Variant report

Variant	rs146505700
Chromosome Location	chr14:38871077-38871078
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	nsv533235	chr14:38558180-39117391	Weak transcription Bivalent/Poised TSS Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv530640	chr14:38702117-38927901	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	esv2754119	chr14:38825349-38988849	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
4	esv1846932	chr14:38842788-38944821	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv510632	chr14:38868313-38939927	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv564409	chr14:38870456-38930054	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:38868600-38879800	Enhancers	Muscle Satellite Cultured Cells	--
2	chr14:38870000-38871800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr14:38870000-38876000	Enhancers	HUVEC	blood vessel
4	chr14:38870400-38871200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr14:38870400-38876200	Enhancers	NHLF	lung
6	chr14:38870800-38872600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr14:38870800-38875800	Enhancers	Hela-S3	cervix
8	chr14:38870800-38876600	Enhancers	NHDF-Ad	bronchial
9	chr14:38870800-38876800	Enhancers	HSMM	muscle
10	chr14:38871000-38871400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr14:38871000-38873200	Weak transcription	Fetal Lung	lung
12	chr14:38871000-38876400	Enhancers	HSMMtube	muscle

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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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