Variant report

Variant	rs7314768
Chromosome Location	chr12:10893159-10893160
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:10891600-10893400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
2	chr12:10891600-10893800	Enhancers	K562	blood
3	chr12:10892000-10893400	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr12:10892200-10893200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr12:10892200-10893400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr12:10892200-10893600	Enhancers	HMEC	breast
7	chr12:10892400-10893400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr12:10892600-10893800	Enhancers	GM12878-XiMat	blood
9	chr12:10892800-10895600	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr12:10892800-10895800	Enhancers	Primary monocytes fromperipheralblood	blood

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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