Variant report

Variant	rs1784473
Chromosome Location	chr8:107768365-107768366
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1580289	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1601249	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1676420	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1681879	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1681904	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1681905	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1784469	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1784472	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1784479	0.81[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs1784480	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1784492	0.81[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1784494	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2126581	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2282509	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2627788	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2627790	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs725906	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs776932	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs776933	0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs776934	0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs776938	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs776939	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs776941	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs776944	0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs776946	0.80[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs776948	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs776949	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs776950	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs776951	0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs776954	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs776960	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs776961	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs776962	0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs776963	0.80[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs776965	0.80[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][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	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
2	nsv1032991	chr8:107756661-107819035	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:83 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:107719600-107775200	Weak transcription	Gastric	stomach
2	chr8:107719600-107777800	Weak transcription	Esophagus	oesophagus
3	chr8:107739000-107775200	Weak transcription	A549	lung
4	chr8:107740000-107775200	Weak transcription	Ovary	ovary
5	chr8:107740200-107783800	Weak transcription	Fetal Brain Male	brain
6	chr8:107740800-107775200	Weak transcription	Brain Substantia Nigra	brain
7	chr8:107749400-107775200	Weak transcription	HMEC	breast
8	chr8:107753200-107771400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
9	chr8:107753600-107777400	Weak transcription	HUVEC	blood vessel
10	chr8:107753800-107775200	Weak transcription	Muscle Satellite Cultured Cells	--
11	chr8:107754200-107775200	Weak transcription	Pancreas	Pancrea
12	chr8:107754800-107775200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr8:107755200-107772000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr8:107755400-107771600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr8:107755800-107771200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr8:107755800-107777800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
17	chr8:107756000-107775000	Weak transcription	Fetal Heart	heart
18	chr8:107756400-107772400	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr8:107756400-107775000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr8:107756400-107777800	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr8:107756600-107769800	Weak transcription	Brain Hippocampus Middle	brain
22	chr8:107756600-107771200	Weak transcription	Skeletal Muscle Female	skeletal muscle
23	chr8:107756600-107772000	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr8:107756600-107772200	Weak transcription	Primary hematopoietic stem cells	blood
25	chr8:107756600-107772400	Weak transcription	Left Ventricle	heart
26	chr8:107756600-107772800	Weak transcription	Primary T cells fromperipheralblood	blood
27	chr8:107756600-107775200	Weak transcription	Brain Angular Gyrus	brain
28	chr8:107756600-107775200	Weak transcription	Brain Anterior Caudate	brain
29	chr8:107756600-107775200	Weak transcription	Fetal Intestine Large	intestine
30	chr8:107756600-107775200	Weak transcription	Fetal Kidney	kidney
31	chr8:107756600-107775200	Weak transcription	Fetal Muscle Leg	muscle
32	chr8:107756600-107775200	Weak transcription	Stomach Smooth Muscle	stomach
33	chr8:107756600-107777400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr8:107756600-107777400	Weak transcription	Psoas Muscle	Psoas
35	chr8:107756600-107777600	Weak transcription	Fetal Brain Female	brain
36	chr8:107756800-107775200	Weak transcription	Brain Cingulate Gyrus	brain
37	chr8:107756800-107775200	Weak transcription	Osteobl	bone
38	chr8:107757000-107768600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr8:107757200-107771400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr8:107757200-107775200	Weak transcription	NHDF-Ad	bronchial
41	chr8:107757600-107771400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr8:107757800-107769000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr8:107758000-107771200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr8:107758000-107771800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr8:107759800-107769800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
46	chr8:107759800-107775200	Weak transcription	Fetal Thymus	thymus
47	chr8:107760200-107773800	Weak transcription	GM12878-XiMat	blood
48	chr8:107760200-107775800	Weak transcription	Right Ventricle	heart
49	chr8:107761400-107777600	Weak transcription	Fetal Stomach	stomach
50	chr8:107761600-107775200	Weak transcription	Fetal Intestine Small	intestine

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