Variant report

Variant	rs11042522
Chromosome Location	chr11:9893276-9893277
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:24)

rs_ID	r²[population]
rs11042504	1.00[EUR][1000 genomes]
rs11042508	1.00[EUR][1000 genomes]
rs11042513	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11042520	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11042537	1.00[EUR][1000 genomes]
rs11042538	1.00[EUR][1000 genomes]
rs12270313	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12285985	1.00[EUR][1000 genomes]
rs12290340	1.00[EUR][1000 genomes]
rs12291871	1.00[EUR][1000 genomes]
rs12294282	1.00[EUR][1000 genomes]
rs12295264	1.00[EUR][1000 genomes]
rs13377352	1.00[EUR][1000 genomes]
rs360121	1.00[EUR][1000 genomes]
rs57108291	1.00[EUR][1000 genomes]
rs57125659	1.00[EUR][1000 genomes]
rs57460369	1.00[EUR][1000 genomes]
rs57669768	1.00[EUR][1000 genomes]
rs60528623	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7116821	1.00[EUR][1000 genomes]
rs7358421	1.00[EUR][1000 genomes]
rs7358470	1.00[EUR][1000 genomes]
rs9630162	1.00[EUR][1000 genomes]
rs9971601	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933855	chr11:9645441-10130519	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	esv3384280	chr11:9766350-9911228	Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
3	esv2762895	chr11:9849511-9954549	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9877800-9897000	Weak transcription	Psoas Muscle	Psoas
2	chr11:9878200-9897000	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr11:9878400-9916200	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr11:9878800-9952200	Weak transcription	Aorta	Aorta
5	chr11:9880200-9913200	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr11:9880600-9893800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr11:9880600-9896400	Weak transcription	Rectal Smooth Muscle	rectum
8	chr11:9880600-9897200	Weak transcription	Ovary	ovary
9	chr11:9880600-9914800	Weak transcription	Placenta	Placenta
10	chr11:9880800-9902200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr11:9881800-9893600	Weak transcription	Adipose Nuclei	Adipose
12	chr11:9881800-9893600	Weak transcription	Fetal Lung	lung
13	chr11:9882400-9929600	Weak transcription	Primary T cells from cord blood	blood
14	chr11:9883800-9896200	Weak transcription	HSMMtube	muscle
15	chr11:9884200-9896800	Weak transcription	HSMM	muscle
16	chr11:9884800-9905400	Weak transcription	NHLF	lung
17	chr11:9885000-9895800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr11:9885200-9897000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr11:9885600-9900400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr11:9885800-9896200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr11:9885800-9905600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr11:9886200-9893600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
23	chr11:9887400-9894200	Weak transcription	Left Ventricle	heart
24	chr11:9890600-9893600	Weak transcription	A549	lung
25	chr11:9890600-9915200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr11:9891400-9916800	Weak transcription	Primary B cells from cord blood	blood
27	chr11:9891600-9893800	Weak transcription	Pancreas	Pancrea
28	chr11:9891600-9902000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr11:9891800-9916600	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chr11:9892200-9893600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr11:9892200-9914600	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr11:9892400-9914400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr11:9892400-9914600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr11:9892400-9921200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr11:9892600-9898000	Weak transcription	Fetal Stomach	stomach
36	chr11:9893200-9894400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
37	chr11:9893200-9895200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast

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