Variant report

Variant	rs11070795
Chromosome Location	chr15:50853372-50853373
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	chr15:50842951..50845112-chr15:50852235..50854464,2	MCF-7	breast:
2	chr15:50646500..50650701-chr15:50853140..50859875,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000104064	Chromatin interaction
ENSG00000244879	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs11635045	0.87[GIH][hapmap];0.91[TSI][hapmap]
rs11636576	0.82[CEU][hapmap];0.85[GIH][hapmap];0.91[TSI][hapmap]
rs11636930	0.81[CHB][hapmap]
rs12324599	0.82[CEU][hapmap];0.82[AMR][1000 genomes]
rs12593931	0.95[CHB][hapmap];0.93[CHD][hapmap];0.86[JPT][hapmap]
rs12708424	0.82[AMR][1000 genomes]
rs3098198	0.89[GIH][hapmap];0.80[MEX][hapmap];0.84[TSI][hapmap]
rs3105592	0.80[CHD][hapmap]
rs3109887	0.89[GIH][hapmap];0.84[TSI][hapmap]
rs3109890	0.81[AMR][1000 genomes]
rs473357	0.82[CEU][hapmap];0.89[GIH][hapmap];0.84[MEX][hapmap];0.98[TSI][hapmap];0.86[AMR][1000 genomes]
rs476733	0.81[AMR][1000 genomes]
rs4775899	0.81[CEU][hapmap];0.89[GIH][hapmap];0.98[TSI][hapmap]
rs480280	0.81[AMR][1000 genomes]
rs493728	0.82[CEU][hapmap];0.86[AMR][1000 genomes]
rs506693	0.82[CEU][hapmap];0.89[GIH][hapmap];0.84[MEX][hapmap];0.98[TSI][hapmap];0.80[AMR][1000 genomes]
rs512708	0.86[AMR][1000 genomes]
rs539383	0.82[CEU][hapmap];0.89[GIH][hapmap];0.84[MEX][hapmap];0.98[TSI][hapmap];0.82[AMR][1000 genomes]
rs567109	0.81[CEU][hapmap];0.85[GIH][hapmap];0.93[TSI][hapmap];0.82[AMR][1000 genomes]
rs577583	0.82[CEU][hapmap];0.86[AMR][1000 genomes]
rs581172	0.82[AMR][1000 genomes]
rs616256	0.82[CEU][hapmap];0.91[GIH][hapmap];0.84[MEX][hapmap];0.98[TSI][hapmap];0.83[AMR][1000 genomes]
rs62019154	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs644890	0.81[CEU][hapmap];0.81[AMR][1000 genomes]
rs679774	0.82[CEU][hapmap];0.89[GIH][hapmap];0.80[MEX][hapmap];0.91[TSI][hapmap]
rs7163283	0.81[CEU][hapmap];0.83[AMR][1000 genomes]
rs7163628	0.86[AMR][1000 genomes]
rs7165721	0.82[CEU][hapmap];0.87[GIH][hapmap];0.84[MEX][hapmap];0.98[TSI][hapmap]
rs7175149	0.86[GIH][hapmap];0.90[TSI][hapmap];0.82[AMR][1000 genomes]
rs7178070	0.82[CEU][hapmap];0.89[GIH][hapmap];0.84[MEX][hapmap];0.98[TSI][hapmap]
rs8023255	0.81[AMR][1000 genomes]
rs8035534	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045456	chr15:50592472-51019873	Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
2	nsv948579	chr15:50645530-51045564	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
3	nsv524613	chr15:50656449-50868779	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv1053966	chr15:50715572-51133186	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
5	nsv542383	chr15:50715572-51133186	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases
6	nsv1043805	chr15:50715572-51208891	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
7	nsv542384	chr15:50715572-51208891	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
8	nsv1047443	chr15:50744781-51647023	Strong transcription Active TSS Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
9	nsv1051990	chr15:50745814-51133186	Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
10	nsv1054970	chr15:50761410-51036625	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
11	nsv457134	chr15:50770868-51184583	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
12	nsv471242	chr15:50770868-51184583	Genic enhancers ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
13	nsv569396	chr15:50770868-51184583	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
14	nsv457135	chr15:50770868-51189707	ZNF genes & repeats Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
15	nsv569397	chr15:50770868-51189707	Strong transcription Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
16	nsv1048621	chr15:50775451-51115535	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
17	nsv1047039	chr15:50782070-51187804	Enhancers Strong transcription Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
18	nsv542385	chr15:50782070-51187804	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
19	nsv457136	chr15:50789125-51294995	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
20	nsv569398	chr15:50789125-51294995	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
21	nsv431389	chr15:50795835-50979738	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
