Variant report

Variant	rs11785871
Chromosome Location	chr8:120925199-120925200
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 106 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:96)

rs_ID	r²[population]
rs10093230	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs10094455	0.86[AFR][1000 genomes]
rs10094458	0.86[AFR][1000 genomes]
rs10094587	0.86[AFR][1000 genomes]
rs10098306	0.90[AFR][1000 genomes]
rs10103058	0.86[AFR][1000 genomes]
rs10103660	0.85[AFR][1000 genomes]
rs10107251	0.81[AFR][1000 genomes]
rs10107579	0.93[AFR][1000 genomes]
rs10110216	0.83[AFR][1000 genomes]
rs10110223	0.83[AFR][1000 genomes]
rs10216503	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs10217083	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs10808505	0.93[AFR][1000 genomes]
rs10955940	0.89[AFR][1000 genomes]
rs10955941	0.85[AFR][1000 genomes]
rs11777705	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs12545854	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12545863	0.93[AFR][1000 genomes];0.85[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs12677814	0.81[AFR][1000 genomes]
rs12681402	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs12681623	0.89[AFR][1000 genomes]
rs13249122	0.91[AFR][1000 genomes]
rs13250594	0.92[AFR][1000 genomes]
rs13253140	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs13257252	0.90[AFR][1000 genomes]
rs13257316	0.86[AFR][1000 genomes]
rs13258592	0.88[AFR][1000 genomes]
rs13259990	0.91[AFR][1000 genomes]
rs13260088	0.86[AFR][1000 genomes]
rs13260933	0.91[AFR][1000 genomes]
rs13261304	0.91[AFR][1000 genomes]
rs13265367	0.85[AFR][1000 genomes]
rs13265546	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs13267896	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs13269024	0.83[AFR][1000 genomes]
rs13275524	0.97[AFR][1000 genomes];0.87[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs13277947	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs13277992	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs13279398	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs13281299	0.91[AFR][1000 genomes]
rs1464276	0.93[AFR][1000 genomes]
rs1607624	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2037346	0.90[AFR][1000 genomes]
rs35272074	0.88[AFR][1000 genomes]
rs4073560	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs4871012	0.91[AFR][1000 genomes]
rs4871013	0.91[AFR][1000 genomes]
rs4871772	0.91[AFR][1000 genomes]
rs4871773	0.88[AFR][1000 genomes]
rs4871787	0.93[AFR][1000 genomes]
rs55892034	0.87[AFR][1000 genomes]
rs56864850	0.86[AFR][1000 genomes]
rs6469861	0.91[AFR][1000 genomes]
rs6469862	0.91[AFR][1000 genomes]
rs6469863	0.91[AFR][1000 genomes]
rs6469864	0.91[AFR][1000 genomes]
rs6469865	0.91[AFR][1000 genomes]
rs6469867	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs6469868	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs6469870	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs6469871	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs6469872	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs6469878	0.93[AFR][1000 genomes]
rs6987580	0.90[AFR][1000 genomes]
rs6988011	0.91[AFR][1000 genomes]
rs6989741	0.90[AFR][1000 genomes]
rs6993375	0.91[AFR][1000 genomes]
rs6993797	0.91[AFR][1000 genomes]
rs6995139	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7002839	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7006905	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7015470	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7387264	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7387694	0.86[AFR][1000 genomes]
rs7388508	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7459671	0.91[AFR][1000 genomes]
rs7461290	0.89[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7462250	0.91[AFR][1000 genomes]
rs7462302	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7465181	0.91[AFR][1000 genomes]
rs7465609	0.83[AFR][1000 genomes]
rs7465612	0.84[AFR][1000 genomes]
rs7814294	0.93[AFR][1000 genomes]
rs7814520	0.89[AFR][1000 genomes]
rs7818471	0.91[AFR][1000 genomes]
rs7824545	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7829901	0.94[AFR][1000 genomes]
rs7832923	0.88[AFR][1000 genomes]
