Variant report

Variant	rs7918734
Chromosome Location	chr10:192533-192534
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr10:185579..190564-chr10:192316..195395,6	MCF-7	breast:
2	chr10:187321..189950-chr10:190667..193548,2	MCF-7	breast:

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs1017361	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1367896	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.87[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1476129	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes]
rs1545003	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2007293	0.87[AMR][1000 genomes]
rs2043201	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2303990	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap]
rs2379050	0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2436024	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2436025	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2436028	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2436031	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2448365	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2448367	0.81[AMR][1000 genomes]
rs2448369	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs2448372	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2448374	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes]
rs2448375	0.83[AMR][1000 genomes]
rs2448376	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2448377	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2448379	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2448382	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes]
rs2496274	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.90[AMR][1000 genomes]
rs2496277	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.90[AMR][1000 genomes]
rs2496279	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes]
rs3001994	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs3123252	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.81[AMR][1000 genomes]
rs3132006	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.86[AMR][1000 genomes]
rs3740303	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[YRI][hapmap]
rs4275539	0.81[AFR][1000 genomes]
rs4331015	0.81[AFR][1000 genomes]
rs4390277	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4411223	0.84[ASN][1000 genomes]
rs4469806	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4469807	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4504990	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4537685	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4582897	0.82[AMR][1000 genomes]
rs4593933	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs4600135	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.86[AMR][1000 genomes]
rs4880517	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes]
rs58496617	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6560723	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6560742	0.82[AMR][1000 genomes]
rs7081782	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7089889	0.82[AFR][1000 genomes]
rs7478542	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7893922	0.84[AFR][1000 genomes];0.88[AMR][1000 genomes]
rs7898275	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7905732	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[AMR][1000 genomes]
rs7910845	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7914050	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7919991	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes]
rs9286070	0.84[ASN][1000 genomes]
rs9329277	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9329281	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9419419	0.90[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9419433	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs9419435	0.81[AMR][1000 genomes]
rs9419436	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes]
rs9419475	1.00[JPT][hapmap]
rs9419499	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes]
rs9419560	0.84[ASN][1000 genomes]
rs9419561	0.84[ASN][1000 genomes]
rs9419562	0.84[ASN][1000 genomes]
rs9419564	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531919	chr10:60001-668649	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats 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	19 gene(s)	inside rSNPs	diseases
2	nsv1040332	chr10:72797-244561	Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv1044775	chr10:72797-250662	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv1047868	chr10:72797-259003	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv1048232	chr10:72797-274675	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:183000-192600	Weak transcription	Primary hematopoietic stem cells	blood
2	chr10:183000-196400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr10:183200-205400	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr10:183400-194600	Weak transcription	Fetal Stomach	stomach
5	chr10:183400-194600	Weak transcription	Gastric	stomach
6	chr10:183400-199400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr10:183400-200800	Weak transcription	Thymus	Thymus
8	chr10:183600-199000	Weak transcription	HSMM	muscle
9	chr10:184400-199600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr10:184400-200200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr10:184600-200000	Weak transcription	NHLF	lung
12	chr10:185200-198000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr10:186200-199800	Weak transcription	Right Ventricle	heart
14	chr10:187400-193600	Weak transcription	Fetal Lung	lung
15	chr10:187400-194400	Weak transcription	HepG2	liver
16	chr10:187400-194600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr10:188000-200400	Weak transcription	Primary B cells from cord blood	blood
18	chr10:188400-193800	Weak transcription	Pancreas	Pancrea
19	chr10:188400-199600	Weak transcription	Ovary	ovary
20	chr10:188400-199600	Weak transcription	Sigmoid Colon	Sigmoid Colon
21	chr10:188800-193800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
22	chr10:188800-202600	Weak transcription	A549	lung
23	chr10:189000-193800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr10:189000-196600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr10:189000-204000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr10:189000-208800	Weak transcription	Small Intestine	intestine
27	chr10:189200-199800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr10:189200-199800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr10:189200-201800	Weak transcription	Brain Hippocampus Middle	brain
30	chr10:189400-200200	Weak transcription	Fetal Heart	heart
31	chr10:189800-192600	Weak transcription	Primary T helper cells PMA-I stimulated	--
32	chr10:190400-193600	Weak transcription	Right Atrium	heart
33	chr10:190400-200200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr10:190400-215200	Weak transcription	Primary T cells fromperipheralblood	blood
35	chr10:190600-192600	Weak transcription	Psoas Muscle	Psoas
36	chr10:190600-196400	Weak transcription	Colon Smooth Muscle	Colon
37	chr10:190600-203200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr10:190600-212800	Weak transcription	Left Ventricle	heart
39	chr10:191400-199800	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr10:192200-193400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
41	chr10:192200-194200	Weak transcription	Dnd41	blood
42	chr10:192400-194600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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