Variant report

Variant	rs11075144
Chromosome Location	chr16:12807223-12807224
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs10852355	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4780472	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs8060606	0.85[EUR][1000 genomes]
rs882908	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9972703	0.85[AMR][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	nsv1043096	chr16:12013915-12840769	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
2	nsv1051242	chr16:12482972-12897243	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv542749	chr16:12482972-12897243	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv1035581	chr16:12516946-12863700	ZNF genes & repeats Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	nsv1051607	chr16:12522130-13347676	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv542750	chr16:12522130-13347676	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
7	nsv1053617	chr16:12730958-12871639	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
8	nsv869284	chr16:12735729-13533462	Enhancers ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
9	nsv1052802	chr16:12766360-12964248	Strong transcription ZNF genes & repeats Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	10 gene(s)	inside rSNPs	diseases
10	nsv1043773	chr16:12791629-12810232	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:41 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:12753400-12836000	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr16:12758400-12818200	Weak transcription	Left Ventricle	heart
3	chr16:12758600-12822400	Weak transcription	HSMMtube	muscle
4	chr16:12780000-12812800	Weak transcription	NH-A	brain
5	chr16:12784400-12815200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr16:12797600-12823200	Weak transcription	Primary T cells from cord blood	blood
7	chr16:12798400-12808800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr16:12798400-12825800	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr16:12798600-12822800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr16:12798600-12825800	Weak transcription	Primary hematopoietic stem cells	blood
11	chr16:12798600-12836800	Weak transcription	Placenta	Placenta
12	chr16:12798800-12810800	Weak transcription	Esophagus	oesophagus
13	chr16:12798800-12814000	Weak transcription	Liver	Liver
14	chr16:12798800-12815200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr16:12798800-12816200	Weak transcription	Duodenum Mucosa	Duodenum
16	chr16:12798800-12817000	Weak transcription	Aorta	Aorta
17	chr16:12798800-12817200	Weak transcription	Muscle Satellite Cultured Cells	--
18	chr16:12798800-12817600	Weak transcription	Fetal Stomach	stomach
19	chr16:12798800-12826600	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr16:12799000-12816600	Weak transcription	Fetal Intestine Small	intestine
21	chr16:12799000-12817400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr16:12799000-12820200	Weak transcription	Ovary	ovary
23	chr16:12799000-12823600	Weak transcription	Adipose Nuclei	Adipose
24	chr16:12799200-12821400	Weak transcription	Sigmoid Colon	Sigmoid Colon
25	chr16:12799400-12823000	Weak transcription	Fetal Intestine Large	intestine
26	chr16:12801000-12815000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr16:12801200-12810400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr16:12801400-12809800	Weak transcription	Brain Hippocampus Middle	brain
29	chr16:12801400-12814800	Weak transcription	Brain Substantia Nigra	brain
30	chr16:12801600-12813200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr16:12801800-12810200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr16:12801800-12816400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr16:12803800-12822400	Weak transcription	Spleen	Spleen
34	chr16:12806200-12808000	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr16:12806200-12808200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr16:12806200-12808200	Weak transcription	HSMM	muscle
37	chr16:12806200-12808800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr16:12806200-12808800	Weak transcription	HepG2	liver
39	chr16:12806200-12818000	Weak transcription	Lung	lung
40	chr16:12806400-12808000	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr16:12807200-12809600	Weak transcription	Primary neutrophils fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links