Variant report

Variant	rs1075063
Chromosome Location	chr12:24979395-24979396
allele	C/T
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	POLR2A	chr12:24978919-24983566	K562	blood:	n/a	n/a

Variant related genes	Relation type
ENSG00000256482	TF binding region

Extended variants
information (count: 102 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:77)

rs_ID	r²[population]
rs10160847	0.91[CHB][hapmap];0.89[JPT][hapmap];0.84[ASN][1000 genomes]
rs10466757	0.95[ASN][1000 genomes]
rs10466800	0.93[ASN][1000 genomes]
rs1054277	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs1054279	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs10743521	0.88[ASN][1000 genomes]
rs10743522	0.88[ASN][1000 genomes]
rs1075061	1.00[CEU][hapmap];0.95[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10771127	1.00[JPT][hapmap]
rs10771138	0.91[CHB][hapmap];0.80[GIH][hapmap];0.82[TSI][hapmap]
rs10842417	0.91[CHB][hapmap];0.89[JPT][hapmap];0.84[ASN][1000 genomes]
rs10842420	0.91[CHB][hapmap];0.96[CHD][hapmap];0.89[GIH][hapmap];0.89[JPT][hapmap];0.86[TSI][hapmap]
rs11047684	0.91[CHB][hapmap]
rs11047686	0.91[CHB][hapmap]
rs11047696	0.88[JPT][hapmap]
rs11609552	0.86[JPT][hapmap]
rs11613673	0.91[CHB][hapmap];0.96[CHD][hapmap];0.89[JPT][hapmap];0.87[ASN][1000 genomes]
rs11615863	0.91[CHB][hapmap];0.89[JPT][hapmap]
rs12227952	0.93[ASN][1000 genomes]
rs12228257	0.95[ASN][1000 genomes]
rs12229422	0.95[ASN][1000 genomes]
rs12296255	0.91[CHB][hapmap]
rs12302883	0.91[CHB][hapmap]
rs12319639	0.91[CHB][hapmap]
rs12424348	0.80[ASW][hapmap];0.91[CHB][hapmap];0.96[CHD][hapmap];0.89[JPT][hapmap];0.92[YRI][hapmap];0.92[ASN][1000 genomes]
rs12425320	0.91[CHB][hapmap]
rs1392195	0.91[CHB][hapmap]
rs1392196	0.91[CHB][hapmap];0.80[GIH][hapmap];0.82[TSI][hapmap]
rs1471844	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs16928089	0.91[CHB][hapmap];0.96[CHD][hapmap];0.89[JPT][hapmap];0.93[ASN][1000 genomes]
rs16928173	0.88[JPT][hapmap]
rs17372766	0.95[ASN][1000 genomes]
rs1872644	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs1872645	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs2046524	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs2062497	0.91[CHB][hapmap]
rs2133582	0.91[CHB][hapmap]
rs2200509	1.00[JPT][hapmap]
rs2220269	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs2220270	0.85[ASN][1000 genomes]
rs2220271	0.82[ASN][1000 genomes]
rs2353478	0.91[CHB][hapmap];0.96[CHD][hapmap];0.89[JPT][hapmap];0.84[ASN][1000 genomes]
rs2353479	0.85[EUR][1000 genomes]
rs2353483	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs3198082	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs3736211	0.91[CHB][hapmap];0.96[CHD][hapmap];0.89[JPT][hapmap];0.93[ASN][1000 genomes]
rs4143212	0.88[JPT][hapmap]
rs4400889	0.84[ASN][1000 genomes]
rs4963805	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4963806	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4963808	0.96[ASN][1000 genomes]
rs4963814	0.84[ASN][1000 genomes]
rs60104197	0.95[ASN][1000 genomes]
rs61914865	0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6487419	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs6487420	0.81[CHB][hapmap];0.89[JPT][hapmap]
rs6487434	0.83[CHB][hapmap]
rs6487437	0.88[CHB][hapmap]
rs7138685	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs71450459	0.89[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs718567	1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs7296211	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs7305794	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs73079552	0.85[ASN][1000 genomes]
rs7308285	0.91[ASN][1000 genomes]
rs7310300	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs7956863	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7961152	1.00[ASW][hapmap];0.96[CEU][hapmap];0.83[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7961688	0.83[ASN][1000 genomes]
rs7961778	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7962203	0.91[CHB][hapmap];1.00[CHD][hapmap];0.89[JPT][hapmap];0.83[ASN][1000 genomes]
rs7966783	0.88[ASN][1000 genomes]
rs7970244	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7976928	1.00[ASW][hapmap];1.00[CEU][hapmap];0.91[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];0.89[JPT][hapmap];0.97[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs937503	0.91[CHB][hapmap]
rs954199	0.83[CHD][hapmap];0.89[JPT][hapmap]
rs9988971	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422312	chr12:24519392-25221686	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv898920	chr12:24648863-25147192	Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv469169	chr12:24692383-25357680	Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	nsv557775	chr12:24692383-25357680	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv932477	chr12:24705151-25346677	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS 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 miRNA target site	30 gene(s)	inside rSNPs	diseases
6	nsv1053309	chr12:24770995-25078227	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
7	nsv1067577	chr12:24791283-25346677	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
8	nsv529514	chr12:24791283-25346677	Enhancers Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
9	nsv1041221	chr12:24880443-25213168	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
