G | A | 1 | a0001c0001t0008 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*644G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 21/21 | 644 | chr17 | 43210718 | ||||||
| chr17:43210945 | G | GA | 3 | a0001c0001t0003 a0001c0001t0006 a0003c0003t0003 |
30 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*874dupA | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 21/21 | 875 | INFO_REALIGN_3_PRIME | chr17 | 43210945 | |||||
| chr17:43211579 | G | A | 1 | a0001c0001t0005 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1505G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 21/21 | 1505 | chr17 | 43211579 | ||||||
| chr17:43211620 | C | G | 1 | a0001c0001t0010 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1546C>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 21/21 | 1546 | chr17 | 43211620 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:43171402 | T | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG00438.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.-10+100T>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43171402 | |||||||
| chr17:43171657 | G | A | 2 | a0002c0002t0002g0037 a0002c0002t0002g0038 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-10+355G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43171657 | |||||||
| chr17:43171662 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-10+360C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43171662 | |||||||
| chr17:43171859 | G | C | 1 | a0001c0001t0001g0039 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-10+557G>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43171859 | |||||||
| chr17:43172057 | GA | G | 5 | a0001c0001t0003g0257 a0001c0001t0003g0258 a0001c0001t0003g0259 others(2): Show |
5 | HG02258.hp1 HG04199.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+764delA | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | 43172057 | ||||||
| chr17:43172091 | G | C | 2 | a0002c0002t0002g0037 a0002c0002t0002g0038 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-10+789G>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43172091 | |||||||
| chr17:43172304 | C | T | 2 | a0001c0001t0001g0254 a0001c0001t0001g0255 |
2 | NA18940.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-10+1002C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43172304 | |||||||
| chr17:43172619 | G | C | 1 | a0003c0003t0003g0016 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-10+1317G>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43172619 | |||||||
| chr17:43172622 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-10+1320G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43172622 | |||||||
| chr17:43172871 | G | T | 1 | a0001c0001t0001g0253 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-10+1569G>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43172871 | |||||||
| chr17:43172995 | T | C | 1 | a0002c0002t0002g0042 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-10+1693T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43172995 | |||||||
| chr17:43173003 | T | C | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.-10+1701T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43173003 | |||||||
| chr17:43173064 | G | A | 2 | a0002c0002t0002g0043 a0002c0002t0002g0044 |
2 | HG02015.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.-10+1762G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43173064 | |||||||
| chr17:43173121 | C | T | 3 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0009c0010t0001g0252 |
3 | NA18977.hp2 NA19060.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-10+1819C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43173121 | |||||||
| chr17:43173179 | C | G | 1 | a0001c0001t0003g0249 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-10+1877C>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43173179 | |||||||
| chr17:43173263 | A | T | 1 | a0002c0002t0002g0118 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-10+1961A>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43173263 | |||||||
| chr17:43173325 | A | G | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.-10+2023A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43173325 | |||||||
| chr17:43173473 | G | A | 99 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(96): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-10+2171G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43173473 | |||||||
| chr17:43173658 | T | C | 13 | a0001c0001t0001g0011 a0001c0001t0001g0124 a0001c0001t0001g0125 others(10): Show |
15 | HG00735.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-9-2133T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43173658 | |||||||
| chr17:43173747 | C | T | 1 | a0002c0002t0002g0117 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-9-2044C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43173747 | |||||||
| chr17:43174070 | T | G | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.-9-1721T>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43174070 | |||||||
| chr17:43174318 | C | A | 1 | a0002c0009t0001g0135 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-9-1473C>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43174318 | |||||||
| chr17:43174341 | A | T | 13 | a0002c0002t0002g0010 a0002c0002t0002g0107 a0002c0002t0002g0108 others(10): Show |
14 | HG00280.hp1 HG02027.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9-1450A>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43174341 | |||||||
| chr17:43174425 | G | A | 3 | a0004c0004t0004g0119 a0004c0004t0004g0120 a0004c0004t0004g0121 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-9-1366G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43174425 | |||||||
| chr17:43174466 | C | T | 1 | a0001c0008t0001g0248 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-9-1325C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43174466 | |||||||
| chr17:43174491 | A | G | 103 | a0001c0001t0001g0094 a0001c0001t0003g0257 a0001c0001t0003g0258 others(100): Show |
125 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.-9-1300A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43174491 | |||||||
| chr17:43174588 | A | G | 1 | a0001c0001t0003g0247 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-9-1203A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43174588 | |||||||
| chr17:43174705 | G | A | 1 | a0002c0002t0002g0045 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-9-1086G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43174705 | |||||||
| chr17:43174881 | G | A | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.-9-910G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43174881 | |||||||
| chr17:43174923 | G | A | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.-9-868G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43174923 | |||||||
| chr17:43174975 | G | A | 6 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(3): Show |
6 | HG02109.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9-816G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43174975 | |||||||
| chr17:43174992 | G | C | 1 | a0001c0001t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-9-799G>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43174992 | |||||||
| chr17:43175016 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-9-775G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43175016 | |||||||
| chr17:43175157 | G | A | 1 | a0002c0002t0002g0046 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-9-634G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43175157 | |||||||
| chr17:43175300 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-9-491C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43175300 | |||||||
| chr17:43175604 | A | G | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.-9-187A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43175604 | |||||||
| chr17:43175631 | T | C | 99 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(96): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.-9-160T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | chr17 | 43175631 | |||||||
| chr17:43175633 | G | GT | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.-9-157dupT | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | 43175633 | ||||||
| chr17:43175980 | G | A | 2 | a0002c0002t0002g0047 a0002c0002t0002g0048 |
2 | HG02004.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.102+79G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | chr17 | 43175980 | |||||||
| chr17:43176078 | A | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.102+177A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | chr17 | 43176078 | |||||||
| chr17:43176119 | G | T | 1 | a0001c0001t0001g0245 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.102+218G>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | chr17 | 43176119 | |||||||
| chr17:43176206 | A | G | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.102+305A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | chr17 | 43176206 | |||||||
| chr17:43176357 | A | T | 1 | a0001c0001t0009g0159 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.102+456A>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | chr17 | 43176357 | |||||||
| chr17:43176801 | T | A | 99 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(96): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.102+900T>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | chr17 | 43176801 | |||||||
| chr17:43176956 | T | G | 1 | a0001c0001t0003g0249 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.103-980T>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | chr17 | 43176956 | |||||||
| chr17:43176993 | A | G | 99 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(96): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.103-943A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | chr17 | 43176993 | |||||||
| chr17:43177099 | C | T | 1 | a0002c0002t0002g0116 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.103-837C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | chr17 | 43177099 | |||||||
| chr17:43177155 | T | C | 99 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(96): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.103-781T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | chr17 | 43177155 | |||||||
