Variant report

Variant	rs73750639
Chromosome Location	chr6:82442191-82442192
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 3 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs11969483	1.00[AMR][1000 genomes]
rs56281911	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1017529	chr6:82411355-82442277	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:82422800-82451800	Weak transcription	Aorta	Aorta
2	chr6:82432800-82442600	Weak transcription	Left Ventricle	heart
3	chr6:82437800-82459400	Weak transcription	Pancreas	Pancrea
4	chr6:82441200-82442200	Enhancers	Right Ventricle	heart
5	chr6:82441200-82442600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr6:82441200-82442800	Enhancers	Right Atrium	heart
7	chr6:82441600-82442400	Enhancers	Pancreatic Islets	Pancreatic Islet
8	chr6:82441800-82442600	Weak transcription	Psoas Muscle	Psoas
9	chr6:82442000-82442800	Enhancers	Fetal Heart	heart
10	chr6:82442000-82445400	Weak transcription	NHDF-Ad	bronchial
11	chr6:82442000-82449600	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr6:82442000-82455000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr6:82442000-82456200	Weak transcription	Small Intestine	intestine

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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