Variant report

Variant	rs588036
Chromosome Location	chr6:150698674-150698675
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs2064214	0.87[CHB][hapmap]
rs581697	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs606775	0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs608175	0.89[CEU][hapmap]
rs609146	0.92[CEU][hapmap];0.93[CHB][hapmap];0.93[GIH][hapmap];0.86[MEX][hapmap];0.91[TSI][hapmap];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs623252	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs627147	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs633945	0.93[ASW][hapmap];1.00[CEU][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];0.81[MKK][hapmap];0.89[TSI][hapmap];0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs634686	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs640074	0.89[CEU][hapmap]
rs641944	0.82[ASN][1000 genomes]
rs649613	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs651777	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs654116	0.93[CHB][hapmap];0.82[ASN][1000 genomes]
rs654928	0.82[ASN][1000 genomes]
rs655254	0.82[ASN][1000 genomes]
rs655401	0.93[CHB][hapmap];0.82[ASN][1000 genomes]
rs655745	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs666147	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs670292	0.93[ASW][hapmap];1.00[CEU][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];0.81[MKK][hapmap];0.89[TSI][hapmap];0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs671753	0.93[CHB][hapmap];0.82[ASN][1000 genomes]
rs672766	1.00[CEU][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs674026	0.85[CEU][hapmap]
rs679249	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs685969	0.82[ASN][1000 genomes]
rs6906028	0.85[CEU][hapmap]
rs6906229	0.92[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6930494	0.87[CHB][hapmap]
rs694326	0.88[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7757225	0.89[CEU][hapmap]
rs7771338	0.87[CHB][hapmap]
rs7772011	0.89[CEU][hapmap]
rs805989	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs805991	0.90[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs805992	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9322260	0.96[CEU][hapmap];0.82[JPT][hapmap]
rs9480339	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9480340	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2763602	chr6:150581193-150720666	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs588036	PPP1R14C	cis	parietal	SCAN
rs588036	ESR1	cis	cerebellum	SCAN
rs588036	RMND1	cis	cerebellum	SCAN

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:150691600-150700200	Weak transcription	Lung	lung
2	chr6:150695400-150703400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr6:150696800-150699200	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr6:150697200-150699200	Enhancers	Fetal Kidney	kidney
5	chr6:150697800-150699000	Enhancers	Liver	Liver
6	chr6:150698000-150698800	Enhancers	Pancreas	Pancrea
7	chr6:150698000-150699000	Enhancers	Fetal Heart	heart
8	chr6:150698000-150699200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr6:150698000-150699200	Enhancers	Fetal Intestine Small	intestine
10	chr6:150698200-150698800	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr6:150698200-150698800	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr6:150698200-150698800	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr6:150698200-150698800	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
14	chr6:150698200-150698800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr6:150698200-150698800	Enhancers	Brain Anterior Caudate	brain
16	chr6:150698200-150698800	Enhancers	Brain Cingulate Gyrus	brain
17	chr6:150698200-150698800	Enhancers	Right Atrium	heart
18	chr6:150698200-150699000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr6:150698200-150699000	Enhancers	Brain Substantia Nigra	brain
20	chr6:150698200-150699000	Enhancers	Osteobl	bone
21	chr6:150698200-150699200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr6:150698200-150699200	Enhancers	Brain Hippocampus Middle	brain
23	chr6:150698400-150698800	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr6:150698400-150698800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr6:150698400-150698800	Enhancers	Adipose Nuclei	Adipose
26	chr6:150698400-150698800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
27	chr6:150698400-150698800	Enhancers	Gastric	stomach
28	chr6:150698400-150698800	Enhancers	Ovary	ovary
29	chr6:150698400-150698800	Enhancers	Skeletal Muscle Female	skeletal muscle
30	chr6:150698400-150698800	Enhancers	Spleen	Spleen
31	chr6:150698400-150698800	Bivalent Enhancer	NH-A	brain
32	chr6:150698400-150699000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr6:150698400-150699000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr6:150698400-150699000	Flanking Active TSS	Duodenum Mucosa	Duodenum
35	chr6:150698400-150699000	Enhancers	Fetal Lung	lung
36	chr6:150698400-150699000	Flanking Active TSS	HepG2	liver
37	chr6:150698400-150699200	Enhancers	Fetal Intestine Large	intestine
38	chr6:150698400-150699200	Enhancers	K562	blood
39	chr6:150698600-150698800	Flanking Active TSS	Brain Angular Gyrus	brain
40	chr6:150698600-150698800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
41	chr6:150698600-150698800	Enhancers	Left Ventricle	heart
42	chr6:150698600-150698800	Bivalent Enhancer	HSMMtube	muscle
43	chr6:150698600-150699000	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr6:150698600-150699000	Enhancers	NHDF-Ad	bronchial
45	chr6:150698600-150699200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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