Variant report

Variant	rs1237203
Chromosome Location	chr11:85395180-85395181
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:85392491-85397452	K562	blood:	n/a	n/a

No data

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:85387868..85389432-chr11:85395056..85397188,2	MCF-7	breast:
2	chr11:85374551..85377717-chr11:85388541..85395552,6	MCF-7	breast:
3	chr11:85337931..85339718-chr11:85394952..85396893,2	K562	blood:
4	chr11:85374139..85377473-chr11:85394538..85397297,3	MCF-7	breast:
5	chr11:85375817..85377426-chr11:85394328..85396398,2	K562	blood:
6	chr11:85394543..85396055-chr11:85509684..85512654,2	MCF-7	breast:
7	chr11:85389569..85392078-chr11:85394347..85396779,2	MCF-7	breast:

No data

Variant related genes	Relation type
CREBZF	TF binding region
ENSG00000150672	Chromatin interaction
ENSG00000171204	Chromatin interaction
ENSG00000137504	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:57)

rs_ID	r²[population]
rs1046216	0.83[ASW][hapmap];0.95[CHB][hapmap];0.87[CHD][hapmap];0.85[JPT][hapmap];0.89[YRI][hapmap];0.87[ASN][1000 genomes]
rs10898410	0.83[MEX][hapmap]
rs11600919	0.90[ASN][1000 genomes]
rs11603256	1.00[CHB][hapmap];0.90[CHD][hapmap];0.90[JPT][hapmap];0.88[ASN][1000 genomes]
rs2117312	0.80[ASN][1000 genomes]
rs2196168	0.89[ASW][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.90[JPT][hapmap];0.89[YRI][hapmap];0.84[ASN][1000 genomes]
rs2290823	0.83[ASW][hapmap];0.86[YRI][hapmap]
rs2374683	0.83[MEX][hapmap]
rs290173	0.86[CHB][hapmap];0.95[JPT][hapmap];0.87[MEX][hapmap];0.85[ASN][1000 genomes]
rs290174	0.85[ASN][1000 genomes]
rs290179	0.81[CHB][hapmap];0.86[CHD][hapmap];0.80[ASN][1000 genomes]
rs290180	0.86[CHB][hapmap];0.92[CHD][hapmap];0.83[ASN][1000 genomes]
rs290181	0.82[ASN][1000 genomes]
rs290183	1.00[CHB][hapmap];0.89[ASN][1000 genomes]
rs290184	0.89[ASW][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.85[JPT][hapmap];0.84[MKK][hapmap];0.89[YRI][hapmap];0.83[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs290185	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.98[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs290190	0.90[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs290191	0.85[ASN][1000 genomes]
rs290193	0.82[JPT][hapmap]
rs290195	0.90[CHB][hapmap];1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs290200	0.86[CHB][hapmap];0.82[CHD][hapmap];1.00[JPT][hapmap];0.81[ASN][1000 genomes]
rs290202	0.90[CHB][hapmap];0.80[CHD][hapmap];1.00[JPT][hapmap];0.83[MEX][hapmap];0.85[ASN][1000 genomes]
rs370385	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3753050	0.89[ASW][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.90[JPT][hapmap];0.84[MKK][hapmap];0.89[YRI][hapmap];0.89[ASN][1000 genomes]
rs3781815	1.00[CHB][hapmap];0.88[JPT][hapmap];0.86[ASN][1000 genomes]
rs3817087	0.88[ASN][1000 genomes]
rs3824956	0.89[ASW][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.85[JPT][hapmap];0.84[MKK][hapmap];0.89[YRI][hapmap];0.88[ASN][1000 genomes]
rs3862782	0.89[ASW][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.90[JPT][hapmap];0.89[YRI][hapmap];0.89[ASN][1000 genomes]
rs431606	0.86[CHB][hapmap];0.97[CHD][hapmap]
rs491867	0.86[CHB][hapmap];0.95[JPT][hapmap]
rs4944530	0.88[ASN][1000 genomes]
rs496187	0.86[CHB][hapmap];0.95[JPT][hapmap]
rs522604	0.81[ASN][1000 genomes]
rs540063	0.80[CHB][hapmap];0.90[JPT][hapmap]
rs550404	0.95[JPT][hapmap]
rs552013	0.85[ASN][1000 genomes]
rs556669	0.95[JPT][hapmap]
rs57296431	0.85[ASN][1000 genomes]
rs575013	0.81[JPT][hapmap]
rs575050	0.81[CHB][hapmap]
rs580459	0.95[JPT][hapmap]
rs589327	0.89[CHB][hapmap];0.85[JPT][hapmap]
rs592460	0.84[CEU][hapmap];1.00[CHB][hapmap];0.85[JPT][hapmap];0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs597480	0.95[JPT][hapmap];0.83[MEX][hapmap]
rs631375	0.82[AMR][1000 genomes]
rs631410	0.86[CHB][hapmap];0.95[JPT][hapmap]
rs641393	0.95[JPT][hapmap];0.83[MEX][hapmap]
rs647912	0.86[CHB][hapmap];0.95[JPT][hapmap];0.83[MEX][hapmap]
rs679204	0.86[CHB][hapmap];0.94[JPT][hapmap]
rs680498	0.85[CHB][hapmap];0.95[JPT][hapmap]
rs7107788	0.89[ASW][hapmap];1.00[CHB][hapmap];0.92[CHD][hapmap];0.90[JPT][hapmap];0.84[MKK][hapmap];0.89[YRI][hapmap];0.88[ASN][1000 genomes]
rs7116195	0.89[ASW][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];0.85[JPT][hapmap];0.89[YRI][hapmap];0.87[ASN][1000 genomes]
rs7119617	0.83[ASW][hapmap];0.85[YRI][hapmap]
rs7925739	0.81[ASN][1000 genomes]
rs7943586	0.83[ASW][hapmap];0.82[YRI][hapmap]
rs881120	0.94[ASW][hapmap];0.84[CEU][hapmap];1.00[CHB][hapmap];0.89[CHD][hapmap];0.85[JPT][hapmap];0.83[MEX][hapmap];0.86[YRI][hapmap];0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs956202	1.00[CHB][hapmap];0.90[JPT][hapmap];0.87[ASN][1000 genomes]

