Variant report

Variant	rs542983623
Chromosome Location	chr6:145392634-145392635
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016747	chr6:144917411-145599874	Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
2	nsv1022965	chr6:145374851-145635385	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1015500	chr6:145388558-145421503	Flanking Active TSS Enhancers Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv830834	chr6:145392073-145556294	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:145388000-145393000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr6:145388000-145393200	Enhancers	NHDF-Ad	bronchial
3	chr6:145388200-145393200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr6:145390600-145393000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr6:145390800-145392800	Enhancers	HSMMtube	muscle
6	chr6:145391000-145393000	Enhancers	Osteobl	bone
7	chr6:145391200-145393000	Enhancers	NHLF	lung
8	chr6:145391400-145393000	Enhancers	Muscle Satellite Cultured Cells	--
9	chr6:145391800-145392800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr6:145391800-145393000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr6:145391800-145393000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr6:145391800-145393000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr6:145391800-145393000	Enhancers	HSMM	muscle
14	chr6:145391800-145393000	Enhancers	NH-A	brain
15	chr6:145391800-145393000	Enhancers	NHEK	skin
16	chr6:145391800-145393200	Enhancers	HMEC	breast

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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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