rs939241	0.95[AFR][1000 genomes];0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs939242	0.95[AFR][1000 genomes];0.83[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs9649947	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs9720591	0.91[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs9721029	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs9721042	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs9987332	0.92[AFR][1000 genomes];0.81[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	nsv949368	chr8:120568034-121019872	Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv1021071	chr8:120589963-120968317	Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
3	nsv891418	chr8:120600965-121301474	Active TSS Flanking Active TSS Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
4	nsv465789	chr8:120636850-120994394	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
5	nsv612111	chr8:120636850-120994394	Flanking Active TSS Weak transcription Genic enhancers Strong transcription Enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
6	nsv427826	chr8:120642181-120953395	Weak transcription Strong transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
7	nsv1027974	chr8:120885478-121079658	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv539739	chr8:120885478-121079658	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv972194	chr8:120898451-120965081	Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv1018953	chr8:120910380-120954832	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:120908800-120926000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr8:120908800-120927600	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr8:120909000-120927200	Weak transcription	Fetal Intestine Large	intestine
4	chr8:120909000-120927600	Weak transcription	Duodenum Mucosa	Duodenum
5	chr8:120910800-120927600	Weak transcription	Small Intestine	intestine
6	chr8:120916200-120927200	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr8:120917800-120927600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr8:120920600-120928800	Weak transcription	Pancreas	Pancrea
9	chr8:120920800-120932800	Weak transcription	Fetal Muscle Trunk	muscle
10	chr8:120921400-120925600	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr8:120921600-120927800	Weak transcription	Hela-S3	cervix
12	chr8:120921800-120931800	Weak transcription	HSMMtube	muscle
13	chr8:120922000-120931200	Enhancers	Psoas Muscle	Psoas
14	chr8:120923000-120935400	Enhancers	Stomach Mucosa	stomach
15	chr8:120923200-120925600	Enhancers	Liver	Liver
16	chr8:120923200-120926200	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr8:120923200-120926200	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr8:120923400-120926000	Weak transcription	Gastric	stomach
19	chr8:120923400-120927400	Enhancers	Left Ventricle	heart
20	chr8:120923600-120925200	Weak transcription	Ovary	ovary
21	chr8:120923600-120926000	Enhancers	Stomach Smooth Muscle	stomach
22	chr8:120923600-120932800	Weak transcription	Lung	lung
23	chr8:120923800-120926200	Enhancers	Brain Angular Gyrus	brain
24	chr8:120923800-120926200	Enhancers	Brain Cingulate Gyrus	brain
25	chr8:120923800-120926200	Enhancers	Brain Substantia Nigra	brain
26	chr8:120923800-120926200	Enhancers	Colon Smooth Muscle	Colon
27	chr8:120924000-120926200	Enhancers	Rectal Smooth Muscle	rectum
28	chr8:120924000-120927400	Weak transcription	Fetal Intestine Small	intestine
29	chr8:120924000-120931800	Weak transcription	Right Atrium	heart
30	chr8:120924400-120925600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr8:120924400-120925800	Enhancers	Brain Anterior Caudate	brain
32	chr8:120924400-120926000	Enhancers	Brain Hippocampus Middle	brain
33	chr8:120924400-120926000	Enhancers	HepG2	liver
34	chr8:120924400-120928000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr8:120924600-120925200	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
36	chr8:120924600-120926400	Enhancers	Primary hematopoietic stem cells	blood
37	chr8:120924600-120928200	Enhancers	Fetal Muscle Leg	muscle
38	chr8:120924800-120925200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
39	chr8:120924800-120926000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr8:120924800-120927000	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr8:120924800-120927400	Weak transcription	Adipose Nuclei	Adipose
42	chr8:120925000-120925400	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr8:120925000-120927000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr8:120925000-120931800	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr8:120925000-120932400	Weak transcription	Right Ventricle	heart
46	chr8:120925000-120932600	Weak transcription	Esophagus	oesophagus

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