Variant report

Variant	rs11202869
Chromosome Location	chr10:90594274-90594275
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs11202866	1.00[YRI][hapmap]
rs11202871	1.00[AFR][1000 genomes]
rs11202905	0.86[AFR][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	nsv529324	chr10:90198865-90738588	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1042848	chr10:90466032-91318474	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
3	nsv540741	chr10:90466032-91318474	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
4	nsv467415	chr10:90478483-90600865	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
5	nsv551840	chr10:90478483-90600865	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases
6	nsv831942	chr10:90564697-90730352	Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:90574200-90598400	Weak transcription	Gastric	stomach
2	chr10:90578000-90607200	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr10:90578600-90611200	Weak transcription	Esophagus	oesophagus
4	chr10:90588800-90595000	Weak transcription	Hela-S3	cervix
5	chr10:90588800-90595200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr10:90589000-90599000	Weak transcription	Fetal Intestine Small	intestine
7	chr10:90589000-90608800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr10:90589400-90595600	Enhancers	Primary T cells fromperipheralblood	blood
9	chr10:90591200-90595200	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr10:90591400-90596000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
11	chr10:90591800-90595600	Weak transcription	GM12878-XiMat	blood
12	chr10:90592200-90595600	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr10:90592200-90596000	Enhancers	Primary hematopoietic stem cells	blood
14	chr10:90592600-90595600	Weak transcription	Primary B cells from peripheral blood	blood
15	chr10:90592600-90596600	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr10:90592800-90594600	Enhancers	Monocytes-CD14+_RO01746	blood
17	chr10:90593000-90595400	Enhancers	Primary B cells from cord blood	blood
18	chr10:90593800-90594800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
19	chr10:90593800-90595200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
20	chr10:90593800-90600800	Weak transcription	Fetal Thymus	thymus
21	chr10:90594000-90594600	Enhancers	Primary neutrophils fromperipheralblood	blood
22	chr10:90594000-90595000	Weak transcription	Primary T cells from cord blood	blood
23	chr10:90594000-90595000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr10:90594000-90595000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
25	chr10:90594000-90595000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr10:90594000-90595000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr10:90594000-90595200	Weak transcription	Primary T helper cells PMA-I stimulated	--
28	chr10:90594000-90595200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
29	chr10:90594000-90595200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
30	chr10:90594000-90595800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr10:90594200-90594600	Weak transcription	Primary T helper cells fromperipheralblood	blood

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