Variant report

Variant	rs7698670
Chromosome Location	chr4:148789542-148789543
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:148605054..148606838-chr4:148786766..148789557,2	MCF-7	breast:
2	chr4:148509882..148511690-chr4:148787031..148789794,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000164169	Chromatin interaction

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:70)

rs_ID	r²[population]
rs10000278	0.94[EUR][1000 genomes]
rs10001688	0.87[EUR][1000 genomes]
rs10001756	0.88[EUR][1000 genomes]
rs10003507	0.90[EUR][1000 genomes]
rs10004138	0.85[EUR][1000 genomes]
rs10004691	0.86[EUR][1000 genomes]
rs10004792	0.90[EUR][1000 genomes]
rs10014593	0.90[EUR][1000 genomes]
rs10014696	0.94[EUR][1000 genomes]
rs10015875	0.88[EUR][1000 genomes]
rs10025069	0.88[EUR][1000 genomes]
rs10026985	0.88[EUR][1000 genomes]
rs10030358	0.90[EUR][1000 genomes]
rs10049932	0.90[EUR][1000 genomes]
rs11099671	0.89[EUR][1000 genomes]
rs11099672	0.91[EUR][1000 genomes]
rs11734553	0.87[EUR][1000 genomes]
rs11735412	0.89[EUR][1000 genomes]
rs11737346	0.91[ASN][1000 genomes]
rs12331562	0.94[EUR][1000 genomes]
rs12509618	0.87[EUR][1000 genomes]
rs12513192	0.90[EUR][1000 genomes]
rs12643550	0.91[EUR][1000 genomes]
rs13129325	0.94[EUR][1000 genomes]
rs13151898	0.87[EUR][1000 genomes]
rs1369958	0.90[EUR][1000 genomes]
rs17024037	0.87[EUR][1000 genomes]
rs17613979	0.90[EUR][1000 genomes]
rs17614025	0.89[EUR][1000 genomes]
rs17676080	0.88[EUR][1000 genomes]
rs2043643	0.90[EUR][1000 genomes]
rs2043645	0.87[EUR][1000 genomes]
rs28576385	0.88[EUR][1000 genomes]
rs28614116	0.87[EUR][1000 genomes]
rs2884400	0.89[EUR][1000 genomes]
rs34970355	0.87[EUR][1000 genomes]
rs35243600	0.87[EUR][1000 genomes]
rs35810358	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35899247	0.87[EUR][1000 genomes]
rs3893175	0.84[EUR][1000 genomes]
rs3990920	0.85[EUR][1000 genomes]
rs4240341	0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4491995	0.90[EUR][1000 genomes]
rs4571312	0.90[EUR][1000 genomes]
rs4627844	0.87[EUR][1000 genomes]
rs4835103	0.87[EUR][1000 genomes]
rs4835109	0.91[EUR][1000 genomes]
rs4835110	0.91[EUR][1000 genomes]
rs4835469	0.84[EUR][1000 genomes]
rs55650760	0.84[EUR][1000 genomes]
rs55820558	0.90[EUR][1000 genomes]
rs62330732	0.85[EUR][1000 genomes]
rs62330735	0.85[EUR][1000 genomes]
rs62330737	0.89[EUR][1000 genomes]
rs6535569	0.80[EUR][1000 genomes]
rs6811769	0.87[EUR][1000 genomes]
rs6818371	0.87[EUR][1000 genomes]
rs6832527	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6840771	0.87[EUR][1000 genomes]
rs6843392	0.88[EUR][1000 genomes]
rs6856273	0.89[EUR][1000 genomes]
rs7656471	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7660508	0.89[EUR][1000 genomes]
rs7677632	0.87[EUR][1000 genomes]
rs893033	0.90[EUR][1000 genomes]
rs9991741	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9994650	0.88[EUR][1000 genomes]
rs9995956	0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9997027	0.94[EUR][1000 genomes]
rs9999321	0.94[EUR][1000 genomes];0.80[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	nsv1028958	chr4:148377752-148793485	Weak transcription Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
2	nsv498083	chr4:148519825-148917583	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
3	nsv880243	chr4:148735644-148879583	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv880244	chr4:148764252-148920089	Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv1029845	chr4:148766290-148916437	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv1030001	chr4:148773479-148916437	Genic enhancers Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:148763200-148796200	Weak transcription	Monocytes-CD14+_RO01746	blood
2	chr4:148766600-148796200	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr4:148767600-148796400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr4:148768400-148815600	Weak transcription	Primary T cells from cord blood	blood
5	chr4:148770400-148796200	Weak transcription	Fetal Kidney	kidney
6	chr4:148772000-148806000	Weak transcription	Fetal Thymus	thymus
7	chr4:148777000-148796200	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr4:148777000-148823000	Weak transcription	Small Intestine	intestine
9	chr4:148777400-148796600	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr4:148777800-148796200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
11	chr4:148779800-148793800	Weak transcription	Fetal Lung	lung
12	chr4:148782000-148799400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr4:148783000-148796200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr4:148783000-148796200	Weak transcription	Thymus	Thymus
15	chr4:148783400-148796400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr4:148783400-148796400	Weak transcription	Lung	lung
17	chr4:148783600-148789800	Weak transcription	Fetal Intestine Small	intestine
18	chr4:148783600-148796200	Weak transcription	Esophagus	oesophagus
19	chr4:148783600-148796200	Weak transcription	Placenta	Placenta
20	chr4:148783800-148790000	Weak transcription	Left Ventricle	heart
21	chr4:148783800-148796200	Weak transcription	Fetal Intestine Large	intestine
22	chr4:148783800-148796200	Weak transcription	Gastric	stomach
23	chr4:148783800-148796200	Weak transcription	Right Ventricle	heart
24	chr4:148784400-148810800	Weak transcription	Fetal Heart	heart
25	chr4:148784600-148796400	Weak transcription	Duodenum Mucosa	Duodenum
26	chr4:148785400-148796200	Weak transcription	GM12878-XiMat	blood
27	chr4:148785600-148796200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr4:148786000-148789800	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr4:148786000-148790200	Strong transcription	HSMM	muscle
30	chr4:148786000-148804000	Weak transcription	Psoas Muscle	Psoas
31	chr4:148786000-148861400	Weak transcription	Pancreas	Pancrea
32	chr4:148786400-148796200	Weak transcription	Skeletal Muscle Male	skeletal muscle
33	chr4:148787000-148794000	Weak transcription	Stomach Smooth Muscle	stomach
34	chr4:148787200-148790400	Strong transcription	Fetal Muscle Trunk	muscle
35	chr4:148787400-148789600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr4:148787400-148789800	Strong transcription	Muscle Satellite Cultured Cells	--
37	chr4:148787400-148795600	Weak transcription	NH-A	brain
38	chr4:148787400-148796200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr4:148787400-148800400	Weak transcription	NHEK	skin
40	chr4:148787600-148796200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr4:148787600-148796200	Weak transcription	Osteobl	bone
42	chr4:148787600-148801600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr4:148787800-148790000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
44	chr4:148787800-148790400	Strong transcription	HSMMtube	muscle
45	chr4:148787800-148791000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr4:148787800-148793600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr4:148788000-148790400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr4:148788000-148790400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr4:148788000-148790600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr4:148788000-148796200	Weak transcription	HUVEC	blood vessel

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