Variant report

Variant	rs16974307
Chromosome Location	chr15:93195462-93195463
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs12443091	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12908852	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1496712	0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1496726	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2254142	0.88[CEU][hapmap];0.92[EUR][1000 genomes]
rs2453901	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs285754	0.89[CEU][hapmap];0.90[EUR][1000 genomes]
rs285755	0.89[CEU][hapmap];0.91[EUR][1000 genomes]
rs285757	0.89[CEU][hapmap];0.91[EUR][1000 genomes]
rs285758	0.89[CEU][hapmap];0.91[EUR][1000 genomes]
rs285766	0.80[CEU][hapmap];0.83[EUR][1000 genomes]
rs285772	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs366789	0.85[EUR][1000 genomes]
rs373481	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs406032	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs413450	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs434826	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs503112	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6496969	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7178546	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs893379	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[YRI][hapmap];0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][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	nsv1037972	chr15:92804908-93270761	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
2	nsv904499	chr15:92914795-93472582	Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	163 gene(s)	inside rSNPs	diseases
3	nsv948738	chr15:93070742-93728147	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	169 gene(s)	inside rSNPs	diseases
4	nsv1049490	chr15:93134405-93591660	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	151 gene(s)	inside rSNPs	diseases
5	nsv1040501	chr15:93177153-93286393	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs16974307	LOC400451	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:93171000-93197400	Weak transcription	Primary T cells from cord blood	blood
2	chr15:93182000-93197800	Weak transcription	Small Intestine	intestine
3	chr15:93182600-93197200	Weak transcription	Fetal Kidney	kidney
4	chr15:93183200-93198400	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr15:93187600-93195800	Weak transcription	Brain Angular Gyrus	brain
6	chr15:93187800-93195600	Weak transcription	Fetal Muscle Trunk	muscle
7	chr15:93189000-93195600	Weak transcription	Rectal Mucosa Donor 31	rectum
8	chr15:93189000-93197000	Weak transcription	Brain Hippocampus Middle	brain
9	chr15:93189400-93197000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr15:93189400-93197000	Weak transcription	Esophagus	oesophagus
11	chr15:93190600-93197000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr15:93191000-93196600	Weak transcription	HSMM	muscle
13	chr15:93191000-93197400	Weak transcription	HSMMtube	muscle
14	chr15:93192000-93196800	Weak transcription	Liver	Liver
15	chr15:93192000-93197400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr15:93192800-93195600	Weak transcription	HUVEC	blood vessel
17	chr15:93193000-93196200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr15:93193800-93199000	Enhancers	Fetal Heart	heart
19	chr15:93194000-93195600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr15:93194000-93196800	Weak transcription	Duodenum Smooth Muscle	Duodenum
21	chr15:93194000-93197200	Weak transcription	Rectal Smooth Muscle	rectum
22	chr15:93194000-93197400	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr15:93194200-93195600	Weak transcription	Fetal Lung	lung
24	chr15:93194200-93195600	Weak transcription	Gastric	stomach
25	chr15:93194200-93195600	Weak transcription	Right Atrium	heart
26	chr15:93194200-93197000	Weak transcription	Ovary	ovary
27	chr15:93194200-93197400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr15:93194200-93198200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr15:93194400-93197400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr15:93194400-93198400	Weak transcription	Brain Anterior Caudate	brain
31	chr15:93194600-93196600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr15:93194600-93197400	Weak transcription	Primary hematopoietic stem cells	blood
33	chr15:93194600-93197600	Weak transcription	Fetal Brain Female	brain
34	chr15:93194600-93198400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr15:93194800-93195600	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr15:93194800-93196000	Enhancers	Colon Smooth Muscle	Colon
37	chr15:93195000-93195800	Transcr. at gene 5' and 3'	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr15:93195000-93197000	Active TSS	GM12878-XiMat	blood
39	chr15:93195000-93197600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr15:93195200-93195800	Enhancers	H9 Cell Line	embryonic stem cell
41	chr15:93195200-93196400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr15:93195200-93196400	Enhancers	Skeletal Muscle Male	skeletal muscle
43	chr15:93195200-93197200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr15:93195200-93197200	Enhancers	Placenta	Placenta
45	chr15:93195200-93199600	Active TSS	Pancreatic Islets	Pancreatic Islet
46	chr15:93195400-93195600	Strong transcription	Fetal Muscle Leg	muscle
47	chr15:93195400-93195600	Flanking Active TSS	Stomach Smooth Muscle	stomach
48	chr15:93195400-93195800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr15:93195400-93195800	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr15:93195400-93195800	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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