Variant report

Variant	rs55861984
Chromosome Location	chr14:66331900-66331901
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs17103072	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2022844	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs59694569	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs61989046	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs61990008	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7153000	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7160924	0.92[EUR][1000 genomes]
rs7494067	0.80[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs7494719	0.88[AMR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8008176	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs8022645	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8022817	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043943	chr14:65782466-66698411	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
2	nsv542120	chr14:65782466-66698411	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	55 gene(s)	inside rSNPs	diseases
3	esv3366524	chr14:65924360-66423862	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
4	nsv1045000	chr14:66010886-66372518	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1042671	chr14:66010886-66399888	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv817409	chr14:66220075-66990168	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
7	nsv564953	chr14:66287921-67046960	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
8	nsv1050485	chr14:66308283-67109270	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
9	nsv832820	chr14:66310846-66362845	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
10	nsv530775	chr14:66316836-67079049	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
11	nsv530793	chr14:66317036-67078908	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:66326800-66332000	Enhancers	Primary T cells fromperipheralblood	blood
2	chr14:66327000-66332200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
3	chr14:66327000-66332400	Enhancers	Primary T helper naive cells from peripheral blood	blood
4	chr14:66327000-66332400	Enhancers	Fetal Thymus	thymus
5	chr14:66327000-66332600	Enhancers	Primary T helper cells fromperipheralblood	blood
6	chr14:66327000-66332600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr14:66328200-66333600	Enhancers	Primary T helper cells PMA-I stimulated	--
8	chr14:66329600-66332400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
9	chr14:66329600-66332400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
10	chr14:66330000-66332400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr14:66330000-66332600	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr14:66330600-66334400	Enhancers	Thymus	Thymus
13	chr14:66330800-66332000	Flanking Active TSS	Dnd41	blood
14	chr14:66330800-66332200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr14:66330800-66332200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr14:66330800-66332400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
17	chr14:66331000-66332400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr14:66331200-66332000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr14:66331200-66332400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr14:66331400-66334400	Enhancers	NHDF-Ad	bronchial
21	chr14:66331400-66335200	Enhancers	Primary T cells from cord blood	blood
22	chr14:66331600-66332000	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr14:66331600-66332000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
24	chr14:66331600-66332000	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr14:66331800-66332000	Enhancers	Brain Germinal Matrix	brain
26	chr14:66331800-66332000	Enhancers	Fetal Stomach	stomach
27	chr14:66331800-66332000	Enhancers	Gastric	stomach
28	chr14:66331800-66332000	Enhancers	Lung	lung
29	chr14:66331800-66332200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
30	chr14:66331800-66332200	Enhancers	Small Intestine	intestine
31	chr14:66331800-66332400	Enhancers	Pancreatic Islets	Pancreatic Islet
32	chr14:66331800-66333800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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