Variant report
Variant | rs6823295 |
---|---|
Chromosome Location | chr4:119050498-119050499 |
allele | C/G |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:0)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
No data |
No data |
No data |
No data |
No data |
rs_ID | r2[population] |
---|---|
rs10008049 | 1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10014096 | 1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs10015232 | 1.00[ASN][1000 genomes] |
rs10016285 | 0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs10020473 | 0.91[ASN][1000 genomes] |
rs10021128 | 0.91[ASN][1000 genomes] |
rs10021781 | 1.00[ASN][1000 genomes] |
rs10023699 | 1.00[ASN][1000 genomes] |
rs10026541 | 0.96[ASN][1000 genomes] |
rs10027013 | 0.87[ASN][1000 genomes] |
rs10027893 | 0.91[ASN][1000 genomes] |
rs10033308 | 0.96[ASN][1000 genomes] |
rs10033412 | 0.98[ASN][1000 genomes] |
rs10440400 | 1.00[ASN][1000 genomes] |
rs11098422 | 0.91[ASN][1000 genomes] |
rs11098424 | 0.95[ASN][1000 genomes] |
rs11098425 | 0.95[ASN][1000 genomes] |
rs11098427 | 0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11098428 | 0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs11722962 | 0.91[ASN][1000 genomes] |
rs11728724 | 0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes] |
rs11730541 | 0.96[ASN][1000 genomes] |
rs11733562 | 0.91[ASN][1000 genomes] |
rs11736688 | 0.96[ASN][1000 genomes] |
rs11937777 | 0.98[ASN][1000 genomes] |
rs11947071 | 0.98[ASN][1000 genomes] |
rs12499751 | 0.91[ASN][1000 genomes] |
rs12505156 | 0.95[ASN][1000 genomes] |
rs12508017 | 0.98[ASN][1000 genomes] |
rs12711064 | 1.00[ASN][1000 genomes] |
rs13104129 | 0.91[ASN][1000 genomes] |
rs13111697 | 1.00[ASN][1000 genomes] |
rs13114621 | 0.98[ASN][1000 genomes] |
rs13114895 | 0.98[ASN][1000 genomes] |
rs13125397 | 0.84[ASN][1000 genomes] |
rs13126882 | 0.96[ASN][1000 genomes] |
rs13127321 | 0.96[ASN][1000 genomes] |
rs13134901 | 0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs13135646 | 0.89[ASN][1000 genomes] |
rs13139875 | 0.91[ASN][1000 genomes] |
rs1319938 | 0.98[ASN][1000 genomes] |
rs1994384 | 0.91[ASN][1000 genomes] |
rs2049362 | 0.95[ASN][1000 genomes] |
rs2140475 | 0.93[ASN][1000 genomes] |
rs2389510 | 0.84[CHB][hapmap];0.91[ASN][1000 genomes] |
rs2389511 | 0.91[ASN][1000 genomes] |
rs2389512 | 0.91[ASN][1000 genomes] |
rs2389513 | 0.95[ASN][1000 genomes] |
rs2389514 | 0.95[ASN][1000 genomes] |
rs2389515 | 0.95[ASN][1000 genomes] |
rs2389516 | 0.95[ASN][1000 genomes] |
rs2389517 | 0.95[ASN][1000 genomes] |
rs2389518 | 0.95[ASN][1000 genomes] |
rs2389519 | 0.95[ASN][1000 genomes] |
rs2389520 | 0.96[ASN][1000 genomes] |
rs2389521 | 0.94[ASN][1000 genomes] |
rs2389522 | 0.96[ASN][1000 genomes] |
rs2389523 | 0.96[ASN][1000 genomes] |
rs2389524 | 0.96[ASN][1000 genomes] |
rs2389525 | 0.98[ASN][1000 genomes] |
rs2389526 | 0.98[ASN][1000 genomes] |
rs2389527 | 0.98[ASN][1000 genomes] |
rs2892787 | 0.91[ASN][1000 genomes] |
rs2892788 | 0.96[ASN][1000 genomes] |
rs2892789 | 0.96[ASN][1000 genomes] |
rs2892790 | 0.96[ASN][1000 genomes] |
rs2892791 | 0.98[ASN][1000 genomes] |
rs2892799 | 0.94[ASN][1000 genomes] |
rs4131600 | 0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4240316 | 0.98[ASN][1000 genomes] |
rs4240317 | 0.98[ASN][1000 genomes] |
rs4240318 | 0.98[ASN][1000 genomes] |
rs4280816 | 0.98[ASN][1000 genomes] |
rs4362895 | 0.83[ASN][1000 genomes] |
rs4397073 | 0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4437319 | 0.91[ASN][1000 genomes] |
rs4452509 | 0.98[ASN][1000 genomes] |
rs4546313 | 0.90[ASN][1000 genomes] |
rs4558930 | 0.89[ASN][1000 genomes] |
rs4566725 | 0.98[ASN][1000 genomes] |
rs4569819 | 0.98[ASN][1000 genomes] |
rs4576085 | 0.98[ASN][1000 genomes] |
rs4616829 | 0.98[ASN][1000 genomes] |
rs4833560 | 1.00[ASN][1000 genomes] |
rs4833561 | 1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4833563 | 1.00[ASN][1000 genomes] |
rs4833566 | 0.92[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes] |
rs4833567 | 0.90[ASN][1000 genomes] |
rs4834656 | 0.91[ASN][1000 genomes] |
rs4834657 | 0.98[ASN][1000 genomes] |
rs4834658 | 0.85[ASN][1000 genomes] |
rs4834660 | 0.82[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4834661 | 1.00[ASN][1000 genomes] |
