Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54700 |
| ensemblid | ENSG00000085721.13 |
| hgncid | 30346 |
| symbol | RRN3 |
| name | RRN3 homolog, RNA polymerase I transcription factor |
| refseq_nuc | NM_018427.5 |
| refseq_prot | NP_060897.3 |
| ensembl_nuc | ENST00000198767.11 |
| ensembl_prot | ENSP00000198767.7 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 15060033 |
| end | 15094272 |
| strand | - |
| ver | v1.2 |
| region | chr16:15060033-15094272 |
| region5000 | chr16:15055033-15099272 |
| regionname0 | RRN3_chr16_15060033_15094272 |
| regionname5000 | RRN3_chr16_15055033_15099272 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 651 | 379 | 83 | 63 | 179 | 13 | 41 | 138 | RRN3_chr16_15055033_15099272 | RRN3 | MAAPL others(646): Show |
chr16 | 15055033 | 15099272 |
| a0002 | 0/0 | 651 | 13 | 0 | 7 | 0 | 3 | 3 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | MAAPL others(646): Show |
chr16 | 15055033 | 15099272 |
| a0003 | 0/0 | 651 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | MAAPL others(646): Show |
chr16 | 15055033 | 15099272 |
| a0004 | 0/1 | 651 | 2 | 0 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | MAAPL others(646): Show |
chr16 | 15055033 | 15099272 |
| a0005 | 0/0 | 651 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | MAAPL others(646): Show |
chr16 | 15055033 | 15099272 |
| a0006 | 0/0 | 651 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | MAAPL others(646): Show |
chr16 | 15055033 | 15099272 |
| a0007 | 0/0 | 651 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | MAAPL others(646): Show |
chr16 | 15055033 | 15099272 |
| a0008 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | MAAPL others(646): Show |
chr16 | 15055033 | 15099272 |
| a0009 | 0/0 | 651 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | MAAPL others(646): Show |
chr16 | 15055033 | 15099272 |
| a0010 | 0/0 | 651 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | MAAPL others(646): Show |
chr16 | 15055033 | 15099272 |
| a0011 | 0/0 | 651 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | MAAPL others(646): Show |
chr16 | 15055033 | 15099272 |
| a0012 | 0/0 | 651 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | MAAPL others(646): Show |
chr16 | 15055033 | 15099272 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1953 | 335 | 63 | 59 | 162 | 13 | 38 | RRN3_chr16_15055033_15099272 | RRN3 | ATGGC others(1948): Show |
chr16 | 15055033 | 15099272 | ||
| a0001c0002 | 0/0 | 1953 | 40 | 19 | 4 | 14 | 0 | 3 | RRN3_chr16_15055033_15099272 | RRN3 | ATGGC others(1948): Show |
chr16 | 15055033 | 15099272 | ||
| a0001c0007 | 0/0 | 1953 | 2 | 0 | 0 | 2 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATGGC others(1948): Show |
chr16 | 15055033 | 15099272 | ||
| a0001c0010 | 0/0 | 1953 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATGGC others(1948): Show |
chr16 | 15055033 | 15099272 | ||
| a0001c0015 | 0/0 | 1953 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATGGC others(1948): Show |
chr16 | 15055033 | 15099272 | ||
| a0002c0003 | 0/0 | 1953 | 13 | 0 | 7 | 0 | 3 | 3 | RRN3_chr16_15055033_15099272 | RRN3 | ATGGC others(1948): Show |
chr16 | 15055033 | 15099272 | ||
| a0003c0004 | 0/0 | 1953 | 3 | 0 | 2 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | ATGGC others(1948): Show |
chr16 | 15055033 | 15099272 | ||
| a0004c0005 | 0/1 | 1953 | 2 | 0 | 0 | 0 | 1 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATGGC others(1948): Show |
chr16 | 15055033 | 15099272 | ||
| a0005c0006 | 0/0 | 1953 | 2 | 2 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATGGC others(1948): Show |
chr16 | 15055033 | 15099272 | ||
| a0006c0016 | 0/0 | 1953 | 1 | 0 | 0 | 0 | 1 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATGGC others(1948): Show |
chr16 | 15055033 | 15099272 | ||
| a0006c0017 | 0/0 | 1953 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATGGC others(1948): Show |
chr16 | 15055033 | 15099272 | ||
| a0007c0008 | 0/0 | 1953 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATGGC others(1948): Show |
chr16 | 15055033 | 15099272 | ||
| a0008c0011 | 0/0 | 1953 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATGGC others(1948): Show |
chr16 | 15055033 | 15099272 | ||
| a0009c0013 | 0/0 | 1953 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATGGC others(1948): Show |
chr16 | 15055033 | 15099272 | ||
| a0010c0009 | 0/0 | 1953 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | ATGGC others(1948): Show |
chr16 | 15055033 | 15099272 | ||
| a0011c0012 | 0/0 | 1953 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATGGC others(1948): Show |
chr16 | 15055033 | 15099272 | ||
| a0012c0014 | 0/0 | 1953 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATGGC others(1948): Show |
chr16 | 15055033 | 15099272 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3706 | 220 | 55 | 35 | 94 | 11 | 25 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0001c0001t0002 | 0/0 | 3706 | 62 | 5 | 11 | 42 | 0 | 4 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0001c0001t0003 | 0/0 | 3706 | 45 | 1 | 12 | 23 | 2 | 7 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0001c0001t0004 | 0/0 | 3706 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0001c0001t0009 | 0/0 | 3706 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0001c0001t0010 | 0/0 | 3706 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0001c0001t0011 | 0/0 | 3706 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0001c0001t0012 | 0/0 | 3706 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0001c0001t0013 | 0/0 | 3706 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0001c0001t0015 | 0/0 | 3706 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0001c0001t0016 | 0/0 | 3706 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0001c0002t0001 | 0/0 | 3706 | 38 | 19 | 3 | 13 | 0 | 3 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0001c0002t0007 | 0/0 | 3706 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0001c0002t0014 | 0/0 | 3706 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0001c0007t0005 | 0/0 | 3706 | 2 | 0 | 0 | 2 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0001c0010t0001 | 0/0 | 3706 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0001c0015t0002 | 0/0 | 3706 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0002c0003t0001 | 0/0 | 3706 | 13 | 0 | 7 | 0 | 3 | 3 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0003c0004t0001 | 0/0 | 3706 | 3 | 0 | 2 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0004c0005t0001 | 0/1 | 3706 | 2 | 0 | 0 | 0 | 1 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0005c0006t0001 | 0/0 | 3706 | 2 | 2 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0006c0016t0006 | 0/0 | 3706 | 1 | 0 | 0 | 0 | 1 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0006c0017t0004 | 0/0 | 3706 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0007c0008t0002 | 0/0 | 3706 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0008c0011t0001 | 0/0 | 3706 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0009c0013t0001 | 0/0 | 3706 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0010c0009t0001 | 0/0 | 3706 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0011c0012t0003 | 0/0 | 3706 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| a0012c0014t0008 | 0/0 | 3706 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | ATCCG others(3701): Show |
chr16 | 15055033 | 15099272 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 20 | 0 | 3 | 16 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0002 | 0/0 | 17 | 6 | 4 | 7 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0009 | 0/0 | 5 | 2 | 0 | 2 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0044 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0053 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0003 | 0/0 | 10 | 1 | 1 | 7 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0010 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0006 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0014 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0028 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0055 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0009g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0010g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0011g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0012g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0013g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0015g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0001t0016g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0004 | 0/0 | 9 | 0 | 1 | 7 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0007g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0002t0014g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0007t0005g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0010t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0001c0015t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0002c0003t0001g0007 | 0/0 | 7 | 0 | 3 | 0 | 2 | 2 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0002c0003t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0002c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0002c0003t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0002c0003t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0002c0003t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0003c0004t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0003c0004t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0003c0004t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0004c0005t0001g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0004c0005t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0005c0006t0001g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0006c0016t0006g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0006c0017t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0007c0008t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0008c0011t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0009c0013t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0010c0009t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0011c0012t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| a0012c0014t0008g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | GBR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00140 | hp1 | a0002 | c0003 | t0001 | g0034 | EUR | GBR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | GBR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00280 | hp1 | a0004 | c0005 | t0001 | g0058 | EUR | FIN | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | FIN | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | CHS | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | CHS | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | CHS | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00597 | hp2 | a0001 | c0001 | t0016 | g0253 | EAS | CHS | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | CHS | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | CHS | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | CHS | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00639 | hp2 | a0001 | c0002 | t0014 | g0143 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0217 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0249 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01074 | hp1 | a0003 | c0004 | t0001 | g0141 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01074 | hp2 | a0002 | c0003 | t0001 | g0107 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01099 | hp1 | a0002 | c0003 | t0001 | g0007 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0210 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01167 | hp1 | a0003 | c0004 | t0001 | g0156 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01175 | hp2 | a0002 | c0003 | t0001 | g0108 | AMR | PUR | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01255 | hp1 | a0002 | c0003 | t0001 | g0109 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01256 | hp2 | a0002 | c0003 | t0001 | g0034 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01261 | hp2 | a0002 | c0003 | t0001 | g0007 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0250 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01358 | hp2 | a0002 | c0003 | t0001 | g0007 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01433 | hp1 | a0001 | c0001 | t0012 | g0252 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01515 | hp1 | a0002 | c0003 | t0001 | g0007 | EUR | IBS | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | IBS | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0055 | EUR | IBS | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01517 | hp1 | a0002 | c0003 | t0001 | g0007 | EUR | IBS | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0055 | EUR | IBS | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0218 | AMR | PEL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | PEL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | PEL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PEL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PEL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PEL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0127 | AMR | PEL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | KHV | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | ACB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | KHV | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02071 | hp2 | a0007 | c0008 | t0002 | g0224 | EAS | KHV | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0173 | AFR | ACB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | PEL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | CDX | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | ACB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02258 | hp2 | a0008 | c0011 | t0001 | g0074 | AFR | ACB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0120 | AFR | ACB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PEL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | ACB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02602 | hp1 | a0001 | c0001 | t0011 | g0067 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0147 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0118 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02735 | hp2 | a0002 | c0003 | t0001 | g0106 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02809 | hp1 | a0005 | c0006 | t0001 | g0054 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | ESN | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ESN | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03017 | hp1 | a0001 | c0001 | t0013 | g0182 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03139 | hp2 | a0005 | c0006 | t0001 | g0054 | AFR | ESN | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03209 | hp1 | a0001 | c0010 | t0001 | g0154 | AFR | MSL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | MSL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03239 | hp2 | a0002 | c0003 | t0001 | g0007 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0225 | AFR | MSL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | MSL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0037 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0037 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | MSL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03579 | hp2 | a0009 | c0013 | t0001 | g0077 | AFR | MSL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0208 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03654 | hp2 | a0002 | c0003 | t0001 | g0007 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0247 | SAS | STU | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0207 | SAS | PJL | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03831 | hp1 | a0010 | c0009 | t0001 | g0169 | SAS | BEB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0251 | SAS | BEB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | STU | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | STU | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | STU | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | STU | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | STU | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | STU | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG04228 | hp1 | a0003 | c0004 | t0001 | g0142 | SAS | STU | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | STU | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | YRI | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | CHB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | CHB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | YRI | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18945 | hp1 | a0011 | c0012 | t0003 | g0136 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18947 | hp2 | a0001 | c0015 | t0002 | g0232 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18964 | hp2 | a0001 | c0001 | t0010 | g0188 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18973 | hp1 | a0001 | c0007 | t0005 | g0049 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18995 | hp1 | a0001 | c0002 | t0007 | g0125 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18998 | hp2 | a0012 | c0014 | t0008 | g0124 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19012 | hp2 | a0001 | c0001 | t0015 | g0226 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19030 | hp1 | a0006 | c0017 | t0004 | g0112 | AFR | LWK | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0060 | AFR | LWK | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19086 | hp2 | a0001 | c0007 | t0005 | g0049 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19091 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0128 | AFR | YRI | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ASW | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | ASW | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA20752 | hp1 | a0006 | c0016 | t0006 | g0056 | EUR | TSI | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | TSI | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | TSI | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | GIH | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | GIH | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0209 | AMR | CLM | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0062 | AFR | ACB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0122 | AFR | ACB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | ACB | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0021 | AFR | USA | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | USA | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | USA | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | LWK | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0117 | AFR | LWK | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| homoSapiens | chm13v2 | a0004 | c0005 | t0001 | g0057 | REF | REF | RRN3_chr16_15055033_15099272 | RRN3 | chr16 | 15055033 | 15099272 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:15061773 | C | T | 1 | a0012 | 1 | NA18998.hp2 | missense_variant | MODERATE | c.1927G>A | p.Val643Met | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 18/18 | 1966/3706 | 1927/1956 | 643/651 | chr16 | 15061773 | |||
| chr16:15065342 | A | G | 1 | a0011 | 1 | NA18945.hp1 | missense_variant | MODERATE | c.1583T>C | p.Ile528Thr | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/18 | 1622/3706 | 1583/1956 | 528/651 | chr16 | 15065342 | |||
| chr16:15065358 | C | T | 1 | a0008 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.1567G>A | p.Val523Ile | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/18 | 1606/3706 | 1567/1956 | 523/651 | chr16 | 15065358 | |||
| chr16:15070211 | T | C | 1 | a0009 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.1303A>G | p.Ile435Val | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 14/18 | 1342/3706 | 1303/1956 | 435/651 | chr16 | 15070211 | |||
| chr16:15073034 | T | C | 2 | a0002 a0005 |
15 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(12): Show |
missense_variant | MODERATE | c.1044A>G | p.Ile348Met | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 12/18 | 1083/3706 | 1044/1956 | 348/651 | chr16 | 15073034 | |||
| chr16:15074824 | C | T | 1 | a0010 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.896G>A | p.Gly299Asp | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 11/18 | 935/3706 | 896/1956 | 299/651 | chr16 | 15074824 | |||
| chr16:15076595 | C | A | 1 | a0002 | 13 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(10): Show |
missense_variant | MODERATE | c.821G>T | p.Cys274Phe | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/18 | 860/3706 | 821/1956 | 274/651 | chr16 | 15076595 | |||
| chr16:15076637 | C | T | 1 | a0007 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.779G>A | p.Arg260Gln | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/18 | 818/3706 | 779/1956 | 260/651 | chr16 | 15076637 | |||
| chr16:15085687 | T | C | 1 | a0006 | 2 | NA19030.hp1 NA20752.hp1 |
missense_variant | MODERATE | c.484A>G | p.Ile162Val | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 6/18 | 523/3706 | 484/1956 | 162/651 | chr16 | 15085687 | |||
| chr16:15091329 | C | T | 1 | a0003 | 3 | HG01074.hp1 HG01167.hp1 HG04228.hp1 |
missense_variant | MODERATE | c.238G>A | p.Asp80Asn | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/18 | 277/3706 | 238/1956 | 80/651 | chr16 | 15091329 | |||
| chr16:15094168 | C | G | 1 | a0004 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.66G>C | p.Lys22Asn | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/18 | 105/3706 | 66/1956 | 22/651 | chr16 | 15094168 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:15070098 | C | T | 1 | a0001c0010 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.1416G>A | p.Lys472Lys | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 14/18 | 1455/3706 | 1416/1956 | 472/651 | chr16 | 15070098 | |||
| chr16:15071246 | G | A | 2 | a0001c0002 a0012c0014 |
41 | HG00639.hp2 HG00733.hp1 HG01109.hp2 others(38): Show |
synonymous_variant | LOW | c.1134C>T | p.Phe378Phe | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 13/18 | 1173/3706 | 1134/1956 | 378/651 | chr16 | 15071246 | |||
| chr16:15074771 | G | A | 1 | a0001c0007 | 2 | NA18973.hp1 NA19086.hp2 |
synonymous_variant | LOW | c.949C>T | p.Leu317Leu | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 11/18 | 988/3706 | 949/1956 | 317/651 | chr16 | 15074771 | |||
| chr16:15080088 | G | A | 1 | a0006c0017 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.675C>T | p.Tyr225Tyr | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/18 | 714/3706 | 675/1956 | 225/651 | chr16 | 15080088 | |||
| chr16:15080094 | T | C | 1 | a0001c0015 | 1 | NA18947.hp2 | splice_region_variant&synonymous_variant | LOW | c.669A>G | p.Glu223Glu | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/18 | 708/3706 | 669/1956 | 223/651 | chr16 | 15080094 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:15060218 | G | A | 1 | a0001c0001t0012 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1526C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 18/18 | 1526 | chr16 | 15060218 | ||||||
| chr16:15060234 | G | A | 1 | a0001c0001t0010 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1510C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 18/18 | 1510 | chr16 | 15060234 | ||||||
| chr16:15060407 | T | C | 1 | a0001c0007t0005 | 2 | NA18973.hp1 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1337A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 18/18 | 1337 | chr16 | 15060407 | ||||||
| chr16:15060881 | G | C | 1 | a0001c0001t0011 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*863C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 18/18 | 863 | chr16 | 15060881 | ||||||
| chr16:15060986 | G | A | 1 | a0001c0001t0015 | 1 | NA19012.hp2 | 3_prime_UTR_variant | MODIFIER | c.*758C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 18/18 | 758 | chr16 | 15060986 | ||||||
| chr16:15061018 | T | C | 1 | a0001c0001t0001 | 4 | HG02145.hp2 HG02818.hp2 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*726A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 18/18 | 726 | chr16 | 15061018 | ||||||
| chr16:15061041 | T | C | 4 | a0001c0001t0003 a0001c0001t0012 a0001c0007t0005 others(1): Show |
49 | HG00609.hp1 HG00621.hp2 HG00642.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*703A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 18/18 | 703 | chr16 | 15061041 | ||||||
| chr16:15061213 | C | T | 1 | a0001c0001t0009 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*531G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 18/18 | 531 | chr16 | 15061213 | ||||||
| chr16:15061264 | G | A | 1 | a0001c0001t0013 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*480C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 18/18 | 480 | chr16 | 15061264 | ||||||