| chr17:43177167 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.103-769G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | chr17 | 43177167 | |||||||
| chr17:43177271 | C | CA | 92 | a0001c0001t0001g0094 a0001c0001t0001g0171 a0001c0001t0001g0172 others(89): Show |
114 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.103-648dupA | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177271 | ||||||
| chr17:43177271 | C | CAA | 9 | a0002c0002t0002g0043 a0002c0002t0002g0047 a0002c0002t0002g0048 others(6): Show |
9 | HG01952.hp1 HG02004.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.103-649_103-648dup others(2): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177271 | ||||||
| chr17:43177298 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | NA18943.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.103-638C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | chr17 | 43177298 | |||||||
| chr17:43177299 | G | GT | 6 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0173 others(3): Show |
6 | HG00621.hp2 HG00741.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-625dupT | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177299 | ||||||
| chr17:43177299 | GT | G | 15 | a0001c0001t0001g0027 a0001c0001t0001g0174 a0001c0001t0001g0175 others(12): Show |
16 | HG00140.hp2 HG00642.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.103-625delT | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177299 | ||||||
| chr17:43177324 | C | A | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 |
3 | HG02257.hp1 HG02451.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.103-612C>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | chr17 | 43177324 | |||||||
| chr17:43177572 | A | AAC | 14 | a0001c0001t0001g0133 a0001c0001t0001g0144 a0001c0001t0001g0145 others(11): Show |
14 | HG00140.hp1 HG01192.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.103-316_103-315dup others(2): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177572 | ||||||
| chr17:43177572 | A | AACAC | 14 | a0001c0001t0001g0011 a0001c0001t0001g0025 a0001c0001t0001g0127 others(11): Show |
17 | HG00735.hp1 HG01070.hp2 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.103-318_103-315dup others(4): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177572 | ||||||
| chr17:43177572 | A | AACACAC | 11 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0125 others(8): Show |
11 | HG00735.hp2 HG00741.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.103-320_103-315dup others(6): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177572 | ||||||
| chr17:43177572 | A | AACACACA others(1): Show |
3 | a0001c0001t0001g0124 a0001c0001t0001g0153 a0001c0001t0003g0136 |
3 | HG03579.hp1 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.103-322_103-315dup others(8): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177572 | ||||||
| chr17:43177572 | A | AACACACA others(3): Show |
5 | a0001c0001t0001g0141 a0001c0001t0001g0182 a0001c0001t0003g0258 others(2): Show |
5 | HG01123.hp1 HG02258.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-324_103-315dup others(10): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177572 | ||||||
| chr17:43177572 | A | AACACACA others(5): Show |
2 | a0001c0001t0001g0149 a0001c0001t0001g0171 |
2 | HG02004.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.103-326_103-315dup others(12): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177572 | ||||||
| chr17:43177572 | A | AACACACA others(7): Show |
2 | a0001c0001t0003g0257 a0003c0003t0003g0016 |
3 | HG02622.hp2 HG02630.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.103-328_103-315dup others(14): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177572 | ||||||
| chr17:43177572 | A | AACACACA others(9): Show |
1 | a0006c0007t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.103-330_103-315dup others(16): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177572 | ||||||
| chr17:43177572 | A | AACACACA others(11): Show |
2 | a0001c0001t0003g0138 a0003c0003t0003g0147 |
2 | HG02280.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.103-332_103-315dup others(18): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177572 | ||||||
| chr17:43177572 | A | AACACACA others(13): Show |
1 | a0003c0003t0003g0146 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.103-334_103-315dup others(20): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177572 | ||||||
| chr17:43177572 | AAC | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(48): Show |
70 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.103-316_103-315del others(2): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177572 | ||||||
| chr17:43177572 | AACAC | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0039 others(13): Show |
21 | HG00423.hp2 HG00544.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.103-318_103-315del others(4): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177572 | ||||||
| chr17:43177572 | AACACAC | A | 14 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0239 others(11): Show |
15 | HG00558.hp1 HG00609.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.103-320_103-315del others(6): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177572 | ||||||
| chr17:43177572 | AACACACA others(1): Show |
A | 38 | a0002c0002t0002g0005 a0002c0002t0002g0006 a0002c0002t0002g0018 others(35): Show |
46 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.103-322_103-315del others(8): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177572 | ||||||
| chr17:43177572 | AACACACA others(3): Show |
A | 43 | a0001c0001t0001g0094 a0001c0001t0003g0170 a0002c0002t0002g0001 others(40): Show |
55 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.103-324_103-315del others(10): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177572 | ||||||
| chr17:43177572 | AACACACA others(5): Show |
A | 9 | a0001c0001t0001g0241 a0002c0002t0002g0024 a0002c0002t0002g0051 others(6): Show |
10 | HG00099.hp1 HG00280.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.103-326_103-315del others(12): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177572 | ||||||
| chr17:43177572 | AACACACA others(7): Show |
A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0242 |
2 | HG00099.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.103-328_103-315del others(14): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177572 | ||||||
| chr17:43177572 | AACACACA others(9): Show |
A | 1 | a0001c0001t0001g0181 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.103-330_103-315del others(16): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177572 | ||||||
| chr17:43177620 | C | CACACACA others(9): Show |
1 | a0001c0001t0001g0148 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.103-315_103-314ins others(16): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177620 | ||||||
| chr17:43177620 | C | CACACACA others(3): Show |
2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG02486.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.103-315_103-314ins others(10): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr17 | 43177620 | ||||||
| chr17:43177799 | G | T | 1 | a0002c0002t0002g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.103-137G>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | chr17 | 43177799 | |||||||
| chr17:43177800 | G | T | 1 | a0002c0002t0002g0038 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.103-136G>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | chr17 | 43177800 | |||||||
| chr17:43177830 | G | A | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.103-106G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | chr17 | 43177830 | |||||||
| chr17:43177859 | T | G | 8 | a0001c0001t0003g0161 a0001c0001t0003g0162 a0001c0001t0003g0163 others(5): Show |
8 | HG01884.hp1 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-77T>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | chr17 | 43177859 | |||||||
| chr17:43177925 | C | T | 1 | a0006c0007t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.103-11C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 2/20 | chr17 | 43177925 | |||||||
| chr17:43178007 | T | C | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.165+9T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 3/20 | chr17 | 43178007 | |||||||
| chr17:43178248 | A | G | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.165+250A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 3/20 | chr17 | 43178248 | |||||||
| chr17:43178366 | CT | C | 98 | a0001c0001t0001g0094 a0001c0001t0003g0166 a0001c0001t0003g0167 others(95): Show |
120 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.165+380delT | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | 43178366 | ||||||
| chr17:43178378 | T | C | 2 | a0002c0002t0002g0045 a0002c0002t0002g0053 |
2 | HG01123.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.165+380T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 3/20 | chr17 | 43178378 | |||||||
| chr17:43178379 | C | T | 2 | a0002c0002t0002g0045 a0002c0002t0002g0053 |
2 | HG01123.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.165+381C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 3/20 | chr17 | 43178379 | |||||||
| chr17:43178695 | A | G | 9 | a0001c0001t0003g0161 a0001c0001t0003g0162 a0001c0001t0003g0163 others(6): Show |
9 | HG01884.hp1 HG02055.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+697A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 3/20 | chr17 | 43178695 | |||||||
| chr17:43178733 | A | G | 2 | a0002c0002t0002g0103 a0002c0002t0002g0104 |
2 | HG00099.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.166-661A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 3/20 | chr17 | 43178733 | |||||||
| chr17:43178768 | CT | C | 14 | a0001c0001t0001g0127 a0001c0001t0001g0188 a0001c0001t0001g0210 others(11): Show |
15 | HG00099.hp2 HG01070.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.166-607delT | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | 43178768 | ||||||
| chr17:43178803 | C | G | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.166-591C>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 3/20 | chr17 | 43178803 | |||||||
