Variant report

Variant	rs2374050
Chromosome Location	chr12:103895177-103895178
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:103890400-103895800	Weak transcription	Thymus	Thymus
2	chr12:103893600-103897200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr12:103893600-103897200	Weak transcription	HMEC	breast
4	chr12:103893600-103897400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr12:103894000-103898000	Weak transcription	GM12878-XiMat	blood
6	chr12:103894200-103895200	Enhancers	Brain Germinal Matrix	brain
7	chr12:103894600-103895200	Weak transcription	Fetal Brain Female	brain
8	chr12:103894800-103896200	Enhancers	Fetal Brain Male	brain

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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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