Variant report

Variant	rs11224429
Chromosome Location	chr11:100619793-100619794
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs11224332	1.00[AMR][1000 genomes]
rs11224341	1.00[AMR][1000 genomes]
rs11224343	1.00[AMR][1000 genomes]
rs11224346	1.00[AMR][1000 genomes]
rs11224385	1.00[AMR][1000 genomes]
rs11224404	1.00[AFR][1000 genomes]
rs11224418	0.90[AFR][1000 genomes]
rs11224428	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11224438	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11224465	1.00[AMR][1000 genomes]
rs11224525	1.00[AMR][1000 genomes]
rs12274762	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12275133	1.00[AMR][1000 genomes]
rs12277269	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12278938	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12279270	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12279931	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12281021	1.00[AMR][1000 genomes]
rs12281097	1.00[AMR][1000 genomes]
rs12284980	1.00[AFR][1000 genomes]
rs12286434	1.00[AMR][1000 genomes]
rs12286625	1.00[AMR][1000 genomes]
rs12287226	1.00[AMR][1000 genomes]
rs12295600	1.00[AMR][1000 genomes]
rs13377291	0.91[YRI][hapmap];0.93[AFR][1000 genomes]
rs56805393	1.00[AMR][1000 genomes]
rs61104011	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73565305	1.00[AMR][1000 genomes]
rs73565310	1.00[AMR][1000 genomes]
rs73565331	1.00[AMR][1000 genomes]
rs73565337	1.00[AMR][1000 genomes]
rs73565348	1.00[AMR][1000 genomes]
rs73567534	1.00[AMR][1000 genomes]
rs73571424	1.00[AMR][1000 genomes]
rs73573332	1.00[AMR][1000 genomes]
rs73573395	0.97[AFR][1000 genomes]
rs73575539	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73580523	1.00[AMR][1000 genomes]
rs7933646	1.00[YRI][hapmap];1.00[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1053430	chr11:99888390-100629136	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1042067	chr11:99889697-100629136	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1037689	chr11:99895378-100624599	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1040942	chr11:99895378-100629136	Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv1045190	chr11:99913193-100627395	Active TSS Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
6	nsv541153	chr11:99913193-100627395	Flanking Active TSS Enhancers Genic enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv529454	chr11:99913394-100627255	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv520995	chr11:100163957-100681211	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	nsv530643	chr11:100196082-100713156	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv898327	chr11:100569021-100631075	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:100598800-100620000	Weak transcription	Gastric	stomach
2	chr11:100599800-100619800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr11:100611400-100622800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr11:100612200-100619800	Weak transcription	Fetal Muscle Trunk	muscle
5	chr11:100612200-100620000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr11:100612400-100619800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr11:100612400-100619800	Weak transcription	H9 Cell Line	embryonic stem cell
8	chr11:100612400-100619800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr11:100612400-100620000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr11:100612400-100620000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr11:100612400-100620000	Weak transcription	Fetal Lung	lung
12	chr11:100612400-100620400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:100612400-100630800	Weak transcription	Right Atrium	heart
14	chr11:100612600-100619800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr11:100613000-100619800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr11:100613000-100620000	Weak transcription	Liver	Liver
17	chr11:100613000-100620000	Weak transcription	Duodenum Mucosa	Duodenum
18	chr11:100613000-100631600	Weak transcription	Ovary	ovary
19	chr11:100613200-100628400	Weak transcription	Fetal Kidney	kidney
20	chr11:100614200-100623800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chr11:100615800-100620200	Weak transcription	Esophagus	oesophagus
22	chr11:100617200-100620000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr11:100617200-100623200	Weak transcription	Right Ventricle	heart
24	chr11:100617600-100619800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr11:100617800-100619800	Weak transcription	Fetal Stomach	stomach
26	chr11:100618800-100620200	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr11:100618800-100620200	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr11:100619200-100623800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr11:100619400-100619800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr11:100619400-100620000	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr11:100619400-100620600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr11:100619400-100622400	ZNF genes & repeats	Fetal Muscle Leg	muscle
33	chr11:100619600-100620000	Weak transcription	H1 Cell Line	embryonic stem cell
34	chr11:100619600-100620600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
35	chr11:100619600-100621200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
36	chr11:100619600-100621200	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
37	chr11:100619600-100621400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
38	chr11:100619600-100621400	ZNF genes & repeats	Fetal Intestine Small	intestine
39	chr11:100619600-100621600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr11:100619600-100621600	ZNF genes & repeats	Fetal Adrenal Gland	Adrenal Gland
41	chr11:100619600-100621600	ZNF genes & repeats	Placenta	Placenta
42	chr11:100619600-100622600	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain

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