| chr17:43178958 | T | G | 1 | a0002c0002t0002g0054 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.166-436T>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 3/20 | chr17 | 43178958 | |||||||
| chr17:43179005 | C | T | 2 | a0001c0001t0006g0160 a0001c0001t0006g0169 |
2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.166-389C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 3/20 | chr17 | 43179005 | |||||||
| chr17:43179021 | C | G | 6 | a0001c0001t0001g0015 a0001c0001t0001g0029 a0001c0001t0001g0033 others(3): Show |
10 | HG01928.hp1 HG01978.hp2 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.166-373C>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 3/20 | chr17 | 43179021 | |||||||
| chr17:43179192 | C | T | 2 | a0002c0002t0002g0097 a0002c0002t0002g0098 |
2 | HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.166-202C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 3/20 | chr17 | 43179192 | |||||||
| chr17:43179271 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.166-123T>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 3/20 | chr17 | 43179271 | |||||||
| chr17:43179289 | C | T | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.166-105C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 3/20 | chr17 | 43179289 | |||||||
| chr17:43179443 | G | A | 99 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(96): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.184+31G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 4/20 | chr17 | 43179443 | |||||||
| chr17:43179580 | T | C | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.184+168T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 4/20 | chr17 | 43179580 | |||||||
| chr17:43179735 | T | C | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | NA18943.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.184+323T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 4/20 | chr17 | 43179735 | |||||||
| chr17:43179767 | GTTTA | G | 3 | a0002c0002t0002g0007 a0002c0002t0002g0077 a0002c0002t0002g0078 |
5 | HG01891.hp2 HG02055.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.184+361_184+364del others(4): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr17 | 43179767 | ||||||
| chr17:43179799 | C | T | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.184+387C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 4/20 | chr17 | 43179799 | |||||||
| chr17:43179900 | T | C | 2 | a0001c0001t0001g0254 a0001c0001t0001g0255 |
2 | NA18940.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.184+488T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 4/20 | chr17 | 43179900 | |||||||
| chr17:43179902 | T | TCTTGAGT others(11): Show |
99 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(96): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.184+491_184+492ins others(18): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr17 | 43179902 | ||||||
| chr17:43179915 | G | A | 3 | a0004c0004t0004g0119 a0004c0004t0004g0120 a0004c0004t0004g0121 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.184+503G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 4/20 | chr17 | 43179915 | |||||||
| chr17:43180313 | T | C | 99 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(96): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.185-482T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 4/20 | chr17 | 43180313 | |||||||
| chr17:43180323 | G | A | 2 | a0001c0001t0006g0160 a0001c0001t0006g0169 |
2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.185-472G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 4/20 | chr17 | 43180323 | |||||||
| chr17:43180346 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.185-449G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 4/20 | chr17 | 43180346 | |||||||
| chr17:43180476 | G | A | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.185-319G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 4/20 | chr17 | 43180476 | |||||||
| chr17:43180717 | A | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0175 |
3 | HG00140.hp2 HG01517.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.185-78A>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 4/20 | chr17 | 43180717 | |||||||
| chr17:43180787 | T | C | 246 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
splice_region_variant&intron_variant | LOW | c.185-8T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 4/20 | chr17 | 43180787 | |||||||
| chr17:43180898 | G | T | 1 | a0001c0001t0001g0175 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.207+81G>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43180898 | |||||||
| chr17:43181020 | C | T | 2 | a0002c0002t0002g0097 a0002c0002t0002g0098 |
2 | HG03017.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.207+203C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43181020 | |||||||
| chr17:43181200 | C | G | 1 | a0001c0001t0001g0025 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.207+383C>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43181200 | |||||||
| chr17:43181531 | G | GGT | 214 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.207+715_207+716ins others(2): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43181531 | ||||||
| chr17:43181615 | G | C | 5 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0139 others(2): Show |
5 | HG02109.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.207+798G>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43181615 | |||||||
| chr17:43181673 | AAAAC | A | 5 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0004c0004t0004g0119 others(2): Show |
5 | HG00642.hp1 HG01106.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.207+865_207+868del others(4): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43181673 | ||||||
| chr17:43181681 | C | A | 1 | a0001c0001t0001g0242 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.207+864C>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43181681 | |||||||
| chr17:43181769 | A | G | 99 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(96): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.207+952A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43181769 | |||||||
| chr17:43181868 | CAGCTACT others(1657): Show |
C | 3 | a0004c0004t0004g0119 a0004c0004t0004g0120 a0004c0004t0004g0121 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.207+1052_207+2715d others(2): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43181868 | |||||||
| chr17:43181999 | C | A | 94 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(91): Show |
115 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.207+1182C>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43181999 | |||||||
| chr17:43182096 | C | G | 1 | a0001c0001t0009g0159 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.207+1279C>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43182096 | |||||||
| chr17:43182211 | C | CT | 92 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(89): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.207+1418dupT | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43182211 | ||||||
| chr17:43182211 | C | CTT | 19 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0032 others(16): Show |
20 | HG00544.hp1 HG00621.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.207+1417_207+1418d others(4): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43182211 | ||||||
| chr17:43182211 | CT | C | 20 | a0001c0001t0001g0011 a0001c0001t0001g0124 a0001c0001t0001g0125 others(17): Show |
22 | HG00558.hp1 HG00735.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.207+1418delT | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43182211 | ||||||
| chr17:43182331 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0214 a0001c0001t0001g0235 |
4 | HG00423.hp2 HG02071.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.207+1514C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43182331 | |||||||
| chr17:43182599 | C | CT | 10 | a0001c0001t0001g0011 a0001c0001t0001g0124 a0001c0001t0001g0125 others(7): Show |
12 | HG00735.hp1 HG02280.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.207+1792dupT | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43182599 | ||||||
| chr17:43182732 | C | T | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.207+1915C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43182732 | |||||||
| chr17:43182786 | C | G | 1 | a0002c0002t0002g0021 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.207+1969C>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43182786 | |||||||
| chr17:43182908 | T | C | 96 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(93): Show |
118 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.207+2091T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43182908 | |||||||
| chr17:43183188 | C | T | 23 | a0002c0002t0002g0001 a0002c0002t0002g0022 a0002c0002t0002g0023 others(20): Show |
28 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.207+2371C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43183188 | |||||||
| chr17:43183362 | G | A | 8 | a0002c0002t0002g0024 a0002c0002t0002g0047 a0002c0002t0002g0048 others(5): Show |
9 | HG00099.hp1 HG00741.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.207+2545G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43183362 | |||||||
| chr17:43183379 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.207+2562C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43183379 | |||||||
| chr17:43183455 | A | G | 96 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(93): Show |
118 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.207+2638A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43183455 | |||||||
| chr17:43183533 | C | T | 3 | a0004c0004t0004g0119 a0004c0004t0004g0120 a0004c0004t0004g0121 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.207+2716C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43183533 | |||||||
| chr17:43183586 | C | T | 1 | a0002c0002t0002g0074 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.208-2664C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43183586 | |||||||
| chr17:43183838 | T | G | 2 | a0001c0001t0003g0258 a0001c0001t0003g0259 |
2 | HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.208-2412T>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43183838 | |||||||
