Variant report

Variant	rs71237210
Chromosome Location	chr8:52367693-52367694
allele	-/AAAAAAAAAAAAAAAA
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932026	chr8:51858658-52758574	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv948338	chr8:52060314-52368754	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv890895	chr8:52190571-52615191	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv817615	chr8:52252405-53023384	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	esv2496359	chr8:52366867-52368305	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
6	esv2236053	chr8:52367315-52367896	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
7	esv3498094	chr8:52367414-52367798	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
8	esv3498093	chr8:52367428-52367772	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
9	esv3498091	chr8:52367431-52367727	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
10	esv3479215	chr8:52367436-52367769	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
11	esv3498090	chr8:52367449-52367746	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
12	esv3479216	chr8:52367451-52367719	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
13	esv3479217	chr8:52367487-52367699	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
14	esv3498092	chr8:52367496-52367714	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
15	esv3479218	chr8:52367503-52367707	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
16	esv3498095	chr8:52367503-52367707	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:52355400-52374000	Weak transcription	Right Ventricle	heart
2	chr8:52356800-52396200	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr8:52365800-52369200	Enhancers	Primary B cells from peripheral blood	blood
4	chr8:52366200-52374000	Weak transcription	Right Atrium	heart
5	chr8:52366400-52374000	Weak transcription	Left Ventricle	heart
6	chr8:52367000-52367800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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