Variant report

Variant	rs2270345
Chromosome Location	chr2:67795610-67795611
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

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	nsv534389	chr2:67388428-68225338	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
2	nsv962033	chr2:67794826-67798059	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67789800-67795800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr2:67790400-67798600	Weak transcription	Pancreas	Pancrea
3	chr2:67793600-67799400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr2:67793800-67799600	Weak transcription	Psoas Muscle	Psoas
5	chr2:67793800-67800400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr2:67793800-67803000	Weak transcription	Fetal Stomach	stomach
7	chr2:67794400-67798200	Weak transcription	Stomach Mucosa	stomach
8	chr2:67794400-67798600	Weak transcription	Left Ventricle	heart
9	chr2:67794400-67798600	Weak transcription	NHLF	lung
10	chr2:67794600-67796200	Enhancers	Hela-S3	cervix
11	chr2:67794600-67799000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr2:67794600-67799400	Weak transcription	HSMMtube	muscle
13	chr2:67794800-67799400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr2:67795200-67796000	Enhancers	Fetal Heart	heart
15	chr2:67795400-67798600	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr2:67795400-67799600	Weak transcription	NH-A	brain
17	chr2:67795600-67797800	Weak transcription	A549	lung
18	chr2:67795600-67799800	Weak transcription	Osteobl	bone
19	chr2:67795600-67802800	Weak transcription	Fetal Lung	lung

Quick Search:

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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