Variant report

Variant	rs2002245
Chromosome Location	chr14:20767872-20767873
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:20767452..20770221-chr14:20798521..20800836,2	K562	blood:

Variant related genes	Relation type
ENSG00000100814	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs1953550	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2318863	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs28436279	0.80[EUR][1000 genomes]
rs3093868	0.81[AMR][1000 genomes]
rs45583431	0.81[AMR][1000 genomes]
rs45622542	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56383558	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61993958	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61993959	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs61995461	0.93[EUR][1000 genomes]
rs61995462	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61995463	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61995493	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61995494	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs61995495	0.93[EUR][1000 genomes]
rs61995497	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs61995498	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61995500	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs61995503	0.81[AMR][1000 genomes]
rs61995504	0.81[AMR][1000 genomes]
rs61995508	0.81[AMR][1000 genomes]
rs61995509	0.81[AMR][1000 genomes]
rs61995513	0.81[AMR][1000 genomes]
rs61995534	0.81[AMR][1000 genomes]
rs61995536	0.81[AMR][1000 genomes]
rs61995537	0.81[AMR][1000 genomes]
rs61995538	0.81[AMR][1000 genomes]
rs61995542	0.81[AMR][1000 genomes]
rs61995544	0.81[AMR][1000 genomes]
rs61995545	0.81[AMR][1000 genomes]
rs72671246	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs72671250	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043923	chr14:20338742-21336425	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	203 gene(s)	inside rSNPs	diseases
2	nsv541970	chr14:20338742-21336425	Strong transcription Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats 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 target site	203 gene(s)	inside rSNPs	diseases
3	nsv1043938	chr14:20427182-20776276	Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
4	nsv541971	chr14:20427182-20776276	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
5	nsv1037160	chr14:20517485-20901811	Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	103 gene(s)	inside rSNPs	diseases
6	nsv541974	chr14:20517485-20901811	Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	103 gene(s)	inside rSNPs	diseases
7	nsv869984	chr14:20732655-20776216	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	esv1806993	chr14:20743269-20841162	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	71 gene(s)	inside rSNPs	diseases
9	nsv534131	chr14:20757405-20886235	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	87 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:20746600-20773200	Weak transcription	Stomach Mucosa	stomach
2	chr14:20749200-20773400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:20754400-20770000	Strong transcription	HUES64 Cell Line	embryonic stem cell
4	chr14:20754400-20770200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr14:20754400-20770800	Strong transcription	Primary T helper cells fromperipheralblood	blood
6	chr14:20754600-20770400	Strong transcription	Duodenum Mucosa	Duodenum
7	chr14:20754600-20770400	Strong transcription	Dnd41	blood
8	chr14:20754800-20770000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
9	chr14:20754800-20770000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr14:20754800-20770200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr14:20754800-20770400	Strong transcription	Primary T cells fromperipheralblood	blood
12	chr14:20754800-20770400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr14:20754800-20770400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr14:20754800-20770400	Strong transcription	Adipose Nuclei	Adipose
15	chr14:20754800-20770400	Strong transcription	Liver	Liver
16	chr14:20754800-20770400	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr14:20754800-20770600	Strong transcription	Primary monocytes fromperipheralblood	blood
18	chr14:20755000-20769800	Strong transcription	Primary T helper cells PMA-I stimulated	--
19	chr14:20755000-20770000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr14:20755000-20770000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
21	chr14:20755000-20770400	Strong transcription	Primary T cells from cord blood	blood
22	chr14:20755000-20770400	Strong transcription	Rectal Mucosa Donor 29	rectum
23	chr14:20755000-20770600	Strong transcription	Stomach Smooth Muscle	stomach
24	chr14:20755200-20769600	Strong transcription	HUES48 Cell Line	embryonic stem cell
25	chr14:20755200-20770000	Strong transcription	Rectal Mucosa Donor 31	rectum
26	chr14:20755200-20770200	Strong transcription	Primary hematopoietic stem cells	blood
27	chr14:20755200-20770200	Strong transcription	Aorta	Aorta
28	chr14:20755200-20770200	Strong transcription	Fetal Brain Female	brain
29	chr14:20755200-20770200	Strong transcription	Left Ventricle	heart
30	chr14:20755200-20770200	Strong transcription	Skeletal Muscle Female	skeletal muscle
31	chr14:20755200-20770400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr14:20755200-20770400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr14:20755200-20770400	Strong transcription	Fetal Muscle Trunk	muscle
34	chr14:20755400-20769800	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr14:20755400-20770200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr14:20755400-20770200	Strong transcription	Primary neutrophils fromperipheralblood	blood
37	chr14:20755400-20770200	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr14:20755400-20770200	Strong transcription	Ovary	ovary
39	chr14:20756400-20770200	Strong transcription	HUES6 Cell Line	embryonic stem cell
40	chr14:20756800-20769800	Strong transcription	Skeletal Muscle Male	skeletal muscle
41	chr14:20757000-20769400	Strong transcription	Primary T killer naive cells fromperipheralblood	blood
42	chr14:20757000-20769400	Strong transcription	Brain Substantia Nigra	brain
43	chr14:20758000-20773200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr14:20758400-20770200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr14:20758400-20770400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr14:20758600-20770400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
47	chr14:20759000-20769400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
48	chr14:20759000-20770400	Strong transcription	Cortex derived primary cultured neurospheres	brain
49	chr14:20759000-20770400	Strong transcription	Duodenum Smooth Muscle	Duodenum
50	chr14:20759000-20770400	Strong transcription	Fetal Intestine Large	intestine

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