Variant report

Variant	rs73343908
Chromosome Location	chr8:125638496-125638497
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:82956061..82958842-chr8:125637568..125639220,2	MCF-7	breast:
2	chr8:125628049..125629556-chr8:125636539..125638565,2	MCF-7	breast:
3	chr8:125631062..125635661-chr8:125637990..125641115,5	MCF-7	breast:
4	chr8:125638065..125640378-chr8:125640492..125642045,2	K562	blood:
5	chr8:125634912..125639122-chr8:125652761..125656973,4	K562	blood:
6	chr8:125552236..125554783-chr8:125637109..125639947,2	MCF-7	breast:
7	chr8:125638351..125644610-chr8:125826258..125829486,6	K562	blood:
8	chr8:125627308..125630217-chr8:125638327..125642424,3	K562	blood:
9	chr8:125636931..125639466-chr8:125722447..125724460,2	MCF-7	breast:
10	chr8:125635200..125638584-chr8:125825947..125829303,4	K562	blood:
11	chr8:125625102..125627021-chr8:125636879..125638991,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000005700	Chromatin interaction
ENSG00000255491	Chromatin interaction
ENSG00000170873	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10110296	1.00[ASN][1000 genomes]
rs13250940	1.00[ASN][1000 genomes]
rs16899702	1.00[ASN][1000 genomes]
rs16899745	1.00[ASN][1000 genomes]
rs28515894	1.00[ASN][1000 genomes]
rs4301438	1.00[ASN][1000 genomes]
rs57360261	1.00[ASN][1000 genomes]
rs59780127	1.00[ASN][1000 genomes]
rs60490907	1.00[ASN][1000 genomes]
rs60740213	1.00[ASN][1000 genomes]
rs61105996	1.00[ASN][1000 genomes]
rs61446370	1.00[ASN][1000 genomes]
rs61712455	1.00[ASN][1000 genomes]
rs72716935	1.00[ASN][1000 genomes]
rs73341805	1.00[ASN][1000 genomes]
rs73341837	1.00[ASN][1000 genomes]
rs73341838	1.00[ASN][1000 genomes]
rs73341884	1.00[ASN][1000 genomes]
rs73341898	1.00[ASN][1000 genomes]
rs73343904	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1027585	chr8:125627924-125707738	Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
2	nsv891434	chr8:125630655-126324432	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125618000-125640400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr8:125619200-125649000	Weak transcription	Colonic Mucosa	Colon
3	chr8:125626400-125638800	Weak transcription	HMEC	breast
4	chr8:125629400-125640200	Enhancers	Fetal Brain Male	brain
5	chr8:125631800-125639200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
6	chr8:125631800-125639200	Weak transcription	Pancreas	Pancrea
7	chr8:125631800-125639800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr8:125632000-125638600	Weak transcription	NHEK	skin
9	chr8:125632200-125638800	Weak transcription	Gastric	stomach
10	chr8:125632400-125640200	Weak transcription	Rectal Smooth Muscle	rectum
11	chr8:125632400-125640600	Weak transcription	Primary hematopoietic stem cells	blood
12	chr8:125633400-125639000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr8:125633400-125639600	Weak transcription	NHDF-Ad	bronchial
14	chr8:125633400-125643200	Weak transcription	Fetal Kidney	kidney
15	chr8:125633800-125638600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
16	chr8:125633800-125638800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr8:125633800-125639200	Weak transcription	Stomach Mucosa	stomach
18	chr8:125633800-125639600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
19	chr8:125633800-125641000	Weak transcription	Osteobl	bone
20	chr8:125633800-125642400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr8:125634200-125639000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr8:125634200-125639600	Weak transcription	GM12878-XiMat	blood
23	chr8:125634400-125641800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr8:125634800-125639800	Weak transcription	Primary T helper cells PMA-I stimulated	--
25	chr8:125634800-125646600	Weak transcription	Primary T cells from cord blood	blood
26	chr8:125635400-125639600	Weak transcription	Primary T helper cells fromperipheralblood	blood
27	chr8:125635400-125640600	Weak transcription	Colon Smooth Muscle	Colon
28	chr8:125635800-125641000	Enhancers	Fetal Thymus	thymus
29	chr8:125635800-125641200	Enhancers	Fetal Muscle Trunk	muscle
30	chr8:125636200-125638800	Enhancers	Fetal Muscle Leg	muscle
31	chr8:125636400-125640600	Strong transcription	Fetal Intestine Small	intestine
32	chr8:125636400-125644400	Enhancers	Brain Inferior Temporal Lobe	brain
33	chr8:125636600-125639200	Genic enhancers	Primary B cells from peripheral blood	blood
34	chr8:125636600-125639600	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr8:125636600-125639800	Enhancers	Adipose Nuclei	Adipose
36	chr8:125636600-125639800	Enhancers	Skeletal Muscle Male	skeletal muscle
37	chr8:125636600-125640000	Enhancers	Brain Angular Gyrus	brain
38	chr8:125636600-125640200	Enhancers	Right Atrium	heart
39	chr8:125636600-125641200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
40	chr8:125636600-125644000	Enhancers	Fetal Heart	heart
41	chr8:125636600-125644200	Enhancers	Placenta	Placenta
42	chr8:125636800-125639800	Enhancers	Left Ventricle	heart
43	chr8:125636800-125640000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr8:125636800-125640200	Enhancers	Liver	Liver
45	chr8:125636800-125641400	Enhancers	Brain Substantia Nigra	brain
46	chr8:125637000-125639000	Weak transcription	Lung	lung
47	chr8:125637000-125639400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr8:125637000-125644200	Enhancers	Thymus	Thymus
49	chr8:125637200-125638800	Enhancers	Primary B cells from cord blood	blood
50	chr8:125637200-125639000	Enhancers	Spleen	Spleen

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links