Variant report

Variant	rs12324775
Chromosome Location	chr15:55524789-55524790
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:55520811..55529435-chr15:55529925..55534726,12	K562	blood:
2	chr15:55524035..55525892-chr15:55526403..55529147,3	K562	blood:
3	chr15:55523127..55525294-chr15:55532956..55534638,2	MCF-7	breast:
4	chr15:55520793..55522811-chr15:55524156..55526936,2	K562	blood:
5	chr15:55524517..55526709-chr15:55528227..55531220,3	MCF-7	breast:
6	chr15:55523751..55526514-chr15:55535362..55537475,2	K562	blood:

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:55)

rs_ID	r²[population]
rs10518803	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs10518805	1.00[CHB][hapmap];0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12324754	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12438278	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12439213	1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12439264	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12439890	1.00[CHB][hapmap]
rs12440497	1.00[CHB][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12440550	1.00[CHB][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12441258	1.00[CHB][hapmap];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12441307	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12442180	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12442887	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12442920	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12442937	1.00[CHB][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16976218	0.90[GIH][hapmap];0.88[TSI][hapmap];0.91[EUR][1000 genomes]
rs16976220	1.00[GIH][hapmap];0.88[TSI][hapmap];0.91[EUR][1000 genomes]
rs16976227	0.90[GIH][hapmap];0.81[EUR][1000 genomes]
rs16976229	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs16976231	0.81[EUR][1000 genomes]
rs17238178	1.00[CHB][hapmap];0.90[TSI][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17238220	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs17819000	1.00[CHB][hapmap];0.90[TSI][hapmap];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17819012	1.00[CHB][hapmap];0.90[TSI][hapmap];0.89[EUR][1000 genomes]
rs28421759	0.86[AFR][1000 genomes]
rs28499877	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28581943	0.90[AFR][1000 genomes]
rs28705006	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55649971	0.91[AFR][1000 genomes]
rs557254	0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56117636	0.95[AFR][1000 genomes]
rs57297946	0.95[AFR][1000 genomes]
rs57535550	0.95[AFR][1000 genomes]
rs57868158	0.91[AFR][1000 genomes]
rs58387023	0.93[AFR][1000 genomes]
rs58708905	0.95[AFR][1000 genomes]
rs59577009	0.91[AFR][1000 genomes]
rs60713987	0.91[AFR][1000 genomes]
rs61638549	1.00[ASN][1000 genomes]
rs6493773	0.82[ASW][hapmap];0.82[LWK][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs7170936	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7171029	0.81[EUR][1000 genomes]
rs7171897	0.81[EUR][1000 genomes]
rs7173803	1.00[ASN][1000 genomes]
rs7177930	1.00[CHB][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74015516	0.93[AFR][1000 genomes]
rs74015520	0.95[AFR][1000 genomes]
rs74015521	0.95[AFR][1000 genomes]
rs74015524	0.91[AFR][1000 genomes]
rs74015535	0.90[AFR][1000 genomes]
rs74015549	0.83[AFR][1000 genomes]
rs8027540	0.83[AFR][1000 genomes]
rs8038540	0.91[AFR][1000 genomes]
rs8039254	1.00[CHB][hapmap];1.00[CHD][hapmap];0.90[GIH][hapmap];0.84[MEX][hapmap];1.00[TSI][hapmap];0.85[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9920531	1.00[CHB][hapmap];0.90[GIH][hapmap];0.88[MEX][hapmap];1.00[TSI][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043176	chr15:55010228-55563000	Genic enhancers Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv1042741	chr15:55068022-55622497	Strong transcription Weak transcription Flanking Active TSS Enhancers 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	31 gene(s)	inside rSNPs	diseases
3	nsv1039471	chr15:55137606-55552555	Enhancers Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv917323	chr15:55290499-56041334	Genic enhancers Active TSS ZNF genes & repeats Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	57 gene(s)	inside rSNPs	diseases
5	nsv1043789	chr15:55400872-56092454	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
6	nsv1049977	chr15:55502508-55555694	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:55489800-55540200	Weak transcription	Esophagus	oesophagus
2	chr15:55490000-55529400	Weak transcription	Rectal Smooth Muscle	rectum
3	chr15:55490000-55562800	Weak transcription	Ovary	ovary
4	chr15:55509400-55541600	Weak transcription	Small Intestine	intestine
5	chr15:55510400-55525000	Weak transcription	Fetal Muscle Trunk	muscle
6	chr15:55510400-55528000	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr15:55512800-55541600	Weak transcription	Colonic Mucosa	Colon
8	chr15:55513400-55532400	Weak transcription	Left Ventricle	heart
9	chr15:55514200-55532000	Weak transcription	Lung	lung
10	chr15:55514200-55532600	Weak transcription	Psoas Muscle	Psoas
11	chr15:55514200-55540400	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr15:55514200-55545200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr15:55514400-55541200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr15:55514600-55534200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr15:55514600-55542600	Weak transcription	Hela-S3	cervix
16	chr15:55514600-55543200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr15:55514800-55532600	Weak transcription	Adipose Nuclei	Adipose
18	chr15:55514800-55539800	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr15:55514800-55560400	Weak transcription	Spleen	Spleen
20	chr15:55515400-55526200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr15:55516000-55559600	Weak transcription	Fetal Stomach	stomach
22	chr15:55516200-55529400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr15:55517600-55542800	Weak transcription	Thymus	Thymus
24	chr15:55517800-55525600	Weak transcription	Primary T cells from cord blood	blood
25	chr15:55517800-55526600	Weak transcription	Fetal Intestine Small	intestine
26	chr15:55517800-55532400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
27	chr15:55517800-55539600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr15:55517800-55542200	Weak transcription	Fetal Thymus	thymus
29	chr15:55517800-55542800	Weak transcription	Primary B cells from peripheral blood	blood
30	chr15:55518000-55539200	Weak transcription	Fetal Lung	lung
31	chr15:55518600-55526200	Weak transcription	Rectal Mucosa Donor 31	rectum
32	chr15:55518600-55527000	Strong transcription	Primary monocytes fromperipheralblood	blood
33	chr15:55518600-55533600	Strong transcription	Monocytes-CD14+_RO01746	blood
34	chr15:55518600-55539400	Weak transcription	Placenta	Placenta
35	chr15:55518800-55541200	Weak transcription	Aorta	Aorta
36	chr15:55519200-55524800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr15:55520000-55525000	Weak transcription	Gastric	stomach
38	chr15:55520600-55526200	Weak transcription	Duodenum Mucosa	Duodenum
39	chr15:55520800-55524800	Weak transcription	Fetal Kidney	kidney
40	chr15:55520800-55528400	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr15:55520800-55574800	Weak transcription	Stomach Smooth Muscle	stomach
42	chr15:55521000-55526200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr15:55521000-55541400	Weak transcription	Fetal Intestine Large	intestine
44	chr15:55521600-55527200	Genic enhancers	K562	blood
45	chr15:55522400-55532400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr15:55522600-55526000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr15:55522600-55526000	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr15:55522600-55526200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
49	chr15:55522600-55529600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
50	chr15:55522800-55525000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood

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