Variant report

Variant	rs62430867
Chromosome Location	chr6:143597941-143597942
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:143570800-143609200	Weak transcription	Fetal Intestine Large	intestine
2	chr6:143583400-143606000	Weak transcription	Fetal Intestine Small	intestine
3	chr6:143583800-143615400	Weak transcription	K562	blood
4	chr6:143589000-143607400	Weak transcription	Aorta	Aorta
5	chr6:143591400-143605200	Weak transcription	Liver	Liver
6	chr6:143592200-143605600	Weak transcription	Adipose Nuclei	Adipose
7	chr6:143593200-143606800	Weak transcription	NHEK	skin
8	chr6:143593400-143607000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr6:143595400-143605400	Weak transcription	HepG2	liver
10	chr6:143595600-143602800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:143597400-143598000	Enhancers	Primary hematopoietic stem cells	blood
12	chr6:143597400-143598200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr6:143597400-143598400	Enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr6:143597600-143598200	Enhancers	Primary monocytes fromperipheralblood	blood
15	chr6:143597600-143598200	Enhancers	Primary B cells from peripheral blood	blood
16	chr6:143597600-143598200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr6:143597800-143598000	Enhancers	GM12878-XiMat	blood

Quick Search:

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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