Variant report

Variant	rs2160013
Chromosome Location	chr7:120725996-120725997
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	chr7:120723060-120727184	K562	blood:	n/a	n/a
2	PML	chr7:120718354-120726378	K562	blood:	n/a	chr7:120719627-120719635 chr7:120725652-120725660 chr7:120724224-120724233 chr7:120723324-120723333
3	POLR2A	chr7:120717974-120727688	K562	blood:	n/a	n/a
4	POLR2A	chr7:120722969-120726383	K562	blood:	n/a	n/a
5	POLR2A	chr7:120716166-120738240	K562	blood:	n/a	n/a
6	POLR2A	chr7:120724469-120726114	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:120674115..120676104-chr7:120725405..120727477,2	K562	blood:
2	chr7:120624020..120645873-chr7:120713358..120727138,77	K562	blood:
3	chr7:120589600..120593889-chr7:120719099..120726294,8	K562	blood:
4	chr7:120621518..120649031-chr7:120712706..120728931,108	K562	blood:
5	chr7:120724755..120727043-chr8:49082625..49084125,2	K562	blood:

Variant related genes	Relation type
RNA5SP241	TF binding region
ENSG00000071243	Chromatin interaction
ENSG00000106034	Chromatin interaction
ENSG00000202225	Chromatin interaction

Extended variants
information (count: 75 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10228942	1.00[JPT][hapmap]
rs1024743	0.91[CEU][hapmap];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10248019	1.00[JPT][hapmap]
rs10268570	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11979342	0.82[EUR][1000 genomes]
rs11981613	0.92[CEU][hapmap];0.82[EUR][1000 genomes]
rs11983939	0.85[EUR][1000 genomes]
rs12706322	0.92[CEU][hapmap]
rs13221538	1.00[JPT][hapmap]
rs13229354	0.92[CEU][hapmap]
rs13233295	0.92[CEU][hapmap]
rs13235373	0.92[CEU][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes]
rs13238393	0.92[CEU][hapmap]
rs1404267	0.90[CEU][hapmap];0.81[EUR][1000 genomes]
rs17143194	0.92[CEU][hapmap];0.81[EUR][1000 genomes]
rs17283542	0.92[CEU][hapmap];1.00[JPT][hapmap];0.87[EUR][1000 genomes]
rs2192289	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2215788	0.87[ASN][1000 genomes]
rs2402554	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2402556	0.95[ASN][1000 genomes]
rs2402561	0.92[CEU][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes]
rs2538491	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2538492	0.95[ASN][1000 genomes]
rs2721349	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs2721374	0.95[ASN][1000 genomes]
rs2721375	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs2908572	1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2908574	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2968344	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34269514	0.87[EUR][1000 genomes]
rs34362455	0.87[EUR][1000 genomes]
rs34385410	0.87[EUR][1000 genomes]
rs34638154	0.87[EUR][1000 genomes]
rs35370706	0.85[EUR][1000 genomes]
rs35411566	0.81[EUR][1000 genomes]
rs4140913	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs4144090	0.92[CEU][hapmap];1.00[JPT][hapmap];0.84[EUR][1000 genomes]
rs4593468	0.84[EUR][1000 genomes]
rs6956851	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs6962260	1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6970001	0.86[AMR][1000 genomes];0.95[ASN][1000 genomes]
rs6976513	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs73433997	0.85[EUR][1000 genomes]
rs73436037	0.81[EUR][1000 genomes]
rs759157	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7790569	0.91[CEU][hapmap];1.00[CHB][hapmap];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7806509	0.82[AMR][1000 genomes]
rs798932	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs798937	1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs798938	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs798939	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs798940	0.92[CEU][hapmap];1.00[JPT][hapmap];0.95[EUR][1000 genomes]
rs798942	0.85[EUR][1000 genomes]
rs798944	0.92[EUR][1000 genomes]
rs798945	0.86[EUR][1000 genomes]
rs798947	0.92[CEU][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes]
rs798948	0.92[EUR][1000 genomes]
rs9641653	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs9690141	0.95[ASN][1000 genomes]
rs9690143	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831114	chr7:120595624-120804510	Weak transcription Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv608327	chr7:120633006-120873078	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	esv2753621	chr7:120635049-120800049	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1023611	chr7:120638930-120881658	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1025430	chr7:120638930-121179289	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
6	nsv1030792	chr7:120662815-120917533	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv1031282	chr7:120667937-120887301	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv539099	chr7:120667937-120887301	Flanking Active TSS Enhancers Genic enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv1019025	chr7:120667937-120918696	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv539100	chr7:120667937-120918696	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	nsv534342	chr7:120667938-120887300	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
12	nsv889118	chr7:120683751-120800837	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
13	nsv889119	chr7:120688463-120800837	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
14	nsv889120	chr7:120691417-120800837	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
15	nsv428506	chr7:120719434-120891759	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:120711400-120790600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr7:120721600-120726200	Weak transcription	Primary B cells from peripheral blood	blood
3	chr7:120722800-120726200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr7:120722800-120726800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr7:120722800-120727400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr7:120723000-120726800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr7:120723200-120727000	Enhancers	Rectal Smooth Muscle	rectum
8	chr7:120724000-120731200	Genic enhancers	K562	blood
9	chr7:120724200-120726200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr7:120724400-120726800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr7:120724400-120727000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr7:120724400-120728200	Enhancers	Adipose Nuclei	Adipose
13	chr7:120724400-120739800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:120724600-120726000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr7:120724600-120727000	Enhancers	Liver	Liver
16	chr7:120724600-120727000	Enhancers	Fetal Heart	heart
17	chr7:120724800-120727200	Enhancers	Ovary	ovary
18	chr7:120725000-120726400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
19	chr7:120725200-120726000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
20	chr7:120725400-120726600	Weak transcription	Psoas Muscle	Psoas
21	chr7:120725400-120726800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:120725400-120727000	Enhancers	Skeletal Muscle Female	skeletal muscle
23	chr7:120725400-120727000	Enhancers	HMEC	breast
24	chr7:120725400-120727000	Enhancers	NH-A	brain
25	chr7:120725400-120727000	Enhancers	NHEK	skin
26	chr7:120725400-120727600	Enhancers	Osteobl	bone
27	chr7:120725400-120728600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr7:120725400-120735000	Weak transcription	Right Ventricle	heart
29	chr7:120725400-120739600	Weak transcription	Left Ventricle	heart
30	chr7:120725600-120726000	Weak transcription	Aorta	Aorta
31	chr7:120725600-120726000	Flanking Active TSS	Colon Smooth Muscle	Colon
32	chr7:120725600-120726200	Flanking Active TSS	Stomach Smooth Muscle	stomach
33	chr7:120725600-120727400	Genic enhancers	HSMM	muscle
34	chr7:120725600-120736800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr7:120725800-120727400	Enhancers	HSMMtube	muscle
36	chr7:120725800-120727800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr7:120725800-120727800	Enhancers	NHLF	lung
38	chr7:120725800-120729200	Enhancers	NHDF-Ad	bronchial
39	chr7:120725800-120744400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
40	chr7:120725800-120761800	Weak transcription	Fetal Stomach	stomach

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