Variant report

Variant	rs4918905
Chromosome Location	chr10:97016553-97016554
allele	A/G
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:12)

rs_ID	r²[population]
rs10786195	0.86[EUR][1000 genomes]
rs11188250	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11188255	0.92[EUR][1000 genomes]
rs11593722	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11594748	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12775067	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1385065	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17110556	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2296961	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35497513	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4918908	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58140424	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv497859	chr10:96058024-97027747	Strong transcription Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	nsv529726	chr10:96632494-97106315	Strong transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	esv15160	chr10:96942869-97074756	Bivalent Enhancer Active TSS Strong transcription Enhancers Weak transcription Flanking Active TSS Genic enhancers 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 miRNA target site	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:96991000-97020400	Weak transcription	Fetal Muscle Leg	muscle
2	chr10:96991000-97024000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr10:96991400-97019000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
4	chr10:96998400-97030200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr10:97000400-97024400	Weak transcription	Fetal Kidney	kidney
6	chr10:97006200-97017600	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr10:97006400-97019600	Weak transcription	K562	blood
8	chr10:97007000-97026400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr10:97007600-97020600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr10:97007800-97020800	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr10:97008000-97016600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr10:97008000-97019400	Weak transcription	Placenta	Placenta
13	chr10:97008000-97020200	Weak transcription	Rectal Smooth Muscle	rectum
14	chr10:97008200-97017800	Weak transcription	Osteobl	bone
15	chr10:97008600-97019800	Weak transcription	HSMM	muscle
16	chr10:97008800-97019800	Weak transcription	Fetal Thymus	thymus
17	chr10:97009000-97019200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr10:97009000-97020400	Weak transcription	Stomach Smooth Muscle	stomach
19	chr10:97009200-97019600	Weak transcription	Esophagus	oesophagus
20	chr10:97009200-97020200	Weak transcription	Pancreas	Pancrea
21	chr10:97009200-97020600	Weak transcription	Fetal Lung	lung
22	chr10:97009200-97028200	Weak transcription	Fetal Muscle Trunk	muscle
23	chr10:97009600-97019600	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr10:97009800-97019200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr10:97009800-97019200	Weak transcription	Small Intestine	intestine
26	chr10:97009800-97019200	Weak transcription	Spleen	Spleen
27	chr10:97009800-97020000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr10:97009800-97020000	Weak transcription	Fetal Heart	heart
29	chr10:97009800-97020400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr10:97009800-97020800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr10:97010000-97017600	Weak transcription	NHLF	lung
32	chr10:97010800-97017400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr10:97011600-97019200	Weak transcription	Aorta	Aorta
34	chr10:97012000-97017400	Weak transcription	Adipose Nuclei	Adipose
35	chr10:97012000-97019800	Weak transcription	Colonic Mucosa	Colon
36	chr10:97012200-97017400	Weak transcription	Left Ventricle	heart
37	chr10:97012200-97017400	Weak transcription	Right Ventricle	heart
38	chr10:97012200-97017600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr10:97012200-97017800	Weak transcription	Gastric	stomach
40	chr10:97012200-97019200	Weak transcription	Lung	lung
41	chr10:97012200-97019600	Weak transcription	Fetal Stomach	stomach
42	chr10:97012200-97019800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr10:97012200-97020200	Weak transcription	Psoas Muscle	Psoas
44	chr10:97014400-97020200	Weak transcription	Stomach Mucosa	stomach
45	chr10:97014600-97019800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr10:97014800-97019800	Weak transcription	HUVEC	blood vessel
47	chr10:97015000-97017400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr10:97015400-97020200	Strong transcription	Rectal Mucosa Donor 31	rectum
49	chr10:97015400-97022000	Strong transcription	Primary B cells from peripheral blood	blood
50	chr10:97015600-97017200	Weak transcription	HepG2	liver

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