Variant report

Variant	rs2444981
Chromosome Location	chr15:33439414-33439415
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs1454987	0.86[CHB][hapmap];0.83[CHD][hapmap];0.85[JPT][hapmap]
rs2085180	0.86[CHB][hapmap];0.86[JPT][hapmap]
rs2257131	0.86[CHB][hapmap];0.81[JPT][hapmap]
rs2444962	0.86[CHB][hapmap];0.95[CHD][hapmap];0.83[GIH][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs2444976	0.90[ASN][1000 genomes]
rs2444979	0.90[ASN][1000 genomes]
rs2444982	1.00[CEU][hapmap];0.90[GIH][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap];0.85[TSI][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2444983	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2468741	0.85[CHB][hapmap];0.86[JPT][hapmap]
rs2468751	0.86[ASN][1000 genomes]
rs2468758	0.95[ASN][1000 genomes]
rs2468759	0.83[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4350544	0.86[JPT][hapmap]
rs4780082	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs5002280	0.86[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv903979	chr15:33144202-33550256	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv1052966	chr15:33149753-33541951	Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv542340	chr15:33149753-33541951	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
4	nsv903981	chr15:33207082-33550256	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
5	nsv568918	chr15:33244672-33446971	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv903982	chr15:33282844-33616150	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
7	nsv903983	chr15:33388030-33550256	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	esv2763091	chr15:33435045-33439414	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33424400-33440600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr15:33427800-33445400	Weak transcription	Right Atrium	heart
3	chr15:33435800-33442200	Weak transcription	Duodenum Mucosa	Duodenum
4	chr15:33438000-33440200	Weak transcription	Fetal Kidney	kidney
5	chr15:33438000-33440600	Weak transcription	Esophagus	oesophagus
6	chr15:33438000-33442000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr15:33438400-33440400	Weak transcription	Fetal Thymus	thymus
8	chr15:33438400-33444800	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr15:33438600-33440400	Weak transcription	Primary monocytes fromperipheralblood	blood
10	chr15:33438600-33441600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr15:33438600-33449800	Weak transcription	NHEK	skin
12	chr15:33438800-33440400	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr15:33438800-33442000	Weak transcription	HMEC	breast
14	chr15:33438800-33442400	Weak transcription	Pancreatic Islets	Pancreatic Islet
15	chr15:33438800-33442800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr15:33438800-33444600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr15:33439000-33445200	Weak transcription	Placenta	Placenta
18	chr15:33439000-33445200	Weak transcription	Lung	lung
19	chr15:33439000-33447200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr15:33439400-33440400	Weak transcription	Fetal Intestine Small	intestine
21	chr15:33439400-33441600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr15:33439400-33441800	Weak transcription	Fetal Intestine Large	intestine

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