10	nsv541425	chr12:24880443-25213168	Bivalent/Poised TSS Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
11	nsv469170	chr12:24891175-25204353	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
12	nsv557776	chr12:24891175-25204353	Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
13	nsv557777	chr12:24891175-25205241	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers 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	16 gene(s)	inside rSNPs	diseases
14	nsv469173	chr12:24891175-25207653	Enhancers Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
15	nsv557778	chr12:24891175-25207653	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
16	nsv1045302	chr12:24921100-25078227	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
17	nsv1049138	chr12:24921100-25164524	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS 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 miRNA target site	13 gene(s)	inside rSNPs	diseases
18	nsv1051319	chr12:24921100-25238936	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
19	nsv1054863	chr12:24941350-25078227	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
20	nsv541426	chr12:24941350-25078227	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
21	nsv1051968	chr12:24941350-25138118	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
22	nsv541427	chr12:24941350-25138118	Active TSS Genic enhancers Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
23	nsv1037288	chr12:24941350-25238936	Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
24	nsv541428	chr12:24941350-25238936	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription 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	14 gene(s)	inside rSNPs	diseases
25	nsv1041218	chr12:24972019-25304356	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:24964000-25013400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr12:24965200-24989800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr12:24965600-24986800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr12:24965600-24989400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
5	chr12:24965600-25004800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:24965800-24989800	Strong transcription	HUES64 Cell Line	embryonic stem cell
7	chr12:24966200-24987800	Strong transcription	HUES48 Cell Line	embryonic stem cell
8	chr12:24966200-24989600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
9	chr12:24966200-25002000	Weak transcription	HepG2	liver
10	chr12:24967000-24989600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr12:24967800-24989000	Weak transcription	Aorta	Aorta
12	chr12:24968000-24990800	Weak transcription	Brain Hippocampus Middle	brain
13	chr12:24968000-25017600	Weak transcription	Fetal Thymus	thymus
14	chr12:24968200-24985000	Weak transcription	Fetal Lung	lung
15	chr12:24968200-24986800	Weak transcription	Thymus	Thymus
16	chr12:24968400-24983600	Weak transcription	Fetal Kidney	kidney
17	chr12:24968400-25007800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr12:24968600-24980600	Weak transcription	Fetal Brain Female	brain
19	chr12:24969000-24991000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr12:24969200-25002200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr12:24969400-24981600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
22	chr12:24969600-24981600	Strong transcription	Dnd41	blood
23	chr12:24969600-24989200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr12:24970000-24986400	Strong transcription	HUVEC	blood vessel
25	chr12:24970400-24985400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr12:24971000-25054800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr12:24971400-24995600	Weak transcription	Brain Angular Gyrus	brain
28	chr12:24972000-24990800	Weak transcription	Fetal Stomach	stomach
29	chr12:24972000-25004200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr12:24972400-24990800	Weak transcription	Placenta	Placenta
31	chr12:24972800-24987000	Strong transcription	HUES6 Cell Line	embryonic stem cell
32	chr12:24973400-24991400	Weak transcription	Fetal Brain Male	brain
33	chr12:24974400-25001800	Weak transcription	Pancreas	Pancrea
34	chr12:24975000-24989200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr12:24975000-24992200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr12:24975200-24980000	Weak transcription	Fetal Muscle Trunk	muscle
37	chr12:24975400-24989400	Weak transcription	Ovary	ovary
38	chr12:24975600-24983200	Weak transcription	Placenta Amnion	Placenta Amnion
39	chr12:24975600-24984000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr12:24975600-24992000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr12:24975600-24993200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr12:24975800-24984200	Weak transcription	NHLF	lung
43	chr12:24975800-24990800	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr12:24976000-24981000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr12:24976200-24980800	Weak transcription	HSMMtube	muscle
46	chr12:24976400-24979600	Strong transcription	ES-I3 Cell Line	embryonic stem cell
47	chr12:24976400-24981400	Strong transcription	HSMM	muscle
48	chr12:24976400-24993400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr12:24977000-24985000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr12:24977000-24989000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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