Variant report

Variant	rs72788909
Chromosome Location	chr2:20571202-20571203
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:20565200-20578400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:20565800-20575200	Weak transcription	NH-A	brain
3	chr2:20569000-20571800	Enhancers	NHEK	skin
4	chr2:20569600-20574200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr2:20569800-20571400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr2:20570200-20574800	Weak transcription	Placenta	Placenta
7	chr2:20570200-20578600	Weak transcription	Ovary	ovary
8	chr2:20570400-20571400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr2:20570800-20571800	Weak transcription	Fetal Brain Male	brain
10	chr2:20571000-20571600	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
11	chr2:20571000-20571600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr2:20571000-20571800	Enhancers	Fetal Stomach	stomach
13	chr2:20571200-20571600	Active TSS	Fetal Lung	lung
14	chr2:20571200-20571600	Active TSS	NHLF	lung
15	chr2:20571200-20571800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr2:20571200-20571800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr2:20571200-20571800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr2:20571200-20571800	Flanking Active TSS	Fetal Brain Female	brain
19	chr2:20571200-20571800	Enhancers	Fetal Muscle Leg	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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