Variant report

Variant	rs61990417
Chromosome Location	chr14:71534826-71534827
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 87 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs10140218	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11623477	1.00[ASN][1000 genomes]
rs11844339	1.00[ASN][1000 genomes]
rs17766986	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs45498105	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs45517434	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4902905	1.00[ASN][1000 genomes]
rs4902908	1.00[ASN][1000 genomes]
rs55896578	1.00[ASN][1000 genomes]
rs55903050	1.00[ASN][1000 genomes]
rs57204407	1.00[ASN][1000 genomes]
rs57723945	1.00[ASN][1000 genomes]
rs58952176	1.00[ASN][1000 genomes]
rs59060154	1.00[ASN][1000 genomes]
rs61988691	1.00[ASN][1000 genomes]
rs61988692	1.00[ASN][1000 genomes]
rs61988693	1.00[ASN][1000 genomes]
rs61988695	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61988719	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61988721	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61988723	1.00[AMR][1000 genomes]
rs61988726	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61988727	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61988728	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61988729	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61988735	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61988736	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61988737	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61988738	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61988740	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs61989175	1.00[ASN][1000 genomes]
rs61989177	1.00[ASN][1000 genomes]
rs61989179	1.00[ASN][1000 genomes]
rs61989180	1.00[ASN][1000 genomes]
rs61989234	1.00[ASN][1000 genomes]
rs61989239	1.00[ASN][1000 genomes]
rs61989240	1.00[ASN][1000 genomes]
rs61990375	1.00[ASN][1000 genomes]
rs61990382	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990383	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990384	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990385	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990404	1.00[ASN][1000 genomes]
rs61990406	1.00[ASN][1000 genomes]
rs61990407	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990408	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990409	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990410	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990411	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990412	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990414	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990416	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990418	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990420	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990451	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990452	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990453	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61990458	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61992061	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61992066	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61992067	1.00[EUR][1000 genomes]
rs61992068	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61992069	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61992070	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61992080	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61992081	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61992086	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61992088	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61992090	1.00[ASN][1000 genomes]
rs61992091	1.00[ASN][1000 genomes]
rs7155259	1.00[ASN][1000 genomes]
rs7156194	1.00[ASN][1000 genomes]
rs7159252	1.00[ASN][1000 genomes]
rs7160587	1.00[ASN][1000 genomes]
rs73289980	1.00[ASN][1000 genomes]
rs7492426	1.00[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	nsv1041980	chr14:71196358-71767339	Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv542125	chr14:71196358-71767339	Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv1035416	chr14:71212882-71623271	Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	nsv542126	chr14:71212882-71623271	Weak transcription Enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv1037839	chr14:71263886-71625114	Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
6	nsv542127	chr14:71263886-71625114	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
7	nsv1038007	chr14:71269747-71667680	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
8	nsv565043	chr14:71395604-71625112	Strong transcription Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
9	nsv1036929	chr14:71469148-71683412	Strong transcription Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	nsv1044090	chr14:71496198-71780026	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
11	esv3430065	chr14:71534649-71536547	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:71495800-71546200	Weak transcription	Stomach Mucosa	stomach
2	chr14:71497000-71554200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:71499600-71540800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr14:71510200-71538200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr14:71511600-71540800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr14:71511600-71541000	Weak transcription	Pancreas	Pancrea
7	chr14:71518200-71544000	Strong transcription	Primary T helper cells PMA-I stimulated	--
8	chr14:71525800-71539800	Weak transcription	Brain Substantia Nigra	brain
9	chr14:71527200-71536200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr14:71527400-71540000	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr14:71527600-71540000	Weak transcription	Brain Angular Gyrus	brain
12	chr14:71528000-71541200	Weak transcription	Small Intestine	intestine
13	chr14:71528000-71543200	Weak transcription	Placenta Amnion	Placenta Amnion
14	chr14:71528200-71539000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr14:71528400-71535600	Weak transcription	Colonic Mucosa	Colon
16	chr14:71528400-71539800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr14:71528400-71540800	Weak transcription	HSMMtube	muscle
18	chr14:71528400-71541200	Weak transcription	Right Ventricle	heart
19	chr14:71528600-71535600	Weak transcription	Left Ventricle	heart
20	chr14:71528600-71536200	Weak transcription	Fetal Kidney	kidney
21	chr14:71528600-71536200	Weak transcription	Stomach Smooth Muscle	stomach
22	chr14:71528600-71536400	Weak transcription	Fetal Brain Male	brain
23	chr14:71528600-71536400	Weak transcription	NHLF	lung
24	chr14:71528600-71536600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
25	chr14:71528600-71537600	Weak transcription	Gastric	stomach
26	chr14:71528600-71539800	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr14:71528600-71539800	Weak transcription	Placenta	Placenta
28	chr14:71528600-71539800	Weak transcription	Lung	lung
29	chr14:71528600-71540000	Weak transcription	Fetal Thymus	thymus
30	chr14:71528600-71540200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr14:71528600-71540200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr14:71528600-71540200	Weak transcription	Aorta	Aorta
33	chr14:71528600-71540200	Weak transcription	Brain Cingulate Gyrus	brain
34	chr14:71528600-71540200	Weak transcription	Esophagus	oesophagus
35	chr14:71528600-71540800	Weak transcription	Colon Smooth Muscle	Colon
36	chr14:71528600-71540800	Weak transcription	A549	lung
37	chr14:71528600-71543200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr14:71528800-71540000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr14:71528800-71540200	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr14:71528800-71540200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr14:71528800-71540200	Weak transcription	Hela-S3	cervix
42	chr14:71528800-71540200	Weak transcription	HepG2	liver
43	chr14:71529000-71536200	Weak transcription	NH-A	brain
44	chr14:71529000-71539600	Weak transcription	Fetal Stomach	stomach
45	chr14:71529000-71539600	Weak transcription	HUVEC	blood vessel
46	chr14:71529000-71539800	Weak transcription	Spleen	Spleen
47	chr14:71529000-71540200	Weak transcription	Thymus	Thymus
48	chr14:71529000-71543000	Weak transcription	Psoas Muscle	Psoas
49	chr14:71529200-71540200	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr14:71529600-71538200	Weak transcription	Fetal Heart	heart

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