| chr17:43184133 | C | G | 9 | a0001c0001t0003g0161 a0001c0001t0003g0162 a0001c0001t0003g0163 others(6): Show |
9 | HG01884.hp1 HG02055.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.208-2117C>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43184133 | |||||||
| chr17:43184227 | CT | C | 6 | a0001c0001t0003g0166 a0002c0002t0002g0057 a0002c0002t0002g0058 others(3): Show |
7 | HG01109.hp1 HG01891.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.208-2008delT | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43184227 | ||||||
| chr17:43184372 | C | CTTTTTTT others(3): Show |
5 | a0001c0001t0001g0127 a0001c0001t0001g0197 a0001c0001t0001g0212 others(2): Show |
5 | HG00099.hp2 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-1876_208-1867d others(12): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43184372 | ||||||
| chr17:43184372 | C | CTTTTTTT others(4): Show |
101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
128 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.208-1877_208-1867d others(13): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43184372 | ||||||
| chr17:43184372 | C | CTTTTTTT others(8): Show |
1 | a0002c0002t0002g0059 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.208-1867_208-1866i others(17): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43184372 | ||||||
| chr17:43184372 | C | CTTTTTTT others(5): Show |
9 | a0001c0001t0001g0133 a0001c0001t0001g0172 a0001c0001t0001g0195 others(6): Show |
9 | HG00609.hp1 HG00609.hp2 HG00642.hp2 others(6): Show |
intron_variant | MODIFIER | c.208-1867_208-1866i others(14): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43184372 | ||||||
| chr17:43184372 | C | CTTTTTTT others(7): Show |
33 | a0002c0002t0002g0001 a0002c0002t0002g0022 a0002c0002t0002g0023 others(30): Show |
39 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.208-1867_208-1866i others(16): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43184372 | ||||||
| chr17:43184372 | C | CTTTTTTT others(8): Show |
55 | a0001c0001t0001g0094 a0002c0002t0002g0005 a0002c0002t0002g0007 others(52): Show |
68 | HG00280.hp1 HG00280.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.208-1867_208-1866i others(17): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43184372 | ||||||
| chr17:43184372 | C | CTTTTTTT others(9): Show |
10 | a0002c0002t0002g0006 a0002c0002t0002g0021 a0002c0002t0002g0038 others(7): Show |
13 | HG00438.hp2 HG01106.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.208-1867_208-1866i others(18): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43184372 | ||||||
| chr17:43184451 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.208-1799C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43184451 | |||||||
| chr17:43184452 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.208-1798G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43184452 | |||||||
| chr17:43184657 | C | T | 3 | a0004c0004t0004g0119 a0004c0004t0004g0120 a0004c0004t0004g0121 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.208-1593C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43184657 | |||||||
| chr17:43184658 | G | A | 1 | a0002c0009t0001g0135 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.208-1592G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43184658 | |||||||
| chr17:43184691 | G | A | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.208-1559G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43184691 | |||||||
| chr17:43184862 | C | T | 1 | a0002c0002t0002g0054 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.208-1388C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43184862 | |||||||
| chr17:43184962 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.208-1288G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43184962 | |||||||
| chr17:43185046 | A | G | 2 | a0002c0002t0002g0043 a0002c0002t0002g0044 |
2 | HG02015.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.208-1204A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43185046 | |||||||
| chr17:43185096 | GA | G | 94 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(91): Show |
116 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.208-1141delA | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43185096 | ||||||
| chr17:43185252 | C | T | 1 | a0003c0003t0003g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.208-998C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43185252 | |||||||
| chr17:43185455 | C | T | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(112): Show |
142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.208-795C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43185455 | |||||||
| chr17:43185462 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.208-788G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43185462 | |||||||
| chr17:43185538 | C | T | 3 | a0004c0004t0004g0119 a0004c0004t0004g0120 a0004c0004t0004g0121 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.208-712C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43185538 | |||||||
| chr17:43185594 | G | A | 1 | a0002c0002t0002g0037 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.208-656G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43185594 | |||||||
| chr17:43185771 | T | C | 1 | a0001c0001t0006g0160 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.208-479T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43185771 | |||||||
| chr17:43185883 | A | C | 99 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(96): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.208-367A>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43185883 | |||||||
| chr17:43185997 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.208-253G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | chr17 | 43185997 | |||||||
| chr17:43186003 | A | AAAAT | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0148 others(2): Show |
5 | HG02723.hp2 HG02886.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.208-202_208-199dup others(4): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43186003 | ||||||
| chr17:43186003 | AAAAT | A | 38 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0124 others(35): Show |
41 | HG00423.hp2 HG00735.hp1 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.208-202_208-199del others(4): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43186003 | ||||||
| chr17:43186003 | AAAATAAA others(1): Show |
A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(90): Show |
117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.208-206_208-199del others(8): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43186003 | ||||||
| chr17:43186003 | AAAATAAA others(5): Show |
A | 90 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(87): Show |
112 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.208-210_208-199del others(12): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43186003 | ||||||
| chr17:43186003 | AAAATAAA others(9): Show |
A | 6 | a0002c0002t0002g0056 a0002c0002t0002g0070 a0002c0002t0002g0071 others(3): Show |
6 | HG00438.hp2 HG00558.hp1 HG00597.hp1 others(3): Show |
intron_variant | MODIFIER | c.208-214_208-199del others(16): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43186003 | ||||||
| chr17:43186159 | T | TA | 3 | a0002c0002t0002g0018 a0002c0002t0002g0045 a0002c0002t0002g0072 |
4 | HG01106.hp1 HG01109.hp2 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.208-90dupA | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | 43186159 | ||||||
| chr17:43186695 | G | A | 2 | a0002c0002t0002g0047 a0002c0002t0002g0048 |
2 | HG02004.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.402+251G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | chr17 | 43186695 | |||||||
| chr17:43186734 | T | C | 3 | a0004c0004t0004g0119 a0004c0004t0004g0120 a0004c0004t0004g0121 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.402+290T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | chr17 | 43186734 | |||||||
| chr17:43186890 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG00438.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.402+446G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | chr17 | 43186890 | |||||||
| chr17:43187217 | T | C | 3 | a0002c0002t0002g0112 a0002c0002t0002g0115 a0002c0002t0002g0118 |
3 | HG00280.hp1 NA19007.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.402+773T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | chr17 | 43187217 | |||||||
| chr17:43187224 | G | A | 6 | a0002c0002t0002g0019 a0002c0002t0002g0043 a0002c0002t0002g0044 others(3): Show |
7 | HG01070.hp1 HG01975.hp2 HG02015.hp1 others(4): Show |
intron_variant | MODIFIER | c.402+780G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | chr17 | 43187224 | |||||||
| chr17:43187273 | C | T | 2 | a0002c0002t0002g0069 a0002c0002t0002g0256 |
2 | NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.402+829C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | chr17 | 43187273 | |||||||
| chr17:43187422 | C | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0229 |
2 | HG02027.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.402+978C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | chr17 | 43187422 | |||||||
| chr17:43187460 | G | A | 1 | a0001c0001t0010g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.402+1016G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | chr17 | 43187460 | |||||||
| chr17:43187470 | G | A | 101 | a0001c0001t0001g0094 a0001c0001t0001g0188 a0001c0001t0001g0189 others(98): Show |
123 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.402+1026G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | chr17 | 43187470 | |||||||
| chr17:43187502 | C | CT | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(97): Show |
126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.402+1082dupT | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr17 | 43187502 | ||||||
| chr17:43187502 | C | CTT | 16 | a0001c0001t0001g0032 a0001c0001t0001g0130 a0001c0001t0001g0174 others(13): Show |
17 | HG00408.hp2 HG00735.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.402+1081_402+1082d others(4): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr17 | 43187502 | ||||||
