Variant report

Variant	rs11593866
Chromosome Location	chr10:112771339-112771340
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr10:112747542..112749737-chr10:112770146..112772624,2	K562	blood:
2	chr10:112768505..112770915-chr10:112771228..112772833,2	K562	blood:
3	chr10:112770762..112772712-chr10:112775005..112777166,2	K562	blood:

Variant related genes	Relation type
ENSG00000221214	Chromatin interaction

Extended variants
information (count: 61 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:51)

rs_ID	r²[population]
rs11195368	0.84[EUR][1000 genomes]
rs11195373	0.84[EUR][1000 genomes]
rs11195376	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11195409	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11592186	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11592376	0.84[EUR][1000 genomes]
rs11593462	0.89[EUR][1000 genomes]
rs11593479	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11593592	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11597120	0.89[EUR][1000 genomes]
rs11597460	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11597928	0.82[EUR][1000 genomes]
rs11812232	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11812855	0.89[EUR][1000 genomes]
rs11813262	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11813593	0.84[EUR][1000 genomes]
rs11814418	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11814686	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11816033	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs11816247	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11816269	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11816396	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11818060	0.89[EUR][1000 genomes]
rs11818747	0.89[EUR][1000 genomes]
rs11818761	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11818771	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11818869	0.84[EUR][1000 genomes]
rs1322997	0.82[EUR][1000 genomes]
rs1327556	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1535559	0.84[EUR][1000 genomes]
rs17128189	0.89[EUR][1000 genomes]
rs1885796	0.84[EUR][1000 genomes]
rs34104444	0.89[EUR][1000 genomes]
rs55647014	0.84[EUR][1000 genomes]
rs55858908	0.84[EUR][1000 genomes]
rs56237211	0.84[EUR][1000 genomes]
rs60633872	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs60681723	0.81[EUR][1000 genomes]
rs61469604	0.89[EUR][1000 genomes]
rs6585018	0.82[EUR][1000 genomes]
rs6585020	0.84[EUR][1000 genomes]
rs7081726	0.89[EUR][1000 genomes]
rs74156305	0.87[EUR][1000 genomes]
rs74156307	0.82[EUR][1000 genomes]
rs74156308	0.84[EUR][1000 genomes]
rs74156309	0.89[EUR][1000 genomes]
rs74156310	0.89[EUR][1000 genomes]
rs74156311	0.89[EUR][1000 genomes]
rs74156320	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs74156323	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7923004	0.89[EUR][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	nsv1035602	chr10:112636053-112781413	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1051327	chr10:112650316-112772917	ZNF genes & repeats Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv540774	chr10:112650316-112772917	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS 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	27 gene(s)	inside rSNPs	diseases
4	nsv831985	chr10:112652089-112803103	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers ZNF genes & repeats 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	28 gene(s)	inside rSNPs	diseases
5	nsv1048809	chr10:112683822-112781413	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
6	nsv1042020	chr10:112686323-112795159	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
7	nsv1048444	chr10:112724159-112795159	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
8	nsv1036202	chr10:112726834-112781413	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
9	nsv1051595	chr10:112730022-112789048	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
10	nsv1047412	chr10:112747749-112781413	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:118 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:112705200-112789800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr10:112707200-112784200	Weak transcription	Left Ventricle	heart
3	chr10:112723200-112783000	Weak transcription	Small Intestine	intestine
4	chr10:112732600-112789400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr10:112732800-112782800	Weak transcription	Esophagus	oesophagus
6	chr10:112732800-112789400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr10:112738000-112782800	Weak transcription	Rectal Smooth Muscle	rectum
8	chr10:112738200-112784600	Weak transcription	Ovary	ovary
9	chr10:112738400-112779400	Weak transcription	HepG2	liver
10	chr10:112739200-112774400	Weak transcription	Gastric	stomach
11	chr10:112740400-112791800	Weak transcription	Colon Smooth Muscle	Colon
12	chr10:112744800-112778800	Weak transcription	Hela-S3	cervix
13	chr10:112745600-112777600	Weak transcription	Pancreas	Pancrea
14	chr10:112746000-112783400	Weak transcription	Colonic Mucosa	Colon
15	chr10:112746800-112782800	Weak transcription	Psoas Muscle	Psoas
16	chr10:112747400-112779800	Weak transcription	Fetal Brain Male	brain
17	chr10:112747600-112785200	Weak transcription	Fetal Brain Female	brain
18	chr10:112749200-112789400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr10:112750400-112785000	Weak transcription	A549	lung
20	chr10:112751800-112772600	Weak transcription	K562	blood
21	chr10:112753000-112772600	Weak transcription	Brain Angular Gyrus	brain
22	chr10:112753200-112779200	Weak transcription	Brain Hippocampus Middle	brain
23	chr10:112753200-112779600	Weak transcription	Brain Anterior Caudate	brain
24	chr10:112753200-112782600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr10:112753200-112784200	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr10:112753400-112776200	Weak transcription	Lung	lung
27	chr10:112753400-112789600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr10:112753800-112775000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
29	chr10:112754000-112782000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr10:112754000-112784800	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr10:112754400-112782600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr10:112754800-112773000	Strong transcription	Monocytes-CD14+_RO01746	blood
33	chr10:112755000-112773000	Strong transcription	Primary monocytes fromperipheralblood	blood
34	chr10:112756800-112777800	Weak transcription	Sigmoid Colon	Sigmoid Colon
35	chr10:112757200-112782400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr10:112757400-112773000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr10:112757400-112775400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr10:112758200-112775000	Strong transcription	GM12878-XiMat	blood
39	chr10:112758200-112783600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr10:112758600-112773200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr10:112759600-112773000	Strong transcription	Primary T helper cells fromperipheralblood	blood
42	chr10:112759800-112773600	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr10:112760200-112773200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr10:112760200-112774600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr10:112760400-112773400	Strong transcription	Primary B cells from peripheral blood	blood
46	chr10:112761000-112774000	Strong transcription	Primary neutrophils fromperipheralblood	blood
47	chr10:112761600-112781400	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr10:112761600-112782800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr10:112761800-112778200	Weak transcription	Fetal Intestine Small	intestine
50	chr10:112761800-112784200	Weak transcription	Spleen	Spleen

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