Variant report

Variant	rs35085433
Chromosome Location	chr8:19184446-19184447
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:19168689..19173779-chr8:19180928..19188121,8	MCF-7	breast:
2	chr8:19174699..19177695-chr8:19183567..19186086,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000104611	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs13264045	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17116609	0.92[EUR][1000 genomes]
rs2410609	0.92[EUR][1000 genomes]
rs3808643	0.91[EUR][1000 genomes]
rs3808644	0.91[EUR][1000 genomes]
rs4075192	0.94[ASN][1000 genomes]
rs56005620	0.87[EUR][1000 genomes]
rs7829274	0.92[EUR][1000 genomes]
rs7832867	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7845057	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1026466	chr8:18433493-19271274	Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Active TSS 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 target site	29 gene(s)	inside rSNPs	diseases
2	nsv539520	chr8:18433493-19271274	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv1015395	chr8:18489538-19370258	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
4	nsv429907	chr8:18578720-19398220	Active TSS Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv917232	chr8:18585309-19208665	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
6	nsv890610	chr8:18749120-19260599	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
7	nsv949745	chr8:18826830-19363963	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
8	nsv1016482	chr8:18834807-19339487	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
9	nsv890614	chr8:18838764-19274793	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
10	nsv533109	chr8:18845845-19456780	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
11	nsv1016993	chr8:18855623-19311731	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
12	nsv949636	chr8:18957705-19664732	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
13	nsv890616	chr8:18989735-19197809	Weak transcription Flanking Active TSS Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
14	nsv1033229	chr8:19081684-19271274	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
15	nsv890621	chr8:19173379-19211220	Genic enhancers Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19172400-19184800	Weak transcription	Stomach Smooth Muscle	stomach
2	chr8:19172400-19187800	Weak transcription	Fetal Heart	heart
3	chr8:19172400-19188000	Weak transcription	Right Ventricle	heart
4	chr8:19172400-19202400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr8:19172600-19202800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr8:19173600-19254800	Weak transcription	Colonic Mucosa	Colon
7	chr8:19173800-19185200	Weak transcription	Sigmoid Colon	Sigmoid Colon
8	chr8:19173800-19205400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr8:19174000-19223600	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr8:19174200-19191400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr8:19174200-19220400	Weak transcription	HSMM	muscle
12	chr8:19174400-19205200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr8:19176600-19187000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr8:19176800-19185600	Strong transcription	Osteobl	bone
15	chr8:19177000-19185400	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr8:19177000-19188800	Strong transcription	A549	lung
17	chr8:19177000-19189600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr8:19177200-19189400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr8:19177400-19184800	Weak transcription	Fetal Lung	lung
20	chr8:19177800-19185600	Strong transcription	Fetal Intestine Small	intestine
21	chr8:19177800-19190600	Weak transcription	Adipose Nuclei	Adipose
22	chr8:19178200-19185400	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr8:19178200-19194400	Strong transcription	Duodenum Mucosa	Duodenum
24	chr8:19178800-19185600	Strong transcription	NHLF	lung
25	chr8:19179800-19185600	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr8:19180000-19188000	Weak transcription	Left Ventricle	heart
27	chr8:19180600-19184600	Enhancers	Fetal Thymus	thymus
28	chr8:19180600-19185800	Strong transcription	Fetal Stomach	stomach
29	chr8:19180600-19187800	Strong transcription	Rectal Mucosa Donor 29	rectum
30	chr8:19181000-19185200	Strong transcription	Fetal Intestine Large	intestine
31	chr8:19181600-19184600	Enhancers	Placenta	Placenta
32	chr8:19181600-19184600	Genic enhancers	Pancreas	Pancrea
33	chr8:19181800-19186600	Weak transcription	Ovary	ovary
34	chr8:19181800-19188000	Weak transcription	Rectal Mucosa Donor 31	rectum
35	chr8:19181800-19204800	Weak transcription	Spleen	Spleen
36	chr8:19182000-19189000	Strong transcription	HepG2	liver
37	chr8:19182000-19190600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
38	chr8:19182600-19184600	Genic enhancers	Esophagus	oesophagus
39	chr8:19182600-19184600	Genic enhancers	Gastric	stomach
40	chr8:19182800-19188000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
41	chr8:19183200-19184600	Enhancers	Stomach Mucosa	stomach
42	chr8:19183200-19185400	Enhancers	Placenta Amnion	Placenta Amnion
43	chr8:19183400-19184600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr8:19183400-19184800	Enhancers	Lung	lung
45	chr8:19183600-19185000	Weak transcription	Hela-S3	cervix
46	chr8:19183800-19189200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr8:19183800-19202600	Weak transcription	Primary T cells from cord blood	blood
48	chr8:19184000-19185000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr8:19184000-19185400	Enhancers	Primary neutrophils fromperipheralblood	blood
50	chr8:19184000-19186800	Strong transcription	Liver	Liver

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