Variant report

Variant	rs11887799
Chromosome Location	chr2:20091399-20091400
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:19977143..19979803-chr2:20091279..20093604,2	K562	blood:

Extended variants
information (count: 23 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10175236	0.80[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10175486	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10190645	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10203067	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10211513	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12328613	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12467740	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12615824	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1462754	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs16987206	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2278528	0.82[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2304589	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28742930	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6716854	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6717139	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6721754	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6757734	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][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	nsv873712	chr2:19955245-20131079	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
2	nsv873713	chr2:19955245-20144372	Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
3	nsv455819	chr2:19987440-20095690	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
4	nsv581155	chr2:19987440-20095690	Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv873714	chr2:20019616-20113088	Active TSS Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	52 gene(s)	inside rSNPs	diseases
6	nsv873715	chr2:20059323-20144372	ZNF genes & repeats Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription 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	51 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11887799	TTC32	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:20068800-20097200	Weak transcription	Aorta	Aorta
2	chr2:20069000-20098200	Weak transcription	Right Atrium	heart
3	chr2:20069800-20097200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr2:20075400-20097600	Weak transcription	Fetal Kidney	kidney
5	chr2:20076400-20093600	Weak transcription	Primary T helper cells PMA-I stimulated	--
6	chr2:20076400-20097200	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr2:20076600-20097400	Weak transcription	Primary hematopoietic stem cells	blood
8	chr2:20076600-20098200	Weak transcription	Fetal Muscle Leg	muscle
9	chr2:20076800-20095400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
10	chr2:20076800-20095800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
11	chr2:20076800-20097200	Weak transcription	Fetal Thymus	thymus
12	chr2:20076800-20098400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr2:20076800-20099800	Weak transcription	Fetal Intestine Large	intestine
14	chr2:20079200-20098600	Weak transcription	Fetal Intestine Small	intestine
15	chr2:20079400-20097200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr2:20079800-20099000	Weak transcription	Thymus	Thymus
17	chr2:20081800-20095200	Weak transcription	Primary T cells from cord blood	blood
18	chr2:20083000-20095400	Weak transcription	Fetal Brain Female	brain
19	chr2:20086400-20097400	Weak transcription	Stomach Smooth Muscle	stomach
20	chr2:20086600-20091800	Weak transcription	Spleen	Spleen
21	chr2:20086600-20095400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chr2:20086600-20097400	Weak transcription	HMEC	breast
23	chr2:20086600-20099800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr2:20087200-20097400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr2:20087400-20097800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr2:20088000-20099600	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr2:20088400-20098200	Weak transcription	Fetal Muscle Trunk	muscle
28	chr2:20088800-20091800	Weak transcription	Fetal Brain Male	brain
29	chr2:20089000-20095200	Weak transcription	Dnd41	blood
30	chr2:20089000-20097200	Weak transcription	Adipose Nuclei	Adipose
31	chr2:20089200-20097200	Weak transcription	Brain Cingulate Gyrus	brain
32	chr2:20089200-20097400	Weak transcription	Brain Anterior Caudate	brain
33	chr2:20089400-20097000	Weak transcription	Brain Hippocampus Middle	brain
34	chr2:20089400-20097200	Weak transcription	Skeletal Muscle Male	skeletal muscle
35	chr2:20089600-20094200	Weak transcription	K562	blood
36	chr2:20089600-20097200	Weak transcription	Skeletal Muscle Female	skeletal muscle
37	chr2:20089600-20097400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr2:20089600-20097400	Weak transcription	NHEK	skin
39	chr2:20089600-20097600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr2:20089600-20098200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr2:20089800-20091800	Enhancers	GM12878-XiMat	blood
42	chr2:20089800-20092800	Weak transcription	NHDF-Ad	bronchial
43	chr2:20089800-20095400	Weak transcription	Brain Angular Gyrus	brain
44	chr2:20089800-20095600	Weak transcription	Osteobl	bone
45	chr2:20089800-20099800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr2:20090000-20092000	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr2:20090200-20092400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr2:20090200-20093400	Weak transcription	Brain Germinal Matrix	brain
49	chr2:20090200-20095000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr2:20090200-20097200	Weak transcription	Fetal Heart	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links