| chr16:15061352 | C | G | 3 | a0001c0001t0004 a0006c0016t0006 a0006c0017t0004 |
3 | HG03453.hp1 NA19030.hp1 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*392G>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 18/18 | 392 | chr16 | 15061352 | ||||||
| chr16:15061361 | T | C | 1 | a0001c0002t0014 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*383A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 18/18 | 383 | chr16 | 15061361 | ||||||
| chr16:15061416 | A | G | 1 | a0012c0014t0008 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*328T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 18/18 | 328 | chr16 | 15061416 | ||||||
| chr16:15061471 | A | G | 1 | a0001c0002t0007 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*273T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 18/18 | 273 | chr16 | 15061471 | ||||||
| chr16:15061550 | G | A | 4 | a0001c0001t0002 a0001c0001t0015 a0001c0015t0002 others(1): Show |
65 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*194C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 18/18 | 194 | chr16 | 15061550 | ||||||
| chr16:15094241 | A | G | 1 | a0006c0016t0006 | 1 | NA20752.hp1 | 5_prime_UTR_variant | MODIFIER | c.-8T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/18 | 8 | chr16 | 15094241 | ||||||
| chr16:15094254 | G | C | 1 | a0001c0001t0016 | 1 | HG00597.hp2 | 5_prime_UTR_variant | MODIFIER | c.-21C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/18 | 21 | chr16 | 15094254 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:15062041 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(145): Show |
237 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1795-136A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 17/17 | chr16 | 15062041 | |||||||
| chr16:15062298 | C | G | 1 | a0001c0001t0002g0233 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1795-393G>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 17/17 | chr16 | 15062298 | |||||||
| chr16:15062299 | G | C | 2 | a0001c0002t0001g0130 a0001c0002t0014g0143 |
2 | HG00639.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1795-394C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 17/17 | chr16 | 15062299 | |||||||
| chr16:15062323 | A | G | 4 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0113 others(1): Show |
8 | HG02145.hp2 HG02257.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1795-418T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 17/17 | chr16 | 15062323 | |||||||
| chr16:15062359 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0113 a0001c0001t0001g0114 |
4 | HG02145.hp2 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1795-454C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 17/17 | chr16 | 15062359 | |||||||
| chr16:15062372 | T | C | 1 | a0001c0001t0002g0227 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1795-467A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 17/17 | chr16 | 15062372 | |||||||
| chr16:15062411 | T | C | 5 | a0001c0001t0003g0014 a0001c0001t0003g0206 a0001c0001t0003g0209 others(2): Show |
8 | HG00735.hp1 HG01123.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1795-506A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 17/17 | chr16 | 15062411 | |||||||
| chr16:15062512 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0190 |
3 | HG02630.hp1 HG03710.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1795-607C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 17/17 | chr16 | 15062512 | |||||||
| chr16:15062685 | C | T | 3 | a0001c0001t0004g0225 a0006c0016t0006g0056 a0006c0017t0004g0112 |
3 | HG03453.hp1 NA19030.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1794+511G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 17/17 | chr16 | 15062685 | |||||||
| chr16:15062724 | A | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(144): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1794+472T>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 17/17 | chr16 | 15062724 | |||||||
| chr16:15063017 | A | C | 1 | a0001c0001t0001g0172 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1794+179T>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 17/17 | chr16 | 15063017 | |||||||
| chr16:15063019 | A | T | 1 | a0001c0001t0001g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1794+177T>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 17/17 | chr16 | 15063019 | |||||||
| chr16:15063078 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1794+118G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 17/17 | chr16 | 15063078 | |||||||
| chr16:15063084 | C | T | 1 | a0001c0001t0001g0012 | 4 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1794+112G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 17/17 | chr16 | 15063084 | |||||||
| chr16:15063111 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1794+85G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 17/17 | chr16 | 15063111 | |||||||
| chr16:15063114 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(144): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1794+82T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 17/17 | chr16 | 15063114 | |||||||
| chr16:15063354 | T | C | 1 | a0001c0001t0003g0220 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1707-71A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15063354 | |||||||
| chr16:15063448 | C | T | 27 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0030 others(24): Show |
41 | HG00639.hp2 HG00733.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1707-165G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15063448 | |||||||
| chr16:15063485 | G | T | 1 | a0001c0001t0001g0160 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1707-202C>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15063485 | |||||||
| chr16:15063636 | C | T | 4 | a0001c0002t0001g0118 a0001c0002t0001g0119 a0001c0002t0001g0120 others(1): Show |
4 | HG02055.hp2 HG02280.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1707-353G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15063636 | |||||||
| chr16:15063649 | G | A | 5 | a0001c0002t0001g0030 a0001c0002t0001g0059 a0001c0002t0001g0060 others(2): Show |
6 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1707-366C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15063649 | |||||||
| chr16:15063704 | C | CA | 108 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(105): Show |
180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.1707-422dupT | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15063704 | |||||||
| chr16:15063704 | C | CAA | 35 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0174 others(32): Show |
51 | HG00323.hp2 HG00423.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.1707-423_1707-422d others(4): Show |
RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15063704 | |||||||
| chr16:15063966 | T | C | 4 | a0001c0001t0003g0055 a0001c0001t0003g0250 a0001c0001t0003g0251 others(1): Show |
5 | HG01346.hp1 HG01433.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1707-683A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15063966 | |||||||
| chr16:15064008 | A | C | 1 | a0001c0001t0001g0066 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1707-725T>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15064008 | |||||||
| chr16:15064059 | T | C | 42 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0022 others(39): Show |
65 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.1707-776A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15064059 | |||||||
| chr16:15064157 | T | A | 1 | a0001c0001t0001g0199 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1707-874A>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15064157 | |||||||
| chr16:15064232 | T | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0025 |
6 | HG01069.hp1 HG01071.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.1707-949A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15064232 | |||||||
| chr16:15064295 | C | A | 1 | a0001c0001t0001g0159 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1706+924G>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15064295 | |||||||
| chr16:15064489 | C | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(189): Show |
308 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.1706+730G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15064489 | |||||||
| chr16:15064507 | G | C | 27 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0030 others(24): Show |
41 | HG00639.hp2 HG00733.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1706+712C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15064507 | |||||||
| chr16:15064519 | G | A | 1 | a0001c0002t0001g0120 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1706+700C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15064519 | |||||||
| chr16:15064545 | T | A | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1706+674A>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15064545 | |||||||
| chr16:15064546 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1706+673C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15064546 | |||||||
| chr16:15064808 | A | G | 1 | a0003c0004t0001g0156 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1706+411T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15064808 | |||||||
| chr16:15064905 | G | A | 1 | a0001c0002t0001g0128 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1706+314C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15064905 | |||||||
| chr16:15064921 | C | G | 2 | a0006c0016t0006g0056 a0006c0017t0004g0112 |
2 | NA19030.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1706+298G>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15064921 | |||||||
| chr16:15065124 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1706+95G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15065124 | |||||||
| chr16:15065144 | C | T | 10 | a0001c0002t0001g0004 a0001c0002t0001g0037 a0001c0002t0001g0038 others(7): Show |
20 | HG00733.hp1 HG01993.hp2 HG02683.hp1 others(17): Show |
intron_variant | MODIFIER | c.1706+75G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 16/17 | chr16 | 15065144 | |||||||
| chr16:15065467 | A | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1554-96T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15065467 | |||||||
| chr16:15065614 | C | CTTATATT others(24): Show |
1 | a0001c0001t0001g0047 | 2 | NA18971.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1554-274_1554-244d others(33): Show |
RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15065614 | |||||||
| chr16:15065643 | T | G | 1 | a0001c0001t0002g0240 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1554-272A>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15065643 | |||||||
| chr16:15066301 | A | C | 1 | a0001c0010t0001g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1554-930T>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15066301 | |||||||
| chr16:15066350 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1554-979G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15066350 | |||||||
| chr16:15066493 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(140): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.1554-1122G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15066493 | |||||||
| chr16:15066589 | C | T | 1 | a0001c0001t0003g0250 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1554-1218G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15066589 | |||||||
| chr16:15066636 | TA | T | 19 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0024 others(16): Show |
29 | HG00099.hp1 HG00140.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.1554-1266delT | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15066636 | |||||||
| chr16:15066666 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1554-1295C>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15066666 | |||||||
| chr16:15066762 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0105 |
2 | HG03098.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1554-1391G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15066762 | |||||||
| chr16:15066767 | G | C | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1554-1396C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15066767 | |||||||
| chr16:15066774 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1553+1395C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15066774 | |||||||
