Variant report

Variant	rs7167892
Chromosome Location	chr15:35192148-35192149
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 102 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs10152246	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10519967	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11073076	0.87[CEU][hapmap];0.87[CHB][hapmap]
rs11633307	0.96[ASN][1000 genomes]
rs11635485	0.95[CEU][hapmap];0.94[CHB][hapmap];0.84[JPT][hapmap];0.95[YRI][hapmap];0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11636350	1.00[CEU][hapmap];0.95[CHB][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11852957	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11855784	0.95[CHB][hapmap];0.90[JPT][hapmap];0.93[ASN][1000 genomes]
rs11857217	0.91[CHB][hapmap];0.90[JPT][hapmap];0.91[ASN][1000 genomes]
rs11858044	0.96[ASN][1000 genomes]
rs12439825	0.90[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap]
rs12442905	0.86[CHB][hapmap]
rs12593379	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12593603	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12593818	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12595318	0.90[ASN][1000 genomes]
rs12898639	0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12899377	0.95[CHB][hapmap];0.89[JPT][hapmap];0.96[ASN][1000 genomes]
rs12901028	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12901394	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12901457	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12901466	0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs12901794	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12901991	0.95[CHB][hapmap];0.90[JPT][hapmap];0.96[ASN][1000 genomes]
rs12902633	0.90[ASN][1000 genomes]
rs12904279	0.90[ASN][1000 genomes]
rs12915053	0.82[EUR][1000 genomes]
rs12915493	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12917386	0.95[CHB][hapmap];0.90[JPT][hapmap];0.93[ASN][1000 genomes]
rs12917597	0.93[ASN][1000 genomes]
rs1376784	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16959966	0.86[CHB][hapmap];0.81[ASN][1000 genomes]
rs2044920	0.95[ASN][1000 genomes]
rs2060809	0.91[CEU][hapmap];0.86[CHB][hapmap]
rs2060810	0.85[CHB][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2060811	0.87[CHB][hapmap]
rs2060812	0.94[CEU][hapmap];0.88[CHB][hapmap];0.83[JPT][hapmap];0.91[YRI][hapmap];0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2123048	0.96[ASN][1000 genomes]
rs2290320	0.86[CHB][hapmap];0.90[JPT][hapmap];0.93[ASN][1000 genomes]
rs2305411	0.95[CEU][hapmap];0.91[CHB][hapmap];0.85[JPT][hapmap];0.92[YRI][hapmap];0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2339746	0.96[ASN][1000 genomes]
rs28498500	0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs28715915	0.82[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs36067547	0.86[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs3743121	0.86[CHB][hapmap];0.84[JPT][hapmap];0.85[ASN][1000 genomes]
rs3816447	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3848167	0.95[CHB][hapmap];0.90[JPT][hapmap];0.93[ASN][1000 genomes]
rs4513050	0.86[CHB][hapmap]
rs4569214	0.95[CHB][hapmap];0.89[JPT][hapmap]
rs4923817	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4923818	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4923845	1.00[CEU][hapmap];0.91[CHB][hapmap];0.85[JPT][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4924324	0.93[ASN][1000 genomes]
rs4924325	0.95[CHB][hapmap];0.90[JPT][hapmap];0.93[ASN][1000 genomes]
rs4924339	0.82[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4924344	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4924355	0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4924357	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4924369	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6495723	0.96[ASN][1000 genomes]
rs6495724	0.95[CHB][hapmap];0.89[JPT][hapmap];0.96[ASN][1000 genomes]
rs6495726	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6495728	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6495729	0.95[CEU][hapmap];0.91[CHB][hapmap];0.85[JPT][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6495730	0.87[CEU][hapmap];0.87[CHB][hapmap]
rs7164151	0.90[CEU][hapmap];0.91[CHB][hapmap]
rs7164169	0.91[CEU][hapmap];0.86[CHB][hapmap]
rs7164266	0.91[CEU][hapmap];0.86[CHB][hapmap]
rs7164977	0.95[CHB][hapmap];0.90[JPT][hapmap];0.96[ASN][1000 genomes]
rs7165835	0.91[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7170280	0.86[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7170737	0.91[ASN][1000 genomes]
rs7171808	0.92[ASN][1000 genomes]
rs7172507	0.85[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs7177962	0.95[CHB][hapmap];0.90[JPT][hapmap];0.93[ASN][1000 genomes]
rs7179833	0.86[CHB][hapmap]
rs7182356	0.86[CHB][hapmap]
rs7182492	0.96[ASN][1000 genomes]
rs7497306	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs8024212	0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs8025770	0.95[CHB][hapmap];0.89[JPT][hapmap];0.94[ASN][1000 genomes]
rs8029192	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8031583	0.96[ASN][1000 genomes]
rs8031677	0.96[ASN][1000 genomes]
