Variant report

Variant	rs13199416
Chromosome Location	chr6:12516759-12516760
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:12516000-12517000	Enhancers	Duodenum Mucosa	Duodenum
2	chr6:12516000-12517000	Enhancers	Fetal Intestine Small	intestine
3	chr6:12516200-12516800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr6:12516200-12516800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr6:12516200-12516800	Enhancers	Fetal Intestine Large	intestine
6	chr6:12516400-12516800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr6:12516400-12516800	Enhancers	Small Intestine	intestine
8	chr6:12516400-12516800	Enhancers	HSMM	muscle
9	chr6:12516400-12517000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr6:12516600-12516800	Flanking Active TSS	Right Atrium	heart
11	chr6:12516600-12516800	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chr6:12516600-12517000	Enhancers	Aorta	Aorta
13	chr6:12516600-12517000	Active TSS	A549	lung
14	chr6:12516600-12530200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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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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