Variant report

Variant	rs12437551
Chromosome Location	chr15:34498405-34498406
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:34495127..34499100-chr15:34500646..34503502,4	MCF-7	breast:
2	chr15:34498121..34503791-chr15:34514506..34519551,14	K562	blood:
3	chr15:34493054..34495397-chr15:34496160..34499059,3	MCF-7	breast:
4	chr15:34497680..34504001-chr15:34514973..34521212,14	K562	blood:

Variant related genes	Relation type
ENSG00000134152	Chromatin interaction
ENSG00000128463	Chromatin interaction

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10775222	0.88[CEU][hapmap];0.93[CHB][hapmap];0.84[JPT][hapmap]
rs10851950	0.80[ASN][1000 genomes]
rs10851952	0.84[ASW][hapmap];0.96[CEU][hapmap];0.93[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];0.91[MEX][hapmap];0.90[MKK][hapmap];0.87[TSI][hapmap];0.91[YRI][hapmap];0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10851955	0.89[ASN][1000 genomes]
rs10851964	0.81[JPT][hapmap]
rs11073010	0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11073014	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11073019	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs11635964	0.96[CEU][hapmap];0.93[CHB][hapmap];0.94[JPT][hapmap];0.91[YRI][hapmap];0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11636442	0.88[CEU][hapmap];0.93[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];0.84[JPT][hapmap];0.82[LWK][hapmap];0.82[MEX][hapmap];0.85[MKK][hapmap];0.83[TSI][hapmap]
rs11852537	0.85[CHB][hapmap];0.84[JPT][hapmap]
rs11854686	0.87[ASN][1000 genomes]
rs11857205	0.87[ASN][1000 genomes]
rs11857684	0.80[CEU][hapmap];0.86[CHB][hapmap];0.84[JPT][hapmap]
rs11858408	0.92[ASN][1000 genomes]
rs12441003	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12442758	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs12591181	0.88[CEU][hapmap];0.84[JPT][hapmap]
rs12592460	0.81[ASN][1000 genomes]
rs12594077	0.86[CHB][hapmap]
rs12917397	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16958835	0.91[CHD][hapmap]
rs1836978	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs1978810	0.80[CEU][hapmap];0.86[CHB][hapmap];0.84[JPT][hapmap];0.87[ASN][1000 genomes]
rs28652966	0.92[ASN][1000 genomes]
rs4381574	0.92[ASN][1000 genomes]
rs4530104	0.81[JPT][hapmap]
rs4577050	0.80[JPT][hapmap]
rs4780226	0.80[ASN][1000 genomes]
rs4780227	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4780229	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs4780231	0.84[JPT][hapmap]
rs56731918	0.90[ASN][1000 genomes]
rs58875083	0.90[ASN][1000 genomes]
rs6495619	0.85[ASN][1000 genomes]
rs6495620	0.84[ASN][1000 genomes]
rs6495621	0.82[ASN][1000 genomes]
rs6495622	0.85[CEU][hapmap];0.93[GIH][hapmap];0.81[TSI][hapmap];0.81[EUR][1000 genomes]
rs6495625	0.82[ASN][1000 genomes]
rs7164448	0.81[ASN][1000 genomes]
rs7168761	0.88[CHD][hapmap]
rs7174014	0.85[ASN][1000 genomes]
rs7174442	0.86[CHB][hapmap];0.88[CHD][hapmap];0.91[MEX][hapmap]
rs7178002	0.94[CHD][hapmap]
rs7178203	0.86[CHB][hapmap];0.88[CHD][hapmap];0.91[MEX][hapmap]
rs7178988	0.80[CEU][hapmap];0.86[CHB][hapmap];0.84[JPT][hapmap];0.90[ASN][1000 genomes]
rs7180920	0.81[ASN][1000 genomes]
rs7181687	0.80[CEU][hapmap];0.86[CHB][hapmap];0.88[CHD][hapmap];0.84[JPT][hapmap];0.91[MEX][hapmap];0.90[ASN][1000 genomes]
rs7181902	0.80[CEU][hapmap];0.86[CHB][hapmap];0.85[CHD][hapmap];0.89[JPT][hapmap];0.91[MEX][hapmap];0.90[ASN][1000 genomes]
rs8025406	0.88[CEU][hapmap];0.93[CHB][hapmap];0.92[CHD][hapmap];1.00[GIH][hapmap];0.89[JPT][hapmap];0.82[LWK][hapmap];0.86[MEX][hapmap];0.85[MKK][hapmap];0.83[TSI][hapmap];0.80[ASN][1000 genomes]
rs8025730	0.86[CHB][hapmap]
rs8026939	0.92[ASN][1000 genomes]
rs8027499	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8027830	0.90[ASN][1000 genomes]
rs8028027	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs8034315	0.90[ASN][1000 genomes]
rs8035493	0.88[CEU][hapmap];0.93[CHB][hapmap];0.84[JPT][hapmap]
rs8035954	0.85[JPT][hapmap]
rs8036468	0.84[ASW][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.84[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs8040071	0.91[CHD][hapmap];0.84[JPT][hapmap];0.82[ASN][1000 genomes]