rs8031861	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs8036690	0.96[ASN][1000 genomes]
rs8037610	0.86[CEU][hapmap];0.87[CHB][hapmap]
rs8040551	0.91[CHB][hapmap];0.84[JPT][hapmap];0.91[ASN][1000 genomes]
rs959478	0.95[CHB][hapmap];0.89[JPT][hapmap];0.96[ASN][1000 genomes]
rs963425	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9672656	0.84[ASN][1000 genomes]
rs9806487	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9920918	0.96[ASN][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	esv3350109	chr15:34668106-35534229	Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv522411	chr15:34953986-35462981	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	43 gene(s)	inside rSNPs	diseases
3	nsv457106	chr15:35049787-35227613	Strong transcription Weak transcription Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv569153	chr15:35049787-35227613	Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	esv2761865	chr15:35101678-35271639	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv832967	chr15:35110102-35267906	Strong transcription Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
7	nsv904071	chr15:35150897-35250771	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv904072	chr15:35150897-35259376	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv569154	chr15:35165366-35259376	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	7 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	chr15:35140400-35221600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr15:35145200-35198200	Weak transcription	Colonic Mucosa	Colon
3	chr15:35176200-35195000	Weak transcription	Brain Substantia Nigra	brain
4	chr15:35184600-35193200	Strong transcription	Cortex derived primary cultured neurospheres	brain
5	chr15:35185200-35205200	Weak transcription	Stomach Mucosa	stomach
6	chr15:35186000-35192200	Weak transcription	Thymus	Thymus
7	chr15:35186000-35192800	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chr15:35186000-35192800	Weak transcription	Stomach Smooth Muscle	stomach
9	chr15:35186000-35193400	Strong transcription	H1 Cell Line	embryonic stem cell
10	chr15:35186000-35194400	Weak transcription	Brain Angular Gyrus	brain
11	chr15:35186000-35195400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr15:35186000-35196600	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr15:35186000-35196600	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr15:35186000-35197600	Weak transcription	Left Ventricle	heart
15	chr15:35186000-35198000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr15:35186000-35198000	Weak transcription	Spleen	Spleen
17	chr15:35186000-35198400	Weak transcription	Aorta	Aorta
18	chr15:35186000-35198400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr15:35186000-35199600	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr15:35186000-35204200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr15:35186000-35206400	Weak transcription	Right Ventricle	heart
22	chr15:35186000-35206600	Weak transcription	Small Intestine	intestine
23	chr15:35186000-35212400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr15:35186000-35212600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr15:35186000-35213000	Strong transcription	Primary monocytes fromperipheralblood	blood
26	chr15:35186000-35220000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr15:35186000-35220000	Weak transcription	Pancreas	Pancrea
28	chr15:35186000-35223200	Weak transcription	Gastric	stomach
29	chr15:35186000-35232000	Weak transcription	Fetal Brain Male	brain
30	chr15:35186200-35192200	Weak transcription	HepG2	liver
31	chr15:35186200-35192600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr15:35186200-35192600	Weak transcription	Brain Germinal Matrix	brain
33	chr15:35186200-35192800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr15:35186200-35192800	Weak transcription	Brain Hippocampus Middle	brain
35	chr15:35186200-35198000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr15:35186200-35198200	Weak transcription	Esophagus	oesophagus
37	chr15:35186200-35198400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr15:35186200-35202200	Weak transcription	NHEK	skin
39	chr15:35186200-35212000	Strong transcription	Primary B cells from peripheral blood	blood
40	chr15:35186200-35212400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr15:35186200-35212400	Strong transcription	Liver	Liver
42	chr15:35186400-35192600	Weak transcription	Fetal Heart	heart
43	chr15:35186400-35195200	Weak transcription	HMEC	breast
44	chr15:35186400-35201000	Weak transcription	Colon Smooth Muscle	Colon
45	chr15:35186400-35205400	Weak transcription	Brain Cingulate Gyrus	brain
46	chr15:35186400-35238800	Strong transcription	Primary T helper cells fromperipheralblood	blood
47	chr15:35186600-35194000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr15:35186600-35195400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr15:35186600-35195400	Strong transcription	Primary T helper cells PMA-I stimulated	--
50	chr15:35186600-35195800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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