Variant report

Variant	rs9886014
Chromosome Location	chr7:16452404-16452405
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:16447322..16450777-chr7:16450983..16453871,4	K562	blood:
2	chr7:16451524..16456332-chr7:16459501..16462581,7	MCF-7	breast:
3	chr7:16451377..16453700-chr7:16455359..16457041,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000214960	Chromatin interaction

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10257743	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10267704	0.83[EUR][1000 genomes]
rs10273034	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17169461	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17169466	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17169476	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1882382	0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1882383	0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1921832	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1921833	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2178599	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2389639	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3763508	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6461256	0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73308344	0.83[EUR][1000 genomes]
rs7803246	0.85[EUR][1000 genomes];0.98[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	nsv1016642	chr7:15884061-16799788	Genic enhancers Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	esv2759514	chr7:16236162-16527390	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	esv2758105	chr7:16272822-16527390	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	esv2757215	chr7:16346139-16458474	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv1031019	chr7:16377519-16458474	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Genic enhancers	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
6	nsv1034151	chr7:16415497-16578081	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16434400-16459000	Weak transcription	Stomach Mucosa	stomach
2	chr7:16440200-16452600	Weak transcription	Pancreas	Pancrea
3	chr7:16440400-16452600	Weak transcription	Gastric	stomach
4	chr7:16440400-16459600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:16443600-16456400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr7:16450000-16459600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr7:16450200-16453000	Enhancers	NHDF-Ad	bronchial
8	chr7:16450600-16459800	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr7:16450800-16453200	Enhancers	Muscle Satellite Cultured Cells	--
10	chr7:16451000-16452600	Weak transcription	Left Ventricle	heart
11	chr7:16451400-16456200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr7:16451800-16453000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr7:16451800-16453000	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr7:16451800-16453000	Enhancers	Fetal Lung	lung
15	chr7:16452200-16453000	Enhancers	Fetal Muscle Leg	muscle
16	chr7:16452200-16453000	Enhancers	Fetal Stomach	stomach
17	chr7:16452200-16453000	Enhancers	HSMMtube	muscle
18	chr7:16452400-16452600	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr7:16452400-16452600	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr7:16452400-16453200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr7:16452400-16457200	Enhancers	K562	blood

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