| chr17:43187502 | CT | C | 107 | a0001c0001t0001g0094 a0001c0001t0001g0141 a0001c0001t0001g0143 others(104): Show |
129 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.402+1082delT | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr17 | 43187502 | ||||||
| chr17:43187502 | CTT | C | 6 | a0001c0001t0003g0139 a0002c0002t0002g0062 a0002c0002t0002g0113 others(3): Show |
6 | HG02615.hp2 HG03195.hp1 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.402+1081_402+1082d others(4): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr17 | 43187502 | ||||||
| chr17:43187525 | T | G | 1 | a0007c0011t0012g0122 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.402+1081T>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | chr17 | 43187525 | |||||||
| chr17:43187657 | C | T | 2 | a0001c0001t0001g0197 a0001c0001t0001g0246 |
2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.402+1213C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | chr17 | 43187657 | |||||||
| chr17:43187680 | T | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(98): Show |
126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.402+1236T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | chr17 | 43187680 | |||||||
| chr17:43187886 | CT | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.403-1134delT | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr17 | 43187886 | ||||||
| chr17:43187886 | CTT | C | 20 | a0001c0001t0001g0127 a0001c0001t0001g0199 a0001c0001t0001g0212 others(17): Show |
20 | HG00099.hp1 HG00099.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.403-1135_403-1134d others(4): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr17 | 43187886 | ||||||
| chr17:43187992 | G | A | 1 | a0002c0002t0002g0064 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.403-1050G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | chr17 | 43187992 | |||||||
| chr17:43188135 | C | G | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.403-907C>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | chr17 | 43188135 | |||||||
| chr17:43188184 | C | T | 1 | a0002c0002t0002g0067 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.403-858C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | chr17 | 43188184 | |||||||
| chr17:43188286 | C | G | 1 | a0002c0009t0001g0135 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.403-756C>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | chr17 | 43188286 | |||||||
| chr17:43188435 | C | A | 1 | a0001c0001t0003g0249 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.403-607C>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | chr17 | 43188435 | |||||||
| chr17:43188672 | A | G | 99 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(96): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.403-370A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | chr17 | 43188672 | |||||||
| chr17:43188856 | T | G | 1 | a0002c0009t0001g0135 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.403-186T>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | chr17 | 43188856 | |||||||
| chr17:43189010 | C | A | 5 | a0001c0001t0001g0174 a0001c0001t0001g0176 a0001c0001t0001g0178 others(2): Show |
5 | HG00642.hp1 HG01106.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.403-32C>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 6/20 | chr17 | 43189010 | |||||||
| chr17:43189411 | C | T | 1 | a0001c0001t0001g0003 | 4 | HG02647.hp2 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.481-177C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 7/20 | chr17 | 43189411 | |||||||
| chr17:43189967 | A | G | 99 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(96): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.695+165A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 8/20 | chr17 | 43189967 | |||||||
| chr17:43190091 | G | GT | 8 | a0002c0002t0002g0023 a0002c0002t0002g0050 a0002c0002t0002g0076 others(5): Show |
9 | HG00423.hp1 HG00621.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.695+289_695+290ins others(1): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 8/20 | chr17 | 43190091 | |||||||
| chr17:43190093 | C | CT | 88 | a0001c0001t0001g0094 a0001c0001t0001g0181 a0001c0001t0001g0196 others(85): Show |
108 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.695+308dupT | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr17 | 43190093 | ||||||
| chr17:43190093 | C | CTT | 8 | a0002c0002t0002g0018 a0002c0002t0002g0038 a0002c0002t0002g0045 others(5): Show |
9 | HG01106.hp1 HG01109.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.695+307_695+308dup others(2): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr17 | 43190093 | ||||||
| chr17:43190093 | C | T | 8 | a0002c0002t0002g0023 a0002c0002t0002g0050 a0002c0002t0002g0076 others(5): Show |
9 | HG00423.hp1 HG00621.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.695+291C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 8/20 | chr17 | 43190093 | |||||||
| chr17:43190093 | CT | C | 8 | a0001c0001t0003g0161 a0001c0001t0003g0162 a0001c0001t0003g0163 others(5): Show |
8 | HG01884.hp1 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.695+308delT | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr17 | 43190093 | ||||||
| chr17:43190296 | A | C | 99 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(96): Show |
121 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.696-313A>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 8/20 | chr17 | 43190296 | |||||||
| chr17:43190364 | G | T | 3 | a0001c0001t0001g0234 a0001c0001t0005g0198 a0001c0001t0005g0216 |
3 | HG03491.hp1 HG03492.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.696-245G>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 8/20 | chr17 | 43190364 | |||||||
| chr17:43191087 | A | G | 6 | a0003c0003t0003g0016 a0003c0003t0003g0026 a0003c0003t0003g0146 others(3): Show |
8 | HG01109.hp1 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.864-285A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 9/20 | chr17 | 43191087 | |||||||
| chr17:43191125 | G | A | 3 | a0004c0004t0004g0119 a0004c0004t0004g0120 a0004c0004t0004g0121 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.864-247G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 9/20 | chr17 | 43191125 | |||||||
| chr17:43191151 | G | A | 2 | a0001c0001t0001g0197 a0001c0001t0001g0246 |
2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.864-221G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 9/20 | chr17 | 43191151 | |||||||
| chr17:43191167 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.864-205T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 9/20 | chr17 | 43191167 | |||||||
| chr17:43191314 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.864-58C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 9/20 | chr17 | 43191314 | |||||||
| chr17:43192020 | C | CT | 196 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.1073+457dupT | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | 43192020 | ||||||
| chr17:43192020 | C | CTT | 16 | a0001c0001t0001g0207 a0001c0001t0001g0228 a0001c0001t0001g0251 others(13): Show |
16 | HG01361.hp1 HG01517.hp1 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.1073+456_1073+457d others(4): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | 43192020 | ||||||
| chr17:43192052 | G | A | 1 | a0001c0001t0006g0160 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1073+471G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 10/20 | chr17 | 43192052 | |||||||
| chr17:43192181 | C | T | 1 | a0009c0010t0001g0252 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1073+600C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 10/20 | chr17 | 43192181 | |||||||
| chr17:43192182 | G | A | 2 | a0002c0002t0002g0086 a0002c0002t0002g0093 |
2 | HG00423.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.1073+601G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 10/20 | chr17 | 43192182 | |||||||
| chr17:43192269 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1073+688G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 10/20 | chr17 | 43192269 | |||||||
| chr17:43192269 | G | T | 1 | a0007c0011t0012g0122 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1073+688G>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 10/20 | chr17 | 43192269 | |||||||
| chr17:43192295 | A | T | 100 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(97): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1073+714A>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 10/20 | chr17 | 43192295 | |||||||
| chr17:43192319 | C | T | 2 | a0003c0003t0003g0146 a0003c0003t0003g0147 |
2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1073+738C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 10/20 | chr17 | 43192319 | |||||||
| chr17:43192385 | G | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0172 a0001c0001t0001g0211 others(2): Show |
6 | HG00609.hp1 HG02165.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074-709G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 10/20 | chr17 | 43192385 | |||||||
| chr17:43192485 | C | T | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1074-609C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 10/20 | chr17 | 43192485 | |||||||
| chr17:43192493 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0205 a0001c0001t0001g0218 others(2): Show |
7 | HG00408.hp2 NA18947.hp2 NA18987.hp1 others(4): Show |
intron_variant | MODIFIER | c.1074-601C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 10/20 | chr17 | 43192493 | |||||||
| chr17:43192571 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1074-523G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 10/20 | chr17 | 43192571 | |||||||
| chr17:43192953 | A | G | 2 | a0001c0001t0001g0194 a0001c0001t0001g0196 |
2 | HG00642.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1074-141A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 10/20 | chr17 | 43192953 | |||||||
| chr17:43194089 | T | A | 1 | a0001c0001t0001g0033 | 2 | NA19065.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1525-261T>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 12/20 | chr17 | 43194089 | |||||||
| chr17:43194239 | T | C | 3 | a0004c0004t0004g0119 a0004c0004t0004g0120 a0004c0004t0004g0121 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1525-111T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 12/20 | chr17 | 43194239 | |||||||
