Variant report

Variant	rs10160911
Chromosome Location	chr12:117773403-117773404
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117771200-117773600	Enhancers	Lung	lung
2	chr12:117771200-117773800	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr12:117771400-117773600	Bivalent Enhancer	Fetal Stomach	stomach
4	chr12:117771400-117773600	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr12:117771600-117776600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr12:117771600-117776600	Weak transcription	A549	lung
7	chr12:117771600-117789000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr12:117771800-117776400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr12:117771800-117776600	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr12:117772000-117776000	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr12:117772200-117776600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr12:117772400-117774400	Enhancers	Psoas Muscle	Psoas
13	chr12:117772800-117773600	Enhancers	NHEK	skin
14	chr12:117773000-117773600	Bivalent Enhancer	Fetal Lung	lung
15	chr12:117773000-117773600	Enhancers	Pancreas	Pancrea
16	chr12:117773000-117773600	Enhancers	Spleen	Spleen
17	chr12:117773200-117779800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr12:117773400-117773800	Enhancers	Skeletal Muscle Female	skeletal muscle

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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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