Variant report

Variant	rs4472803
Chromosome Location	chr15:33125971-33125972
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs17228788	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17228795	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17228801	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17228808	1.00[ASN][1000 genomes]
rs17228815	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17228822	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17816405	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17816411	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17816417	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2167509	1.00[CEU][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2339160	1.00[CEU][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34696684	1.00[ASN][1000 genomes]
rs4238561	1.00[ASN][1000 genomes]
rs4337273	1.00[CEU][hapmap]
rs7171257	1.00[YRI][hapmap]
rs7174704	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs74011986	1.00[ASN][1000 genomes]
rs7494771	1.00[CEU][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8026518	1.00[YRI][hapmap];0.94[AFR][1000 genomes]
rs8040200	1.00[YRI][hapmap];0.94[AFR][1000 genomes]
rs896506	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][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	esv2422296	chr15:32798938-33221215	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv456785	chr15:32926076-33352989	Genic enhancers Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
3	nsv568913	chr15:32926076-33352989	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	nsv482680	chr15:32958401-33154005	Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	nsv832961	chr15:33021177-33134988	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv832962	chr15:33111517-33239736	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:33061200-33141000	Weak transcription	Placenta	Placenta
2	chr15:33096200-33154000	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr15:33096400-33159000	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr15:33103800-33139200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr15:33111200-33130000	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr15:33112000-33126800	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr15:33112000-33130600	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr15:33117000-33126800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr15:33117800-33130800	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr15:33117800-33131000	Weak transcription	Stomach Smooth Muscle	stomach
11	chr15:33118600-33159000	Weak transcription	Gastric	stomach
12	chr15:33119400-33131600	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr15:33120400-33127400	Enhancers	NHLF	lung
14	chr15:33121400-33126600	Enhancers	NHDF-Ad	bronchial
15	chr15:33121800-33130600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr15:33122800-33127800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr15:33122800-33130400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr15:33123000-33130800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr15:33123800-33127000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr15:33124400-33130200	Weak transcription	A549	lung
21	chr15:33124600-33131200	Weak transcription	Lung	lung
22	chr15:33124800-33126200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr15:33124800-33126400	Enhancers	Osteobl	bone
24	chr15:33124800-33126800	Enhancers	HUVEC	blood vessel
25	chr15:33125000-33126600	Enhancers	HSMMtube	muscle
26	chr15:33125400-33126200	Enhancers	NH-A	brain
27	chr15:33125600-33126200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr15:33125600-33126200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
29	chr15:33125600-33126200	Enhancers	HMEC	breast
30	chr15:33125600-33126800	Enhancers	HSMM	muscle
31	chr15:33125600-33127200	Enhancers	GM12878-XiMat	blood
32	chr15:33125800-33126600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr15:33125800-33126800	Enhancers	Muscle Satellite Cultured Cells	--
34	chr15:33125800-33127200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr15:33125800-33129200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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