Variant report

Variant	rs16893393
Chromosome Location	chr6:82445150-82445151
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82422800-82451800	Weak transcription	Aorta	Aorta
2	chr6:82437800-82459400	Weak transcription	Pancreas	Pancrea
3	chr6:82442000-82445400	Weak transcription	NHDF-Ad	bronchial
4	chr6:82442000-82449600	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr6:82442000-82455000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr6:82442000-82456200	Weak transcription	Small Intestine	intestine
7	chr6:82442600-82454400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr6:82442800-82447600	Weak transcription	Right Ventricle	heart
9	chr6:82443200-82449600	Weak transcription	Left Ventricle	heart
10	chr6:82444200-82445400	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr6:82444600-82446200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr6:82444600-82446200	Enhancers	HMEC	breast
13	chr6:82444800-82446400	Enhancers	Placenta	Placenta
14	chr6:82444800-82455600	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr6:82445000-82445400	Weak transcription	NHEK	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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