Variant report

Variant	rs776953
Chromosome Location	chr8:107723733-107723734
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1080965	0.81[AMR][1000 genomes]
rs1552302	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1580428	0.87[CEU][hapmap];0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1580429	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1676418	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1676419	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs1681881	0.82[CEU][hapmap]
rs1681887	0.88[CEU][hapmap]
rs1784468	0.81[AMR][1000 genomes]
rs1784470	0.82[CEU][hapmap];0.81[AMR][1000 genomes]
rs1784476	0.81[AMR][1000 genomes]
rs1784478	0.82[CEU][hapmap];0.81[AMR][1000 genomes]
rs1784493	0.87[CEU][hapmap]
rs702776	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs763904	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs776935	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs776936	0.82[CEU][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs776937	0.82[CEU][hapmap];0.81[AMR][1000 genomes]
rs776942	0.87[CEU][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs776943	0.94[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs776952	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs776956	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs776957	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs776958	0.82[EUR][1000 genomes]
rs776966	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs776967	0.82[CEU][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs776968	0.82[CEU][hapmap];0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs812907	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs936737	0.81[AMR][1000 genomes]

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	nsv831419	chr8:107624709-107827801	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:107679200-107738200	Weak transcription	Right Ventricle	heart
2	chr8:107681200-107730200	Weak transcription	Small Intestine	intestine
3	chr8:107690200-107730600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr8:107692000-107738400	Weak transcription	Colon Smooth Muscle	Colon
5	chr8:107692800-107725800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr8:107694600-107738000	Weak transcription	Fetal Heart	heart
7	chr8:107695000-107725800	Weak transcription	NHLF	lung
8	chr8:107696000-107737200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr8:107697800-107723800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
10	chr8:107698200-107731000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
11	chr8:107707800-107737800	Weak transcription	Brain Inferior Temporal Lobe	brain
12	chr8:107708800-107725600	Weak transcription	Fetal Brain Male	brain
13	chr8:107710000-107723800	Weak transcription	Fetal Muscle Leg	muscle
14	chr8:107710400-107724600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr8:107710400-107725400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:107710400-107735600	Weak transcription	Fetal Intestine Small	intestine
17	chr8:107710400-107738200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr8:107710400-107755400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr8:107711800-107738200	Weak transcription	Brain Angular Gyrus	brain
20	chr8:107717200-107737200	Weak transcription	Brain Hippocampus Middle	brain
21	chr8:107717800-107726000	Weak transcription	Brain Substantia Nigra	brain
22	chr8:107718000-107728600	Strong transcription	Primary monocytes fromperipheralblood	blood
23	chr8:107718600-107723800	Strong transcription	Primary hematopoietic stem cells	blood
24	chr8:107718600-107726400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr8:107718600-107727600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr8:107718800-107723800	Strong transcription	Primary B cells from peripheral blood	blood
27	chr8:107719000-107738200	Weak transcription	NHEK	skin
28	chr8:107719200-107725400	Weak transcription	Pancreas	Pancrea
29	chr8:107719200-107742400	Weak transcription	Stomach Mucosa	stomach
30	chr8:107719400-107723800	Weak transcription	A549	lung
31	chr8:107719400-107723800	Weak transcription	NH-A	brain
32	chr8:107719400-107725400	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr8:107719600-107723800	Weak transcription	HUVEC	blood vessel
34	chr8:107719600-107725400	Weak transcription	H9 Cell Line	embryonic stem cell
35	chr8:107719600-107726200	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr8:107719600-107729800	Weak transcription	Spleen	Spleen
37	chr8:107719600-107731000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
38	chr8:107719600-107732400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr8:107719600-107737000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr8:107719600-107737400	Weak transcription	Psoas Muscle	Psoas
41	chr8:107719600-107738000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr8:107719600-107738200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr8:107719600-107738400	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr8:107719600-107739600	Weak transcription	Left Ventricle	heart
45	chr8:107719600-107762400	Weak transcription	Lung	lung
46	chr8:107719600-107765600	Weak transcription	Colonic Mucosa	Colon
47	chr8:107719600-107775200	Weak transcription	Gastric	stomach
48	chr8:107719600-107777800	Weak transcription	Esophagus	oesophagus
49	chr8:107719800-107730200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
50	chr8:107719800-107731200	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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