Variant report

Variant	rs73576660
Chromosome Location	chr6:143644803-143644804
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:143642600-143675600	Weak transcription	Left Ventricle	heart
2	chr6:143643000-143645600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr6:143643400-143645000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr6:143643800-143646200	Weak transcription	HSMM	muscle
5	chr6:143643800-143653600	Weak transcription	Ovary	ovary
6	chr6:143643800-143661200	Weak transcription	Aorta	Aorta
7	chr6:143644000-143645000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr6:143644000-143645000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr6:143644400-143645000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr6:143644400-143646000	Enhancers	Fetal Brain Male	brain
11	chr6:143644600-143645400	Enhancers	Liver	Liver
12	chr6:143644600-143648600	Enhancers	NHEK	skin
13	chr6:143644600-143650400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr6:143644800-143645000	Enhancers	Pancreas	Pancrea
15	chr6:143644800-143646000	Enhancers	Fetal Heart	heart
16	chr6:143644800-143652200	Enhancers	HMEC	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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