Variant report

Variant	rs718742
Chromosome Location	chr8:10614275-10614276
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	chr8:10613644..10615982-chr8:10616006..10618005,2	MCF-7	breast:

Extended variants
information (count: 116 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:101)

rs_ID	r²[population]
rs10089615	0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs10091836	0.80[ASN][1000 genomes]
rs10092781	0.81[CHB][hapmap];0.80[ASN][1000 genomes]
rs10097283	0.86[CHB][hapmap];0.83[ASN][1000 genomes]
rs10099021	0.88[CHD][hapmap]
rs10100265	0.91[CHB][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs10105487	0.95[JPT][hapmap]
rs10107180	0.90[CHD][hapmap]
rs10107289	0.92[ASN][1000 genomes]
rs10109416	0.80[CEU][hapmap]
rs10113332	0.88[CHD][hapmap]
rs10113343	0.82[CHB][hapmap];0.80[ASN][1000 genomes]
rs10481451	0.83[CHD][hapmap];0.82[JPT][hapmap];0.82[ASN][1000 genomes]
rs1073913	0.97[ASN][1000 genomes]
rs10903330	0.90[JPT][hapmap]
rs1115866	0.95[CHB][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs1115867	0.93[ASN][1000 genomes]
rs1124010	0.83[ASN][1000 genomes]
rs11250069	0.84[ASN][1000 genomes]
rs11250073	0.95[CHB][hapmap];0.94[JPT][hapmap]
rs11250074	0.95[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs11250077	0.91[CHB][hapmap];0.90[CHD][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs11250078	0.83[JPT][hapmap]
rs11250080	0.84[CEU][hapmap];0.83[GIH][hapmap];0.85[JPT][hapmap];0.84[MEX][hapmap];0.82[TSI][hapmap]
rs11993903	0.85[JPT][hapmap]
rs12542888	0.86[CHB][hapmap];0.90[CHD][hapmap];0.83[ASN][1000 genomes]
rs12676417	0.90[JPT][hapmap];0.80[ASN][1000 genomes]
rs13276026	0.94[ASN][1000 genomes]
rs1430867	0.84[ASN][1000 genomes]
rs17152302	0.84[ASN][1000 genomes]
rs17152305	0.84[ASN][1000 genomes]
rs1821002	0.93[ASN][1000 genomes]
rs1897207	0.97[ASN][1000 genomes]
rs1968400	0.99[ASN][1000 genomes]
rs1968401	0.99[ASN][1000 genomes]
rs2005309	0.88[ASN][1000 genomes]
rs2116092	0.84[ASN][1000 genomes]
rs2116093	0.99[ASN][1000 genomes]
rs2116095	0.95[CHB][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs2280047	0.82[ASN][1000 genomes]
rs2409663	0.95[CHB][hapmap];0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs2409669	1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2409672	0.83[ASN][1000 genomes]
rs2409674	0.82[ASN][1000 genomes]
rs2409675	0.83[ASN][1000 genomes]
rs28570522	0.93[ASN][1000 genomes]
rs2898248	0.91[CHB][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs2898251	0.97[ASN][1000 genomes]
rs4240669	0.93[ASN][1000 genomes]
rs4240670	0.94[JPT][hapmap]
rs4321967	0.95[CHB][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs4504595	0.86[ASN][1000 genomes]
rs4593498	0.86[ASN][1000 genomes]
rs4840512	0.83[ASN][1000 genomes]
rs4840513	0.99[ASN][1000 genomes]
rs4840516	0.81[CHD][hapmap];0.90[JPT][hapmap]
rs4840517	0.81[CHD][hapmap];0.92[GIH][hapmap];0.90[JPT][hapmap];0.84[MEX][hapmap];0.85[TSI][hapmap]
rs4841436	0.81[ASN][1000 genomes]
rs4841437	0.83[ASN][1000 genomes]
rs4841441	0.93[ASN][1000 genomes]
rs6601513	0.82[ASN][1000 genomes]
rs6601521	0.91[CHB][hapmap];0.91[CHD][hapmap];0.95[JPT][hapmap];0.93[ASN][1000 genomes]
rs6601522	1.00[CHB][hapmap];0.97[CHD][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs6601523	0.91[CHB][hapmap];0.90[JPT][hapmap];0.93[ASN][1000 genomes]
rs6601525	0.83[CHB][hapmap];0.90[CHD][hapmap];0.80[ASN][1000 genomes]
rs6601529	0.90[JPT][hapmap]
rs6601530	0.90[JPT][hapmap]
rs6981530	0.84[ASN][1000 genomes]
rs6984744	0.96[ASN][1000 genomes]
rs6985218	0.85[CHD][hapmap]
rs6989072	0.81[ASN][1000 genomes]
rs6989370	0.99[ASN][1000 genomes]
rs6993841	0.86[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs6994595	0.80[ASN][1000 genomes]
rs7002117	0.98[ASN][1000 genomes]
rs7002137	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7002282	0.90[JPT][hapmap]
rs7005905	0.82[CHB][hapmap];0.80[CHD][hapmap]
rs7014285	0.84[ASN][1000 genomes]
rs718741	0.99[ASN][1000 genomes]
rs733395	0.82[ASN][1000 genomes]
rs733396	0.82[ASN][1000 genomes]
rs73542560	0.84[ASN][1000 genomes]
rs73544343	0.81[ASN][1000 genomes]