| chr16:15067072 | T | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(143): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1553+1097A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15067072 | |||||||
| chr16:15067239 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0139 |
4 | HG01884.hp1 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1553+930G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15067239 | |||||||
| chr16:15067256 | T | C | 3 | a0001c0001t0004g0225 a0006c0016t0006g0056 a0006c0017t0004g0112 |
3 | HG03453.hp1 NA19030.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1553+913A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15067256 | |||||||
| chr16:15067305 | A | T | 1 | a0001c0001t0001g0245 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1553+864T>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15067305 | |||||||
| chr16:15067432 | A | AGAGGGTT others(4): Show |
146 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(143): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1553+736_1553+737i others(13): Show |
RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15067432 | |||||||
| chr16:15067476 | C | G | 3 | a0001c0001t0003g0048 a0001c0001t0003g0204 a0001c0001t0003g0217 |
4 | HG00642.hp2 NA18941.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.1553+693G>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15067476 | |||||||
| chr16:15067591 | T | C | 42 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0022 others(39): Show |
65 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.1553+578A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15067591 | |||||||
| chr16:15067811 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1553+358C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15067811 | |||||||
| chr16:15067888 | G | A | 1 | a0001c0010t0001g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1553+281C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15067888 | |||||||
| chr16:15068052 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(140): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.1553+117G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 15/17 | chr16 | 15068052 | |||||||
| chr16:15068286 | T | TA | 22 | a0001c0002t0001g0004 a0001c0002t0001g0030 a0001c0002t0001g0037 others(19): Show |
33 | HG00639.hp2 HG00733.hp1 HG01993.hp2 others(30): Show |
intron_variant | MODIFIER | c.1445-10dupT | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 14/17 | chr16 | 15068286 | |||||||
| chr16:15068286 | T | TAA | 3 | a0001c0002t0001g0021 a0001c0002t0001g0036 a0001c0002t0001g0129 |
6 | HG01109.hp2 HG02451.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1445-11_1445-10dup others(2): Show |
RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 14/17 | chr16 | 15068286 | |||||||
| chr16:15068339 | C | T | 1 | a0005c0006t0001g0054 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1445-62G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 14/17 | chr16 | 15068339 | |||||||
| chr16:15068494 | C | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(140): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.1445-217G>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 14/17 | chr16 | 15068494 | |||||||
| chr16:15068924 | A | G | 1 | a0003c0004t0001g0141 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1445-647T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 14/17 | chr16 | 15068924 | |||||||
| chr16:15069148 | G | A | 4 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0006c0016t0006g0056 others(1): Show |
4 | HG02818.hp1 HG03041.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1445-871C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 14/17 | chr16 | 15069148 | |||||||
| chr16:15069228 | G | T | 4 | a0001c0001t0001g0171 a0001c0001t0001g0177 a0001c0001t0001g0185 others(1): Show |
4 | HG03669.hp2 HG03688.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.1444+842C>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 14/17 | chr16 | 15069228 | |||||||
| chr16:15069231 | C | T | 1 | a0001c0001t0002g0050 | 2 | NA18982.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1444+839G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 14/17 | chr16 | 15069231 | |||||||
| chr16:15069394 | T | A | 1 | a0001c0001t0001g0197 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1444+676A>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 14/17 | chr16 | 15069394 | |||||||
| chr16:15069546 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1444+524G>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 14/17 | chr16 | 15069546 | |||||||
| chr16:15069886 | C | G | 1 | a0001c0001t0001g0012 | 4 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1444+184G>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 14/17 | chr16 | 15069886 | |||||||
| chr16:15069943 | AG | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0113 a0001c0001t0001g0114 |
4 | HG02145.hp2 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1444+126delC | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 14/17 | chr16 | 15069943 | |||||||
| chr16:15069952 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1444+118C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 14/17 | chr16 | 15069952 | |||||||
| chr16:15070060 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1444+10G>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 14/17 | chr16 | 15070060 | |||||||
| chr16:15070273 | C | A | 1 | a0001c0001t0001g0095 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1260-19G>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 13/17 | chr16 | 15070273 | |||||||
| chr16:15070289 | A | T | 27 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0030 others(24): Show |
41 | HG00639.hp2 HG00733.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1260-35T>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 13/17 | chr16 | 15070289 | |||||||
| chr16:15070302 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1260-48G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 13/17 | chr16 | 15070302 | |||||||
| chr16:15070360 | T | C | 1 | a0005c0006t0001g0054 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1260-106A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 13/17 | chr16 | 15070360 | |||||||
| chr16:15070423 | G | C | 6 | a0002c0003t0001g0007 a0002c0003t0001g0034 a0002c0003t0001g0106 others(3): Show |
13 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.1260-169C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 13/17 | chr16 | 15070423 | |||||||
| chr16:15070432 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0096 others(1): Show |
10 | HG02109.hp2 HG02559.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1260-178C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 13/17 | chr16 | 15070432 | |||||||
| chr16:15070816 | A | T | 142 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(139): Show |
231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.1259+305T>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 13/17 | chr16 | 15070816 | |||||||
| chr16:15071291 | C | G | 1 | a0001c0001t0001g0170 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1129-40G>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 12/17 | chr16 | 15071291 | |||||||
| chr16:15071322 | A | G | 1 | a0001c0001t0001g0168 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1129-71T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 12/17 | chr16 | 15071322 | |||||||
| chr16:15071426 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1129-175G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 12/17 | chr16 | 15071426 | |||||||
| chr16:15071515 | C | T | 1 | a0006c0017t0004g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1129-264G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 12/17 | chr16 | 15071515 | |||||||
| chr16:15071539 | G | A | 1 | a0001c0010t0001g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1129-288C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 12/17 | chr16 | 15071539 | |||||||
| chr16:15071835 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0139 |
4 | HG01884.hp1 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1129-584G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 12/17 | chr16 | 15071835 | |||||||
| chr16:15072129 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1128+821T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 12/17 | chr16 | 15072129 | |||||||
| chr16:15072134 | T | A | 27 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0030 others(24): Show |
41 | HG00639.hp2 HG00733.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1128+816A>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 12/17 | chr16 | 15072134 | |||||||
| chr16:15072140 | C | A | 1 | a0001c0001t0003g0208 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1128+810G>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 12/17 | chr16 | 15072140 | |||||||
| chr16:15072204 | C | T | 3 | a0001c0001t0001g0157 a0001c0001t0001g0195 a0001c0001t0001g0200 |
3 | HG00642.hp1 HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1128+746G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 12/17 | chr16 | 15072204 | |||||||
| chr16:15072215 | A | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0139 |
4 | HG01884.hp1 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1128+735T>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 12/17 | chr16 | 15072215 | |||||||
| chr16:15072245 | CA | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(123): Show |
204 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.1128+704delT | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 12/17 | chr16 | 15072245 | |||||||
| chr16:15072245 | CAA | C | 27 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0030 others(24): Show |
41 | HG00639.hp2 HG00733.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.1128+703_1128+704d others(4): Show |
RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 12/17 | chr16 | 15072245 | |||||||
| chr16:15072375 | A | G | 105 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(102): Show |
171 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.1128+575T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 12/17 | chr16 | 15072375 | |||||||
| chr16:15072574 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1128+376C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 12/17 | chr16 | 15072574 | |||||||
| chr16:15072588 | T | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(140): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.1128+362A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 12/17 | chr16 | 15072588 | |||||||
| chr16:15072662 | G | A | 1 | a0001c0001t0002g0239 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1128+288C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 12/17 | chr16 | 15072662 | |||||||
| chr16:15072808 | G | A | 1 | a0001c0010t0001g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1128+142C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 12/17 | chr16 | 15072808 | |||||||
| chr16:15073198 | G | A | 1 | a0001c0001t0003g0249 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.998-118C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 11/17 | chr16 | 15073198 | |||||||
| chr16:15073370 | C | A | 1 | a0001c0001t0002g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.998-290G>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 11/17 | chr16 | 15073370 | |||||||
| chr16:15073382 | A | C | 1 | a0001c0001t0001g0186 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.998-302T>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 11/17 | chr16 | 15073382 | |||||||
| chr16:15073415 | C | T | 1 | a0001c0001t0003g0027 | 3 | NA18960.hp2 NA18993.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.998-335G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 11/17 | chr16 | 15073415 | |||||||
| chr16:15073470 | A | C | 1 | a0001c0001t0001g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.998-390T>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 11/17 | chr16 | 15073470 | |||||||
| chr16:15073522 | T | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(140): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.998-442A>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 11/17 | chr16 | 15073522 | |||||||
| chr16:15073581 | C | A | 1 | a0001c0001t0002g0229 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.998-501G>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 11/17 | chr16 | 15073581 | |||||||
