Variant report

Variant	rs35672192
Chromosome Location	chr14:64365894-64365895
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 48 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs12879641	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12880477	0.83[ASN][1000 genomes]
rs12881241	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12882341	0.84[ASN][1000 genomes]
rs12882972	0.86[ASN][1000 genomes]
rs12883728	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12884259	0.90[AMR][1000 genomes];0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12887573	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12889107	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12889504	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12892555	0.87[ASN][1000 genomes]
rs12894035	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12894619	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12896216	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12898127	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13379083	0.84[ASN][1000 genomes]
rs17101419	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17101437	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17225497	0.82[ASN][1000 genomes]
rs1959033	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2356994	0.83[ASN][1000 genomes]
rs28494507	0.87[ASN][1000 genomes]
rs28783479	0.84[ASN][1000 genomes]
rs34252863	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34292510	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34294645	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs35103832	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs35244884	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35353466	0.90[AMR][1000 genomes];0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35499091	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35635100	0.86[ASN][1000 genomes]
rs35752453	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35773852	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs35860218	0.86[ASN][1000 genomes]
rs57010514	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs71416311	0.86[ASN][1000 genomes]
rs71416313	0.86[ASN][1000 genomes]
rs71416318	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs71437513	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs8003797	0.86[ASN][1000 genomes]
rs9707777	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915909	chr14:63620440-64560369	Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv1038825	chr14:64109441-64491720	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv1037140	chr14:64248421-64442980	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv542119	chr14:64248421-64442980	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv564904	chr14:64346190-64416898	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	esv1793389	chr14:64346190-64457224	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
7	nsv826965	chr14:64360774-64366612	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64337800-64403800	Weak transcription	Thymus	Thymus
2	chr14:64339400-64366800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr14:64341400-64366800	Weak transcription	Primary T cells from cord blood	blood
4	chr14:64342800-64368400	Weak transcription	Esophagus	oesophagus
5	chr14:64349400-64366600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr14:64349600-64366000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr14:64352800-64366800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr14:64357800-64366600	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr14:64358200-64375800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr14:64358200-64377600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr14:64358400-64366000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr14:64358800-64377600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr14:64359000-64366400	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr14:64359000-64367800	Weak transcription	Duodenum Mucosa	Duodenum
15	chr14:64360600-64382200	Weak transcription	Psoas Muscle	Psoas
16	chr14:64360800-64367000	Weak transcription	HUES6 Cell Line	embryonic stem cell
17	chr14:64360800-64374200	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr14:64360800-64377800	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr14:64361200-64373600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr14:64361400-64369800	Weak transcription	Colonic Mucosa	Colon
21	chr14:64363200-64366200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr14:64363400-64366200	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr14:64363400-64368400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr14:64363400-64374400	Weak transcription	Fetal Intestine Small	intestine
25	chr14:64363400-64375200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr14:64363400-64375400	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr14:64363600-64367600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr14:64363600-64368200	Weak transcription	Liver	Liver
29	chr14:64363800-64375400	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr14:64364400-64366200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
31	chr14:64364400-64385200	Weak transcription	Pancreas	Pancrea
32	chr14:64364600-64366400	Weak transcription	Dnd41	blood
33	chr14:64364600-64366600	Weak transcription	HUVEC	blood vessel
34	chr14:64364600-64375400	Weak transcription	Aorta	Aorta
35	chr14:64364600-64387800	Weak transcription	HMEC	breast
36	chr14:64364800-64375400	Weak transcription	Hela-S3	cervix
37	chr14:64365000-64366600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
38	chr14:64365000-64366800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr14:64365000-64367000	Weak transcription	Right Atrium	heart
40	chr14:64365000-64367200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr14:64365000-64367200	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr14:64365000-64367400	Weak transcription	HSMM	muscle
43	chr14:64365000-64367600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr14:64365000-64368400	Weak transcription	Ovary	ovary
45	chr14:64365000-64368800	Weak transcription	Muscle Satellite Cultured Cells	--
46	chr14:64365000-64369600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr14:64365000-64374200	Weak transcription	Brain Germinal Matrix	brain
48	chr14:64365000-64375000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr14:64365000-64375000	Weak transcription	Fetal Kidney	kidney
50	chr14:64365000-64430200	Weak transcription	Fetal Brain Male	brain

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