rs736668	0.82[ASN][1000 genomes]
rs736669	0.82[ASN][1000 genomes]
rs752446	0.91[CHB][hapmap];0.92[CHD][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs7813706	0.93[ASN][1000 genomes]
rs7814142	0.93[ASN][1000 genomes]
rs7814757	0.84[JPT][hapmap]
rs7823088	0.80[ASN][1000 genomes]
rs7826180	0.92[CHD][hapmap];0.80[ASN][1000 genomes]
rs7826189	0.82[CHB][hapmap];0.92[CHD][hapmap];0.80[ASN][1000 genomes]
rs7826218	0.83[ASN][1000 genomes]
rs7826392	0.82[ASN][1000 genomes]
rs7826458	0.90[CHD][hapmap]
rs7834466	0.95[CHB][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs891556	0.88[ASN][1000 genomes]
rs919555	0.84[ASN][1000 genomes]
rs9329231	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9969626	0.90[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022994	chr8:10190618-10660122	Strong transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv539466	chr8:10190618-10660122	Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	nsv917085	chr8:10237508-10828204	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv1022582	chr8:10571218-10636162	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	nsv539468	chr8:10571218-10636162	Bivalent/Poised TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
6	nsv1026802	chr8:10576444-10754489	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
7	nsv539469	chr8:10576444-10754489	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
8	nsv1017836	chr8:10591801-10803617	Enhancers ZNF genes & repeats Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
9	nsv1034988	chr8:10591801-10804243	Genic enhancers Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	14 gene(s)	inside rSNPs	diseases
10	nsv519768	chr8:10600254-10691993	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
11	nsv1024806	chr8:10605438-10662555	Weak transcription Strong transcription Genic enhancers Enhancers Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv831232	chr8:10606053-10774948	Flanking Active TSS Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
13	nsv1031709	chr8:10610545-10657726	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
14	esv2764105	chr8:10610557-10657726	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
15	nsv519376	chr8:10611708-10691993	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10609600-10616200	Weak transcription	Primary T cells from cord blood	blood
2	chr8:10610000-10621400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:10610600-10620400	Weak transcription	HepG2	liver
4	chr8:10610800-10622200	Weak transcription	Primary B cells from cord blood	blood
5	chr8:10610800-10662000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr8:10611200-10624400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr8:10612600-10617600	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr8:10612600-10621600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr8:10612800-10621600	Weak transcription	Spleen	Spleen
10	chr8:10613200-10622600	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr8:10613400-10621600	Weak transcription	Aorta	Aorta
12	chr8:10613600-10614800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr8:10613600-10614800	Enhancers	HMEC	breast
14	chr8:10613600-10618400	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr8:10613600-10618800	Weak transcription	Fetal Muscle Leg	muscle
16	chr8:10613800-10617800	Weak transcription	Ovary	ovary
17	chr8:10614000-10614800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr8:10614000-10614800	Enhancers	Esophagus	oesophagus
19	chr8:10614000-10614800	Enhancers	Placenta	Placenta
20	chr8:10614200-10614400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr8:10614200-10614800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr8:10614200-10614800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr8:10614200-10614800	Enhancers	Hela-S3	cervix
24	chr8:10614200-10614800	Enhancers	NHEK	skin
25	chr8:10614200-10616600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr8:10614200-10621400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood

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