Variant report

Variant	rs10414433
Chromosome Location	chr19:38544631-38544632
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 40 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10413751	1.00[CEU][hapmap];0.90[YRI][hapmap];0.91[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10421137	0.82[CHB][hapmap]
rs1612361	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1614979	0.82[CEU][hapmap]
rs1654338	0.81[CHB][hapmap]
rs1654341	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1654343	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1654347	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1654349	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1654350	0.88[EUR][1000 genomes]
rs1654352	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1654365	0.82[CEU][hapmap]
rs1725458	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1725462	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1725470	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1725475	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1725476	0.89[EUR][1000 genomes]
rs1725504	0.82[CEU][hapmap]
rs1725507	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1725508	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1725509	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1725510	0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1725512	0.83[CEU][hapmap]
rs28587798	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4802233	0.83[CEU][hapmap]
rs57585457	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs57999412	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7257303	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs734365	0.98[ASN][1000 genomes]
rs855597	0.82[AMR][1000 genomes]
rs855600	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs855601	0.89[CEU][hapmap];0.80[EUR][1000 genomes]
rs855603	0.82[CEU][hapmap]
rs855605	0.98[ASN][1000 genomes]
rs855636	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs855637	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs941040	0.83[CEU][hapmap]

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	nsv949296	chr19:38034722-38763140	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
2	nsv1060359	chr19:38512719-38552438	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1062518	chr19:38540454-38564913	Enhancers Strong transcription Genic enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS	TF binding region Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10414433	DPF1	cis	Skin Sun Exposed Lower leg	GTEx

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:38521800-38548600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr19:38522000-38553600	Weak transcription	Stomach Smooth Muscle	stomach
3	chr19:38526800-38545600	Weak transcription	Stomach Mucosa	stomach
4	chr19:38527800-38548800	Weak transcription	Right Atrium	heart
5	chr19:38527800-38551800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr19:38528200-38573200	Weak transcription	Left Ventricle	heart
7	chr19:38529000-38548600	Weak transcription	Pancreas	Pancrea
8	chr19:38531400-38550800	Weak transcription	NHLF	lung
9	chr19:38534800-38545400	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr19:38537800-38545400	Weak transcription	Fetal Stomach	stomach
11	chr19:38537800-38548800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr19:38537800-38548800	Weak transcription	Esophagus	oesophagus
13	chr19:38538000-38548800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr19:38538400-38552800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr19:38539000-38545200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
16	chr19:38539000-38545400	Weak transcription	Gastric	stomach
17	chr19:38539000-38572000	Weak transcription	Right Ventricle	heart
18	chr19:38539200-38545200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr19:38539200-38545200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
20	chr19:38539200-38545400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr19:38539200-38545400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr19:38539200-38548800	Weak transcription	Colonic Mucosa	Colon
23	chr19:38539200-38548800	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr19:38539200-38591200	Weak transcription	Small Intestine	intestine
25	chr19:38539600-38545400	Weak transcription	HSMM	muscle
26	chr19:38540200-38545200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr19:38540200-38545200	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr19:38540200-38545400	Weak transcription	Fetal Lung	lung
29	chr19:38540200-38545400	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr19:38540200-38545400	Weak transcription	Skeletal Muscle Male	skeletal muscle
31	chr19:38540200-38548600	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr19:38540400-38545000	Weak transcription	Fetal Muscle Leg	muscle
33	chr19:38540400-38545200	Weak transcription	Osteobl	bone
34	chr19:38540400-38551600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr19:38540600-38545000	Weak transcription	Fetal Muscle Trunk	muscle
36	chr19:38540600-38545200	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr19:38540600-38545400	Weak transcription	Lung	lung
38	chr19:38540600-38545400	Weak transcription	Thymus	Thymus
39	chr19:38540600-38545400	Weak transcription	Spleen	Spleen
40	chr19:38540600-38545400	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr19:38540600-38545600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
42	chr19:38540600-38548800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
43	chr19:38540600-38549000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
44	chr19:38540800-38545000	Weak transcription	Fetal Thymus	thymus
45	chr19:38540800-38545200	Weak transcription	Primary hematopoietic stem cells	blood
46	chr19:38540800-38545400	Weak transcription	Primary monocytes fromperipheralblood	blood
47	chr19:38540800-38545600	Weak transcription	Primary neutrophils fromperipheralblood	blood
48	chr19:38540800-38548800	Weak transcription	Primary T helper cells fromperipheralblood	blood
49	chr19:38540800-38549800	Weak transcription	Primary T helper cells PMA-I stimulated	--
50	chr19:38541000-38545200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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