| chr16:15073683 | A | G | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0004g0225 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.998-603T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 11/17 | chr16 | 15073683 | |||||||
| chr16:15073730 | T | C | 1 | a0001c0001t0001g0031 | 2 | HG02083.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.998-650A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 11/17 | chr16 | 15073730 | |||||||
| chr16:15073954 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.997+769T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 11/17 | chr16 | 15073954 | |||||||
| chr16:15074112 | G | T | 1 | a0007c0008t0002g0224 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.997+611C>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 11/17 | chr16 | 15074112 | |||||||
| chr16:15074222 | T | C | 1 | a0001c0002t0001g0117 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.997+501A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 11/17 | chr16 | 15074222 | |||||||
| chr16:15074224 | C | G | 1 | a0001c0001t0001g0053 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.997+499G>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 11/17 | chr16 | 15074224 | |||||||
| chr16:15074415 | A | G | 1 | a0001c0002t0001g0120 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.997+308T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 11/17 | chr16 | 15074415 | |||||||
| chr16:15074903 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(106): Show |
176 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.859-42A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15074903 | |||||||
| chr16:15074971 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.859-110A>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15074971 | |||||||
| chr16:15075067 | T | A | 1 | a0001c0001t0003g0210 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.859-206A>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15075067 | |||||||
| chr16:15075096 | A | T | 43 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0022 others(40): Show |
66 | HG00423.hp2 HG00558.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.859-235T>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15075096 | |||||||
| chr16:15075101 | T | A | 27 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0030 others(24): Show |
41 | HG00639.hp2 HG00733.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.859-240A>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15075101 | |||||||
| chr16:15075163 | T | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0031 a0001c0001t0001g0081 others(4): Show |
10 | HG00280.hp1 HG00323.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.859-302A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15075163 | |||||||
| chr16:15075201 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.859-340C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15075201 | |||||||
| chr16:15075211 | G | A | 1 | a0001c0001t0003g0210 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.859-350C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15075211 | |||||||
| chr16:15075250 | C | CA | 34 | a0001c0001t0001g0019 a0001c0001t0001g0079 a0001c0001t0001g0080 others(31): Show |
38 | HG00140.hp1 HG00621.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.859-390dupT | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15075250 | |||||||
| chr16:15075250 | C | T | 2 | a0001c0002t0001g0037 a0001c0002t0001g0127 |
3 | HG01993.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.859-389G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15075250 | |||||||
| chr16:15075295 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.859-434G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15075295 | |||||||
| chr16:15075370 | T | A | 1 | a0001c0001t0001g0081 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.859-509A>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15075370 | |||||||
| chr16:15075435 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.859-574G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15075435 | |||||||
| chr16:15075463 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.859-602C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15075463 | |||||||
| chr16:15075584 | G | C | 1 | a0001c0002t0001g0127 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.859-723C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15075584 | |||||||
| chr16:15075589 | AAAAG | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(142): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.859-732_859-729del others(4): Show |
RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15075589 | |||||||
| chr16:15075725 | T | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0091 |
3 | HG02622.hp2 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.858+833A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15075725 | |||||||
| chr16:15075804 | G | A | 2 | a0001c0001t0001g0039 a0001c0010t0001g0154 |
3 | HG02896.hp1 HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.858+754C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15075804 | |||||||
| chr16:15075928 | C | T | 1 | a0001c0001t0002g0223 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.858+630G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15075928 | |||||||
| chr16:15076088 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.858+470C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15076088 | |||||||
| chr16:15076207 | A | T | 1 | a0006c0017t0004g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.858+351T>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15076207 | |||||||
| chr16:15076215 | C | T | 9 | a0001c0001t0002g0022 a0001c0001t0002g0041 a0001c0001t0002g0042 others(6): Show |
13 | HG00423.hp2 HG00639.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.858+343G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15076215 | |||||||
| chr16:15076420 | T | G | 1 | a0001c0001t0001g0113 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.858+138A>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 10/17 | chr16 | 15076420 | |||||||
| chr16:15076660 | A | T | 1 | a0001c0001t0002g0223 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.766-10T>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15076660 | |||||||
| chr16:15076766 | A | G | 1 | a0002c0003t0001g0106 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.766-116T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15076766 | |||||||
| chr16:15076882 | G | A | 1 | a0001c0001t0001g0192 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.766-232C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15076882 | |||||||
| chr16:15076963 | T | C | 1 | a0001c0001t0003g0055 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.766-313A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15076963 | |||||||
| chr16:15076971 | C | A | 5 | a0001c0001t0003g0055 a0001c0001t0003g0210 a0001c0001t0003g0250 others(2): Show |
6 | HG01106.hp1 HG01346.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-321G>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15076971 | |||||||
| chr16:15076979 | A | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(144): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.766-329T>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15076979 | |||||||
| chr16:15076980 | C | CT | 137 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(134): Show |
223 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.766-331dupA | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15076980 | |||||||
| chr16:15076980 | C | CTT | 5 | a0001c0001t0001g0180 a0001c0001t0003g0207 a0001c0002t0001g0021 others(2): Show |
8 | HG01109.hp2 HG01167.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.766-332_766-331dup others(2): Show |
RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15076980 | |||||||
| chr16:15077049 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(113): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.766-399C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15077049 | |||||||
| chr16:15077123 | T | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(144): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.766-473A>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15077123 | |||||||
| chr16:15077169 | G | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG00733.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.766-519C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15077169 | |||||||
| chr16:15077224 | C | T | 3 | a0001c0001t0002g0029 a0001c0001t0002g0050 a0001c0001t0002g0222 |
6 | HG02071.hp1 HG02523.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.766-574G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15077224 | |||||||
| chr16:15077270 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.766-620G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15077270 | |||||||
| chr16:15077284 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.766-634A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15077284 | |||||||
| chr16:15077335 | G | T | 1 | a0001c0015t0002g0232 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.766-685C>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15077335 | |||||||
| chr16:15077351 | T | A | 1 | a0001c0001t0003g0212 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.766-701A>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15077351 | |||||||
| chr16:15077378 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.766-728A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15077378 | |||||||
| chr16:15077398 | A | G | 7 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(4): Show |
13 | HG00738.hp2 HG00741.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.766-748T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15077398 | |||||||
| chr16:15077408 | A | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(144): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.766-758T>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15077408 | |||||||
| chr16:15077470 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0139 |
4 | HG01884.hp1 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-820G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15077470 | |||||||
| chr16:15077590 | C | G | 1 | a0001c0001t0011g0067 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.766-940G>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15077590 | |||||||
| chr16:15077591 | G | C | 11 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0157 others(8): Show |
14 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.766-941C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15077591 | |||||||
| chr16:15077655 | C | G | 22 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0036 others(19): Show |
35 | HG00639.hp2 HG00733.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.766-1005G>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15077655 | |||||||
| chr16:15078045 | T | C | 1 | a0001c0001t0003g0206 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.766-1395A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15078045 | |||||||
| chr16:15078084 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.766-1434A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15078084 | |||||||
| chr16:15078143 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.766-1493T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15078143 | |||||||
| chr16:15078261 | T | C | 19 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0024 others(16): Show |
29 | HG00099.hp1 HG00140.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.766-1611A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15078261 | |||||||
| chr16:15078346 | G | A | 1 | a0001c0001t0003g0204 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.765+1652C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15078346 | |||||||
| chr16:15078373 | T | A | 1 | a0001c0001t0003g0212 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.765+1625A>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15078373 | |||||||
| chr16:15078414 | T | A | 2 | a0001c0001t0002g0051 a0001c0001t0002g0230 |
3 | HG00673.hp2 NA18952.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.765+1584A>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15078414 | |||||||
