Variant report

Variant	rs10861216
Chromosome Location	chr12:104801819-104801820
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10735392	0.84[CEU][hapmap]
rs10735393	0.84[CEU][hapmap]
rs10745995	0.84[CEU][hapmap]
rs10745996	0.84[CEU][hapmap]
rs10778326	0.81[JPT][hapmap]
rs10861204	0.85[CEU][hapmap]
rs12425334	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12425523	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13377715	0.94[ASN][1000 genomes]
rs17035504	1.00[CEU][hapmap];0.94[CHB][hapmap];0.93[JPT][hapmap];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs17035521	0.86[EUR][1000 genomes]
rs17202862	0.92[CEU][hapmap]
rs1922264	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4246269	0.85[CEU][hapmap]
rs4246271	0.85[CEU][hapmap]
rs4403872	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4630362	0.92[CEU][hapmap]
rs4964288	0.84[CEU][hapmap]
rs4964752	0.84[CEU][hapmap]
rs4964761	0.84[CEU][hapmap]
rs4964779	0.84[CEU][hapmap]
rs4964789	0.82[ASN][1000 genomes]
rs56831540	0.86[ASN][1000 genomes]
rs57710522	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs57954752	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs59348790	0.90[ASN][1000 genomes]
rs60394569	0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6539137	0.82[CEU][hapmap]
rs7294997	0.81[CEU][hapmap]
rs73183716	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs73183722	0.83[EUR][1000 genomes]
rs73183723	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7486552	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7962423	0.85[CEU][hapmap]
rs9739833	0.85[CEU][hapmap]

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	nsv899494	chr12:104561521-104806232	Flanking Active TSS Weak transcription Genic enhancers Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:104800800-104802200	Enhancers	Hela-S3	cervix
2	chr12:104800800-104803600	Enhancers	HUVEC	blood vessel
3	chr12:104801000-104802200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr12:104801200-104803600	Enhancers	Fetal Heart	heart
5	chr12:104801200-104804600	Enhancers	Pancreas	Pancrea
6	chr12:104801400-104803000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr12:104801600-104803800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr12:104801800-104802000	Enhancers	Small Intestine	intestine
9	chr12:104801800-104802200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr12:104801800-104802200	Flanking Active TSS	Duodenum Mucosa	Duodenum
11	chr12:104801800-104802200	Enhancers	Fetal Intestine Large	intestine
12	chr12:104801800-104802400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr12:104801800-104802400	Flanking Active TSS	A549	lung
14	chr12:104801800-104802800	Enhancers	Gastric	stomach
15	chr12:104801800-104802800	Enhancers	Ovary	ovary
16	chr12:104801800-104803000	Enhancers	Fetal Thymus	thymus
17	chr12:104801800-104803200	Enhancers	Fetal Intestine Small	intestine
18	chr12:104801800-104803600	Enhancers	Placenta	Placenta
19	chr12:104801800-104803600	Enhancers	K562	blood

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