Variant report

Variant	rs1893198
Chromosome Location	chr18:9248150-9248151
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr18:9247837-9248216	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:9240868..9244297-chr18:9247072..9249031,3	K562	blood:
2	chr18:9240868..9242942-chr18:9247072..9249031,2	K562	blood:

Variant related genes	Relation type
ENSG00000207092	TF binding region

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10451358	0.82[CHB][hapmap];0.90[CHD][hapmap]
rs11660603	0.84[CHD][hapmap]
rs11661711	0.90[CHD][hapmap];0.91[JPT][hapmap]
rs12150725	1.00[ASN][1000 genomes]
rs12958093	0.90[ASN][1000 genomes]
rs1443596	0.82[CHB][hapmap];0.90[CHD][hapmap]
rs17413793	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs2028656	0.82[CHB][hapmap]
rs2155707	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs28418978	0.94[ASN][1000 genomes]
rs34310409	0.99[ASN][1000 genomes]
rs34452937	0.90[ASN][1000 genomes]
rs4078337	0.95[CHB][hapmap];0.91[JPT][hapmap]
rs4131992	0.95[CHB][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs4148966	1.00[CEU][hapmap]
rs4148967	0.95[JPT][hapmap]
rs4603624	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs4797356	0.95[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap]
rs4797361	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4798772	0.94[CEU][hapmap];0.95[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[TSI][hapmap]
rs4798776	0.86[CHB][hapmap]
rs4798778	0.95[CHD][hapmap];0.95[JPT][hapmap]
rs4798782	0.89[ASN][1000 genomes]
rs4798784	0.96[ASN][1000 genomes]
rs4798785	0.82[CHB][hapmap];0.90[CHD][hapmap]
rs4798786	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[LWK][hapmap];1.00[MEX][hapmap];0.96[MKK][hapmap];1.00[TSI][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4798788	0.88[ASN][1000 genomes]
rs4798789	0.82[CHB][hapmap]
rs4798790	0.82[CHB][hapmap]
rs4798791	0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs56317320	0.81[ASN][1000 genomes]
rs6506644	0.90[CHD][hapmap]
rs6506648	0.82[CHB][hapmap];0.90[CHD][hapmap]
rs6506649	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7228251	0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs7229883	0.90[CHD][hapmap]
rs7231452	0.82[CHB][hapmap];0.90[CHD][hapmap]
rs7232337	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7235514	0.90[CHD][hapmap]
rs7504603	0.81[JPT][hapmap]
rs7506008	0.96[ASN][1000 genomes]
rs7506291	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs8087306	0.91[JPT][hapmap]
rs8089693	0.95[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8092135	0.82[CHB][hapmap];0.90[CHD][hapmap]
rs8097848	0.93[ASN][1000 genomes]
rs874250	0.82[CHB][hapmap];0.90[CHD][hapmap]
rs894755	1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs9304033	0.96[ASN][1000 genomes]
rs9304034	0.96[ASN][1000 genomes]
rs9304036	1.00[ASN][1000 genomes]
rs977581	0.95[CHB][hapmap];0.91[JPT][hapmap]
rs9944905	0.90[ASN][1000 genomes]
rs9945360	0.95[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap]
rs9946468	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs9946475	0.96[ASN][1000 genomes]
rs9946695	0.94[CEU][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];0.93[MEX][hapmap];0.91[TSI][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9946852	0.87[ASN][1000 genomes]
rs9947027	0.91[JPT][hapmap]
rs9948560	0.94[CHB][hapmap];0.89[JPT][hapmap];0.90[ASN][1000 genomes]
rs9959998	0.90[ASN][1000 genomes]
rs9960129	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];1.00[ASN][1000 genomes]
rs998171	0.82[CHB][hapmap];0.90[CHD][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916373	chr18:9026803-9592201	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS 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 miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv431971	chr18:9081185-9326852	Flanking Active TSS Active TSS Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	nsv1056407	chr18:9144345-9553764	Strong transcription Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
4	nsv1055696	chr18:9191679-9309805	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	nsv458023	chr18:9240413-9357786	Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
6	nsv576447	chr18:9240413-9357786	ZNF genes & repeats Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv2201	chr18:9247631-9279825	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:9192200-9284000	Weak transcription	NHEK	skin
2	chr18:9211800-9254800	Weak transcription	NH-A	brain
3	chr18:9212200-9254200	Weak transcription	Hela-S3	cervix
4	chr18:9216000-9250000	Weak transcription	Small Intestine	intestine
5	chr18:9216000-9289600	Weak transcription	HMEC	breast
6	chr18:9228200-9258000	Weak transcription	Fetal Heart	heart
7	chr18:9232600-9254200	Weak transcription	HUVEC	blood vessel
8	chr18:9232600-9261400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chr18:9232800-9273000	Weak transcription	Fetal Kidney	kidney
10	chr18:9233200-9249600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr18:9233200-9264200	Weak transcription	Brain Anterior Caudate	brain
12	chr18:9233400-9256400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr18:9233400-9265800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr18:9234200-9253600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr18:9234200-9264200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr18:9234400-9254200	Weak transcription	Fetal Thymus	thymus
17	chr18:9234400-9280400	Weak transcription	Psoas Muscle	Psoas
18	chr18:9234600-9256400	Weak transcription	Brain Germinal Matrix	brain
19	chr18:9234600-9264800	Weak transcription	Colonic Mucosa	Colon
20	chr18:9234600-9278000	Weak transcription	Brain Angular Gyrus	brain
21	chr18:9234800-9252200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr18:9234800-9252200	Weak transcription	Ovary	ovary
23	chr18:9234800-9254200	Weak transcription	A549	lung
24	chr18:9234800-9256800	Weak transcription	Fetal Brain Female	brain
25	chr18:9234800-9264200	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr18:9234800-9264800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr18:9234800-9264800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr18:9234800-9264800	Weak transcription	Lung	lung
29	chr18:9234800-9264800	Weak transcription	Pancreas	Pancrea
30	chr18:9234800-9290000	Weak transcription	NHLF	lung
31	chr18:9235000-9251400	Weak transcription	Fetal Intestine Small	intestine
32	chr18:9235000-9257000	Weak transcription	Fetal Muscle Trunk	muscle
33	chr18:9235000-9264600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
34	chr18:9235000-9264800	Weak transcription	Gastric	stomach
35	chr18:9235000-9264800	Weak transcription	Right Ventricle	heart
36	chr18:9235000-9285400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr18:9235200-9260800	Weak transcription	Esophagus	oesophagus
38	chr18:9235200-9264200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr18:9235200-9264600	Weak transcription	Rectal Smooth Muscle	rectum
40	chr18:9235400-9264800	Weak transcription	Fetal Stomach	stomach
41	chr18:9235400-9270800	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr18:9235600-9258200	Weak transcription	Cortex derived primary cultured neurospheres	brain
43	chr18:9235600-9264600	Weak transcription	Stomach Smooth Muscle	stomach
44	chr18:9235800-9260800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr18:9235800-9264800	Weak transcription	Thymus	Thymus
46	chr18:9236200-9253400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr18:9236600-9264200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
48	chr18:9237000-9264200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
49	chr18:9239600-9264600	Weak transcription	HepG2	liver
50	chr18:9240400-9264800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin

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