| chr16:15078472 | A | G | 1 | a0001c0001t0003g0216 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.765+1526T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15078472 | |||||||
| chr16:15078723 | G | A | 1 | a0001c0001t0002g0231 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.765+1275C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15078723 | |||||||
| chr16:15078812 | C | T | 1 | a0001c0001t0001g0012 | 4 | HG02257.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.765+1186G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15078812 | |||||||
| chr16:15078812 | CT | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(136): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.765+1185delA | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15078812 | |||||||
| chr16:15078819 | T | C | 40 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0022 others(37): Show |
63 | HG00423.hp2 HG00597.hp1 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.765+1179A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15078819 | |||||||
| chr16:15078882 | G | T | 2 | a0001c0001t0003g0203 a0001c0001t0003g0205 |
2 | HG00609.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.765+1116C>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15078882 | |||||||
| chr16:15078995 | T | A | 1 | a0001c0001t0001g0082 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.765+1003A>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15078995 | |||||||
| chr16:15079013 | T | C | 2 | a0001c0001t0001g0083 a0001c0001t0001g0086 |
2 | NA18944.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.765+985A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079013 | |||||||
| chr16:15079020 | C | T | 1 | a0001c0001t0003g0216 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.765+978G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079020 | |||||||
| chr16:15079053 | G | A | 1 | a0001c0001t0003g0211 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.765+945C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079053 | |||||||
| chr16:15079092 | G | A | 2 | a0006c0016t0006g0056 a0006c0017t0004g0112 |
2 | NA19030.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.765+906C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079092 | |||||||
| chr16:15079148 | A | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0139 |
4 | HG01884.hp1 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.765+850T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079148 | |||||||
| chr16:15079171 | A | AC | 145 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(142): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.765+826_765+827ins others(1): Show |
RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079171 | |||||||
| chr16:15079172 | A | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(142): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.765+826T>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079172 | |||||||
| chr16:15079274 | C | A | 1 | a0001c0001t0002g0240 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.765+724G>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079274 | |||||||
| chr16:15079300 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.765+698C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079300 | |||||||
| chr16:15079596 | CT | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(136): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.765+401delA | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079596 | |||||||
| chr16:15079623 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.765+375G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079623 | |||||||
| chr16:15079631 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(140): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.765+367G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079631 | |||||||
| chr16:15079686 | G | A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(140): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.765+312C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079686 | |||||||
| chr16:15079712 | C | T | 1 | a0002c0003t0001g0109 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.765+286G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079712 | |||||||
| chr16:15079761 | T | G | 1 | a0002c0003t0001g0109 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.765+237A>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079761 | |||||||
| chr16:15079768 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.765+230A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079768 | |||||||
| chr16:15079786 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.765+212C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079786 | |||||||
| chr16:15079811 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.765+187C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079811 | |||||||
| chr16:15079828 | C | A | 1 | a0001c0002t0001g0117 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.765+170G>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079828 | |||||||
| chr16:15079868 | A | T | 1 | a0001c0001t0003g0220 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.765+130T>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079868 | |||||||
| chr16:15079889 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(113): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.765+109C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079889 | |||||||
| chr16:15079889 | G | C | 3 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0085 |
3 | NA19004.hp2 NA19054.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.765+109C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 9/17 | chr16 | 15079889 | |||||||
| chr16:15080283 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.667-187G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15080283 | |||||||
| chr16:15080637 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0139 |
4 | HG01884.hp1 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.667-541G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15080637 | |||||||
| chr16:15080713 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.667-617G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15080713 | |||||||
| chr16:15080714 | G | A | 19 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0024 others(16): Show |
29 | HG00099.hp1 HG00140.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.667-618C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15080714 | |||||||
| chr16:15080746 | C | T | 3 | a0001c0001t0001g0071 a0001c0002t0001g0122 a0001c0002t0001g0128 |
3 | HG02486.hp1 HG02818.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.667-650G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15080746 | |||||||
| chr16:15080804 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.667-708G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15080804 | |||||||
| chr16:15080833 | T | TGA | 189 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(186): Show |
305 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.667-739_667-738dup others(2): Show |
RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15080833 | |||||||
| chr16:15080836 | C | T | 2 | a0006c0016t0006g0056 a0006c0017t0004g0112 |
2 | NA19030.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.667-740G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15080836 | |||||||
| chr16:15080952 | G | T | 1 | a0001c0001t0001g0132 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.667-856C>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15080952 | |||||||
| chr16:15080989 | A | G | 1 | a0002c0003t0001g0034 | 2 | HG00140.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.667-893T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15080989 | |||||||
| chr16:15080998 | G | C | 1 | a0001c0001t0001g0086 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.667-902C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15080998 | |||||||
| chr16:15081020 | T | C | 1 | a0001c0001t0011g0067 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.667-924A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15081020 | |||||||
| chr16:15081097 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0193 |
4 | HG03704.hp1 HG03834.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.667-1001G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15081097 | |||||||
| chr16:15081255 | C | T | 11 | a0001c0001t0001g0025 a0001c0001t0001g0045 a0001c0001t0001g0157 others(8): Show |
14 | HG00323.hp2 HG00642.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.667-1159G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15081255 | |||||||
| chr16:15081397 | C | T | 1 | a0006c0017t0004g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.667-1301G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15081397 | |||||||
| chr16:15081440 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.667-1344A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15081440 | |||||||
| chr16:15081755 | C | T | 6 | a0001c0001t0001g0016 a0001c0001t0001g0070 a0001c0001t0001g0097 others(3): Show |
8 | NA18939.hp1 NA18946.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.667-1659G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15081755 | |||||||
| chr16:15082140 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.666+1373G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15082140 | |||||||
| chr16:15082529 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.666+984C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15082529 | |||||||
| chr16:15082565 | C | T | 1 | a0001c0001t0011g0067 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.666+948G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15082565 | |||||||
| chr16:15082877 | A | G | 1 | a0001c0002t0001g0117 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.666+636T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15082877 | |||||||
| chr16:15082932 | T | C | 1 | a0001c0001t0003g0203 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.666+581A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15082932 | |||||||
| chr16:15082935 | A | G | 1 | a0001c0001t0003g0203 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.666+578T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15082935 | |||||||
| chr16:15082995 | AG | A | 1 | a0001c0001t0001g0025 | 3 | HG01069.hp1 HG01071.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.666+517delC | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15082995 | |||||||
| chr16:15083032 | C | A | 1 | a0001c0001t0001g0184 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.666+481G>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15083032 | |||||||
| chr16:15083164 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.666+349C>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15083164 | |||||||
| chr16:15083175 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.666+338G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15083175 | |||||||
| chr16:15083196 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0193 |
4 | HG03704.hp1 HG03834.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.666+317G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15083196 | |||||||
| chr16:15083272 | G | A | 1 | a0006c0016t0006g0056 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.666+241C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15083272 | |||||||
| chr16:15083324 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0113 a0001c0001t0001g0114 |
4 | HG02145.hp2 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.666+189C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15083324 | |||||||
| chr16:15083411 | G | A | 3 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0139 |
4 | HG01884.hp1 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+102C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15083411 | |||||||
| chr16:15083459 | A | G | 1 | a0005c0006t0001g0054 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.666+54T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 8/17 | chr16 | 15083459 | |||||||
| chr16:15083747 | G | A | 2 | a0001c0002t0001g0120 a0001c0002t0001g0121 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.597-165C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 7/17 | chr16 | 15083747 | |||||||
| chr16:15083786 | A | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(142): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.597-204T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 7/17 | chr16 | 15083786 | |||||||
