Variant report

Variant	rs17101804
Chromosome Location	chr10:89599749-89599750
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:89592800-89603200	Weak transcription	Aorta	Aorta
2	chr10:89593400-89600800	Weak transcription	A549	lung
3	chr10:89597400-89600800	Weak transcription	Hela-S3	cervix
4	chr10:89597800-89600200	Weak transcription	Fetal Intestine Large	intestine
5	chr10:89597800-89602200	Weak transcription	GM12878-XiMat	blood
6	chr10:89597800-89603000	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr10:89597800-89604000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr10:89599000-89599800	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr10:89599400-89601000	Weak transcription	Stomach Mucosa	stomach
10	chr10:89599400-89601600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr10:89599600-89600400	Weak transcription	Fetal Intestine Small	intestine

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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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