Variant report

Variant	rs11597133
Chromosome Location	chr10:5631773-5631774
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:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr10:5625670..5627432-chr10:5629113..5631880,2	K562	blood:
2	chr10:5631393..5632960-chr10:5641583..5643544,2	MCF-7	breast:
3	chr10:5631327..5633176-chr10:5653154..5654967,2	MCF-7	breast:
4	chr10:5616972..5619862-chr10:5631106..5633140,2	K562	blood:
5	chr10:5623673..5635207-chr10:5656121..5669428,27	MCF-7	breast:
6	chr10:5558375..5560423-chr10:5631236..5633723,2	MCF-7	breast:
7	chr10:5630058..5631900-chr10:5703072..5705315,2	MCF-7	breast:
8	chr10:5533762..5535661-chr10:5631397..5633599,2	MCF-7	breast:
9	chr10:5624590..5636573-chr10:5652742..5661113,15	MCF-7	breast:
10	chr10:5584975..5598212-chr10:5621607..5634806,86	MCF-7	breast:
11	chr10:5486586..5497147-chr10:5622068..5633259,25	MCF-7	breast:
12	chr10:5629660..5633537-chr10:5634085..5636643,3	K562	blood:
13	chr10:5528878..5533686-chr10:5631469..5634620,4	MCF-7	breast:
14	chr10:5487228..5489563-chr10:5631145..5633414,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000231483	Chromatin interaction
ENSG00000173848	Chromatin interaction
ENSG00000228685	Chromatin interaction
ENSG00000228951	Chromatin interaction

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10904528	0.95[EUR][1000 genomes]
rs11254973	1.00[MEX][hapmap]
rs11256654	1.00[MEX][hapmap]
rs11597288	0.81[CEU][hapmap];0.83[GIH][hapmap];0.84[MKK][hapmap];0.85[TSI][hapmap]
rs11597591	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11599233	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11599647	0.82[AMR][1000 genomes]
rs12359886	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1575	1.00[MEX][hapmap]
rs17137747	1.00[MEX][hapmap]
rs57446863	0.88[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv534685	chr10:4914018-5853324	Weak transcription Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Genic enhancers 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	68 gene(s)	inside rSNPs	diseases
2	nsv932104	chr10:5203626-5641023	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
3	nsv549886	chr10:5205437-5632060	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
4	nsv1054865	chr10:5225305-5638119	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	45 gene(s)	inside rSNPs	diseases
5	nsv831774	chr10:5463556-5657421	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
6	nsv894798	chr10:5503610-5670275	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
7	nsv523491	chr10:5542109-5720067	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
8	esv2757364	chr10:5557024-5720512	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
9	esv2759729	chr10:5557024-5804780	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:5625000-5631800	Weak transcription	K562	blood
2	chr10:5625000-5632400	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr10:5625200-5634400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr10:5626000-5634600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr10:5626200-5636200	Weak transcription	Primary B cells from cord blood	blood
6	chr10:5626400-5633600	Enhancers	Fetal Thymus	thymus
7	chr10:5626600-5631800	Enhancers	Fetal Heart	heart
8	chr10:5627400-5639400	Enhancers	Fetal Muscle Leg	muscle
9	chr10:5628200-5631800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr10:5628200-5631800	Weak transcription	HSMM	muscle
11	chr10:5628400-5631800	Weak transcription	NHDF-Ad	bronchial
12	chr10:5628600-5633200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr10:5628600-5634400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr10:5628600-5636200	Weak transcription	Fetal Kidney	kidney
15	chr10:5628800-5632000	Enhancers	Adipose Nuclei	Adipose
16	chr10:5628800-5633400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr10:5629000-5635000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr10:5629400-5631800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr10:5629400-5634600	Enhancers	Placenta	Placenta
20	chr10:5629800-5631800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr10:5629800-5632000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr10:5629800-5632000	Enhancers	Skeletal Muscle Female	skeletal muscle
23	chr10:5629800-5632200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr10:5629800-5632800	Weak transcription	Fetal Intestine Small	intestine
25	chr10:5629800-5633000	Weak transcription	Fetal Intestine Large	intestine
26	chr10:5629800-5634200	Weak transcription	Pancreas	Pancrea
27	chr10:5630000-5631800	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr10:5630000-5631800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr10:5630000-5631800	Weak transcription	HUVEC	blood vessel
30	chr10:5630000-5634200	Weak transcription	Right Atrium	heart
31	chr10:5630000-5636200	Weak transcription	Fetal Lung	lung
32	chr10:5630400-5632600	Enhancers	Hela-S3	cervix
33	chr10:5630400-5633200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr10:5630400-5633800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr10:5630600-5631800	Weak transcription	Stomach Smooth Muscle	stomach
36	chr10:5630600-5632000	Enhancers	HMEC	breast
37	chr10:5630800-5632400	Enhancers	NHEK	skin
38	chr10:5630800-5633800	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr10:5630800-5636400	Weak transcription	Left Ventricle	heart
40	chr10:5631000-5632800	Enhancers	A549	lung
41	chr10:5631000-5633400	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr10:5631000-5634800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr10:5631200-5632000	Enhancers	Esophagus	oesophagus
44	chr10:5631200-5632400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr10:5631200-5632400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr10:5631200-5632400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr10:5631200-5632400	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr10:5631200-5632600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr10:5631200-5633200	Enhancers	HUES64 Cell Line	embryonic stem cell
50	chr10:5631200-5636200	Weak transcription	Lung	lung

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