Variant report

Variant	rs56970966
Chromosome Location	chr3:42895869-42895870
allele	C/G
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	chr3:42890200-42897400	Strong transcription	Placenta	Placenta
2	chr3:42892400-42896000	Enhancers	K562	blood
3	chr3:42893400-42898400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr3:42893400-42906000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr3:42893600-42897600	Enhancers	Liver	Liver
6	chr3:42894200-42896800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr3:42894200-42896800	Weak transcription	Stomach Mucosa	stomach
8	chr3:42894400-42896800	Weak transcription	Fetal Intestine Large	intestine
9	chr3:42894800-42897000	Weak transcription	Primary B cells from peripheral blood	blood
10	chr3:42894800-42897400	Weak transcription	Primary B cells from cord blood	blood
11	chr3:42894800-42912800	Weak transcription	Right Atrium	heart
12	chr3:42895400-42896000	Enhancers	Skeletal Muscle Female	skeletal muscle
13	chr3:42895400-42896600	Weak transcription	Fetal Intestine Small	intestine
14	chr3:42895600-42896000	Flanking Active TSS	HepG2	liver
15	chr3:42895800-42896000	Enhancers	Aorta	Aorta
16	chr3:42895800-42896800	Weak transcription	Pancreas	Pancrea

Quick Search:

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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