Variant report

Variant	rs58207285
Chromosome Location	chr6:107185091-107185092
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:107179800-107197600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:107180600-107187000	Weak transcription	Stomach Mucosa	stomach
3	chr6:107183200-107185400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr6:107184000-107188400	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr6:107184200-107185200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:107184200-107185200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr6:107184200-107185600	Enhancers	NHEK	skin
8	chr6:107184200-107185800	Enhancers	Placenta	Placenta
9	chr6:107184200-107186400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr6:107184200-107186800	Weak transcription	Primary B cells from cord blood	blood
11	chr6:107184200-107187200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr6:107184200-107188400	Enhancers	HMEC	breast
13	chr6:107184800-107187000	Weak transcription	Primary B cells from peripheral blood	blood
14	chr6:107184800-107187000	Weak transcription	Liver	Liver
15	chr6:107185000-107188200	Weak transcription	Pancreas	Pancrea

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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