Variant report

Variant	rs7680972
Chromosome Location	chr4:100882127-100882128
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:100872600-100886000	Weak transcription	Primary T cells from cord blood	blood
2	chr4:100872600-100886000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr4:100872600-100886200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr4:100877400-100885400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr4:100880400-100889600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr4:100881200-100882800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:100881600-100883000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr4:100881800-100882600	Enhancers	Dnd41	blood
9	chr4:100881800-100882800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:100881800-100882800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr4:100882000-100882400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr4:100882000-100882600	Enhancers	NHEK	skin
13	chr4:100882000-100882600	Enhancers	Osteobl	bone
14	chr4:100882000-100883200	Enhancers	Muscle Satellite Cultured Cells	--

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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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