Variant report

Variant	rs11601125
Chromosome Location	chr11:9895925-9895926
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10500709	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11042505	0.80[EUR][1000 genomes]
rs11042521	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11042525	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11042526	0.85[CEU][hapmap]
rs11601212	1.00[ASN][1000 genomes]
rs11601940	1.00[ASN][1000 genomes]
rs11603291	0.85[CEU][hapmap];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12416694	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12416904	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12416993	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12419046	1.00[ASN][1000 genomes]
rs12419471	1.00[ASN][1000 genomes]
rs17269812	1.00[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17355675	0.82[CEU][hapmap]
rs4910075	0.86[CEU][hapmap]
rs55693083	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55782221	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61876873	1.00[ASN][1000 genomes]
rs61876881	1.00[ASN][1000 genomes]
rs61876891	1.00[ASN][1000 genomes]
rs61876894	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][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:38 , 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	chr11:9880600-9896400	Weak transcription	Rectal Smooth Muscle	rectum
7	chr11:9880600-9897200	Weak transcription	Ovary	ovary
8	chr11:9880600-9914800	Weak transcription	Placenta	Placenta
9	chr11:9880800-9902200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr11:9882400-9929600	Weak transcription	Primary T cells from cord blood	blood
11	chr11:9883800-9896200	Weak transcription	HSMMtube	muscle
12	chr11:9884200-9896800	Weak transcription	HSMM	muscle
13	chr11:9884800-9905400	Weak transcription	NHLF	lung
14	chr11:9885200-9897000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr11:9885600-9900400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr11:9885800-9896200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr11:9885800-9905600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr11:9890600-9915200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr11:9891400-9916800	Weak transcription	Primary B cells from cord blood	blood
20	chr11:9891600-9902000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr11:9891800-9916600	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr11:9892200-9914600	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr11:9892400-9914400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr11:9892400-9914600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr11:9892400-9921200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr11:9892600-9898000	Weak transcription	Fetal Stomach	stomach
27	chr11:9894000-9896800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr11:9894000-9910600	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr11:9894200-9897800	Weak transcription	Stomach Smooth Muscle	stomach
30	chr11:9894200-9915200	Weak transcription	Fetal Muscle Trunk	muscle
31	chr11:9894400-9896800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr11:9894400-9897000	Weak transcription	Fetal Lung	lung
33	chr11:9894400-9903200	Weak transcription	A549	lung
34	chr11:9894400-9907400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr11:9894400-9916600	Weak transcription	Primary hematopoietic stem cells	blood
36	chr11:9894400-9978600	Weak transcription	Left Ventricle	heart
37	chr11:9895200-9897600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr11:9895800-9897200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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