Variant report

Variant	rs73692987
Chromosome Location	chr8:94987299-94987300
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:94706032..94706941-chr8:94987049..94988013,6	MCF-7	breast:
2	chr8:94834234..94835361-chr8:94986945..94988056,10	MCF-7	breast:
3	chr8:94967615..94969465-chr8:94986791..94988525,2	MCF-7	breast:
4	chr8:94928011..94930237-chr8:94986282..94987918,2	MCF-7	breast:
5	chr8:94834485..94835366-chr8:94987131..94988250,3	MCF-7	breast:
6	chr8:94577380..94578327-chr8:94987091..94988044,4	MCF-7	breast:
7	chr8:94706225..94706994-chr8:94987102..94988018,5	K562	blood:
8	chr8:94834240..94835236-chr8:94986891..94987651,6	K562	blood:
9	chr8:94705840..94710154-chr8:94987193..94989140,3	MCF-7	breast:

No data

No data

No data

Extended variants
information (count: 3 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11997831	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754970	chr8:94675324-94991724	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
2	nsv518975	chr8:94985722-94992958	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:94986600-94987400	Enhancers	Fetal Intestine Small	intestine
2	chr8:94986800-94987400	Enhancers	Fetal Intestine Large	intestine
3	chr8:94987000-94987800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
4	chr8:94987200-94987600	Enhancers	Primary T regulatory cells fromperipheralblood	blood

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

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