Variant report

Variant	rs73863341
Chromosome Location	chr3:101267749-101267750
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:101263600-101268000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr3:101263800-101267800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr3:101263800-101267800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
4	chr3:101266600-101267800	Enhancers	HepG2	liver
5	chr3:101267200-101268400	Enhancers	Fetal Intestine Small	intestine
6	chr3:101267400-101268400	Enhancers	K562	blood
7	chr3:101267600-101268400	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr3:101267600-101268400	Enhancers	Primary T cells from cord blood	blood

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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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