Variant report

Variant	rs72948656
Chromosome Location	chr2:114564473-114564474
allele	C/T
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	chr2:114563200-114565800	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr2:114563600-114564800	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr2:114563800-114564600	Enhancers	Fetal Intestine Small	intestine
4	chr2:114563800-114564600	Enhancers	Rectal Mucosa Donor 29	rectum
5	chr2:114563800-114564600	Enhancers	Sigmoid Colon	Sigmoid Colon
6	chr2:114563800-114564800	Enhancers	Fetal Intestine Large	intestine
7	chr2:114563800-114565400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr2:114564000-114564600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr2:114564000-114564800	Enhancers	Hela-S3	cervix
10	chr2:114564200-114564600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr2:114564200-114564600	Flanking Active TSS	A549	lung
12	chr2:114564200-114566400	Weak transcription	K562	blood
13	chr2:114564400-114564600	Enhancers	Small Intestine	intestine
14	chr2:114564400-114564800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr2:114564400-114564800	Enhancers	HepG2	liver

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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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