Variant report

Variant	rs1359701
Chromosome Location	chr9:12777126-12777127
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:12716514..12718700-chr9:12776478..12778096,2	MCF-7	breast:
2	chr9:12775994..12778011-chr9:12786037..12787743,2	K562	blood:
3	chr9:12771458..12774120-chr9:12775878..12777874,2	K562	blood:
4	chr9:12776291..12778540-chr9:12858744..12861808,3	MCF-7	breast:
5	chr9:12774109..12791345-chr9:12812800..12822770,37	MCF-7	breast:
6	chr9:12776937..12779598-chr9:12883479..12885184,2	MCF-7	breast:
7	chr9:12773974..12784053-chr9:12813051..12820453,19	MCF-7	breast:

Variant related genes	Relation type
ENSG00000235448	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10120667	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10120695	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10756411	0.94[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10756412	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10756413	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10809839	0.83[CEU][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10809840	0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10809841	0.83[CEU][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10809842	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10809843	0.88[JPT][hapmap]
rs10960792	0.83[CEU][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1326800	1.00[CEU][hapmap];0.82[CHB][hapmap];0.94[JPT][hapmap];0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2147250	0.84[JPT][hapmap]
rs2181817	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2382371	0.88[JPT][hapmap]
rs7468492	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2759671	chr9:12235048-12784092	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1034393	chr9:12278703-12798236	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv869288	chr9:12286919-12816766	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv498136	chr9:12387840-12984158	Genic enhancers Enhancers Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
5	nsv1029415	chr9:12424340-12794623	Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv540064	chr9:12424340-12794623	Transcr. at gene 5' and 3' Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	esv2422212	chr9:12448789-13127738	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
8	esv2758182	chr9:12621991-12784092	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv1030835	chr9:12717405-12840928	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
10	nsv892573	chr9:12730636-12874703	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers 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	10 gene(s)	inside rSNPs	diseases
11	nsv892574	chr9:12754969-12918226	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 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	chr9:12774600-12778000	Active TSS	NHDF-Ad	bronchial
2	chr9:12774800-12777200	Active TSS	Psoas Muscle	Psoas
3	chr9:12774800-12777200	Active TSS	Osteobl	bone
4	chr9:12774800-12777400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr9:12774800-12777400	Active TSS	Brain Angular Gyrus	brain
6	chr9:12774800-12777400	Active TSS	Brain Anterior Caudate	brain
7	chr9:12774800-12777400	Active TSS	Brain Hippocampus Middle	brain
8	chr9:12774800-12777400	Active TSS	Fetal Muscle Trunk	muscle
9	chr9:12774800-12777400	Active TSS	Ovary	ovary
10	chr9:12774800-12777400	Active TSS	A549	lung
11	chr9:12774800-12777600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr9:12774800-12777600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
13	chr9:12774800-12777800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr9:12774800-12777800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr9:12774800-12778000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr9:12774800-12778000	Active TSS	Colon Smooth Muscle	Colon
17	chr9:12774800-12778000	Active TSS	Fetal Intestine Large	intestine
18	chr9:12774800-12778000	Active TSS	Rectal Smooth Muscle	rectum
19	chr9:12774800-12778000	Active TSS	NHEK	skin
20	chr9:12774800-12778200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr9:12774800-12778200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr9:12774800-12778200	Active TSS	Aorta	Aorta
23	chr9:12774800-12778200	Active TSS	Fetal Stomach	stomach
24	chr9:12774800-12778200	Active TSS	Right Atrium	heart
25	chr9:12774800-12778400	Active TSS	NHLF	lung
26	chr9:12774800-12779000	Active TSS	Pancreatic Islets	Pancreatic Islet
27	chr9:12774800-12779000	Active TSS	Stomach Smooth Muscle	stomach
28	chr9:12775000-12777200	Active TSS	Fetal Intestine Small	intestine
29	chr9:12775000-12777400	Active TSS	Colonic Mucosa	Colon
30	chr9:12775000-12777400	Active TSS	Lung	lung
31	chr9:12775000-12779200	Active TSS	Rectal Mucosa Donor 29	rectum
32	chr9:12775800-12779000	Active TSS	Duodenum Smooth Muscle	Duodenum
33	chr9:12776200-12778200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr9:12776200-12779200	ZNF genes & repeats	Fetal Brain Male	brain
35	chr9:12776400-12777800	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
36	chr9:12776400-12778400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr9:12776600-12777200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
38	chr9:12776600-12777200	Flanking Active TSS	HSMM	muscle
39	chr9:12776600-12777400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr9:12776600-12778600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr9:12776600-12778600	Flanking Active TSS	Adipose Nuclei	Adipose
42	chr9:12776600-12778600	Flanking Active TSS	Hela-S3	cervix
43	chr9:12776600-12779200	Transcr. at gene 5' and 3'	Fetal Lung	lung
44	chr9:12776800-12777200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr9:12776800-12777200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr9:12776800-12777200	Active TSS	Fetal Brain Female	brain
47	chr9:12776800-12777400	Active TSS	HepG2	liver
48	chr9:12776800-12778200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr9:12776800-12778200	Active TSS	Fetal Kidney	kidney
50	chr9:12776800-12778200	Active TSS	Placenta	Placenta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links