Variant report

Variant	rs7149766
Chromosome Location	chr14:64343229-64343230
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11158512	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11158516	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12587472	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12588087	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12894053	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12894864	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1959034	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1959035	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2210650	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2275018	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2357002	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2357003	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs34780876	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4902247	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4902248	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6573534	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7145657	0.85[ASN][1000 genomes]
rs7146821	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7157314	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7158974	0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7160127	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7493416	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8005899	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8015158	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8015354	0.88[AFR][1000 genomes];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8022917	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs945030	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs954730	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9707224	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs998241	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 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

No data

Chromatin state (count:99 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64321400-64350200	Weak transcription	Fetal Stomach	stomach
2	chr14:64327400-64355200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr14:64327600-64360000	Weak transcription	Gastric	stomach
4	chr14:64330200-64343600	Weak transcription	Brain Germinal Matrix	brain
5	chr14:64331200-64356400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr14:64335200-64360000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr14:64336800-64362800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr14:64337000-64343600	Weak transcription	Fetal Intestine Large	intestine
9	chr14:64337000-64357200	Weak transcription	Duodenum Mucosa	Duodenum
10	chr14:64337000-64365200	Weak transcription	Fetal Thymus	thymus
11	chr14:64337600-64343600	Weak transcription	A549	lung
12	chr14:64337800-64403800	Weak transcription	Thymus	Thymus
13	chr14:64338000-64353800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr14:64338000-64355200	Weak transcription	Primary B cells from cord blood	blood
15	chr14:64339400-64366800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr14:64340200-64344000	Enhancers	Left Ventricle	heart
17	chr14:64340400-64343600	Enhancers	Right Atrium	heart
18	chr14:64340400-64345600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr14:64340600-64343600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr14:64340600-64343800	Enhancers	Psoas Muscle	Psoas
21	chr14:64340600-64345000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr14:64340600-64345200	Enhancers	Rectal Mucosa Donor 31	rectum
23	chr14:64341000-64356400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr14:64341000-64357200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr14:64341200-64344000	Weak transcription	Pancreatic Islets	Pancreatic Islet
26	chr14:64341200-64345000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr14:64341200-64346200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr14:64341200-64348400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr14:64341200-64348600	Weak transcription	Primary B cells from peripheral blood	blood
30	chr14:64341200-64348800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr14:64341200-64351000	Weak transcription	Right Ventricle	heart
32	chr14:64341200-64352200	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr14:64341200-64352400	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr14:64341200-64354000	Weak transcription	Dnd41	blood
35	chr14:64341200-64354800	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr14:64341200-64356400	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr14:64341200-64356400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
38	chr14:64341200-64356600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr14:64341200-64357000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr14:64341200-64357200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr14:64341200-64357200	Weak transcription	Fetal Lung	lung
42	chr14:64341200-64357200	Weak transcription	Fetal Muscle Leg	muscle
43	chr14:64341400-64344800	Weak transcription	Colonic Mucosa	Colon
44	chr14:64341400-64352400	Weak transcription	HUES6 Cell Line	embryonic stem cell
45	chr14:64341400-64352600	Weak transcription	Stomach Mucosa	stomach
46	chr14:64341400-64356600	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr14:64341400-64356600	Weak transcription	Fetal Kidney	kidney
48	chr14:64341400-64366800	Weak transcription	Primary T cells from cord blood	blood
49	chr14:64341600-64345000	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr14:64341800-64345000	Enhancers	Rectal Mucosa Donor 29	rectum

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