Variant report

Variant	rs7303535
Chromosome Location	chr12:117311569-117311570
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs12303592	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12308184	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12310988	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12312336	1.00[EUR][1000 genomes]
rs12317933	1.00[AMR][1000 genomes]
rs16947036	1.00[EUR][1000 genomes]
rs16947049	1.00[EUR][1000 genomes]
rs56748568	1.00[EUR][1000 genomes]
rs57370760	1.00[EUR][1000 genomes]
rs58984530	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61306390	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73395528	1.00[EUR][1000 genomes]
rs73405130	1.00[EUR][1000 genomes]
rs7967445	1.00[AMR][1000 genomes]

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:117298400-117311800	Weak transcription	Right Atrium	heart
2	chr12:117300000-117314200	Weak transcription	Thymus	Thymus
3	chr12:117303000-117311600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr12:117303000-117312200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr12:117303000-117313600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr12:117306400-117312400	Weak transcription	Primary B cells from cord blood	blood
7	chr12:117311400-117312000	Enhancers	Fetal Thymus	thymus
8	chr12:117311400-117312000	Enhancers	Dnd41	blood

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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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