Variant report

Variant	rs7153729
Chromosome Location	chr14:63991736-63991737
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:63989618..63991820-chr14:63993862..63996489,2	MCF-7	breast:
2	chr14:63989432..63993660-chr14:63995210..63997319,3	MCF-7	breast:
3	chr14:63990536..63993005-chr14:64106908..64108647,2	MCF-7	breast:
4	chr14:63989950..63993504-chr14:63993757..63996174,3	K562	blood:
5	chr14:63989950..63993504-chr14:63993757..63996174,4	K562	blood:

Variant related genes	Relation type
ENSG00000140006	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10136489	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10139904	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10142811	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10143003	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10148041	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10150465	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10467817	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10498508	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12050157	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12323619	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12433448	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28479545	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28688632	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28712544	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28834707	0.88[EUR][1000 genomes]
rs3783738	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4902233	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4902234	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs55858056	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs60971465	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs61983974	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61983975	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61984001	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61984002	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61984003	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61984005	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7145363	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7145769	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7151914	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7158543	0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs72716312	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv527251	chr14:63400786-64068806	Flanking Bivalent TSS/Enh Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv520528	chr14:63400786-64157117	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv530774	chr14:63591348-64029881	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv915909	chr14:63620440-64560369	Active TSS Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	67 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:63951000-64003200	Weak transcription	Ovary	ovary
2	chr14:63960000-64005000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr14:63960200-64008600	Weak transcription	HSMMtube	muscle
4	chr14:63967600-63996400	Weak transcription	Fetal Muscle Trunk	muscle
5	chr14:63970200-64008600	Weak transcription	Aorta	Aorta
6	chr14:63971200-64000800	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr14:63972000-64000200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr14:63972200-64003400	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr14:63972400-64002800	Weak transcription	HMEC	breast
10	chr14:63972600-64008800	Weak transcription	Esophagus	oesophagus
11	chr14:63974800-64007800	Weak transcription	Fetal Brain Male	brain
12	chr14:63975000-64008800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr14:63975200-64000600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr14:63975600-64005800	Weak transcription	K562	blood
15	chr14:63977200-64002400	Weak transcription	HSMM	muscle
16	chr14:63978200-63993200	Weak transcription	Thymus	Thymus
17	chr14:63978400-63999400	Weak transcription	Primary hematopoietic stem cells	blood
18	chr14:63978800-63992800	Weak transcription	Fetal Thymus	thymus
19	chr14:63978800-63993200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr14:63979200-64002600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr14:63980800-64000400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr14:63980800-64008000	Weak transcription	Small Intestine	intestine
23	chr14:63981600-63996400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr14:63981600-63997600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr14:63981600-64002800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr14:63981800-63997400	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr14:63981800-64003200	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr14:63981800-64004400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr14:63981800-64008000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr14:63982000-64001600	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr14:63982000-64002800	Weak transcription	HUVEC	blood vessel
32	chr14:63983400-64000600	Weak transcription	A549	lung
33	chr14:63983400-64002800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr14:63983600-63999400	Weak transcription	Fetal Brain Female	brain
35	chr14:63983600-64000800	Weak transcription	Osteobl	bone
36	chr14:63983600-64003000	Weak transcription	Hela-S3	cervix
37	chr14:63983600-64003000	Weak transcription	NH-A	brain
38	chr14:63983600-64003200	Weak transcription	NHDF-Ad	bronchial
39	chr14:63984400-63996600	Weak transcription	Primary T helper cells PMA-I stimulated	--
40	chr14:63984400-64002000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr14:63986400-64000800	Weak transcription	Placenta	Placenta
42	chr14:63987600-64000800	Weak transcription	NHEK	skin
43	chr14:63987800-63999400	Weak transcription	Primary neutrophils fromperipheralblood	blood
44	chr14:63988200-63992600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr14:63988400-63993200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr14:63988400-64002800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr14:63988600-63996400	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr14:63988600-63999400	Weak transcription	Fetal Muscle Leg	muscle
49	chr14:63988800-64008200	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr14:63989200-63992800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell

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