| chr17:43194266 | G | A | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1525-84G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 12/20 | chr17 | 43194266 | |||||||
| chr17:43194713 | A | T | 1 | a0008c0006t0002g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1674+214A>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 13/20 | chr17 | 43194713 | |||||||
| chr17:43194715 | C | T | 1 | a0008c0006t0002g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1674+216C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 13/20 | chr17 | 43194715 | |||||||
| chr17:43194716 | T | A | 1 | a0008c0006t0002g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1674+217T>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 13/20 | chr17 | 43194716 | |||||||
| chr17:43194721 | T | A | 1 | a0008c0006t0002g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1674+222T>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 13/20 | chr17 | 43194721 | |||||||
| chr17:43194726 | T | G | 1 | a0008c0006t0002g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1674+227T>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 13/20 | chr17 | 43194726 | |||||||
| chr17:43194727 | G | A | 1 | a0008c0006t0002g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1674+228G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 13/20 | chr17 | 43194727 | |||||||
| chr17:43194728 | C | T | 1 | a0008c0006t0002g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1674+229C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 13/20 | chr17 | 43194728 | |||||||
| chr17:43194729 | C | G | 1 | a0008c0006t0002g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1674+230C>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 13/20 | chr17 | 43194729 | |||||||
| chr17:43194731 | C | T | 1 | a0008c0006t0002g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1674+232C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 13/20 | chr17 | 43194731 | |||||||
| chr17:43194781 | T | C | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1675-183T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 13/20 | chr17 | 43194781 | |||||||
| chr17:43195155 | G | A | 3 | a0002c0002t0002g0075 a0002c0002t0002g0079 a0002c0002t0002g0080 |
3 | HG01943.hp1 HG02300.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1750+116G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/20 | chr17 | 43195155 | |||||||
| chr17:43195292 | C | T | 1 | a0003c0003t0003g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1750+253C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/20 | chr17 | 43195292 | |||||||
| chr17:43195407 | T | A | 1 | a0008c0006t0002g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1750+368T>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/20 | chr17 | 43195407 | |||||||
| chr17:43195409 | T | A | 1 | a0008c0006t0002g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1750+370T>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/20 | chr17 | 43195409 | |||||||
| chr17:43195411 | G | T | 1 | a0008c0006t0002g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1750+372G>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/20 | chr17 | 43195411 | |||||||
| chr17:43195414 | G | T | 1 | a0008c0006t0002g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1750+375G>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/20 | chr17 | 43195414 | |||||||
| chr17:43195416 | C | T | 1 | a0008c0006t0002g0089 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1750+377C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/20 | chr17 | 43195416 | |||||||
| chr17:43195535 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0230 |
3 | HG00609.hp2 NA19064.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1750+496G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/20 | chr17 | 43195535 | |||||||
| chr17:43195593 | G | T | 1 | a0001c0001t0001g0229 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1750+554G>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/20 | chr17 | 43195593 | |||||||
| chr17:43195651 | CA | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
133 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1750+632delA | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr17 | 43195651 | ||||||
| chr17:43195651 | CAA | C | 100 | a0001c0001t0001g0094 a0001c0001t0001g0184 a0001c0001t0001g0185 others(97): Show |
120 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1750+631_1750+632d others(4): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr17 | 43195651 | ||||||
| chr17:43195651 | CAAA | C | 4 | a0002c0002t0002g0006 a0002c0002t0002g0046 a0002c0002t0002g0066 others(1): Show |
6 | HG01257.hp1 HG01258.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.1750+630_1750+632d others(5): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr17 | 43195651 | ||||||
| chr17:43195799 | T | C | 100 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(97): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1751-682T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/20 | chr17 | 43195799 | |||||||
| chr17:43195804 | G | A | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.1751-677G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/20 | chr17 | 43195804 | |||||||
| chr17:43196070 | G | A | 9 | a0001c0001t0003g0161 a0001c0001t0003g0162 a0001c0001t0003g0163 others(6): Show |
9 | HG01884.hp1 HG02055.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1751-411G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/20 | chr17 | 43196070 | |||||||
| chr17:43196120 | C | CA | 8 | a0001c0001t0001g0128 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG01884.hp2 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1751-345dupA | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr17 | 43196120 | ||||||
| chr17:43196131 | A | C | 100 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(97): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.1751-350A>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/20 | chr17 | 43196131 | |||||||
| chr17:43196172 | T | C | 1 | a0007c0011t0012g0122 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1751-309T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/20 | chr17 | 43196172 | |||||||
| chr17:43196205 | T | TA | 65 | a0001c0001t0001g0094 a0002c0002t0002g0005 a0002c0002t0002g0006 others(62): Show |
81 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1751-275dupA | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr17 | 43196205 | ||||||
| chr17:43196409 | A | G | 8 | a0001c0001t0003g0161 a0001c0001t0003g0162 a0001c0001t0003g0163 others(5): Show |
8 | HG01884.hp1 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1751-72A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 14/20 | chr17 | 43196409 | |||||||
| chr17:43197295 | G | A | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.2026+189G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43197295 | |||||||
| chr17:43197319 | T | A | 100 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(97): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.2026+213T>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43197319 | |||||||
| chr17:43197411 | C | T | 3 | a0004c0004t0004g0119 a0004c0004t0004g0120 a0004c0004t0004g0121 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2026+305C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43197411 | |||||||
| chr17:43197443 | C | T | 1 | a0001c0001t0003g0247 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2026+337C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43197443 | |||||||
| chr17:43197505 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2026+399C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43197505 | |||||||
| chr17:43197518 | C | CA | 87 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(84): Show |
108 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.2026+425dupA | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | 43197518 | ||||||
| chr17:43197518 | C | CAA | 8 | a0002c0002t0002g0024 a0002c0002t0002g0047 a0002c0002t0002g0051 others(5): Show |
9 | HG00099.hp1 HG00741.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.2026+424_2026+425d others(4): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | 43197518 | ||||||
| chr17:43197553 | T | C | 13 | a0001c0001t0001g0011 a0001c0001t0001g0124 a0001c0001t0001g0125 others(10): Show |
15 | HG00735.hp1 HG02145.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.2026+447T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43197553 | |||||||
| chr17:43197579 | A | C | 1 | a0002c0009t0001g0135 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2026+473A>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43197579 | |||||||
| chr17:43197696 | A | G | 100 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(97): Show |
122 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.2026+590A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43197696 | |||||||
| chr17:43197704 | G | A | 1 | a0002c0002t0002g0076 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2026+598G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43197704 | |||||||
| chr17:43197809 | G | T | 1 | a0002c0009t0001g0135 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2026+703G>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43197809 | |||||||
| chr17:43197964 | C | T | 1 | a0001c0001t0009g0159 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2026+858C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43197964 | |||||||
| chr17:43198171 | A | G | 4 | a0001c0001t0003g0165 a0001c0001t0003g0166 a0001c0001t0003g0167 others(1): Show |
4 | HG01884.hp1 HG02486.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2026+1065A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43198171 | |||||||
| chr17:43198420 | C | T | 1 | a0003c0003t0003g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2026+1314C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43198420 | |||||||
| chr17:43198660 | A | T | 1 | a0002c0002t0002g0043 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.2027-1507A>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43198660 | |||||||
| chr17:43198758 | A | C | 6 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(3): Show |
