Variant report

Variant	rs74096144
Chromosome Location	chr1:85254835-85254836
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85241000-85263600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr1:85251200-85261600	Weak transcription	Right Atrium	heart
3	chr1:85251400-85255000	Weak transcription	NHEK	skin
4	chr1:85251800-85263400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr1:85254600-85255000	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr1:85254600-85255000	Enhancers	Placenta	Placenta
7	chr1:85254800-85255000	Enhancers	Fetal Intestine Large	intestine
8	chr1:85254800-85255200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr1:85254800-85255600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr1:85254800-85255600	Enhancers	HMEC	breast
11	chr1:85254800-85255800	Enhancers	Breast Myoepithelial Primary Cells	Breast

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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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