Variant report

Variant	rs17107610
Chromosome Location	chr14:70477022-70477023
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr14:70476343..70479164-chr14:70482815..70484444,2	MCF-7	breast:
2	chr14:70469751..70473498-chr14:70474814..70477907,3	MCF-7	breast:
3	chr14:70475248..70477475-chr14:70478520..70481359,3	MCF-7	breast:
4	chr14:70469147..70471287-chr14:70474432..70477104,2	MCF-7	breast:

Extended variants
information (count: 38 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1005543	0.82[CHB][hapmap]
rs10134291	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs10134965	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11158827	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];0.91[JPT][hapmap];0.85[LWK][hapmap];0.83[MEX][hapmap];0.86[YRI][hapmap];0.80[AFR][1000 genomes];0.99[ASN][1000 genomes]
rs12050076	0.85[CHD][hapmap]
rs12050089	0.95[ASN][1000 genomes]
rs12101270	0.95[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs12433177	0.84[CHD][hapmap]
rs12885068	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs12885683	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs12887943	0.95[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs12889195	0.95[ASN][1000 genomes]
rs12890357	0.85[ASN][1000 genomes]
rs1459704	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1471243	0.92[CEU][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17107547	0.83[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs227416	0.95[GIH][hapmap]
rs227419	0.93[GIH][hapmap]
rs227425	1.00[GIH][hapmap]
rs227426	0.95[GIH][hapmap]
rs227437	0.83[CHB][hapmap];0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs2281663	0.82[CHB][hapmap];0.81[CHD][hapmap]
rs34311408	0.95[ASN][1000 genomes]
rs3825739	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs56242824	0.95[ASN][1000 genomes]
rs57609901	0.95[ASN][1000 genomes]
rs67294558	0.86[ASN][1000 genomes]
rs7141378	0.94[ASN][1000 genomes]
rs7151788	0.92[CEU][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7157226	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs7160726	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs8010305	0.82[CHB][hapmap];0.83[CHD][hapmap];0.84[MEX][hapmap]
rs8012912	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs8015491	0.86[JPT][hapmap]
rs8016522	0.82[CHB][hapmap];0.81[CHD][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv456336	chr14:70081956-70574149	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
2	nsv565007	chr14:70081956-70574149	Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
3	nsv832824	chr14:70320639-70511401	Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs17107610	SMOC1	cis	Artery Tibial	GTEx

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70439800-70477200	Weak transcription	Spleen	Spleen
2	chr14:70450600-70477200	Weak transcription	Fetal Brain Female	brain
3	chr14:70457800-70484800	Weak transcription	Brain Substantia Nigra	brain
4	chr14:70458600-70480800	Weak transcription	Brain Germinal Matrix	brain
5	chr14:70459000-70484800	Weak transcription	Gastric	stomach
6	chr14:70466200-70484800	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr14:70468400-70484400	Weak transcription	A549	lung
8	chr14:70469800-70484800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr14:70470400-70479800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr14:70472200-70481400	Weak transcription	Fetal Muscle Leg	muscle
11	chr14:70472400-70485400	Strong transcription	Hela-S3	cervix
12	chr14:70474400-70477400	Enhancers	Fetal Stomach	stomach
13	chr14:70475200-70479200	Strong transcription	Liver	Liver
14	chr14:70475400-70477200	Enhancers	Duodenum Smooth Muscle	Duodenum
15	chr14:70475600-70478600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr14:70475600-70478600	Enhancers	HMEC	breast
17	chr14:70475800-70478400	Enhancers	NHEK	skin
18	chr14:70475800-70479000	Enhancers	Breast Myoepithelial Primary Cells	Breast
19	chr14:70475800-70480200	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr14:70475800-70484800	Weak transcription	Brain Hippocampus Middle	brain
21	chr14:70475800-70487200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr14:70476000-70478400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr14:70476000-70480200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
24	chr14:70476000-70500000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr14:70476200-70478400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr14:70476200-70479800	Enhancers	GM12878-XiMat	blood
27	chr14:70476200-70480200	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr14:70476200-70482200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr14:70476200-70490600	Weak transcription	Fetal Brain Male	brain
30	chr14:70476200-70499000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr14:70476600-70478400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr14:70476600-70480200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr14:70476600-70480600	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr14:70476800-70477200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr14:70476800-70477200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr14:70476800-70477800	Enhancers	Placenta	Placenta
37	chr14:70477000-70477400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr14:70477000-70477400	Enhancers	Esophagus	oesophagus
39	chr14:70477000-70479000	Strong transcription	HepG2	liver
40	chr14:70477000-70479200	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr14:70477000-70479200	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr14:70477000-70483000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr14:70477000-70484200	Strong transcription	Cortex derived primary cultured neurospheres	brain

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