| chr16:15083838 | T | A | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(103): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.597-256A>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 7/17 | chr16 | 15083838 | |||||||
| chr16:15083944 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.597-362C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 7/17 | chr16 | 15083944 | |||||||
| chr16:15083968 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(142): Show |
234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.597-386C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 7/17 | chr16 | 15083968 | |||||||
| chr16:15084000 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.597-418C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 7/17 | chr16 | 15084000 | |||||||
| chr16:15084019 | A | G | 1 | a0001c0001t0002g0236 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.597-437T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 7/17 | chr16 | 15084019 | |||||||
| chr16:15084273 | G | C | 1 | a0001c0001t0003g0212 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.596+369C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 7/17 | chr16 | 15084273 | |||||||
| chr16:15084321 | A | AT | 143 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(140): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.596+320dupA | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 7/17 | chr16 | 15084321 | |||||||
| chr16:15084457 | TAA | T | 36 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0022 others(33): Show |
58 | HG00423.hp2 HG00597.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.596+183_596+184del others(2): Show |
RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 7/17 | chr16 | 15084457 | |||||||
| chr16:15084756 | G | C | 1 | a0001c0001t0003g0219 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.533-51C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 6/17 | chr16 | 15084756 | |||||||
| chr16:15084831 | C | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(112): Show |
190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.533-126G>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 6/17 | chr16 | 15084831 | |||||||
| chr16:15085008 | G | A | 2 | a0001c0002t0001g0130 a0001c0002t0014g0143 |
2 | HG00639.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.533-303C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 6/17 | chr16 | 15085008 | |||||||
| chr16:15085009 | C | A | 2 | a0001c0002t0001g0130 a0001c0002t0014g0143 |
2 | HG00639.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.533-304G>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 6/17 | chr16 | 15085009 | |||||||
| chr16:15085304 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.532+335C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 6/17 | chr16 | 15085304 | |||||||
| chr16:15085326 | C | CT | 145 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(142): Show |
235 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.532+312dupA | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 6/17 | chr16 | 15085326 | |||||||
| chr16:15085522 | T | C | 1 | a0001c0001t0003g0213 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.532+117A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 6/17 | chr16 | 15085522 | |||||||
| chr16:15085756 | A | G | 2 | a0006c0016t0006g0056 a0006c0017t0004g0112 |
2 | NA19030.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.473-58T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 5/17 | chr16 | 15085756 | |||||||
| chr16:15085802 | G | C | 1 | a0001c0002t0001g0127 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.473-104C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 5/17 | chr16 | 15085802 | |||||||
| chr16:15085829 | C | T | 143 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(140): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.473-131G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 5/17 | chr16 | 15085829 | |||||||
| chr16:15085841 | T | C | 13 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(10): Show |
21 | HG00438.hp1 HG00673.hp1 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.473-143A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 5/17 | chr16 | 15085841 | |||||||
| chr16:15085911 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.473-213G>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 5/17 | chr16 | 15085911 | |||||||
| chr16:15085931 | A | G | 10 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(7): Show |
16 | HG00738.hp2 HG00741.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.472+198T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 5/17 | chr16 | 15085931 | |||||||
| chr16:15085998 | T | C | 29 | a0001c0002t0001g0004 a0001c0002t0001g0021 a0001c0002t0001g0030 others(26): Show |
43 | HG00639.hp2 HG00733.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.472+131A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 5/17 | chr16 | 15085998 | |||||||
| chr16:15086088 | G | A | 1 | a0006c0016t0006g0056 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.472+41C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 5/17 | chr16 | 15086088 | |||||||
| chr16:15086339 | T | G | 1 | a0001c0001t0001g0246 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.342+26A>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 4/17 | chr16 | 15086339 | |||||||
| chr16:15086354 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.342+11C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 4/17 | chr16 | 15086354 | |||||||
| chr16:15086491 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.253-37A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15086491 | |||||||
| chr16:15086567 | A | C | 2 | a0006c0016t0006g0056 a0006c0017t0004g0112 |
2 | NA19030.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.253-113T>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15086567 | |||||||
| chr16:15086887 | T | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0139 |
4 | HG01884.hp1 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.253-433A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15086887 | |||||||
| chr16:15087003 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.253-549C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15087003 | |||||||
| chr16:15087021 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.253-567G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15087021 | |||||||
| chr16:15087025 | G | A | 1 | a0001c0001t0002g0137 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.253-571C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15087025 | |||||||
| chr16:15087179 | G | C | 1 | a0001c0001t0003g0220 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.253-725C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15087179 | |||||||
| chr16:15087421 | G | C | 1 | a0001c0001t0001g0243 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.253-967C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15087421 | |||||||
| chr16:15087463 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0159 a0001c0001t0001g0160 others(2): Show |
12 | HG03834.hp1 NA18939.hp2 NA18941.hp2 others(9): Show |
intron_variant | MODIFIER | c.253-1009G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15087463 | |||||||
| chr16:15087472 | C | T | 2 | a0001c0001t0001g0068 a0001c0001t0001g0069 |
2 | NA19054.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.253-1018G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15087472 | |||||||
| chr16:15087631 | C | T | 1 | a0001c0001t0002g0151 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.253-1177G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15087631 | |||||||
| chr16:15087670 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(82): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.253-1216A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15087670 | |||||||
| chr16:15087734 | T | A | 1 | a0001c0001t0001g0145 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.253-1280A>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15087734 | |||||||
| chr16:15087846 | A | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(110): Show |
185 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.253-1392T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15087846 | |||||||
| chr16:15087903 | T | C | 1 | a0001c0002t0001g0128 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.253-1449A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15087903 | |||||||
| chr16:15087982 | T | G | 12 | a0001c0002t0001g0004 a0001c0002t0001g0037 a0001c0002t0001g0038 others(9): Show |
22 | HG00733.hp1 HG01993.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.253-1528A>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15087982 | |||||||
| chr16:15088116 | CAAAA | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0139 |
3 | HG01884.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.253-1666_253-1663d others(6): Show |
RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15088116 | |||||||
| chr16:15088118 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.253-1664T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15088118 | |||||||
| chr16:15088281 | G | C | 1 | a0001c0001t0010g0188 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.253-1827C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15088281 | |||||||
| chr16:15088360 | G | A | 1 | a0001c0002t0001g0129 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.253-1906C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15088360 | |||||||
| chr16:15088565 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.253-2111C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15088565 | |||||||
| chr16:15088671 | T | C | 1 | a0006c0017t0004g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.253-2217A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15088671 | |||||||
| chr16:15088922 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.252+2393A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15088922 | |||||||
| chr16:15089049 | T | A | 1 | a0001c0001t0001g0105 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.252+2266A>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089049 | |||||||
| chr16:15089063 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.252+2252C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089063 | |||||||
| chr16:15089261 | A | T | 1 | a0001c0001t0001g0090 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.252+2054T>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089261 | |||||||
| chr16:15089354 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0132 a0001c0001t0001g0139 |
4 | HG01884.hp1 HG02615.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.252+1961G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089354 | |||||||
| chr16:15089567 | A | G | 1 | a0001c0002t0001g0116 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.252+1748T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089567 | |||||||
| chr16:15089571 | C | G | 1 | a0001c0002t0001g0116 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.252+1744G>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089571 | |||||||
| chr16:15089605 | C | T | 7 | a0001c0001t0001g0020 a0001c0001t0001g0026 a0001c0001t0001g0043 others(4): Show |
13 | HG00738.hp2 HG00741.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.252+1710G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089605 | |||||||
| chr16:15089629 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0200 |
2 | HG00642.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.252+1686G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089629 | |||||||
| chr16:15089732 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0113 a0001c0001t0001g0114 |
4 | HG02145.hp2 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.252+1583C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089732 | |||||||
| chr16:15089754 | T | C | 1 | a0001c0001t0003g0201 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.252+1561A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089754 | |||||||
| chr16:15089755 | G | A | 1 | a0001c0001t0003g0201 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.252+1560C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089755 | |||||||
| chr16:15089756 | C | T | 7 | a0001c0001t0003g0201 a0002c0003t0001g0007 a0002c0003t0001g0034 others(4): Show |