6 | HG02109.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2027-1409A>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43198758 | |||||||
| chr17:43199023 | A | C | 1 | a0002c0002t0002g0074 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2027-1144A>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43199023 | |||||||
| chr17:43199082 | G | A | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.2027-1085G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43199082 | |||||||
| chr17:43199087 | AT | A | 105 | a0001c0001t0001g0094 a0001c0001t0001g0200 a0001c0001t0001g0218 others(102): Show |
127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.2027-1064delT | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | 43199087 | ||||||
| chr17:43199383 | T | A | 93 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(90): Show |
115 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.2027-784T>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43199383 | |||||||
| chr17:43199558 | G | A | 2 | a0002c0002t0002g0037 a0002c0002t0002g0038 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2027-609G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43199558 | |||||||
| chr17:43199570 | T | C | 2 | a0002c0002t0002g0047 a0002c0002t0002g0048 |
2 | HG02004.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.2027-597T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43199570 | |||||||
| chr17:43199577 | G | A | 1 | a0002c0002t0002g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2027-590G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43199577 | |||||||
| chr17:43199714 | A | G | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.2027-453A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43199714 | |||||||
| chr17:43199718 | T | C | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2027-449T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43199718 | |||||||
| chr17:43199973 | A | G | 9 | a0001c0001t0003g0161 a0001c0001t0003g0162 a0001c0001t0003g0163 others(6): Show |
9 | HG01884.hp1 HG02055.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2027-194A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 16/20 | chr17 | 43199973 | |||||||
| chr17:43200626 | C | T | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.2468+18C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 17/20 | chr17 | 43200626 | |||||||
| chr17:43200669 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2468+61G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 17/20 | chr17 | 43200669 | |||||||
| chr17:43200867 | G | GT | 104 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0094 others(101): Show |
126 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.2468+278dupT | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr17 | 43200867 | ||||||
| chr17:43200867 | G | GTT | 13 | a0001c0001t0003g0247 a0002c0002t0002g0055 a0002c0002t0002g0065 others(10): Show |
13 | HG00438.hp2 HG00597.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.2468+277_2468+278d others(4): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr17 | 43200867 | ||||||
| chr17:43201071 | G | A | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.2468+463G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 17/20 | chr17 | 43201071 | |||||||
| chr17:43201081 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2468+473C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 17/20 | chr17 | 43201081 | |||||||
| chr17:43201094 | C | G | 15 | a0001c0001t0001g0014 a0001c0001t0001g0031 a0001c0001t0001g0039 others(12): Show |
18 | HG00408.hp2 HG00544.hp1 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.2468+486C>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 17/20 | chr17 | 43201094 | |||||||
| chr17:43201260 | G | A | 1 | a0006c0007t0001g0123 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2469-426G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 17/20 | chr17 | 43201260 | |||||||
| chr17:43201393 | A | G | 39 | a0002c0002t0002g0006 a0002c0002t0002g0007 a0002c0002t0002g0017 others(36): Show |
48 | HG00280.hp2 HG00438.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.2469-293A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 17/20 | chr17 | 43201393 | |||||||
| chr17:43201451 | A | G | 233 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(230): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.2469-235A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 17/20 | chr17 | 43201451 | |||||||
| chr17:43201618 | T | G | 2 | a0002c0002t0002g0007 a0002c0002t0002g0077 |
4 | HG02055.hp2 HG02976.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2469-68T>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 17/20 | chr17 | 43201618 | |||||||
| chr17:43201789 | C | T | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.2563+9C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 18/20 | chr17 | 43201789 | |||||||
| chr17:43201816 | G | T | 2 | a0001c0001t0003g0258 a0001c0001t0003g0259 |
2 | HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2563+36G>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 18/20 | chr17 | 43201816 | |||||||
| chr17:43201901 | C | T | 8 | a0002c0002t0002g0024 a0002c0002t0002g0047 a0002c0002t0002g0048 others(5): Show |
9 | HG00099.hp1 HG00741.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.2563+121C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 18/20 | chr17 | 43201901 | |||||||
| chr17:43201902 | A | G | 106 | a0001c0001t0001g0094 a0001c0001t0003g0136 a0001c0001t0003g0137 others(103): Show |
128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.2563+122A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 18/20 | chr17 | 43201902 | |||||||
| chr17:43201961 | T | C | 2 | a0001c0001t0006g0160 a0001c0001t0006g0169 |
2 | HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2563+181T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 18/20 | chr17 | 43201961 | |||||||
| chr17:43201994 | A | G | 106 | a0001c0001t0001g0094 a0001c0001t0003g0136 a0001c0001t0003g0137 others(103): Show |
128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.2563+214A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 18/20 | chr17 | 43201994 | |||||||
| chr17:43202095 | A | C | 1 | a0001c0001t0001g0229 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2563+315A>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 18/20 | chr17 | 43202095 | |||||||
| chr17:43202166 | C | T | 3 | a0001c0001t0003g0166 a0001c0001t0003g0167 a0001c0001t0003g0168 |
3 | HG02486.hp1 HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2563+386C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 18/20 | chr17 | 43202166 | |||||||
| chr17:43202172 | T | G | 3 | a0004c0004t0004g0119 a0004c0004t0004g0120 a0004c0004t0004g0121 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2563+392T>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 18/20 | chr17 | 43202172 | |||||||
| chr17:43202179 | G | GA | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(109): Show |
139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.2563+417dupA | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | 43202179 | ||||||
| chr17:43202179 | G | GAA | 96 | a0001c0001t0001g0035 a0001c0001t0001g0094 a0001c0001t0001g0128 others(93): Show |
118 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.2563+416_2563+417d others(4): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | 43202179 | ||||||
| chr17:43202523 | T | A | 94 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(91): Show |
116 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.2564-132T>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 18/20 | chr17 | 43202523 | |||||||
| chr17:43202523 | TA | T | 9 | a0001c0001t0001g0220 a0001c0001t0001g0243 a0001c0001t0001g0244 others(6): Show |
9 | HG02615.hp2 HG02895.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.2564-116delA | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | 43202523 | ||||||
| chr17:43202601 | A | G | 2 | a0001c0001t0003g0257 a0001c0001t0003g0260 |
2 | HG04199.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2564-54A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 18/20 | chr17 | 43202601 | |||||||
| chr17:43202796 | G | T | 3 | a0004c0004t0004g0119 a0004c0004t0004g0120 a0004c0004t0004g0121 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2621+84G>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 19/20 | chr17 | 43202796 | |||||||
| chr17:43202871 | A | G | 106 | a0001c0001t0001g0094 a0001c0001t0003g0136 a0001c0001t0003g0137 others(103): Show |
128 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.2621+159A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 19/20 | chr17 | 43202871 | |||||||
| chr17:43202976 | C | T | 11 | a0001c0001t0001g0013 a0001c0001t0001g0199 a0001c0001t0001g0213 others(8): Show |
13 | HG02015.hp2 HG02155.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.2621+264C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 19/20 | chr17 | 43202976 | |||||||
| chr17:43203292 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2622-389C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 19/20 | chr17 | 43203292 | |||||||
| chr17:43203427 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2622-254G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 19/20 | chr17 | 43203427 | |||||||
| chr17:43203938 | CT | C | 102 | a0001c0001t0001g0094 a0001c0001t0003g0136 a0001c0001t0003g0137 others(99): Show |
124 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.2727+169delT | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | 43203938 | ||||||
| chr17:43204089 | C | A | 6 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(3): Show |
6 | HG02109.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2727+303C>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43204089 | |||||||
| chr17:43204228 | G | A | 3 | a0001c0001t0003g0170 a0001c0001t0006g0160 a0001c0001t0006g0169 |
3 | HG01884.hp2 HG02451.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2727+442G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43204228 | |||||||
| chr17:43204380 | C | T | 10 | a0001c0001t0001g0011 a0001c0001t0001g0124 a0001c0001t0001g0125 others(7): Show |
