Variant report
Variant | rs10919300 |
---|---|
Chromosome Location | chr1:170068509-170068510 |
allele | A/C |
Outlinks | Ensembl   UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:2)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
No data |
No data |
(count:2 , 50 per page) page:
1
No data |
No data |
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rs_ID | r2[population] |
---|---|
rs10919276 | 1.00[EUR][1000 genomes] |
rs10919288 | 1.00[EUR][1000 genomes] |
rs10919294 | 1.00[ASW][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs10919295 | 1.00[EUR][1000 genomes] |
rs10919296 | 1.00[EUR][1000 genomes] |
rs10919308 | 1.00[EUR][1000 genomes] |
rs12025296 | 1.00[EUR][1000 genomes] |
rs12061373 | 1.00[EUR][1000 genomes] |
rs12061626 | 1.00[EUR][1000 genomes] |
rs12066551 | 1.00[EUR][1000 genomes] |
rs12071325 | 1.00[EUR][1000 genomes] |
rs12073288 | 1.00[EUR][1000 genomes] |
rs12075569 | 1.00[EUR][1000 genomes] |
rs12076018 | 1.00[EUR][1000 genomes] |
rs12077685 | 1.00[EUR][1000 genomes] |
rs12077708 | 1.00[EUR][1000 genomes] |
rs12079608 | 1.00[EUR][1000 genomes] |
rs12087450 | 1.00[EUR][1000 genomes] |
rs12088186 | 1.00[EUR][1000 genomes] |
rs12090220 | 1.00[EUR][1000 genomes] |
rs12091389 | 1.00[EUR][1000 genomes] |
rs12095784 | 1.00[ASW][hapmap];1.00[EUR][1000 genomes] |
rs16862886 | 1.00[EUR][1000 genomes] |
rs16862978 | 1.00[EUR][1000 genomes] |
rs2103641 | 1.00[EUR][1000 genomes] |
rs2779706 | 1.00[MEX][hapmap] |
rs2806492 | 1.00[MEX][hapmap] |
rs2901261 | 1.00[TSI][hapmap];1.00[EUR][1000 genomes] |
rs4279900 | 1.00[EUR][1000 genomes] |
rs57038529 | 1.00[EUR][1000 genomes] |
rs73023529 | 1.00[EUR][1000 genomes] |
rs73023593 | 1.00[EUR][1000 genomes] |
rs73041148 | 1.00[EUR][1000 genomes] |
rs73041149 | 1.00[EUR][1000 genomes] |
rs74122312 | 1.00[EUR][1000 genomes] |
rs74122421 | 1.00[EUR][1000 genomes] |
rs74122422 | 1.00[EUR][1000 genomes] |
rs74122452 | 1.00[EUR][1000 genomes] |
rs989054 | 1.00[TSI][hapmap];1.00[EUR][1000 genomes] |

No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
---|---|---|---|---|---|---|---|
1 | nsv1014033 | chr1:169968488-170453021 | Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 18 gene(s) | inside rSNPs | diseases |
2 | nsv535200 | chr1:169968488-170453021 | Weak transcription Flanking Active TSS Strong transcription Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 18 gene(s) | inside rSNPs | diseases |
3 | nsv999310 | chr1:170065943-170223350 | Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 8 gene(s) | inside rSNPs | diseases |
No data |
No. | Chromosome Location | Chromatin state | Cell line | Tissue |
---|---|---|---|---|
1 | chr1:170068200-170068600 | Enhancers | HUES48 Cell Line | embryonic stem cell |