Variant report

Variant	rs528721176
Chromosome Location	chr2:205539369-205539370
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 6 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv998485	chr2:205407813-206184006	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv536122	chr2:205407813-206184006	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv875722	chr2:205462099-205572718	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv875723	chr2:205489653-205612846	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1010210	chr2:205489653-206076013	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv584243	chr2:205539092-205630618	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:205520800-205542800	Weak transcription	Psoas Muscle	Psoas
2	chr2:205521000-205546200	Weak transcription	Aorta	Aorta
3	chr2:205528000-205546200	Weak transcription	Pancreas	Pancrea
4	chr2:205531200-205545200	Weak transcription	Rectal Smooth Muscle	rectum
5	chr2:205532200-205539800	Enhancers	HUVEC	blood vessel
6	chr2:205535200-205545200	Weak transcription	Colon Smooth Muscle	Colon
7	chr2:205535400-205542200	Weak transcription	HSMMtube	muscle
8	chr2:205535400-205545600	Weak transcription	Fetal Lung	lung
9	chr2:205537400-205539800	Genic enhancers	HSMM	muscle
10	chr2:205538000-205539400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr2:205538000-205539400	Enhancers	NHEK	skin
12	chr2:205538000-205539600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr2:205538200-205539400	Enhancers	Muscle Satellite Cultured Cells	--
14	chr2:205538200-205539400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr2:205538200-205539400	Enhancers	NH-A	brain
16	chr2:205538200-205539400	Enhancers	Osteobl	bone
17	chr2:205538400-205539600	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr2:205539200-205543600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	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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