Variant report

Variant	rs13036626
Chromosome Location	chr20:25159593-25159594
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:25046140..25046670-chr20:25159575..25160213,2	MCF-7	breast:
2	chr20:24972385..24977147-chr20:25157333..25161116,4	MCF-7	breast:
3	chr20:24975144..24976098-chr20:25159512..25160449,4	MCF-7	breast:
4	chr20:25119381..25120394-chr20:25159500..25160482,5	MCF-7	breast:
5	chr20:24980779..24981584-chr20:25159554..25160358,4	MCF-7	breast:
6	chr20:24972851..24974876-chr20:25158706..25161889,3	MCF-7	breast:
7	chr20:25140270..25141974-chr20:25158745..25161206,2	MCF-7	breast:
8	chr20:25119381..25120481-chr20:25159221..25160482,27	MCF-7	breast:
9	chr20:25125758..25128401-chr20:25158133..25159893,2	MCF-7	breast:
10	chr20:25057340..25057881-chr20:25159450..25160139,2	MCF-7	breast:
11	chr20:25159530..25160087-chr20:25276913..25277799,2	MCF-7	breast:
12	chr20:25046117..25046996-chr20:25159492..25160465,5	MCF-7	breast:
13	chr20:25159426..25161850-chr20:25175828..25177766,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000230725	Chromatin interaction
ENSG00000197586	Chromatin interaction
ENSG00000101474	Chromatin interaction

Extended variants
information (count: 86 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs11698226	0.93[ASN][1000 genomes]
rs11699149	0.86[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs11699219	0.92[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs13037201	0.85[ASN][1000 genomes]
rs13037374	0.85[ASN][1000 genomes]
rs13041051	0.91[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs2038182	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2057042	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2103715	0.93[ASN][1000 genomes]
rs2179639	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35047430	0.94[ASN][1000 genomes]
rs35231728	0.85[ASN][1000 genomes]
rs35910458	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs36115891	0.93[ASN][1000 genomes]
rs4482560	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4815374	0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4815388	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4815389	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4815392	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6037024	0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6037029	0.82[JPT][hapmap]
rs6037032	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6037033	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6037034	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6037049	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6037052	0.87[ASN][1000 genomes]
rs6050342	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6050345	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6050348	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6050353	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6050359	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6050370	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6050372	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap]
rs6050374	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs6050390	0.93[ASN][1000 genomes]
rs6050397	0.92[ASN][1000 genomes]
rs6050399	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6050400	0.93[ASN][1000 genomes]
rs6050403	0.86[CHB][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs6050404	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6050406	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6050408	0.82[ASN][1000 genomes]
rs6050409	0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6050410	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6050411	0.87[ASN][1000 genomes]
rs6050412	0.87[ASN][1000 genomes]
rs6050413	0.85[ASN][1000 genomes]
rs6050415	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6050418	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6050419	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6050421	0.83[ASN][1000 genomes]
rs6107013	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6115069	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6132812	0.93[ASN][1000 genomes]
rs6132816	0.87[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs6138515	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs6138519	0.93[ASN][1000 genomes]
rs6138520	0.93[ASN][1000 genomes]
rs6138521	0.93[ASN][1000 genomes]
rs6138528	0.86[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6138530	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6138531	0.86[ASN][1000 genomes]
rs6138532	0.91[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs6138533	0.85[ASN][1000 genomes]
rs6515614	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8115505	0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8122274	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs910102	0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062140	chr20:24807962-25304054	Strong transcription Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv544219	chr20:24807962-25304054	Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv1056345	chr20:24819570-25168159	Flanking Active TSS Bivalent Enhancer Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	nsv1055341	chr20:24848416-25302271	Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
5	nsv1063494	chr20:25067286-25468557	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
6	nsv1063016	chr20:25067286-25475629	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised 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 miRNA target site	53 gene(s)	inside rSNPs	diseases
7	nsv1065101	chr20:25068046-25466542	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
8	nsv544220	chr20:25068046-25466542	Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Bivalent TSS/Enh 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	53 gene(s)	inside rSNPs	diseases
9	nsv531480	chr20:25070067-25472684	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
10	nsv585746	chr20:25071454-25470056	Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
11	nsv1062742	chr20:25071454-25475629	Enhancers Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
12	nsv949389	chr20:25071454-25506582	Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
13	nsv531481	chr20:25080583-25448944	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
14	nsv949479	chr20:25096494-25467359	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
15	nsv1061109	chr20:25101715-25472685	Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
16	nsv544221	chr20:25101715-25472685	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
17	nsv1066667	chr20:25133066-25238976	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
18	nsv544222	chr20:25133066-25238976	Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs13036626	FAM182B	cis	Artery Tibial	GTEx

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:25155800-25161600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr20:25157000-25160200	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr20:25158000-25160600	Enhancers	NHEK	skin
4	chr20:25158000-25160800	Enhancers	HMEC	breast
5	chr20:25158200-25160200	Enhancers	Hela-S3	cervix
6	chr20:25158200-25160400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr20:25158200-25160400	Enhancers	NH-A	brain
8	chr20:25158200-25160400	Enhancers	Osteobl	bone
9	chr20:25158200-25160600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr20:25158200-25160800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr20:25158400-25159600	Enhancers	Placenta Amnion	Placenta Amnion
12	chr20:25158400-25160000	Enhancers	Ovary	ovary
13	chr20:25158400-25160200	Enhancers	Colon Smooth Muscle	Colon
14	chr20:25158400-25160400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr20:25158600-25159800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr20:25158600-25159800	Enhancers	HSMM	muscle
17	chr20:25158600-25160000	Enhancers	HSMMtube	muscle
18	chr20:25158600-25160400	Enhancers	Muscle Satellite Cultured Cells	--
19	chr20:25158600-25160600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr20:25158600-25160600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr20:25158600-25160800	Enhancers	NHLF	lung
22	chr20:25158800-25159600	Enhancers	Esophagus	oesophagus
23	chr20:25158800-25159600	Enhancers	Right Ventricle	heart
24	chr20:25158800-25160000	Enhancers	Gastric	stomach
25	chr20:25158800-25160000	Enhancers	Pancreas	Pancrea
26	chr20:25158800-25160000	Enhancers	Right Atrium	heart
27	chr20:25158800-25160600	Enhancers	NHDF-Ad	bronchial
28	chr20:25158800-25160800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr20:25158800-25160800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr20:25159200-25159600	Enhancers	Placenta	Placenta
31	chr20:25159200-25159600	Enhancers	Rectal Smooth Muscle	rectum
32	chr20:25159200-25160000	Enhancers	Stomach Smooth Muscle	stomach
33	chr20:25159200-25160600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr20:25159200-25160800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr20:25159400-25159600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr20:25159400-25159600	Enhancers	Lung	lung
37	chr20:25159400-25159800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr20:25159400-25159800	Enhancers	HUVEC	blood vessel
39	chr20:25159400-25160000	Enhancers	Duodenum Smooth Muscle	Duodenum
40	chr20:25159400-25160000	Flanking Active TSS	A549	lung
41	chr20:25159400-25160200	Enhancers	Adipose Nuclei	Adipose
42	chr20:25159400-25160200	Enhancers	Fetal Heart	heart
43	chr20:25159400-25160200	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr20:25159400-25160800	Enhancers	HepG2	liver

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