Variant report

Variant	rs7915127
Chromosome Location	chr10:49720374-49720375
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	SPI1	chr10:49719823-49720410	HL-60	blood:	n/a	chr10:49720134-49720147 chr10:49720136-49720145 chr10:49720060-49720069 chr10:49720133-49720146
2	POLR2A	chr10:49720176-49721069	U87	brain:	n/a	n/a
3	POLR2A	chr10:49720154-49721069	U87	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr10:49718293..49721279-chr10:50504590..50507564,3	K562	blood:
2	chr10:49714562..49719396-chr10:49719920..49724610,6	K562	blood:
3	chr10:49719894..49722832-chr10:49724239..49726454,2	MCF-7	breast:

Variant related genes	Relation type
ARHGAP22-IT1	TF binding region
ENSG00000177354	Chromatin interaction
ENSG00000236208	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10857587	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10857588	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10857589	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11101354	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11101355	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11101357	0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11596336	0.86[ASN][1000 genomes]
rs12777174	0.86[ASN][1000 genomes]
rs12777190	0.86[ASN][1000 genomes]
rs12779617	0.84[ASN][1000 genomes]
rs1816888	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1900022	0.86[ASN][1000 genomes]
rs34279198	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs34552122	0.86[ASN][1000 genomes]
rs34774310	0.86[ASN][1000 genomes]
rs3910907	0.86[ASN][1000 genomes]
rs7910353	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7911247	0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7915233	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[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	nsv895371	chr10:49492075-50232180	Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	35 gene(s)	inside rSNPs	diseases
2	nsv895372	chr10:49576878-49933488	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv467191	chr10:49669142-49735563	Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv550813	chr10:49669142-49735563	Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv550814	chr10:49705142-49735563	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	nsv516006	chr10:49707942-49723300	Weak transcription Strong transcription ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:49698000-49731200	Weak transcription	Aorta	Aorta
2	chr10:49706000-49723400	Weak transcription	NH-A	brain
3	chr10:49709200-49720600	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr10:49714000-49727200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr10:49715800-49727800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr10:49716800-49721400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr10:49717200-49721400	Weak transcription	HSMM	muscle
8	chr10:49717400-49721000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr10:49717400-49721200	Weak transcription	HMEC	breast
10	chr10:49717400-49726200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr10:49717800-49720400	Weak transcription	HSMMtube	muscle
12	chr10:49718200-49723600	Weak transcription	HUVEC	blood vessel
13	chr10:49718400-49720800	Strong transcription	Osteobl	bone
14	chr10:49719000-49720400	Enhancers	Brain Substantia Nigra	brain
15	chr10:49719200-49720600	Enhancers	Primary hematopoietic stem cells	blood
16	chr10:49719200-49720600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr10:49719200-49721200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr10:49719200-49721200	Weak transcription	NHLF	lung
19	chr10:49719200-49721400	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr10:49719400-49720600	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr10:49719400-49721000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr10:49719400-49721000	Enhancers	Fetal Stomach	stomach
23	chr10:49719400-49721200	Enhancers	Primary monocytes fromperipheralblood	blood
24	chr10:49719400-49721400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr10:49719400-49725800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr10:49719600-49721000	Enhancers	Adipose Nuclei	Adipose
27	chr10:49719600-49721600	Enhancers	GM12878-XiMat	blood
28	chr10:49719800-49720400	Enhancers	Primary B cells from peripheral blood	blood
29	chr10:49719800-49720600	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr10:49719800-49720600	Enhancers	Brain Anterior Caudate	brain
31	chr10:49719800-49720800	Enhancers	Brain Cingulate Gyrus	brain
32	chr10:49719800-49721000	Genic enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr10:49719800-49721400	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr10:49719800-49721600	Enhancers	K562	blood
35	chr10:49720000-49720400	Enhancers	Primary B cells from cord blood	blood
36	chr10:49720000-49720400	Enhancers	Fetal Muscle Leg	muscle
37	chr10:49720200-49721400	Weak transcription	NHDF-Ad	bronchial

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