Variant report

Variant	rs10107762
Chromosome Location	chr8:125578635-125578636
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr8:125549460..125555106-chr8:125573452..125578755,9	MCF-7	breast:
2	chr8:125572972..125577628-chr8:125578200..125582090,6	MCF-7	breast:
3	chr8:125572673..125575871-chr8:125577015..125582400,6	K562	blood:
4	chr8:125577321..125579071-chr8:125580874..125582837,2	MCF-7	breast:
5	chr8:125551552..125553200-chr8:125577686..125580051,3	K562	blood:
6	chr8:125577831..125580093-chr8:125580434..125583329,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000147684	Chromatin interaction
ENSG00000170873	Chromatin interaction
ENSG00000147687	Chromatin interaction

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10046739	1.00[CEU][hapmap];0.92[CHB][hapmap];0.96[CHD][hapmap];1.00[JPT][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];0.89[MKK][hapmap];1.00[TSI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13251109	1.00[ASW][hapmap];1.00[CEU][hapmap];0.92[CHB][hapmap];0.96[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.92[TSI][hapmap];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13258027	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13261695	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16899660	1.00[ASW][hapmap]
rs16899708	1.00[CEU][hapmap];0.92[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16899748	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs34263543	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3829034	0.84[GIH][hapmap]
rs3857946	1.00[ASW][hapmap];0.89[CEU][hapmap];0.84[TSI][hapmap];0.83[EUR][1000 genomes]
rs4007921	1.00[ASW][hapmap];1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];0.86[JPT][hapmap];0.92[TSI][hapmap];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs59807139	0.81[AFR][1000 genomes]
rs67077163	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531508	chr8:125390194-125587953	Flanking Active TSS Strong transcription Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	84 gene(s)	inside rSNPs	diseases
2	nsv525649	chr8:125565328-125600818	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1024804	chr8:125575803-125600950	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1025014	chr8:125578314-125600950	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:91 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:125553800-125581200	Strong transcription	Fetal Brain Female	brain
2	chr8:125566000-125602400	Weak transcription	Aorta	Aorta
3	chr8:125566200-125590400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr8:125566400-125600600	Weak transcription	NHEK	skin
5	chr8:125566800-125581400	Weak transcription	HSMM	muscle
6	chr8:125567000-125590200	Weak transcription	Fetal Brain Male	brain
7	chr8:125570000-125584800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr8:125570800-125605000	Weak transcription	Colon Smooth Muscle	Colon
9	chr8:125571800-125581200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr8:125574400-125609400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr8:125574800-125580600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr8:125574800-125581000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr8:125574800-125590200	Weak transcription	HMEC	breast
14	chr8:125575200-125578800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr8:125575400-125589200	Weak transcription	Esophagus	oesophagus
16	chr8:125575600-125600600	Weak transcription	Fetal Kidney	kidney
17	chr8:125575800-125581000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr8:125575800-125589200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr8:125576000-125578800	Weak transcription	Brain Anterior Caudate	brain
20	chr8:125576200-125578800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chr8:125576400-125578800	Weak transcription	Fetal Muscle Trunk	muscle
22	chr8:125576400-125583200	Weak transcription	Pancreas	Pancrea
23	chr8:125576600-125578800	Weak transcription	Brain Hippocampus Middle	brain
24	chr8:125576600-125579200	Genic enhancers	Liver	Liver
25	chr8:125576600-125583600	Strong transcription	Cortex derived primary cultured neurospheres	brain
26	chr8:125576600-125591400	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr8:125576800-125578800	Weak transcription	Brain Cingulate Gyrus	brain
28	chr8:125576800-125578800	Weak transcription	Fetal Stomach	stomach
29	chr8:125576800-125590200	Weak transcription	Rectal Smooth Muscle	rectum
30	chr8:125576800-125598200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr8:125577000-125578800	Weak transcription	Spleen	Spleen
32	chr8:125577000-125579000	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr8:125577200-125578800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr8:125577200-125578800	Weak transcription	Fetal Heart	heart
35	chr8:125577200-125578800	Enhancers	Fetal Lung	lung
36	chr8:125577200-125579800	Weak transcription	Psoas Muscle	Psoas
37	chr8:125577200-125580600	Strong transcription	Brain Inferior Temporal Lobe	brain
38	chr8:125577200-125581200	Weak transcription	Right Ventricle	heart
39	chr8:125577200-125581800	Strong transcription	Brain Germinal Matrix	brain
40	chr8:125577200-125591400	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr8:125577400-125579000	Enhancers	HUVEC	blood vessel
42	chr8:125577400-125579200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
43	chr8:125577400-125579800	Enhancers	Primary T cells fromperipheralblood	blood
44	chr8:125577400-125582000	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr8:125577400-125586600	Weak transcription	Brain Angular Gyrus	brain
46	chr8:125577400-125589800	Weak transcription	NHLF	lung
47	chr8:125577600-125579200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr8:125577600-125579200	Enhancers	Primary T cells from cord blood	blood
49	chr8:125577600-125579200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
50	chr8:125577600-125579400	Enhancers	Primary T killer memory cells from peripheral blood	blood

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