Variant report

Variant	rs1441738
Chromosome Location	chr10:90677586-90677587
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs10887867	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10887870	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11202890	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11202906	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11202907	0.87[EUR][1000 genomes]
rs11595119	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12248284	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12254084	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12256739	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17114152	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs17114161	0.97[ASN][1000 genomes]
rs17114327	0.90[EUR][1000 genomes]
rs1977388	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2119685	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4431933	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7078383	0.90[EUR][1000 genomes]
rs7085698	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7090631	0.92[EUR][1000 genomes]
rs7098235	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs72809324	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72809325	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7897521	0.90[EUR][1000 genomes]
rs7915393	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529324	chr10:90198865-90738588	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases
2	nsv1042848	chr10:90466032-91318474	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
3	nsv540741	chr10:90466032-91318474	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
4	nsv831942	chr10:90564697-90730352	Flanking Active TSS Genic enhancers Weak transcription Enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv831943	chr10:90664836-90865834	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:79 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:90642000-90684800	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr10:90642000-90686400	Weak transcription	Brain Cingulate Gyrus	brain
3	chr10:90647400-90681000	Weak transcription	Aorta	Aorta
4	chr10:90654000-90687400	Weak transcription	Right Ventricle	heart
5	chr10:90655200-90701400	Weak transcription	Gastric	stomach
6	chr10:90657600-90677600	Weak transcription	Lung	lung
7	chr10:90657600-90686400	Weak transcription	Rectal Smooth Muscle	rectum
8	chr10:90658600-90686000	Weak transcription	Brain Anterior Caudate	brain
9	chr10:90659600-90689800	Weak transcription	Esophagus	oesophagus
10	chr10:90660400-90695000	Weak transcription	Fetal Brain Male	brain
11	chr10:90660600-90688200	Strong transcription	Dnd41	blood
12	chr10:90661600-90678400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr10:90661600-90687600	Strong transcription	Primary T helper cells fromperipheralblood	blood
14	chr10:90661600-90688800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
15	chr10:90661600-90692200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr10:90662000-90683000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr10:90662600-90687600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
18	chr10:90662800-90688800	Strong transcription	Primary B cells from peripheral blood	blood
19	chr10:90664200-90694600	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr10:90664400-90679400	Weak transcription	Thymus	Thymus
21	chr10:90664400-90679600	Weak transcription	Ovary	ovary
22	chr10:90664400-90683800	Weak transcription	Colonic Mucosa	Colon
23	chr10:90664400-90685600	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr10:90664400-90691200	Weak transcription	Small Intestine	intestine
25	chr10:90664400-90694800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
26	chr10:90664600-90685400	Weak transcription	Fetal Muscle Trunk	muscle
27	chr10:90666000-90692200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr10:90667600-90685800	Weak transcription	Colon Smooth Muscle	Colon
29	chr10:90668200-90683200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr10:90668400-90694800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
31	chr10:90668600-90685800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr10:90669800-90689200	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr10:90670200-90680400	Strong transcription	Primary T helper cells PMA-I stimulated	--
34	chr10:90672200-90677600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr10:90672200-90683800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr10:90672400-90679000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
37	chr10:90673800-90678800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr10:90673800-90681000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
39	chr10:90674800-90679600	Strong transcription	Primary T helper memory cells from peripheral blood 1	blood
40	chr10:90675000-90677600	Strong transcription	Fetal Intestine Large	intestine
41	chr10:90675000-90678000	Strong transcription	Rectal Mucosa Donor 31	rectum
42	chr10:90675000-90679200	Strong transcription	Rectal Mucosa Donor 29	rectum
43	chr10:90675000-90680000	Strong transcription	Primary T cells from cord blood	blood
44	chr10:90675000-90682200	Strong transcription	GM12878-XiMat	blood
45	chr10:90675200-90679800	Strong transcription	Duodenum Mucosa	Duodenum
46	chr10:90675600-90677600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
47	chr10:90675600-90679000	Strong transcription	A549	lung
48	chr10:90675600-90681000	Weak transcription	Right Atrium	heart
49	chr10:90675600-90685600	Weak transcription	Brain Angular Gyrus	brain
50	chr10:90675800-90677600	Weak transcription	Adipose Nuclei	Adipose

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