14 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.252+1559G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089756 | |||||||
| chr16:15089757 | G | A | 1 | a0001c0001t0002g0235 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.252+1558C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089757 | |||||||
| chr16:15089786 | C | CA | 76 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0033 others(73): Show |
116 | HG00280.hp1 HG00558.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.252+1528dupT | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089786 | |||||||
| chr16:15089786 | C | CAA | 21 | a0001c0001t0001g0012 a0001c0001t0001g0105 a0001c0001t0001g0215 others(18): Show |
31 | HG00597.hp1 HG00621.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.252+1527_252+1528d others(4): Show |
RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089786 | |||||||
| chr16:15089786 | CAA | C | 4 | a0002c0003t0001g0007 a0002c0003t0001g0034 a0002c0003t0001g0106 others(1): Show |
11 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.252+1527_252+1528d others(4): Show |
RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089786 | |||||||
| chr16:15089786 | CAAAA | C | 21 | a0001c0001t0001g0013 a0001c0001t0001g0026 a0001c0001t0001g0039 others(18): Show |
31 | HG00639.hp2 HG00738.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.252+1525_252+1528d others(6): Show |
RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089786 | |||||||
| chr16:15089786 | CAAAAA | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(78): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.252+1524_252+1528d others(7): Show |
RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089786 | |||||||
| chr16:15089786 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0002g0222 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.252+1518_252+1528d others(13): Show |
RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089786 | |||||||
| chr16:15089803 | A | AC | 3 | a0001c0001t0002g0131 a0001c0001t0002g0149 a0001c0001t0002g0150 |
3 | HG00423.hp2 NA18978.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.252+1511_252+1512i others(3): Show |
RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089803 | |||||||
| chr16:15089850 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.252+1465A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089850 | |||||||
| chr16:15089967 | G | C | 1 | a0001c0001t0001g0140 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.252+1348C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089967 | |||||||
| chr16:15089968 | G | C | 2 | a0006c0016t0006g0056 a0006c0017t0004g0112 |
2 | NA19030.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.252+1347C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15089968 | |||||||
| chr16:15090020 | C | A | 1 | a0001c0001t0002g0042 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.252+1295G>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15090020 | |||||||
| chr16:15090210 | T | TA | 34 | a0001c0001t0001g0215 a0001c0001t0002g0214 a0001c0001t0003g0006 others(31): Show |
51 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.252+1104dupT | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15090210 | |||||||
| chr16:15090400 | T | C | 42 | a0001c0001t0002g0003 a0001c0001t0002g0010 a0001c0001t0002g0022 others(39): Show |
65 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.252+915A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15090400 | |||||||
| chr16:15090652 | A | G | 1 | a0001c0001t0003g0250 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.252+663T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15090652 | |||||||
| chr16:15090843 | T | C | 6 | a0002c0003t0001g0007 a0002c0003t0001g0034 a0002c0003t0001g0106 others(3): Show |
13 | HG00140.hp1 HG01074.hp2 HG01099.hp1 others(10): Show |
intron_variant | MODIFIER | c.252+472A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15090843 | |||||||
| chr16:15090873 | G | GT | 6 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0078 others(3): Show |
8 | HG00609.hp1 HG01496.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.252+441dupA | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15090873 | |||||||
| chr16:15090873 | GT | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(100): Show |
173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.252+441delA | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15090873 | |||||||
| chr16:15091094 | C | A | 1 | a0001c0001t0001g0243 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.252+221G>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15091094 | |||||||
| chr16:15091106 | T | C | 1 | a0001c0010t0001g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.252+209A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 3/17 | chr16 | 15091106 | |||||||
| chr16:15091415 | G | C | 1 | a0001c0001t0001g0111 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.196-44C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 2/17 | chr16 | 15091415 | |||||||
| chr16:15091593 | A | G | 1 | a0001c0001t0011g0067 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.196-222T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 2/17 | chr16 | 15091593 | |||||||
| chr16:15091642 | C | G | 1 | a0001c0001t0001g0155 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.196-271G>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 2/17 | chr16 | 15091642 | |||||||
| chr16:15091650 | G | C | 1 | a0006c0016t0006g0056 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.196-279C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 2/17 | chr16 | 15091650 | |||||||
| chr16:15091657 | G | A | 1 | a0006c0016t0006g0056 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.196-286C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 2/17 | chr16 | 15091657 | |||||||
| chr16:15091683 | C | G | 1 | a0001c0010t0001g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.196-312G>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 2/17 | chr16 | 15091683 | |||||||
| chr16:15091893 | T | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0138 a0001c0001t0001g0144 others(4): Show |
11 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.196-522A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 2/17 | chr16 | 15091893 | |||||||
| chr16:15091950 | G | A | 3 | a0001c0001t0002g0040 a0001c0001t0002g0147 a0001c0001t0002g0148 |
4 | HG02622.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+559C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 2/17 | chr16 | 15091950 | |||||||
| chr16:15092071 | C | T | 9 | a0001c0001t0002g0022 a0001c0001t0002g0041 a0001c0001t0002g0042 others(6): Show |
13 | HG00423.hp2 HG00639.hp1 HG01257.hp1 others(10): Show |
intron_variant | MODIFIER | c.195+438G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 2/17 | chr16 | 15092071 | |||||||
| chr16:15092136 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.195+373C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 2/17 | chr16 | 15092136 | |||||||
| chr16:15092201 | G | C | 1 | a0001c0001t0003g0248 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.195+308C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 2/17 | chr16 | 15092201 | |||||||
| chr16:15092223 | C | T | 3 | a0001c0001t0002g0040 a0001c0001t0002g0147 a0001c0001t0002g0148 |
4 | HG02622.hp1 HG02717.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.195+286G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 2/17 | chr16 | 15092223 | |||||||
| chr16:15092248 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.195+261G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 2/17 | chr16 | 15092248 | |||||||
| chr16:15092343 | G | C | 1 | a0001c0001t0001g0053 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.195+166C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 2/17 | chr16 | 15092343 | |||||||
| chr16:15092762 | T | C | 1 | a0005c0006t0001g0054 | 2 | HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.90-148A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15092762 | |||||||
| chr16:15092781 | A | G | 1 | a0001c0001t0002g0146 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.90-167T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15092781 | |||||||
| chr16:15092827 | G | C | 2 | a0001c0002t0001g0130 a0001c0002t0014g0143 |
2 | HG00639.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.90-213C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15092827 | |||||||
| chr16:15092841 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.90-227T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15092841 | |||||||
| chr16:15092843 | C | G | 1 | a0001c0001t0001g0144 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.90-229G>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15092843 | |||||||
| chr16:15092864 | C | T | 28 | a0001c0001t0001g0020 a0001c0002t0001g0004 a0001c0002t0001g0021 others(25): Show |
44 | HG00639.hp2 HG00733.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.90-250G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15092864 | |||||||
| chr16:15093204 | A | T | 1 | a0001c0002t0001g0115 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.90-590T>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15093204 | |||||||
| chr16:15093293 | C | T | 2 | a0003c0004t0001g0141 a0003c0004t0001g0142 |
2 | HG01074.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.90-679G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15093293 | |||||||
| chr16:15093300 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.90-686C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15093300 | |||||||
| chr16:15093316 | T | G | 1 | a0001c0001t0003g0249 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.90-702A>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15093316 | |||||||
| chr16:15093355 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.90-741T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15093355 | |||||||
| chr16:15093397 | C | A | 1 | a0001c0001t0001g0111 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.89+748G>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15093397 | |||||||
| chr16:15093438 | T | C | 4 | a0001c0001t0003g0055 a0001c0001t0003g0250 a0001c0001t0003g0251 others(1): Show |
5 | HG01346.hp1 HG01433.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.89+707A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15093438 | |||||||
| chr16:15093448 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.89+697T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15093448 | |||||||
| chr16:15093504 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.89+641A>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15093504 | |||||||
| chr16:15093886 | A | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | HG02257.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.89+259T>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15093886 | |||||||
| chr16:15093894 | G | A | 4 | a0001c0002t0001g0030 a0001c0002t0001g0060 a0001c0002t0001g0061 others(1): Show |
5 | HG02109.hp1 HG02559.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.89+251C>T | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15093894 | |||||||
| chr16:15093921 | A | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0113 a0001c0001t0001g0114 |
4 | HG02145.hp2 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.89+224T>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15093921 | |||||||
| chr16:15093936 | C | G | 1 | a0006c0017t0004g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.89+209G>C | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15093936 | |||||||
| chr16:15093947 | G | C | 189 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(186): Show |
298 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(295): Show |
intron_variant | MODIFIER | c.89+198C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15093947 | |||||||
| chr16:15094055 | G | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0011 others(143): Show |
234 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.89+90C>G | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15094055 | |||||||
| chr16:15094079 | C | T | 5 | a0001c0002t0001g0030 a0001c0002t0001g0059 a0001c0002t0001g0060 others(2): Show |
6 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.89+66G>A | RRN3 | ENSG00000085721.13 | transcript | ENST00000198767.11 | protein_coding | 1/17 | chr16 | 15094079 |