Variant report

Variant	rs61774767
Chromosome Location	chr1:56159210-56159211
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:56135800-56162000	Weak transcription	Aorta	Aorta
2	chr1:56155800-56160000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr1:56156400-56159800	Weak transcription	Osteobl	bone
4	chr1:56156400-56160400	Weak transcription	Spleen	Spleen
5	chr1:56156600-56159800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr1:56156600-56160400	Weak transcription	Adipose Nuclei	Adipose
7	chr1:56156800-56159600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr1:56156800-56159600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr1:56158400-56170800	Enhancers	NHDF-Ad	bronchial
10	chr1:56159000-56159400	Enhancers	Fetal Heart	heart
11	chr1:56159000-56162800	Enhancers	Fetal Muscle Leg	muscle
12	chr1:56159200-56161200	Enhancers	Fetal Intestine Large	intestine
13	chr1:56159200-56162200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr1:56159200-56163800	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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