Variant report

Variant	rs73606356
Chromosome Location	chr12:1101839-1101840
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	FOS	chr12:1101295-1101980	MCF10A-Er-Src	breast:	n/a	n/a
2	CEBPB	chr12:1101784-1101984	IMR90	lung:	n/a	n/a
3	MXI1	chr12:1098181-1102272	SK-N-SH	brain:	n/a	n/a
4	POLR2A	chr12:1098283-1102022	MCF10A-Er-Src	breast:	n/a	n/a
5	CHD1	chr12:1098198-1102295	IMR90	lung:	n/a	chr12:1100770-1100780 chr12:1100805-1100815
6	MYC	chr12:1101262-1101894	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:1057369..1058961-chr12:1099742..1102215,2	K562	blood:
2	chr12:1099319..1102192-chr19:46282612..46285259,2	MCF-7	breast:
3	chr12:1097166..1102781-chr12:1103327..1109862,10	MCF-7	breast:

Variant related genes	Relation type
RAD52	TF binding region
ENSG00000250132	TF binding region
ENSG00000082805	Chromatin interaction
ENSG00000002016	Chromatin interaction
ENSG00000104936	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs57242706	1.00[AMR][1000 genomes]
rs58007194	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60162523	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60487933	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73606369	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73606383	1.00[AMR][1000 genomes]
rs73606389	1.00[AMR][1000 genomes]
rs73606395	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73608411	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049944	chr12:282465-1232077	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
2	nsv541306	chr12:282465-1232077	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
3	nsv949469	chr12:380411-1122450	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
4	nsv556892	chr12:673515-1210884	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription 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	60 gene(s)	inside rSNPs	diseases
5	nsv898576	chr12:813411-1553450	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS 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 miRNA target site	56 gene(s)	inside rSNPs	diseases
6	nsv948760	chr12:863833-1542875	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers 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 miRNA target site	42 gene(s)	inside rSNPs	diseases
7	nsv1052589	chr12:910460-1421493	ZNF genes & repeats Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers 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	34 gene(s)	inside rSNPs	diseases
8	nsv1045278	chr12:920251-1697030	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
9	nsv529398	chr12:941915-1741311	Weak transcription Strong transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
10	nsv468960	chr12:975276-1455106	Enhancers Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
11	nsv556941	chr12:975276-1455106	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer 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	33 gene(s)	inside rSNPs	diseases
12	nsv1044329	chr12:985144-1403020	Genic enhancers Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
13	nsv541340	chr12:985144-1403020	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
14	nsv470256	chr12:998365-1438761	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
15	nsv492321	chr12:1011692-1388512	Weak transcription Active TSS Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats 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	33 gene(s)	inside rSNPs	diseases
16	nsv898579	chr12:1013176-1510505	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
17	nsv898580	chr12:1024688-1569097	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS 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	37 gene(s)	inside rSNPs	diseases
18	nsv1036488	chr12:1041097-1445923	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS 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	33 gene(s)	inside rSNPs	diseases
19	nsv1037825	chr12:1045734-1432940	Bivalent/Poised TSS Weak transcription Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
20	nsv541342	chr12:1045734-1432940	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
21	nsv868854	chr12:1045935-1354083	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
22	nsv468962	chr12:1047531-1119958	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
23	nsv556942	chr12:1047531-1119958	Flanking Active TSS Weak transcription Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
24	esv2762958	chr12:1049279-1554962	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers 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	37 gene(s)	inside rSNPs	diseases
25	nsv1052559	chr12:1077964-1588543	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
26	nsv898581	chr12:1084783-1527359	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
27	nsv1041799	chr12:1091294-1304839	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
28	nsv541343	chr12:1091294-1304839	Flanking Active TSS Weak transcription Enhancers Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
29	esv3357464	chr12:1099316-1101864	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:1099200-1102000	Active TSS	Brain Angular Gyrus	brain
2	chr12:1099200-1102000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
3	chr12:1099400-1102000	Active TSS	H1 Cell Line	embryonic stem cell
4	chr12:1099400-1102000	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr12:1099400-1102000	Active TSS	iPS-20b Cell Line	embryonic stem cell
6	chr12:1099400-1102200	Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr12:1099800-1102200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr12:1100200-1102000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr12:1100800-1102000	Flanking Active TSS	Dnd41	blood
10	chr12:1101000-1102000	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr12:1101000-1102000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr12:1101000-1102000	Flanking Active TSS	Fetal Brain Female	brain
13	chr12:1101000-1102200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr12:1101000-1102200	Flanking Active TSS	Osteobl	bone
15	chr12:1101000-1104400	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr12:1101000-1123000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr12:1101200-1102000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
18	chr12:1101200-1102000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
19	chr12:1101200-1102000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr12:1101200-1102000	Flanking Active TSS	Brain Anterior Caudate	brain
21	chr12:1101200-1102000	Flanking Active TSS	Brain Cingulate Gyrus	brain
22	chr12:1101200-1102000	Flanking Active TSS	Hela-S3	cervix
23	chr12:1101200-1102200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr12:1101200-1102200	Enhancers	Sigmoid Colon	Sigmoid Colon
25	chr12:1101200-1102200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
26	chr12:1101200-1112800	Weak transcription	Gastric	stomach
27	chr12:1101200-1112800	Weak transcription	Ovary	ovary
28	chr12:1101200-1137000	Weak transcription	Lung	lung
29	chr12:1101400-1102000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
30	chr12:1101400-1102000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
31	chr12:1101400-1102000	Flanking Active TSS	HepG2	liver
32	chr12:1101400-1102200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr12:1101400-1102200	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
34	chr12:1101400-1102200	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr12:1101400-1102200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
36	chr12:1101400-1102200	Flanking Active TSS	A549	lung
37	chr12:1101400-1103800	Enhancers	Liver	Liver
38	chr12:1101400-1113000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr12:1101400-1115400	Weak transcription	Esophagus	oesophagus
40	chr12:1101600-1102000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr12:1101600-1102000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr12:1101600-1102000	Enhancers	Primary neutrophils fromperipheralblood	blood
43	chr12:1101600-1102000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
44	chr12:1101600-1102000	Enhancers	Primary T helper cells fromperipheralblood	blood
45	chr12:1101600-1102000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
46	chr12:1101600-1102000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr12:1101600-1102000	Enhancers	Brain Germinal Matrix	brain
48	chr12:1101600-1102000	Enhancers	Duodenum Mucosa	Duodenum
49	chr12:1101600-1102000	Enhancers	Fetal Intestine Small	intestine
50	chr12:1101600-1102000	Active TSS	Psoas Muscle	Psoas

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