Variant report

Variant	rs6748537
Chromosome Location	chr2:205343209-205343210
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs10181861	1.00[GIH][hapmap]
rs16836294	1.00[GIH][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv964353	chr2:205303005-205473935	Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	esv34706	chr2:205309211-205348724	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1012465	chr2:205335630-205349444	Enhancers Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv2756958	chr2:205342727-205348724	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	esv2759110	chr2:205342727-205348724	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:205337400-205344000	Weak transcription	K562	blood
2	chr2:205338200-205350400	Weak transcription	NHLF	lung
3	chr2:205340600-205344000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr2:205341400-205345200	Weak transcription	Fetal Kidney	kidney
5	chr2:205341400-205345800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr2:205341400-205348400	Weak transcription	HSMMtube	muscle
7	chr2:205341600-205344200	Weak transcription	Osteobl	bone
8	chr2:205341600-205351400	Weak transcription	Aorta	Aorta
9	chr2:205342400-205343600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr2:205342400-205344400	Weak transcription	NHDF-Ad	bronchial
11	chr2:205342400-205344600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr2:205342600-205343800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr2:205342600-205345400	Enhancers	NHEK	skin
14	chr2:205342800-205344200	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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