Variant report

Variant	rs67366717
Chromosome Location	chr15:59612868-59612869
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs11071428	1.00[ASN][1000 genomes]
rs11071429	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11071430	0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11071431	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11071432	0.81[AMR][1000 genomes]
rs11637840	0.82[EUR][1000 genomes]
rs11854697	0.82[EUR][1000 genomes]
rs12593179	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12595769	0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12902525	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs16941337	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17236578	0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs61692274	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6494102	0.83[AMR][1000 genomes]
rs67017396	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67552459	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7163650	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7164494	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7168263	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7170390	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7171696	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7177871	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7177984	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs73426976	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8033217	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8033386	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs965929	0.88[AMR][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	nsv527307	chr15:59103328-60018487	Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
2	nsv934082	chr15:59608605-59733211	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
3	nsv457175	chr15:59609753-59681214	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
4	nsv569603	chr15:59609753-59681214	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
5	nsv471246	chr15:59610743-59681214	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59600000-59627400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr15:59606400-59614000	Weak transcription	Fetal Intestine Small	intestine
3	chr15:59606600-59621200	Weak transcription	Fetal Kidney	kidney
4	chr15:59606800-59615600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr15:59606800-59621400	Weak transcription	Gastric	stomach
6	chr15:59606800-59623000	Weak transcription	Lung	lung
7	chr15:59606800-59631600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr15:59607000-59620200	Weak transcription	Esophagus	oesophagus
9	chr15:59608600-59615000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr15:59608600-59619000	Weak transcription	Sigmoid Colon	Sigmoid Colon
11	chr15:59608600-59619400	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr15:59608600-59621400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr15:59608600-59621400	Weak transcription	Ovary	ovary
14	chr15:59608600-59622600	Weak transcription	Brain Inferior Temporal Lobe	brain
15	chr15:59608600-59623200	Weak transcription	Psoas Muscle	Psoas
16	chr15:59608600-59623400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr15:59608600-59625800	Weak transcription	HMEC	breast
18	chr15:59608800-59621400	Weak transcription	Duodenum Mucosa	Duodenum
19	chr15:59609600-59619000	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr15:59609800-59620200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr15:59609800-59620400	Weak transcription	HSMM	muscle
22	chr15:59609800-59620800	Weak transcription	NH-A	brain
23	chr15:59609800-59621400	Weak transcription	Pancreas	Pancrea
24	chr15:59610000-59619000	Weak transcription	Stomach Mucosa	stomach
25	chr15:59610200-59613200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr15:59610200-59617600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr15:59610200-59620400	Weak transcription	Osteobl	bone
28	chr15:59610200-59623000	Weak transcription	Left Ventricle	heart
29	chr15:59610200-59627200	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr15:59610400-59617400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr15:59610600-59613400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr15:59610600-59616200	Weak transcription	NHDF-Ad	bronchial
33	chr15:59610600-59620400	Weak transcription	Fetal Heart	heart
34	chr15:59610600-59623000	Weak transcription	Aorta	Aorta
35	chr15:59611200-59613200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr15:59611200-59617600	Weak transcription	Hela-S3	cervix
37	chr15:59611200-59617800	Weak transcription	NHEK	skin
38	chr15:59612200-59625800	Weak transcription	HUVEC	blood vessel
39	chr15:59612400-59614200	ZNF genes & repeats	A549	lung
40	chr15:59612600-59614000	ZNF genes & repeats	GM12878-XiMat	blood

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