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	nsv1051155	chr11:85006564-85721261	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv541110	chr11:85006564-85721261	Enhancers Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
3	esv2758279	chr11:85180480-85603988	Flanking Active TSS Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
4	esv2759845	chr11:85180480-85603988	Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
5	nsv898048	chr11:85206156-85404138	Flanking Active TSS Genic enhancers Active TSS Weak transcription Strong transcription Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
6	nsv468768	chr11:85395180-85436352	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv555632	chr11:85395180-85436352	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs1237203	ME3	cis	cerebellum	SCAN
rs1237203	GRM5	cis	parietal	SCAN
rs1237203	SYTL2	cis	Muscle Skeletal	GTEx
rs1237203	RHBG	trans	parietal	SCAN

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:85392400-85396200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr11:85392400-85396200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:85394000-85396200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr11:85394000-85427400	Weak transcription	Small Intestine	intestine
5	chr11:85394200-85395200	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr11:85394200-85395600	Weak transcription	Fetal Stomach	stomach
7	chr11:85394200-85395600	Weak transcription	HepG2	liver
8	chr11:85394200-85395600	Weak transcription	HSMM	muscle
9	chr11:85394200-85395600	Enhancers	NHDF-Ad	bronchial
10	chr11:85394200-85395800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr11:85394200-85395800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr11:85394200-85395800	Weak transcription	Brain Angular Gyrus	brain
13	chr11:85394200-85395800	Weak transcription	Colon Smooth Muscle	Colon
14	chr11:85394200-85395800	Weak transcription	Fetal Heart	heart
15	chr11:85394200-85395800	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr11:85394200-85396000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr11:85394200-85396000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
18	chr11:85394200-85396000	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr11:85394200-85396000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr11:85394200-85396000	Weak transcription	Adipose Nuclei	Adipose
21	chr11:85394200-85396000	Weak transcription	Brain Cingulate Gyrus	brain
22	chr11:85394200-85396000	Weak transcription	Brain Hippocampus Middle	brain
23	chr11:85394200-85396000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr11:85394200-85396000	Weak transcription	Brain Substantia Nigra	brain
25	chr11:85394200-85396000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr11:85394200-85396000	Weak transcription	Fetal Muscle Trunk	muscle
27	chr11:85394200-85396000	Weak transcription	Placenta	Placenta
28	chr11:85394200-85396000	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr11:85394200-85396000	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr11:85394200-85396000	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chr11:85394200-85396000	Weak transcription	Stomach Mucosa	stomach
32	chr11:85394200-85396000	Weak transcription	Spleen	Spleen
33	chr11:85394200-85396000	Weak transcription	NH-A	brain
34	chr11:85394200-85396200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr11:85394200-85396200	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr11:85394200-85396200	Weak transcription	Gastric	stomach
37	chr11:85394200-85396200	Weak transcription	Left Ventricle	heart
38	chr11:85394200-85396200	Weak transcription	Lung	lung
39	chr11:85394200-85396200	Weak transcription	Psoas Muscle	Psoas
40	chr11:85394200-85396200	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr11:85394200-85396400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr11:85394200-85396400	Weak transcription	Fetal Brain Male	brain
43	chr11:85394200-85396400	Weak transcription	Fetal Thymus	thymus
44	chr11:85394200-85396400	Weak transcription	NHEK	skin
45	chr11:85394200-85396800	Weak transcription	Esophagus	oesophagus
46	chr11:85394200-85396800	Weak transcription	Fetal Brain Female	brain
47	chr11:85394200-85396800	Weak transcription	Thymus	Thymus
48	chr11:85394200-85401800	Weak transcription	Primary T cells from cord blood	blood
49	chr11:85394200-85404200	Weak transcription	Sigmoid Colon	Sigmoid Colon
50	chr11:85394200-85406200	Weak transcription	Primary T helper cells fromperipheralblood	blood

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