Variant report

Variant	rs560445992
Chromosome Location	chr8:66811594-66811595
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3446467	chr8:66749863-67667068	Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	nsv1023239	chr8:66775321-66904124	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv3344263	chr8:66811573-66813646	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:66810600-66813400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr8:66810800-66811600	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr8:66810800-66811600	Enhancers	Stomach Mucosa	stomach
4	chr8:66810800-66813200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:66810800-66813400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr8:66811000-66811600	Enhancers	Duodenum Mucosa	Duodenum
7	chr8:66811000-66813200	Enhancers	HMEC	breast
8	chr8:66811200-66811600	Enhancers	Primary T cells fromperipheralblood	blood
9	chr8:66811200-66811600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr8:66811200-66811600	Enhancers	Esophagus	oesophagus
11	chr8:66811200-66811600	Enhancers	Fetal Intestine Small	intestine
12	chr8:66811200-66811800	Enhancers	Small Intestine	intestine
13	chr8:66811400-66811800	Flanking Active TSS	NHEK	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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