Variant report

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10868005	1.00[CEU][hapmap];0.86[YRI][hapmap];0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10868006	1.00[CEU][hapmap];0.86[YRI][hapmap];0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11140078	1.00[CEU][hapmap];0.86[YRI][hapmap];0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11140082	1.00[CEU][hapmap];0.92[YRI][hapmap];0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11140083	1.00[CEU][hapmap];0.92[YRI][hapmap];0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4537377	1.00[CEU][hapmap];0.86[YRI][hapmap];0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4636280	1.00[CEU][hapmap];0.92[YRI][hapmap];0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7023220	0.84[YRI][hapmap];0.91[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs8181122	0.84[YRI][hapmap];0.93[AFR][1000 genomes];0.82[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1046491	chr9:85861492-86063992	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv893512	chr9:86022215-86323309	Flanking Active TSS Bivalent Enhancer Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:23 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:86013400-86041000	Weak transcription	Aorta	Aorta
2	chr9:86021200-86041600	Weak transcription	Right Ventricle	heart
3	chr9:86034600-86039000	Weak transcription	Right Atrium	heart
4	chr9:86035400-86041400	Weak transcription	Psoas Muscle	Psoas
5	chr9:86036800-86041200	Weak transcription	Primary neutrophils fromperipheralblood	blood
6	chr9:86037200-86039200	Enhancers	HepG2	liver
7	chr9:86037400-86039000	Enhancers	Ovary	ovary
8	chr9:86037600-86041000	Weak transcription	Adipose Nuclei	Adipose
9	chr9:86037800-86047200	Weak transcription	Fetal Stomach	stomach
10	chr9:86038000-86041400	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr9:86038200-86039200	Enhancers	Left Ventricle	heart
12	chr9:86038200-86040400	Enhancers	Pancreas	Pancrea
13	chr9:86038400-86039000	Weak transcription	Gastric	stomach
14	chr9:86038400-86045800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr9:86038400-86046600	Weak transcription	Rectal Smooth Muscle	rectum
16	chr9:86038600-86039200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr9:86038600-86040400	Enhancers	Rectal Mucosa Donor 31	rectum
18	chr9:86038600-86041400	Weak transcription	Stomach Smooth Muscle	stomach
19	chr9:86038800-86039200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr9:86038800-86039200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr9:86038800-86039200	Enhancers	Fetal Muscle Leg	muscle
22	chr9:86038800-86040000	Enhancers	Fetal Lung	lung
23	chr9:86038800-86040400	Enhancers	Fetal Intestine Large	intestine

Quick Search: