Variant report

Variant	rs12882429
Chromosome Location	chr14:64351059-64351060
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:64350604..64352187-chr14:64354098..64356730,2	MCF-7	breast:
2	chr14:64350600..64353514-chr7:30543619..30546570,2	MCF-7	breast:
3	chr14:64349303..64352052-chr2:9373051..9375606,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000006625	Chromatin interaction

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs11158520	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11850711	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12588807	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12588955	0.86[ASN][1000 genomes]
rs12589453	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12878037	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12878348	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12879374	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12881942	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12888489	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12888712	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs12891546	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12894963	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17751301	1.00[CEU][hapmap]
rs17824268	1.00[CEU][hapmap];0.88[JPT][hapmap]
rs33976862	1.00[CEU][hapmap];0.86[JPT][hapmap];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs34328391	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs34451919	0.86[ASN][1000 genomes]
rs34556545	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs34561759	1.00[ASN][1000 genomes]
rs35009554	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35033077	0.83[ASN][1000 genomes]
rs35168922	1.00[ASN][1000 genomes]
rs35302448	1.00[ASN][1000 genomes]
rs35581544	0.85[AMR][1000 genomes]
rs35984502	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs3818774	0.97[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs4459477	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs4899120	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4902250	1.00[ASN][1000 genomes]
rs6573539	0.92[EUR][1000 genomes]
rs66684280	1.00[ASN][1000 genomes]
rs67289344	1.00[ASN][1000 genomes]
rs71416319	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7144308	0.86[ASN][1000 genomes]
rs7401191	1.00[ASN][1000 genomes]
rs8015210	1.00[CEU][hapmap];0.88[JPT][hapmap]
rs8023195	1.00[CHB][hapmap];1.00[JPT][hapmap]

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	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
2	nsv1038825	chr14:64109441-64491720	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
3	nsv1037140	chr14:64248421-64442980	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv542119	chr14:64248421-64442980	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv564904	chr14:64346190-64416898	Weak transcription Genic enhancers Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	esv1793389	chr14:64346190-64457224	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:64327400-64355200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr14:64327600-64360000	Weak transcription	Gastric	stomach
3	chr14:64331200-64356400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr14:64335200-64360000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr14:64336800-64362800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr14:64337000-64357200	Weak transcription	Duodenum Mucosa	Duodenum
7	chr14:64337000-64365200	Weak transcription	Fetal Thymus	thymus
8	chr14:64337800-64403800	Weak transcription	Thymus	Thymus
9	chr14:64338000-64353800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr14:64338000-64355200	Weak transcription	Primary B cells from cord blood	blood
11	chr14:64339400-64366800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr14:64341000-64356400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr14:64341000-64357200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr14:64341200-64352200	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr14:64341200-64352400	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr14:64341200-64354000	Weak transcription	Dnd41	blood
17	chr14:64341200-64354800	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr14:64341200-64356400	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr14:64341200-64356400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr14:64341200-64356600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr14:64341200-64357000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr14:64341200-64357200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr14:64341200-64357200	Weak transcription	Fetal Lung	lung
24	chr14:64341200-64357200	Weak transcription	Fetal Muscle Leg	muscle
25	chr14:64341400-64352400	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chr14:64341400-64352600	Weak transcription	Stomach Mucosa	stomach
27	chr14:64341400-64356600	Weak transcription	Primary T helper cells fromperipheralblood	blood
28	chr14:64341400-64356600	Weak transcription	Fetal Kidney	kidney
29	chr14:64341400-64366800	Weak transcription	Primary T cells from cord blood	blood
30	chr14:64342400-64354800	Weak transcription	Aorta	Aorta
31	chr14:64342400-64357200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr14:64342600-64352000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
33	chr14:64342600-64352400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
34	chr14:64342600-64357400	Weak transcription	Duodenum Smooth Muscle	Duodenum
35	chr14:64342800-64351600	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr14:64342800-64352400	Weak transcription	Adipose Nuclei	Adipose
37	chr14:64342800-64354200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr14:64342800-64357000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr14:64342800-64357200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr14:64342800-64360400	Weak transcription	Stomach Smooth Muscle	stomach
41	chr14:64342800-64360400	Weak transcription	Hela-S3	cervix
42	chr14:64342800-64368400	Weak transcription	Esophagus	oesophagus
43	chr14:64343600-64359400	Weak transcription	Fetal Muscle Trunk	muscle
44	chr14:64344000-64357200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr14:64344000-64357200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr14:64344200-64352000	Weak transcription	Brain Germinal Matrix	brain
47	chr14:64344400-64351200	Weak transcription	Pancreatic Islets	Pancreatic Islet
48	chr14:64344400-64356600	Weak transcription	GM12878-XiMat	blood
49	chr14:64344400-64357000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr14:64344400-64357400	Weak transcription	Fetal Intestine Large	intestine

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