22	nsv1036081	chr15:50818569-51097229	Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
23	nsv1043387	chr15:50822035-50940979	Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
24	nsv1055112	chr15:50822035-51133186	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
25	nsv1050385	chr15:50843495-50949798	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
26	nsv1042372	chr15:50846461-51208891	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases
27	nsv542386	chr15:50846461-51208891	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	63 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11070795	TRPM7	cis	lymphoblastoid	seeQTL

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:50837000-50862200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr15:50837000-50882800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:50843600-50860800	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr15:50844000-50855200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr15:50844200-50862200	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr15:50846000-50950800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr15:50846200-50867000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr15:50846600-50858600	Weak transcription	Skeletal Muscle Female	skeletal muscle
9	chr15:50846800-50860800	Weak transcription	NHLF	lung
10	chr15:50847000-50853400	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr15:50847000-50920600	Weak transcription	Aorta	Aorta
12	chr15:50847400-50855200	Weak transcription	HUVEC	blood vessel
13	chr15:50847600-50854400	Weak transcription	Fetal Muscle Leg	muscle
14	chr15:50847600-50865200	Weak transcription	Rectal Smooth Muscle	rectum
15	chr15:50847600-50866400	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr15:50847800-50872200	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr15:50848000-50855000	Weak transcription	Fetal Brain Female	brain
18	chr15:50848000-50855200	Weak transcription	Right Ventricle	heart
19	chr15:50848000-50868200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr15:50848400-50855000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr15:50848400-50864800	Weak transcription	Brain Hippocampus Middle	brain
22	chr15:50848600-50855000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr15:50848800-50855200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr15:50848800-50894800	Strong transcription	Liver	Liver
25	chr15:50849000-50854600	Weak transcription	Thymus	Thymus
26	chr15:50849000-50856400	Strong transcription	A549	lung
27	chr15:50849000-50860600	Weak transcription	Brain Anterior Caudate	brain
28	chr15:50849000-50861200	Weak transcription	NH-A	brain
29	chr15:50849000-50868800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
30	chr15:50849000-50894600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr15:50849200-50853400	Weak transcription	Primary T cells from cord blood	blood
32	chr15:50849200-50855000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr15:50849200-50864200	Weak transcription	Colonic Mucosa	Colon
34	chr15:50849200-50869000	Weak transcription	Esophagus	oesophagus
35	chr15:50849200-50874400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr15:50849200-50883600	Weak transcription	Pancreas	Pancrea
37	chr15:50849200-50883600	Weak transcription	Small Intestine	intestine
38	chr15:50849400-50869000	Weak transcription	Gastric	stomach
39	chr15:50849600-50853400	Weak transcription	Primary T helper cells fromperipheralblood	blood
40	chr15:50849600-50860800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr15:50849600-50863400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr15:50849600-50864000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr15:50849600-50866000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
44	chr15:50849600-50871800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr15:50849800-50862400	Strong transcription	Primary monocytes fromperipheralblood	blood
46	chr15:50849800-50872800	Strong transcription	Fetal Intestine Large	intestine
47	chr15:50850000-50854800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr15:50850000-50864800	Weak transcription	Colon Smooth Muscle	Colon
49	chr15:50850000-50865400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chr15:50850200-50854800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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