Variant report

Variant	rs73688489
Chromosome Location	chr8:85270131-85270132
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs7823245	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831374	chr8:85103604-85308976	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	esv2764062	chr8:85251665-85270692	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
3	nsv6281	chr8:85256650-85271875	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
4	nsv437075	chr8:85257540-85271329	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
5	nsv437076	chr8:85257540-85271644	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
6	nsv1026499	chr8:85257555-85270837	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
7	nsv1030318	chr8:85257555-85271329	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
8	esv1806721	chr8:85257984-85274061	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
9	esv3358179	chr8:85259847-85270795	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
10	esv3335073	chr8:85260297-85270145	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
11	nsv611657	chr8:85261157-85271329	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
12	nsv611658	chr8:85261157-85272419	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
13	esv1794533	chr8:85261383-85270257	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
14	esv1820118	chr8:85261383-85270257	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
15	esv1832616	chr8:85261383-85270257	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
16	esv1847459	chr8:85261383-85270257	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
17	esv2761218	chr8:85262883-85270945	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
18	esv3388861	chr8:85269047-85271245	Weak transcription	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:85267200-85272200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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