Variant report

Variant	rs9920531
Chromosome Location	chr15:55520514-55520515
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:55518640..55522590-chr15:55581375..55583917,4	K562	blood:
2	chr15:55519854..55522805-chr15:55537341..55539230,2	MCF-7	breast:
3	chr15:55520021..55524159-chr15:55571941..55574919,3	K562	blood:

Variant related genes	Relation type
ENSG00000069974	Chromatin interaction

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10518803	1.00[CHB][hapmap];0.83[ASN][1000 genomes]
rs10518805	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12324754	0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12324775	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12438278	0.96[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12439213	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12439264	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12439890	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs12440497	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12440550	1.00[CEU][hapmap];1.00[CHB][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12441258	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12441307	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12442180	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12442887	0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12442920	0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12442937	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs16976218	1.00[CEU][hapmap];1.00[GIH][hapmap];0.88[TSI][hapmap];0.87[EUR][1000 genomes]
rs16976220	1.00[CEU][hapmap];1.00[GIH][hapmap];0.88[TSI][hapmap];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs16976227	1.00[CEU][hapmap];1.00[GIH][hapmap]
rs16976229	1.00[CEU][hapmap]
rs16976231	1.00[CEU][hapmap]
rs17238178	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[TSI][hapmap];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17238220	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs17819000	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[TSI][hapmap];0.93[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs17819012	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[TSI][hapmap];0.93[EUR][1000 genomes]
rs28499877	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs28705006	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs557254	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61638549	0.83[ASN][1000 genomes]
rs7170936	0.83[ASN][1000 genomes]
rs7171029	1.00[CEU][hapmap]
rs7171897	1.00[CEU][hapmap]
rs7173803	0.83[ASN][1000 genomes]
rs7177930	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs8039254	0.88[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[GIH][hapmap];0.89[LWK][hapmap];0.94[MEX][hapmap];0.82[MKK][hapmap];1.00[TSI][hapmap];0.85[AFR][1000 genomes];0.94[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:84 , 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	chr15:55508600-55522600	Weak transcription	Colon Smooth Muscle	Colon
5	chr15:55509400-55541600	Weak transcription	Small Intestine	intestine
6	chr15:55510400-55522600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
7	chr15:55510400-55525000	Weak transcription	Fetal Muscle Trunk	muscle
8	chr15:55510400-55528000	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr15:55510600-55523800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr15:55510800-55521000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr15:55512800-55541600	Weak transcription	Colonic Mucosa	Colon
12	chr15:55513400-55532400	Weak transcription	Left Ventricle	heart
13	chr15:55514200-55521400	Weak transcription	HUVEC	blood vessel
14	chr15:55514200-55522000	Weak transcription	NH-A	brain
15	chr15:55514200-55522200	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr15:55514200-55523000	Weak transcription	NHEK	skin
17	chr15:55514200-55532000	Weak transcription	Lung	lung
18	chr15:55514200-55532600	Weak transcription	Psoas Muscle	Psoas
19	chr15:55514200-55540400	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr15:55514200-55545200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr15:55514400-55521800	Weak transcription	Fetal Brain Female	brain
22	chr15:55514400-55541200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr15:55514600-55522400	Weak transcription	HMEC	breast
24	chr15:55514600-55522600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr15:55514600-55534200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr15:55514600-55542600	Weak transcription	Hela-S3	cervix
27	chr15:55514600-55543200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr15:55514800-55522400	Weak transcription	Sigmoid Colon	Sigmoid Colon
29	chr15:55514800-55532600	Weak transcription	Adipose Nuclei	Adipose
30	chr15:55514800-55539800	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr15:55514800-55560400	Weak transcription	Spleen	Spleen
32	chr15:55515200-55522200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr15:55515400-55526200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr15:55516000-55524600	Genic enhancers	Primary neutrophils fromperipheralblood	blood
35	chr15:55516000-55559600	Weak transcription	Fetal Stomach	stomach
36	chr15:55516200-55529400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr15:55517200-55520800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr15:55517600-55521600	Strong transcription	K562	blood
39	chr15:55517600-55522400	Weak transcription	Pancreas	Pancrea
40	chr15:55517600-55542800	Weak transcription	Thymus	Thymus
41	chr15:55517800-55522000	Weak transcription	Stomach Mucosa	stomach
42	chr15:55517800-55522400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr15:55517800-55525600	Weak transcription	Primary T cells from cord blood	blood
44	chr15:55517800-55526600	Weak transcription	Fetal Intestine Small	intestine
45	chr15:55517800-55532400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr15:55517800-55539600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr15:55517800-55542200	Weak transcription	Fetal Thymus	thymus
48	chr15:55517800-55542800	Weak transcription	Primary B cells from peripheral blood	blood
49	chr15:55518000-55521600	Strong transcription	Primary T helper cells PMA-I stimulated	--
50	chr15:55518000-55522200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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