Variant report

Variant	rs13111327
Chromosome Location	chr4:47012036-47012037
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs13139021	0.87[EUR][1000 genomes]
rs13139768	0.94[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs35982616	0.96[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs3934674	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3934675	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:46997600-47013200	Weak transcription	Right Ventricle	heart
2	chr4:47010200-47012200	Weak transcription	Fetal Heart	heart
3	chr4:47011600-47013400	Enhancers	Stomach Mucosa	stomach
4	chr4:47011800-47012600	Enhancers	Primary T helper cells PMA-I stimulated	--
5	chr4:47011800-47012600	Enhancers	Primary T killer memory cells from peripheral blood	blood
6	chr4:47012000-47012400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
7	chr4:47012000-47012400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
8	chr4:47012000-47012600	Enhancers	Primary T helper naive cells from peripheral blood	blood
9	chr4:47012000-47012600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
10	chr4:47012000-47012800	Enhancers	Primary T helper cells fromperipheralblood	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

what's new

Quick links