Variant report

Variant	rs73708258
Chromosome Location	chr8:129960908-129960909
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:129959000-129964000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr8:129959200-129961200	Genic enhancers	Dnd41	blood
3	chr8:129960000-129965200	Weak transcription	Fetal Muscle Leg	muscle
4	chr8:129960600-129963000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr8:129960600-129963000	Enhancers	HMEC	breast
6	chr8:129960600-129963200	Enhancers	HSMM	muscle
7	chr8:129960800-129961200	Enhancers	Monocytes-CD14+_RO01746	blood
8	chr8:129960800-129961400	Enhancers	Muscle Satellite Cultured Cells	--
9	chr8:129960800-129961400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr8:129960800-129961600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr8:129960800-129963200	Enhancers	NHDF-Ad	bronchial

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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