Variant report

Variant	rs10845567
Chromosome Location	chr12:12662972-12662973
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	GATA3	chr12:12662782-12663695	SK-N-SH	brain:	n/a	chr12:12662896-12662906
2	PBX3	chr12:12662771-12663750	SK-N-SH	brain:	n/a	chr12:12663108-12663117
3	JUND	chr12:12662860-12663670	SK-N-SH	brain:	n/a	chr12:12663109-12663118 chr12:12663151-12663162
4	RXRA	chr12:12662857-12663549	SK-N-SH	brain:	n/a	chr12:12663224-12663233
5	EP300	chr12:12662757-12663695	SK-N-SH	brain:	n/a	n/a
6	RAD21	chr12:12662801-12667120	SK-N-SH	brain:	n/a	chr12:12664792-12664801
7	MAX	chr12:12662962-12663587	SK-N-SH	brain:	n/a	n/a
8	TCF12	chr12:12662591-12663740	SK-N-SH	brain:	n/a	n/a
9	EP300	chr12:12662792-12663662	SK-N-SH	brain:	n/a	n/a
10	EP300	chr12:12662971-12663474	SK-N-SH_RA	brain:	n/a	n/a
11	TCF12	chr12:12662775-12663603	SK-N-SH	brain:	n/a	n/a
12	MEF2A	chr12:12662877-12663604	SK-N-SH	brain:	n/a	n/a
13	PBX3	chr12:12662885-12663669	SK-N-SH	brain:	n/a	chr12:12663108-12663117
14	MAX	chr12:12662928-12663491	SK-N-SH	brain:	n/a	n/a
15	TEAD4	chr12:12662811-12663535	SK-N-SH	brain:	n/a	n/a
16	EP300	chr12:12661255-12667747	SK-N-SH	brain:	n/a	chr12:12661260-12661274 chr12:12662415-12662429 chr12:12667385-12667399 chr12:12661255-12661269 chr12:12661301-12661311
17	EP300	chr12:12662946-12663396	SK-N-SH_RA	brain:	n/a	n/a
18	POLR2A	chr12:12662875-12663616	SK-N-SH	brain:	n/a	n/a
19	NFIC	chr12:12662779-12663657	SK-N-SH	brain:	n/a	n/a
20	FOSL2	chr12:12662880-12663820	SK-N-SH	brain:	n/a	chr12:12663109-12663118 chr12:12663151-12663162
21	JUND	chr12:12662807-12663615	SK-N-SH	brain:	n/a	chr12:12663109-12663118 chr12:12662847-12662858 chr12:12663151-12663162
22	GATA3	chr12:12662718-12663750	SK-N-SH	brain:	n/a	chr12:12662896-12662906
23	MXI1	chr12:12662618-12666979	SK-N-SH	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr12:12658416..12661022-chr12:12661661..12664149,3	K562	blood:
2	chr12:12662519..12664795-chr12:12714606..12716959,2	K562	blood:
3	chr12:12652832..12655883-chr12:12662875..12665481,3	MCF-7	breast:
4	chr12:1874559..1877368-chr12:12662625..12665193,2	MCF-7	breast:

Variant related genes	Relation type
DUSP16	TF binding region
ENSG00000111266	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10743988	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10743989	0.81[AMR][1000 genomes]
rs10772570	0.80[ASN][1000 genomes]
rs10845552	0.83[CEU][hapmap];0.89[CHB][hapmap];0.82[AMR][1000 genomes]
rs10845559	0.95[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10845560	0.95[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10845563	0.80[AFR][1000 genomes]
rs10845572	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs11054937	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11054940	1.00[CHB][hapmap];0.94[ASN][1000 genomes]
rs11054941	0.95[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11054942	0.94[CHB][hapmap];0.94[ASN][1000 genomes]
rs11054947	0.92[ASN][1000 genomes]
rs11613385	1.00[CHB][hapmap];0.81[JPT][hapmap];0.92[ASN][1000 genomes]
rs12422540	0.95[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1558822	0.94[ASN][1000 genomes]
rs2111271	0.92[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2417190	0.94[CHB][hapmap];0.80[JPT][hapmap];0.92[ASN][1000 genomes]
rs3815591	0.89[ASN][1000 genomes]
rs4255620	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4763832	0.85[ASN][1000 genomes]
rs4763833	1.00[CHB][hapmap];0.90[ASN][1000 genomes]
rs7137455	0.94[CHB][hapmap];0.95[ASN][1000 genomes]
rs7294378	0.92[ASN][1000 genomes]
rs7295305	0.94[CHB][hapmap];0.91[ASN][1000 genomes]
rs7295427	0.87[ASN][1000 genomes]
rs7310652	0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7972902	1.00[CHB][hapmap];0.94[ASN][1000 genomes]
rs933575	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs962927	0.87[CEU][hapmap]
rs962928	0.95[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758295	chr12:12620654-12783124	Active TSS Weak transcription Flanking Active TSS Strong transcription 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	25 gene(s)	inside rSNPs	diseases
2	esv2759880	chr12:12620654-12783124	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
3	nsv898811	chr12:12655443-12928295	Flanking Active TSS Weak transcription Enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' 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	41 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:12630800-12681000	Weak transcription	Colonic Mucosa	Colon
2	chr12:12634400-12685200	Weak transcription	Hela-S3	cervix
3	chr12:12639400-12679600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr12:12641600-12663600	Weak transcription	Lung	lung
5	chr12:12641600-12686200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr12:12652800-12665000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
7	chr12:12653800-12669000	Weak transcription	Fetal Muscle Trunk	muscle
8	chr12:12654400-12667200	Weak transcription	Primary T cells from cord blood	blood
9	chr12:12656000-12666400	Weak transcription	Spleen	Spleen
10	chr12:12656800-12670800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr12:12659000-12667000	Weak transcription	Fetal Thymus	thymus
12	chr12:12659000-12669200	Weak transcription	Primary T cells fromperipheralblood	blood
13	chr12:12659400-12663800	Enhancers	Brain Angular Gyrus	brain
14	chr12:12659400-12665200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr12:12659600-12663200	Weak transcription	Rectal Mucosa Donor 29	rectum
16	chr12:12659600-12663800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
17	chr12:12659600-12664000	Enhancers	NHLF	lung
18	chr12:12659600-12664600	Enhancers	Osteobl	bone
19	chr12:12659600-12665800	Enhancers	Brain Cingulate Gyrus	brain
20	chr12:12659800-12663000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr12:12659800-12664600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
22	chr12:12659800-12664600	Weak transcription	Thymus	Thymus
23	chr12:12659800-12665200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
24	chr12:12659800-12665600	Weak transcription	Fetal Intestine Small	intestine
25	chr12:12659800-12667800	Enhancers	Brain Hippocampus Middle	brain
26	chr12:12659800-12669000	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr12:12659800-12669800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
28	chr12:12659800-12670800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr12:12659800-12674200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr12:12659800-12678600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr12:12660000-12664400	Enhancers	NHDF-Ad	bronchial
32	chr12:12660000-12664600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr12:12660000-12665000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
34	chr12:12660000-12665200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr12:12660000-12668600	Enhancers	Brain Substantia Nigra	brain
36	chr12:12660000-12670200	Weak transcription	Duodenum Mucosa	Duodenum
37	chr12:12660000-12681800	Weak transcription	Fetal Kidney	kidney
38	chr12:12660200-12670000	Weak transcription	Fetal Lung	lung
39	chr12:12660400-12663000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr12:12660400-12663000	Weak transcription	Fetal Intestine Large	intestine
41	chr12:12660400-12663000	Weak transcription	HSMMtube	muscle
42	chr12:12660400-12663400	Weak transcription	Liver	Liver
43	chr12:12660400-12663400	Weak transcription	Small Intestine	intestine
44	chr12:12660400-12663600	Weak transcription	Gastric	stomach
45	chr12:12660400-12664800	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr12:12660400-12664800	Weak transcription	Skeletal Muscle Male	skeletal muscle
47	chr12:12660400-12665600	Weak transcription	Colon Smooth Muscle	Colon
48	chr12:12660400-12666000	Weak transcription	Placenta	Placenta
49	chr12:12660400-12666400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr12:12660400-12666400	Weak transcription	Aorta	Aorta

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