Variant report

Variant	rs2248343
Chromosome Location	chr12:104820932-104820933
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	chr12:104808800-104824200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr12:104816200-104824000	Weak transcription	Aorta	Aorta
3	chr12:104820200-104821400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr12:104820200-104821800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
5	chr12:104820200-104821800	Enhancers	HMEC	breast
6	chr12:104820400-104821400	Enhancers	HSMMtube	muscle
7	chr12:104820400-104821600	Enhancers	NHEK	skin
8	chr12:104820600-104821200	Enhancers	NH-A	brain
9	chr12:104820600-104821200	Enhancers	NHLF	lung
10	chr12:104820600-104821400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr12:104820800-104821000	Enhancers	GM12878-XiMat	blood
12	chr12:104820800-104821200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr12:104820800-104821200	Enhancers	NHDF-Ad	bronchial
14	chr12:104820800-104821600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	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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