Variant report

Variant	rs7313778
Chromosome Location	chr12:83120119-83120120
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:83118472..83120538-chr12:83125588..83127513,2	MCF-7	breast:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10506878	0.89[EUR][1000 genomes]
rs10862497	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11115342	0.87[EUR][1000 genomes]
rs11115348	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11115353	0.83[EUR][1000 genomes]
rs11115355	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11610988	0.91[EUR][1000 genomes]
rs11611431	0.89[EUR][1000 genomes]
rs11613168	0.91[EUR][1000 genomes]
rs11614435	0.83[EUR][1000 genomes]
rs11615763	0.91[EUR][1000 genomes]
rs11615765	0.91[EUR][1000 genomes]
rs12305736	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12307168	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12422405	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12423043	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12426166	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13377925	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17009851	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17009854	0.82[EUR][1000 genomes]
rs17009856	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs17009882	0.89[EUR][1000 genomes]
rs17009885	0.89[EUR][1000 genomes]
rs17009891	0.91[EUR][1000 genomes]
rs17009893	0.91[EUR][1000 genomes]
rs17009899	0.91[EUR][1000 genomes]
rs1922576	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1922579	0.80[EUR][1000 genomes]
rs4620789	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4882428	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs56298822	0.82[EUR][1000 genomes]
rs61485473	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6539683	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7134747	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7134766	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7135486	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72615654	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7294890	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7303469	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74106267	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7961953	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7975647	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1053093	chr12:82645292-83287809	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
2	nsv541551	chr12:82645292-83287809	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv899348	chr12:82744187-83169297	Enhancers Strong transcription Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
4	nsv427917	chr12:82917031-83279712	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv521849	chr12:83013783-83991479	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv469490	chr12:83089431-83507269	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
7	nsv559542	chr12:83089431-83507269	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases
8	esv2758315	chr12:83101045-83357621	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
9	esv2759911	chr12:83101045-83357621	Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	esv2755991	chr12:83105631-83248605	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv469491	chr12:83108395-83203742	Enhancers Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	nsv559543	chr12:83108395-83203742	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:83086600-83122200	Weak transcription	Fetal Muscle Trunk	muscle
2	chr12:83093200-83122400	Weak transcription	Gastric	stomach
3	chr12:83098000-83121200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr12:83099200-83122400	Weak transcription	Esophagus	oesophagus
5	chr12:83102400-83138800	Weak transcription	Fetal Kidney	kidney
6	chr12:83102600-83122200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr12:83102600-83122400	Weak transcription	Lung	lung
8	chr12:83102600-83140600	Weak transcription	Pancreas	Pancrea
9	chr12:83102800-83122400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr12:83102800-83134000	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr12:83103200-83124000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr12:83106000-83122200	Weak transcription	Fetal Intestine Small	intestine
13	chr12:83106800-83133800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr12:83107000-83127800	Weak transcription	Fetal Muscle Leg	muscle
15	chr12:83107400-83121200	Weak transcription	Fetal Stomach	stomach
16	chr12:83109200-83120400	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr12:83109600-83120600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr12:83112600-83124200	Weak transcription	Fetal Lung	lung
19	chr12:83113000-83138600	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr12:83113200-83124600	Weak transcription	Fetal Brain Male	brain
21	chr12:83115200-83138200	Weak transcription	Brain Cingulate Gyrus	brain
22	chr12:83115400-83138800	Weak transcription	Brain Anterior Caudate	brain
23	chr12:83115600-83121600	Weak transcription	Brain Hippocampus Middle	brain
24	chr12:83115800-83121600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr12:83115800-83122400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr12:83115800-83138000	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr12:83116000-83121800	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr12:83117800-83122200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr12:83118600-83121600	Weak transcription	Primary monocytes fromperipheralblood	blood
30	chr12:83118800-83124800	Weak transcription	Rectal Smooth Muscle	rectum
31	chr12:83119800-83134200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr12:83120000-83120200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr12:83120000-83121400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr12:83120000-83121600	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr12:83120000-83121800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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