Variant report

Variant	rs374913938
Chromosome Location	chr2:12155019-12155020
allele	G/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	nsv1003899	chr2:11789374-12248081	Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
2	nsv999704	chr2:12153766-12243960	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:12153600-12155600	Enhancers	HSMM	muscle
2	chr2:12153800-12155200	Enhancers	NHDF-Ad	bronchial
3	chr2:12153800-12155200	Enhancers	NHLF	lung
4	chr2:12153800-12155400	Enhancers	Muscle Satellite Cultured Cells	--
5	chr2:12153800-12155400	Enhancers	HSMMtube	muscle
6	chr2:12154000-12155200	Enhancers	Fetal Muscle Leg	muscle
7	chr2:12154000-12155400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr2:12154800-12156400	Weak transcription	Spleen	Spleen
9	chr2:12155000-12158600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr2:12155000-12158600	Weak transcription	Primary B cells from peripheral blood	blood
11	chr2:12155000-12159200	Weak transcription	Primary B cells from cord blood	blood
12	chr2:12155000-12164000	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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