Variant report

Variant	rs10850618
Chromosome Location	chr12:116789154-116789155
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 7 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:7)

rs_ID	r²[population]
rs10850619	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11068003	0.85[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs11068006	0.85[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs11068007	0.85[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs12230486	1.00[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12371905	0.85[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs57615867	0.89[EUR][1000 genomes]

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:116784400-116796600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr12:116784600-116795200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr12:116784800-116789600	Weak transcription	Fetal Muscle Leg	muscle
4	chr12:116787000-116791000	Weak transcription	Fetal Intestine Large	intestine
5	chr12:116787400-116790200	Weak transcription	Liver	Liver
6	chr12:116787400-116791200	Weak transcription	Duodenum Mucosa	Duodenum
7	chr12:116787400-116792200	Weak transcription	K562	blood
8	chr12:116787400-116796000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr12:116787400-116796600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr12:116788400-116792400	Weak transcription	Fetal Thymus	thymus
11	chr12:116788400-116792800	Weak transcription	A549	lung
12	chr12:116788400-116796600	Weak transcription	Placenta	Placenta

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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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