Variant report

Variant	rs1265327
Chromosome Location	chr4:75095061-75095062
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:75094355..75095090-chr4:75547966..75548494,2	K562	blood:
2	chr4:75091219..75093823-chr4:75093870..75096715,2	MCF-7	breast:
3	chr4:75054721..75055635-chr4:75094051..75095124,3	K562	blood:
4	chr4:75093762..75095528-chr4:75175394..75177161,2	MCF-7	breast:
5	chr4:75094225..75095673-chr4:75176947..75177967,4	MCF-7	breast:
6	chr4:75094222..75095380-chr4:75595823..75596616,3	K562	blood:
7	chr4:75093661..75096004-chr4:75147885..75149545,2	K562	blood:

Extended variants
information (count: 98 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs10009707	0.85[EUR][1000 genomes]
rs10010575	0.84[TSI][hapmap]
rs10013212	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10017409	0.86[TSI][hapmap];0.82[EUR][1000 genomes]
rs10017417	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10018373	0.95[CEU][hapmap];1.00[TSI][hapmap];0.92[EUR][1000 genomes]
rs10019396	0.90[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10023519	0.86[TSI][hapmap];0.84[EUR][1000 genomes]
rs10026687	0.84[EUR][1000 genomes]
rs10028285	0.81[EUR][1000 genomes]
rs10433673	0.92[EUR][1000 genomes]
rs10938112	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11724468	0.86[CEU][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11731340	0.87[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11737662	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.91[MEX][hapmap];0.81[MKK][hapmap];1.00[TSI][hapmap];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11945418	0.89[EUR][1000 genomes]
rs1246575	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1246577	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[YRI][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1246578	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.81[MEX][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1246579	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1246580	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1246582	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1246584	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1246586	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1246587	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1246588	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1246590	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1246591	0.90[CEU][hapmap];0.86[CHB][hapmap];0.97[CHD][hapmap];0.97[GIH][hapmap];0.92[JPT][hapmap];0.86[MEX][hapmap];1.00[TSI][hapmap];0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1246594	0.95[CEU][hapmap];0.91[EUR][1000 genomes]
rs1246597	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12500697	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13116896	0.92[EUR][1000 genomes]
rs13142241	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1371796	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1371797	0.92[JPT][hapmap];0.84[EUR][1000 genomes]
rs1380561	1.00[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1460016	0.94[TSI][hapmap];0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1460017	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16850862	0.82[EUR][1000 genomes]
rs17232394	0.84[EUR][1000 genomes]
rs17829765	0.80[TSI][hapmap]
rs1964526	0.92[EUR][1000 genomes]
rs2045616	0.86[TSI][hapmap]
rs2045618	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2061508	0.86[TSI][hapmap];0.84[EUR][1000 genomes]
rs2367555	0.90[EUR][1000 genomes]
rs2367745	0.85[CEU][hapmap];0.89[EUR][1000 genomes]
rs28378517	0.87[EUR][1000 genomes]
rs28436705	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs28539097	0.84[EUR][1000 genomes]
rs28592249	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28644493	0.85[EUR][1000 genomes]
rs28695994	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4371587	0.85[EUR][1000 genomes]
rs4502653	0.84[EUR][1000 genomes]
rs4577545	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4694184	0.87[EUR][1000 genomes]
rs488440	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.92[JPT][hapmap];0.82[MEX][hapmap];0.82[MKK][hapmap];1.00[TSI][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs536541	0.84[EUR][1000 genomes]
rs565831	0.84[EUR][1000 genomes]
rs62312513	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62312515	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs62312545	0.84[EUR][1000 genomes]
rs6446983	0.84[EUR][1000 genomes]
rs6446984	0.86[TSI][hapmap];0.84[EUR][1000 genomes]
rs6446985	0.84[EUR][1000 genomes]
rs6811214	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6814880	0.86[TSI][hapmap]
rs6819605	0.86[TSI][hapmap];0.82[EUR][1000 genomes]
rs6821664	0.86[TSI][hapmap];0.85[EUR][1000 genomes]
rs6835734	0.86[TSI][hapmap]
rs6854203	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6854723	0.88[TSI][hapmap];0.84[EUR][1000 genomes]
