Variant report

Variant	rs7665261
Chromosome Location	chr4:26464043-26464044
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:26458000-26466000	Enhancers	Fetal Stomach	stomach
2	chr4:26460200-26464800	Weak transcription	HSMMtube	muscle
3	chr4:26461400-26465400	Weak transcription	HepG2	liver
4	chr4:26461800-26465800	Weak transcription	Fetal Thymus	thymus
5	chr4:26462000-26464200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr4:26462000-26464200	Weak transcription	Stomach Smooth Muscle	stomach
7	chr4:26462200-26464200	Weak transcription	Osteobl	bone
8	chr4:26462600-26464200	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr4:26463400-26464200	Enhancers	Rectal Smooth Muscle	rectum
10	chr4:26463600-26465000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr4:26463600-26465000	Enhancers	Fetal Muscle Leg	muscle
12	chr4:26463600-26465600	Enhancers	Colon Smooth Muscle	Colon
13	chr4:26464000-26464400	Enhancers	Pancreas	Pancrea

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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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