12 | HG00735.hp1 HG02280.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.2727+594C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43204380 | |||||||
| chr17:43204514 | A | C | 1 | a0001c0001t0001g0232 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2727+728A>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43204514 | |||||||
| chr17:43204532 | T | G | 1 | a0001c0001t0007g0131 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2727+746T>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43204532 | |||||||
| chr17:43204542 | A | G | 105 | a0001c0001t0001g0094 a0001c0001t0003g0136 a0001c0001t0003g0137 others(102): Show |
127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.2727+756A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43204542 | |||||||
| chr17:43204582 | G | A | 1 | a0002c0002t0002g0102 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2727+796G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43204582 | |||||||
| chr17:43204627 | C | G | 6 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(3): Show |
6 | HG02109.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2727+841C>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43204627 | |||||||
| chr17:43204792 | C | A | 1 | a0002c0002t0002g0079 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2727+1006C>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43204792 | |||||||
| chr17:43204813 | T | TA | 35 | a0001c0001t0001g0011 a0001c0001t0001g0124 a0001c0001t0001g0125 others(32): Show |
39 | HG00735.hp1 HG01243.hp2 HG01257.hp1 others(36): Show |
intron_variant | MODIFIER | c.2727+1045dupA | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | 43204813 | ||||||
| chr17:43204813 | T | TAA | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.2727+1044_2727+104 others(6): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | 43204813 | ||||||
| chr17:43204904 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2727+1118T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43204904 | |||||||
| chr17:43204928 | A | G | 96 | a0001c0001t0001g0094 a0001c0001t0001g0237 a0002c0002t0002g0001 others(93): Show |
118 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(115): Show |
intron_variant | MODIFIER | c.2727+1142A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43204928 | |||||||
| chr17:43205078 | G | A | 3 | a0004c0004t0004g0119 a0004c0004t0004g0120 a0004c0004t0004g0121 |
3 | HG02615.hp2 NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2727+1292G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43205078 | |||||||
| chr17:43205136 | G | A | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(217): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.2727+1350G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43205136 | |||||||
| chr17:43205548 | T | C | 1 | a0001c0008t0001g0248 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2727+1762T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43205548 | |||||||
| chr17:43205628 | A | G | 105 | a0001c0001t0001g0094 a0001c0001t0003g0136 a0001c0001t0003g0137 others(102): Show |
127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.2727+1842A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43205628 | |||||||
| chr17:43205877 | C | CA | 8 | a0001c0001t0001g0181 a0001c0001t0001g0192 a0001c0001t0001g0201 others(5): Show |
8 | HG01106.hp2 HG02300.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2727+2111dupA | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | 43205877 | ||||||
| chr17:43205877 | C | CAA | 8 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0003g0138 others(5): Show |
8 | HG02109.hp2 HG02818.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.2727+2110_2727+211 others(6): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | 43205877 | ||||||
| chr17:43205877 | C | CAAA | 65 | a0001c0001t0001g0094 a0002c0002t0002g0005 a0002c0002t0002g0006 others(62): Show |
81 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.2727+2109_2727+211 others(7): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | 43205877 | ||||||
| chr17:43205877 | C | CAAAA | 24 | a0002c0002t0002g0001 a0002c0002t0002g0020 a0002c0002t0002g0022 others(21): Show |
30 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(27): Show |
intron_variant | MODIFIER | c.2727+2108_2727+211 others(8): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | 43205877 | ||||||
| chr17:43205998 | T | G | 1 | a0002c0002t0002g0047 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2727+2212T>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43205998 | |||||||
| chr17:43206133 | G | A | 95 | a0001c0001t0001g0094 a0002c0002t0002g0001 a0002c0002t0002g0005 others(92): Show |
117 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.2727+2347G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43206133 | |||||||
| chr17:43206175 | CA | C | 6 | a0001c0001t0001g0185 a0001c0001t0001g0202 a0001c0001t0001g0225 others(3): Show |
6 | HG01099.hp2 HG01433.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.2727+2404delA | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | 43206175 | ||||||
| chr17:43206299 | G | T | 1 | a0002c0002t0002g0103 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2727+2513G>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43206299 | |||||||
| chr17:43206316 | C | G | 1 | a0001c0001t0001g0221 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2727+2530C>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43206316 | |||||||
| chr17:43206335 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2727+2549C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43206335 | |||||||
| chr17:43206336 | G | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0214 a0001c0001t0001g0235 |
4 | HG00423.hp2 HG02071.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.2727+2550G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43206336 | |||||||
| chr17:43206473 | T | C | 3 | a0002c0002t0002g0076 a0002c0002t0002g0086 a0002c0002t0002g0093 |
3 | HG00423.hp1 HG00621.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.2727+2687T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43206473 | |||||||
| chr17:43206654 | C | CA | 3 | a0001c0001t0001g0003 a0002c0002t0002g0052 a0002c0002t0002g0102 |
6 | HG02647.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2727+2881dupA | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | 43206654 | ||||||
| chr17:43206880 | T | C | 1 | a0003c0003t0003g0016 | 2 | HG02622.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.2728-3021T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43206880 | |||||||
| chr17:43206933 | C | T | 1 | a0001c0001t0001g0012 | 3 | NA18992.hp2 NA19003.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2728-2968C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43206933 | |||||||
| chr17:43207076 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0193 |
2 | HG02004.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.2728-2825G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43207076 | |||||||
| chr17:43207210 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2728-2691G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43207210 | |||||||
| chr17:43207328 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2728-2573A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43207328 | |||||||
| chr17:43207537 | C | A | 1 | a0002c0002t0002g0256 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2728-2364C>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43207537 | |||||||
| chr17:43207570 | T | C | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(112): Show |
142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2728-2331T>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43207570 | |||||||
| chr17:43207873 | G | A | 1 | a0007c0011t0012g0122 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2728-2028G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43207873 | |||||||
| chr17:43208078 | G | C | 1 | a0007c0011t0012g0122 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2728-1823G>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43208078 | |||||||
| chr17:43208979 | A | C | 1 | a0002c0002t0002g0044 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2728-922A>C | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43208979 | |||||||
| chr17:43209024 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2728-877A>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43209024 | |||||||
| chr17:43209138 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2728-763G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43209138 | |||||||
| chr17:43209140 | G | A | 1 | a0001c0001t0014g0238 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2728-761G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43209140 | |||||||
| chr17:43209181 | G | A | 1 | a0004c0004t0004g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2728-720G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43209181 | |||||||
| chr17:43209323 | G | A | 97 | a0002c0002t0002g0001 a0002c0002t0002g0005 a0002c0002t0002g0006 others(94): Show |
119 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.2728-578G>A | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43209323 | |||||||
| chr17:43209450 | T | G | 1 | a0001c0001t0001g0032 | 2 | NA18993.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.2728-451T>G | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43209450 | |||||||
| chr17:43209732 | C | T | 4 | a0002c0002t0002g0019 a0002c0002t0002g0049 a0002c0002t0002g0059 others(1): Show |
5 | HG01070.hp1 HG01975.hp2 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.2728-169C>T | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | chr17 | 43209732 | |||||||
| chr17:43209862 | AT | A | 80 | a0001c0001t0001g0028 a0001c0001t0001g0126 a0001c0001t0001g0201 others(77): Show |
94 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.2728-22delT | NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | 43209862 | ||||||
| chr17:43209862 | ATT | A | 7 | a0002c0002t0002g0006 a0002c0002t0002g0021 a0002c0002t0002g0062 others(4): Show |
10 | HG01099.hp2 HG01192.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2728-23_2728-22del others(2): Show |
NBR1 | ENSG00000188554.15 | transcript | ENST00000590996.6 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | 43209862 |