Variant report

Variant	rs61687461
Chromosome Location	chr22:31545771-31545772
allele	A/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	chr22:31544600-31546200	Enhancers	Placenta Amnion	Placenta Amnion
2	chr22:31544800-31545800	Enhancers	HepG2	liver
3	chr22:31544800-31546800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr22:31545200-31551000	Weak transcription	Fetal Muscle Leg	muscle
5	chr22:31545200-31555400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr22:31545200-31555600	Weak transcription	Fetal Intestine Small	intestine
7	chr22:31545400-31546600	Weak transcription	Adipose Nuclei	Adipose
8	chr22:31545400-31546600	Weak transcription	Osteobl	bone
9	chr22:31545400-31549600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr22:31545400-31549800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr22:31545400-31550800	Weak transcription	Ovary	ovary
12	chr22:31545400-31551000	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr22:31545400-31551000	Weak transcription	Skeletal Muscle Female	skeletal muscle
14	chr22:31545600-31550800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr22:31545600-31551000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr22:31545600-31551000	Weak transcription	Colon Smooth Muscle	Colon

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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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