Variant report

Variant	rs557198
Chromosome Location	chr11:107261619-107261620
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs2508682	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs473551	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs524448	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs542307	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs555032	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs591528	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs601236	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs607042	1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs638504	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs665203	1.00[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs673140	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7926690	1.00[AMR][1000 genomes]
rs7933722	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv898364	chr11:106944975-107285636	Strong transcription Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv898365	chr11:106944975-107430300	ZNF genes & repeats Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv898366	chr11:106944975-107433835	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv898367	chr11:106944975-107443420	Strong transcription Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv898369	chr11:106958304-107443420	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv898370	chr11:107027991-107430300	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv898372	chr11:107049968-107433835	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv1038368	chr11:107116577-107664181	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
9	nsv541163	chr11:107116577-107664181	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
10	nsv898373	chr11:107124903-107433835	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
11	nsv832261	chr11:107145901-107321562	Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv898374	chr11:107156880-107263130	Strong transcription Weak transcription ZNF genes & repeats Active TSS Enhancers Genic enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
13	esv2756363	chr11:107189790-107376790	ZNF genes & repeats Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
14	nsv556376	chr11:107250851-107486598	Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:107195000-107299200	Weak transcription	Colon Smooth Muscle	Colon
2	chr11:107240600-107261800	Weak transcription	Fetal Lung	lung
3	chr11:107241600-107327800	Weak transcription	HSMMtube	muscle
4	chr11:107243800-107267600	Weak transcription	Gastric	stomach
5	chr11:107249000-107267600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr11:107250200-107261800	Weak transcription	Psoas Muscle	Psoas
7	chr11:107252400-107267800	Weak transcription	Right Ventricle	heart
8	chr11:107252600-107267800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr11:107252600-107281200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr11:107252600-107323800	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr11:107255000-107327600	Weak transcription	Fetal Heart	heart
12	chr11:107256600-107263000	Weak transcription	Brain Angular Gyrus	brain
13	chr11:107256600-107264000	Weak transcription	NH-A	brain
14	chr11:107256600-107298000	Weak transcription	Brain Substantia Nigra	brain
15	chr11:107256600-107327600	Weak transcription	NHDF-Ad	bronchial
16	chr11:107256800-107262400	Weak transcription	Osteobl	bone
17	chr11:107256800-107268200	Weak transcription	A549	lung
18	chr11:107256800-107274800	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr11:107257000-107262000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr11:107257200-107263000	Weak transcription	Skeletal Muscle Male	skeletal muscle
21	chr11:107257200-107269600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr11:107257200-107275000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr11:107257400-107268000	Weak transcription	HepG2	liver
24	chr11:107257600-107262200	Weak transcription	NHEK	skin
25	chr11:107257600-107267600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr11:107257600-107267800	Weak transcription	HMEC	breast
27	chr11:107257800-107263200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr11:107257800-107263600	Strong transcription	Primary B cells from peripheral blood	blood
29	chr11:107257800-107268000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr11:107258200-107263600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
31	chr11:107258200-107265600	Strong transcription	Primary T helper cells fromperipheralblood	blood
32	chr11:107258400-107262200	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr11:107258400-107263200	Strong transcription	Sigmoid Colon	Sigmoid Colon
34	chr11:107258400-107263400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr11:107258400-107263600	Strong transcription	Primary T cells fromperipheralblood	blood
36	chr11:107258400-107263800	Strong transcription	Adipose Nuclei	Adipose
37	chr11:107258400-107263800	Strong transcription	Liver	Liver
38	chr11:107258400-107265800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr11:107258600-107281600	Weak transcription	Fetal Brain Male	brain
40	chr11:107258800-107267600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr11:107258800-107277000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr11:107258800-107291800	Weak transcription	Colonic Mucosa	Colon
43	chr11:107258800-107324200	Weak transcription	Small Intestine	intestine
44	chr11:107259000-107264200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
45	chr11:107259000-107280400	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr11:107259200-107299600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr11:107259400-107263800	Strong transcription	Primary T helper cells PMA-I stimulated	--
48	chr11:107259400-107267400	Weak transcription	Fetal Intestine Small	intestine
49	chr11:107259400-107267400	Weak transcription	Fetal Stomach	stomach
50	chr11:107259400-107268000	Weak transcription	K562	blood

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