Variant report

Variant	rs11756772
Chromosome Location	chr6:33532820-33532821
allele	C/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	chr6:33516800-33537600	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr6:33521200-33533800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr6:33530400-33533000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr6:33530400-33534400	Weak transcription	HMEC	breast
5	chr6:33530400-33534600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:33530400-33536800	Weak transcription	K562	blood
7	chr6:33530400-33537600	Weak transcription	GM12878-XiMat	blood
8	chr6:33530400-33538800	Weak transcription	Esophagus	oesophagus
9	chr6:33531000-33538200	Weak transcription	Primary T cells from cord blood	blood
10	chr6:33531400-33538400	Weak transcription	Osteobl	bone
11	chr6:33532200-33533000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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