Variant report

Variant	rs8018707
Chromosome Location	chr14:35766030-35766031
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:35765428..35767078-chr14:35809489..35811845,2	MCF-7	breast:
2	chr12:69885101..69887587-chr14:35765375..35767747,2	MCF-7	breast:
3	chr14:35757780..35767592-chr14:35866063..35878024,53	MCF-7	breast:
4	chr14:35761890..35767767-chr14:35871223..35875046,8	K562	blood:
5	chr14:35745539..35747078-chr14:35765050..35766913,2	K562	blood:
6	chr14:35683125..35684934-chr14:35764206..35766874,2	MCF-7	breast:
7	chr14:35757192..35766588-chr14:35865950..35877395,53	MCF-7	breast:

Variant related genes	Relation type
ENSG00000100906	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10130007	0.88[EUR][1000 genomes]
rs10132938	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs10133402	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10134499	1.00[CEU][hapmap];0.83[YRI][hapmap];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10134666	1.00[CEU][hapmap]
rs10136494	1.00[EUR][1000 genomes]
rs10137095	1.00[EUR][1000 genomes]
rs10137440	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs10137488	1.00[EUR][1000 genomes]
rs10140636	0.83[EUR][1000 genomes]
rs10140985	0.91[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.88[EUR][1000 genomes]
rs10141688	1.00[CEU][hapmap];0.83[EUR][1000 genomes]
rs10143083	0.89[EUR][1000 genomes]
rs10144186	0.89[AFR][1000 genomes]
rs10147734	0.91[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.83[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10148143	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10148234	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10148868	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs10148872	0.82[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.83[EUR][1000 genomes]
rs10149412	1.00[CEU][hapmap];0.88[YRI][hapmap];0.83[EUR][1000 genomes]
rs10151128	0.86[AFR][1000 genomes]
rs10467707	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs10715	0.91[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.88[EUR][1000 genomes]
rs11156879	1.00[EUR][1000 genomes]
rs11156880	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs11547365	1.00[EUR][1000 genomes]
rs11851831	0.82[ASW][hapmap];1.00[CEU][hapmap];0.94[GIH][hapmap]
rs12323542	1.00[CEU][hapmap];0.88[EUR][1000 genomes]
rs13393	1.00[EUR][1000 genomes]
rs17597267	0.82[ASW][hapmap]
rs17597281	0.82[ASW][hapmap]
rs2415281	0.88[EUR][1000 genomes]
rs28460322	0.88[EUR][1000 genomes]
rs57606486	1.00[EUR][1000 genomes]
rs58058174	0.94[EUR][1000 genomes]
rs7145488	0.94[GIH][hapmap]
rs7154775	0.91[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap]
rs8004205	0.88[EUR][1000 genomes]
rs8017330	0.82[ASW][hapmap]
rs8017676	0.91[ASW][hapmap];0.88[LWK][hapmap];0.94[MKK][hapmap]
rs9322944	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs9322945	1.00[EUR][1000 genomes]
rs9322946	1.00[CEU][hapmap];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949617	chr14:35379923-35825436	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	73 gene(s)	inside rSNPs	diseases
2	nsv870305	chr14:35488290-35852349	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
3	nsv1053604	chr14:35548276-35825805	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	nsv1052392	chr14:35563220-35893309	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	83 gene(s)	inside rSNPs	diseases
5	nsv542036	chr14:35563220-35893309	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	83 gene(s)	inside rSNPs	diseases
6	nsv1038396	chr14:35714499-35788189	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	nsv1045288	chr14:35735886-35788189	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv1043840	chr14:35739319-35791879	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35761800-35767400	Transcr. at gene 5' and 3'	Dnd41	blood
2	chr14:35762600-35774400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:35762600-35778400	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr14:35762800-35768200	Enhancers	Primary neutrophils fromperipheralblood	blood
5	chr14:35762800-35778600	Weak transcription	H9 Cell Line	embryonic stem cell
6	chr14:35762800-35778800	Weak transcription	Aorta	Aorta
7	chr14:35763200-35766200	Enhancers	Fetal Brain Male	brain
8	chr14:35763200-35777000	Weak transcription	HUES48 Cell Line	embryonic stem cell
9	chr14:35763200-35778000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr14:35763200-35780000	Weak transcription	Fetal Kidney	kidney
11	chr14:35763200-35789600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr14:35763600-35775000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr14:35763600-35776800	Weak transcription	Fetal Muscle Trunk	muscle
14	chr14:35763600-35777000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
15	chr14:35763600-35778800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr14:35763800-35766800	Weak transcription	Colon Smooth Muscle	Colon
17	chr14:35763800-35767000	Enhancers	Left Ventricle	heart
18	chr14:35763800-35768200	Weak transcription	NH-A	brain
19	chr14:35763800-35777200	Weak transcription	Placenta	Placenta
20	chr14:35763800-35777600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr14:35763800-35777800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr14:35763800-35777800	Weak transcription	HSMM	muscle
23	chr14:35763800-35778600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr14:35763800-35778600	Weak transcription	Colonic Mucosa	Colon
25	chr14:35763800-35778600	Weak transcription	Esophagus	oesophagus
26	chr14:35763800-35778600	Weak transcription	Ovary	ovary
27	chr14:35763800-35779200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
28	chr14:35764000-35767000	Enhancers	Skeletal Muscle Female	skeletal muscle
29	chr14:35764000-35767200	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr14:35764000-35767600	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr14:35764000-35768400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr14:35764000-35769200	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr14:35764000-35769800	Weak transcription	Brain Cingulate Gyrus	brain
34	chr14:35764000-35770000	Enhancers	Adipose Nuclei	Adipose
35	chr14:35764000-35771000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr14:35764000-35771600	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr14:35764000-35771600	Enhancers	Primary T cells fromperipheralblood	blood
38	chr14:35764000-35772600	Weak transcription	Rectal Smooth Muscle	rectum
39	chr14:35764000-35778200	Weak transcription	Brain Hippocampus Middle	brain
40	chr14:35764000-35778600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr14:35764000-35779200	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr14:35764200-35767200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr14:35764200-35768400	Weak transcription	Primary B cells from cord blood	blood
44	chr14:35764200-35768800	Weak transcription	NHDF-Ad	bronchial
45	chr14:35764200-35777000	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr14:35764200-35777200	Weak transcription	Osteobl	bone
47	chr14:35764200-35778200	Weak transcription	Stomach Smooth Muscle	stomach
48	chr14:35764400-35766200	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr14:35764400-35766800	Weak transcription	Brain Substantia Nigra	brain
50	chr14:35764400-35767800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood

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