Variant report

Variant	rs2032025
Chromosome Location	chr10:22972673-22972674
allele	A/C
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:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:22921738..22922640-chr10:22971944..22972725,4	MCF-7	breast:
2	chr10:22912213..22914953-chr10:22971125..22973700,2	MCF-7	breast:
3	chr10:22954085..22955881-chr10:22969545..22973376,3	K562	blood:
4	chr10:22972373..22974105-chr10:23339764..23342277,2	K562	blood:
5	chr10:22972317..22974563-chr10:23000781..23004617,5	K562	blood:
6	chr10:22970742..22972969-chr10:23383375..23385316,2	MCF-7	breast:
7	chr10:22970833..22976396-chr10:22998694..23005048,8	K562	blood:
8	chr10:22947999..22952068-chr10:22969856..22973732,4	MCF-7	breast:
9	chr10:22969549..22974031-chr10:22999027..23004713,8	MCF-7	breast:
10	chr10:22972222..22972916-chr10:23370100..23370969,2	MCF-7	breast:
11	chr10:22969827..22972889-chr10:22996962..23000466,4	K562	blood:
12	chr10:22918230..22923281-chr10:22970702..22974726,7	K562	blood:
13	chr10:22915388..22917585-chr10:22971336..22974325,2	MCF-7	breast:
14	chr10:22871878..22873453-chr10:22971882..22972856,4	MCF-7	breast:
15	chr10:22970725..22973853-chr10:23334957..23339214,5	K562	blood:
16	chr10:22907517..22909327-chr10:22970416..22973310,2	MCF-7	breast:
17	chr10:22968680..22970834-chr10:22971018..22973569,2	K562	blood:
18	chr10:22920959..22922895-chr10:22971419..22973698,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000150867	Chromatin interaction
ENSG00000148450	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs16922601	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs16922612	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs2032026	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2032027	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58854363	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs7078735	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs74121869	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs74121888	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs74121889	0.86[EUR][1000 genomes]
rs74121890	0.94[AMR][1000 genomes];0.86[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	esv1830947	chr10:22881196-23004381	Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv831809	chr10:22918101-23069676	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:109 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:22958600-22975400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
2	chr10:22959200-22980000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr10:22961800-22979600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr10:22962600-22974600	Weak transcription	Fetal Muscle Trunk	muscle
5	chr10:22964000-22973600	Weak transcription	Psoas Muscle	Psoas
6	chr10:22968200-22973000	Enhancers	HUVEC	blood vessel
7	chr10:22968400-22973600	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr10:22968400-22976000	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr10:22969400-22976600	Enhancers	Brain Cingulate Gyrus	brain
10	chr10:22969600-22973200	Enhancers	NH-A	brain
11	chr10:22969800-22974000	Enhancers	Brain Angular Gyrus	brain
12	chr10:22969800-22975200	Enhancers	Primary hematopoietic stem cells	blood
13	chr10:22969800-22975200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr10:22969800-22975600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr10:22969800-22976000	Enhancers	Brain Anterior Caudate	brain
16	chr10:22970000-22973000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr10:22970000-22973200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr10:22970000-22974200	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr10:22970000-22974600	Enhancers	Stomach Mucosa	stomach
20	chr10:22970000-22975200	Enhancers	HSMM	muscle
21	chr10:22970200-22972800	Flanking Active TSS	Primary T cells from cord blood	blood
22	chr10:22970200-22972800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr10:22970200-22973000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr10:22970200-22973000	Enhancers	NHDF-Ad	bronchial
25	chr10:22970200-22973200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr10:22970200-22973200	Enhancers	Osteobl	bone
27	chr10:22970200-22973400	Enhancers	Liver	Liver
28	chr10:22970200-22973800	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr10:22970200-22974000	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr10:22970200-22974000	Enhancers	Muscle Satellite Cultured Cells	--
31	chr10:22970200-22974800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr10:22970200-22975000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr10:22970400-22972800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr10:22970400-22974000	Enhancers	NHLF	lung
35	chr10:22970400-22977800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr10:22970600-22989000	Weak transcription	Esophagus	oesophagus
37	chr10:22970800-22972800	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr10:22970800-22973000	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr10:22970800-22973000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
40	chr10:22970800-22973000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr10:22970800-22973800	Enhancers	Fetal Heart	heart
42	chr10:22971000-22972800	Enhancers	Hela-S3	cervix
43	chr10:22971000-22973200	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr10:22971000-22973200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
45	chr10:22971000-22973200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
46	chr10:22971000-22973200	Flanking Active TSS	A549	lung
47	chr10:22971000-22974000	Flanking Active TSS	GM12878-XiMat	blood
48	chr10:22971000-22974400	Enhancers	HSMMtube	muscle
49	chr10:22971000-22974600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
50	chr10:22971200-22973000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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