rs8040732	0.93[CHB][hapmap];0.87[CHD][hapmap];0.91[MEX][hapmap]
rs8041977	0.81[ASN][1000 genomes]
rs8043216	0.93[CHB][hapmap];0.94[JPT][hapmap];0.91[YRI][hapmap];0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9920654	0.80[ASN][1000 genomes]
rs9972505	0.80[CEU][hapmap];0.86[CHB][hapmap];0.85[CHD][hapmap];0.84[JPT][hapmap];0.90[MEX][hapmap];0.90[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1035579	chr15:34363159-34501115	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34454600-34501200	Weak transcription	Colonic Mucosa	Colon
2	chr15:34454800-34501000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr15:34464600-34500400	Weak transcription	Hela-S3	cervix
4	chr15:34466400-34500400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr15:34467000-34500800	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr15:34467200-34500200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr15:34471000-34501000	Weak transcription	Aorta	Aorta
8	chr15:34471600-34500400	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr15:34473400-34500400	Weak transcription	HSMMtube	muscle
10	chr15:34475000-34500400	Weak transcription	Stomach Smooth Muscle	stomach
11	chr15:34475600-34499800	Weak transcription	Ovary	ovary
12	chr15:34475600-34500000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr15:34475600-34500400	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr15:34475600-34500400	Weak transcription	Colon Smooth Muscle	Colon
15	chr15:34475600-34500400	Weak transcription	HUVEC	blood vessel
16	chr15:34476200-34499600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr15:34476200-34500000	Weak transcription	Fetal Brain Female	brain
18	chr15:34476400-34500800	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr15:34476800-34499800	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr15:34477000-34499800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
21	chr15:34477200-34500000	Weak transcription	Liver	Liver
22	chr15:34477600-34501000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
23	chr15:34477600-34501200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr15:34478000-34500200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr15:34478800-34500000	Weak transcription	Fetal Intestine Large	intestine
26	chr15:34478800-34500400	Weak transcription	Thymus	Thymus
27	chr15:34478800-34500800	Weak transcription	Primary hematopoietic stem cells	blood
28	chr15:34479200-34500000	Weak transcription	Esophagus	oesophagus
29	chr15:34479200-34500800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr15:34479200-34501000	Weak transcription	Gastric	stomach
31	chr15:34479400-34500800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
32	chr15:34479400-34501000	Weak transcription	Left Ventricle	heart
33	chr15:34479400-34501600	Weak transcription	Lung	lung
34	chr15:34479600-34500800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr15:34479600-34501800	Weak transcription	Spleen	Spleen
36	chr15:34480000-34500000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr15:34480000-34500800	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr15:34480400-34500400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr15:34480600-34498600	Weak transcription	Fetal Intestine Small	intestine
40	chr15:34481000-34500400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr15:34481000-34500800	Weak transcription	Brain Cingulate Gyrus	brain
42	chr15:34482800-34500800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr15:34483000-34500400	Weak transcription	GM12878-XiMat	blood
44	chr15:34483000-34500600	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr15:34483200-34500000	Weak transcription	NHDF-Ad	bronchial
46	chr15:34483200-34501000	Weak transcription	Primary B cells from peripheral blood	blood
47	chr15:34485400-34500400	Weak transcription	Brain Hippocampus Middle	brain
48	chr15:34485600-34500800	Weak transcription	Brain Substantia Nigra	brain
49	chr15:34486200-34498800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr15:34486400-34501600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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