rs4834664 | 0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4834665 | 0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs4834666 | 0.96[ASN][1000 genomes] |
rs581739 | 0.89[ASN][1000 genomes] |
rs582448 | 1.00[JPT][hapmap];0.88[ASN][1000 genomes] |
rs586073 | 0.80[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes] |
rs586224 | 1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs593966 | 0.89[ASN][1000 genomes] |
rs597881 | 0.89[ASN][1000 genomes] |
rs607961 | 0.90[ASN][1000 genomes] |
rs608228 | 0.88[ASN][1000 genomes] |
rs610222 | 0.87[ASN][1000 genomes] |
rs613083 | 1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes] |
rs613443 | 0.89[ASN][1000 genomes] |
rs615165 | 0.82[ASN][1000 genomes] |
rs615837 | 0.87[ASN][1000 genomes] |
rs617140 | 0.85[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes] |
rs62328865 | 0.89[ASN][1000 genomes] |
rs62328871 | 0.88[ASN][1000 genomes] |
rs625546 | 0.87[ASN][1000 genomes] |
rs627249 | 0.80[CEU][hapmap];0.84[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes] |
rs641962 | 0.89[ASN][1000 genomes] |
rs644797 | 0.84[ASN][1000 genomes] |
rs6534082 | 0.96[ASN][1000 genomes] |
rs662086 | 0.89[ASN][1000 genomes] |
rs674514 | 0.87[ASN][1000 genomes] |
rs678177 | 0.90[ASN][1000 genomes] |
rs6820061 | 0.98[ASN][1000 genomes] |
rs6820108 | 0.95[ASN][1000 genomes] |
rs6823125 | 0.82[AFR][1000 genomes];0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs6825105 | 0.98[ASN][1000 genomes] |
rs6828552 | 1.00[ASN][1000 genomes] |
rs6837896 | 0.95[ASN][1000 genomes] |
rs6842393 | 0.98[ASN][1000 genomes] |
rs6842719 | 0.81[ASN][1000 genomes] |
rs6848037 | 0.98[ASN][1000 genomes] |
rs6848598 | 0.98[ASN][1000 genomes] |
rs6851494 | 0.99[ASN][1000 genomes] |
rs6857041 | 1.00[ASN][1000 genomes] |
rs6857232 | 1.00[ASN][1000 genomes] |
rs705838 | 0.85[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes] |
rs705841 | 0.81[ASN][1000 genomes] |
rs7435948 | 1.00[ASN][1000 genomes] |
rs7439663 | 0.98[ASN][1000 genomes] |
rs7655439 | 0.96[ASN][1000 genomes] |
rs7655519 | 0.96[ASN][1000 genomes] |
rs7671232 | 0.98[ASN][1000 genomes] |
rs7671359 | 0.98[ASN][1000 genomes] |
rs7671434 | 0.96[ASN][1000 genomes] |
rs7671515 | 0.98[ASN][1000 genomes] |
rs7671562 | 0.98[ASN][1000 genomes] |
rs7677274 | 0.91[ASN][1000 genomes] |
rs7679658 | 0.98[ASN][1000 genomes] |
rs7681830 | 0.95[ASN][1000 genomes] |
rs7685325 | 0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |
rs7686670 | 0.93[ASN][1000 genomes] |
rs7695706 | 0.98[ASN][1000 genomes] |
rs7699653 | 0.88[ASN][1000 genomes] |
rs788647 | 0.92[JPT][hapmap];0.83[ASN][1000 genomes] |
rs788650 | 0.85[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes] |
rs788651 | 0.91[JPT][hapmap];0.83[ASN][1000 genomes] |
rs788655 | 0.85[CHB][hapmap];1.00[JPT][hapmap];0.83[ASN][1000 genomes] |
rs788658 | 0.81[ASN][1000 genomes] |
rs788661 | 0.88[ASN][1000 genomes] |
rs788662 | 0.92[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes] |
rs788668 | 0.85[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes] |
rs9307452 | 1.00[ASN][1000 genomes] |
rs9637622 | 0.98[ASN][1000 genomes] |
rs9637623 | 0.98[ASN][1000 genomes] |
rs9790637 | 0.98[ASN][1000 genomes] |
rs9995675 | 0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv519017 | chr4:118828807-119771481 | Strong transcription Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 39 gene(s) | inside rSNPs | diseases |
2 | nsv1009076 | chr4:118949490-119269424 | Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
3 | nsv1001236 | chr4:118949490-119271243 | Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 22 gene(s) | inside rSNPs | diseases |
4 | nsv1008236 | chr4:118989467-119154024 | ZNF genes & repeats Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
5 | nsv999152 | chr4:119001143-119138322 | Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
6 | esv34038 | chr4:119035124-119455391 | Enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA target site | 23 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr4:119041600-119053000 | Weak transcription | H1 BMP4 Derived Trophoblast Cultured Cells | ES cell derived |
2 | chr4:119050200-119052200 | ZNF genes & repeats | Dnd41 | blood |