Variant report

Variant	rs8024266
Chromosome Location	chr15:43066681-43066682
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs11070377	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11070378	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11632809	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11854550	0.92[CEU][hapmap];0.89[EUR][1000 genomes]
rs16957167	0.94[ASW][hapmap];0.95[CHB][hapmap];1.00[CHD][hapmap];0.85[GIH][hapmap];0.84[JPT][hapmap];0.96[LWK][hapmap];0.85[MKK][hapmap];0.86[YRI][hapmap];0.91[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs16957168	0.83[YRI][hapmap]
rs1915243	0.86[YRI][hapmap]
rs2139655	0.92[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.95[EUR][1000 genomes]
rs28722903	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34302400	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35554267	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4924696	0.92[CEU][hapmap]
rs6493065	1.00[CEU][hapmap];0.95[MEX][hapmap];0.90[TSI][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7181238	1.00[CEU][hapmap];0.82[MEX][hapmap];0.85[TSI][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7182141	0.90[YRI][hapmap]
rs8028167	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs8030696	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8042738	0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8042980	0.88[EUR][1000 genomes]
rs9269	0.83[YRI][hapmap]
rs9920092	0.92[CEU][hapmap];0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9920562	0.92[CEU][hapmap];0.82[MEX][hapmap];0.90[TSI][hapmap];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9920624	0.92[CEU][hapmap];0.82[MEX][hapmap];0.95[TSI][hapmap];0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9920935	1.00[CEU][hapmap];0.95[MEX][hapmap];0.91[TSI][hapmap];0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv528725	chr15:42755555-43104406	Weak transcription Active TSS Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
2	nsv427959	chr15:42931181-43207353	Weak transcription Flanking Active TSS Strong transcription Enhancers 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 target site	10 gene(s)	inside rSNPs	diseases
3	nsv977054	chr15:43015821-43171355	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
4	nsv1050128	chr15:43056145-43262736	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv542368	chr15:43056145-43262736	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv525461	chr15:43062548-43482127	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs8024266	CCNDBP1	cis	Lymphoblastoid	GTEx
rs8024266	EIF3J	cis	parietal	SCAN

Chromatin state (count:111 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:43029800-43071000	Weak transcription	Pancreas	Pancrea
2	chr15:43030000-43067200	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr15:43030000-43093600	Weak transcription	Colonic Mucosa	Colon
4	chr15:43038400-43067400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr15:43045400-43068000	Weak transcription	Fetal Heart	heart
6	chr15:43045600-43074400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr15:43051800-43069400	Weak transcription	Gastric	stomach
8	chr15:43051800-43070600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr15:43051800-43074600	Weak transcription	Right Ventricle	heart
10	chr15:43051800-43075000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr15:43051800-43083800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr15:43052000-43074600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
13	chr15:43053600-43112200	Weak transcription	Rectal Smooth Muscle	rectum
14	chr15:43054000-43074600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr15:43054000-43080200	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr15:43054600-43067200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr15:43054600-43068600	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr15:43054800-43067200	Weak transcription	Duodenum Mucosa	Duodenum
19	chr15:43054800-43146000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
20	chr15:43055600-43066800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr15:43056800-43067200	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr15:43056800-43068200	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr15:43056800-43116800	Weak transcription	HepG2	liver
24	chr15:43057600-43107000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr15:43060800-43122200	Weak transcription	GM12878-XiMat	blood
26	chr15:43061000-43067400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
27	chr15:43061200-43074600	Weak transcription	HSMMtube	muscle
28	chr15:43062200-43067200	Weak transcription	Osteobl	bone
29	chr15:43062200-43069600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr15:43062600-43066800	Weak transcription	Primary neutrophils fromperipheralblood	blood
31	chr15:43062600-43070200	Strong transcription	Primary T cells from cord blood	blood
32	chr15:43062600-43087800	Weak transcription	K562	blood
33	chr15:43062800-43070200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr15:43062800-43075200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr15:43062800-43088600	Weak transcription	NHDF-Ad	bronchial
36	chr15:43063000-43083200	Weak transcription	Fetal Intestine Small	intestine
37	chr15:43063000-43093000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
38	chr15:43063200-43074600	Weak transcription	Hela-S3	cervix
39	chr15:43063400-43070000	Strong transcription	Monocytes-CD14+_RO01746	blood
40	chr15:43063400-43093600	Weak transcription	Esophagus	oesophagus
41	chr15:43063400-43136200	Weak transcription	Psoas Muscle	Psoas
42	chr15:43063600-43069400	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr15:43063600-43069600	Strong transcription	Primary B cells from cord blood	blood
44	chr15:43063800-43069600	Strong transcription	Primary B cells from peripheral blood	blood
45	chr15:43063800-43070000	Strong transcription	Primary monocytes fromperipheralblood	blood
46	chr15:43064000-43068000	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
47	chr15:43064000-43068800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
48	chr15:43064000-43068800	Strong transcription	NHEK	skin
49	chr15:43064000-43069400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
50	chr15:43064000-43069600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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