rs6858809	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7659389	0.85[EUR][1000 genomes]
rs7663269	0.84[TSI][hapmap]
rs7665105	0.85[EUR][1000 genomes]
rs7670535	0.85[EUR][1000 genomes]
rs7672588	0.84[EUR][1000 genomes]
rs7676371	0.84[EUR][1000 genomes]
rs7678292	0.85[EUR][1000 genomes]
rs7681137	0.92[JPT][hapmap];0.82[TSI][hapmap];0.84[EUR][1000 genomes]
rs7681763	0.84[EUR][1000 genomes]
rs7681912	0.86[CEU][hapmap];0.94[TSI][hapmap];0.90[EUR][1000 genomes]
rs7683181	0.90[EUR][1000 genomes]
rs9992393	1.00[CHB][hapmap];0.91[JPT][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9997322	0.88[TSI][hapmap];0.84[EUR][1000 genomes]
rs9997788	0.85[CEU][hapmap];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv525980	chr4:74731526-75382209	Strong transcription Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1004768	chr4:74774372-75109579	Weak transcription Enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
3	nsv1006218	chr4:74782324-75105424	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
4	nsv594683	chr4:75013441-75106485	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	nsv1013260	chr4:75013441-75121643	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv1002907	chr4:75013441-75131443	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
7	nsv1004706	chr4:75014770-75121643	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
8	nsv594684	chr4:75015750-75106485	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	nsv437397	chr4:75077057-75095061	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv1009099	chr4:75089233-75726206	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs1265327	ANKRD56	cis	parietal	SCAN
rs1265327	CCDC158	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:75056800-75096600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr4:75064200-75096400	Weak transcription	Skeletal Muscle Female	skeletal muscle
3	chr4:75067800-75097000	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr4:75068400-75096600	Weak transcription	Adipose Nuclei	Adipose
5	chr4:75071800-75096400	Weak transcription	Rectal Mucosa Donor 29	rectum
6	chr4:75072200-75099200	Weak transcription	Ovary	ovary
7	chr4:75075000-75095800	Weak transcription	Primary T cells from cord blood	blood
8	chr4:75080600-75109600	Weak transcription	Primary hematopoietic stem cells	blood
9	chr4:75080800-75095400	Weak transcription	Fetal Thymus	thymus
10	chr4:75084200-75096400	Weak transcription	GM12878-XiMat	blood
11	chr4:75085400-75102600	Weak transcription	Brain Hippocampus Middle	brain
12	chr4:75086000-75096400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr4:75086200-75117600	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr4:75090200-75095400	Weak transcription	Monocytes-CD14+_RO01746	blood
15	chr4:75090200-75095800	Weak transcription	A549	lung
16	chr4:75090200-75096400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr4:75090200-75096400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr4:75090200-75096400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr4:75090200-75096400	Weak transcription	HSMM	muscle
20	chr4:75090200-75097000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
21	chr4:75090400-75096400	Weak transcription	HMEC	breast
22	chr4:75090400-75102200	Weak transcription	Pancreas	Pancrea
23	chr4:75091600-75096600	Weak transcription	Left Ventricle	heart
24	chr4:75091800-75103200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr4:75093000-75105000	Weak transcription	Lung	lung
26	chr4:75093000-75117400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr4:75093200-75100600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr4:75093600-75101000	Weak transcription	Liver	Liver
29	chr4:75094200-75096400	Enhancers	Muscle Satellite Cultured Cells	--
30	chr4:75094200-75096400	Enhancers	NHDF-Ad	bronchial
31	chr4:75094400-75096400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr4:75094400-75096400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr4:75094400-75096400	Enhancers	Osteobl	bone
34	chr4:75094600-75096400	Enhancers	Hela-S3	cervix
35	chr4:75094600-75096400	Enhancers	HUVEC	blood vessel
36	chr4:75094800-75095200	Enhancers	NHEK	skin
37	chr4:75094800-75096400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr4:75095000-75095600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr4:75095000-75095600	Enhancers	NHLF	lung
40	chr4:75095000-75095800	Enhancers	HSMMtube	muscle
41	chr4:75095000-75096400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr4:75095000-75096400	Enhancers	Rectal Mucosa Donor 31	rectum
43	chr4:75095000-75097200	Enhancers	NH-A	brain
44	chr4:75095000-75097400	Enhancers	Primary hematopoietic stem cells short term culture	blood
45	chr4:75095000-75098400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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