Variant report

Variant	rs931765
Chromosome Location	chr8:49387578-49387579
allele	A/G
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	chr8:49380200-49390400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr8:49384600-49387600	Weak transcription	Fetal Muscle Trunk	muscle
3	chr8:49385800-49387800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr8:49386600-49387800	Enhancers	Fetal Intestine Large	intestine
5	chr8:49386800-49387600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr8:49386800-49387600	Weak transcription	Fetal Muscle Leg	muscle
7	chr8:49386800-49390200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:49386800-49390800	Weak transcription	NHLF	lung
9	chr8:49386800-49391400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr8:49386800-49394600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr8:49387000-49388200	Weak transcription	Osteobl	bone
12	chr8:49387000-49388400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr8:49387000-49388600	Weak transcription	NHDF-Ad	bronchial
14	chr8:49387000-49390200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	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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