Variant report

Variant	rs1145076
Chromosome Location	chr15:45684508-45684509
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:45681835..45684781-chr15:45687815..45690039,2	K562	blood:
2	chr15:45681804..45684538-chr15:45877408..45879902,2	K562	blood:

Variant related genes	Relation type
ENSG00000260170	Chromatin interaction
ENSG00000104164	Chromatin interaction
ENSG00000171766	Chromatin interaction

Extended variants
information (count: 94 )
Associated
traits (count: 20 )

rSNPs within LD-proxies of this variant (count:88)

rs_ID	r²[population]
rs1049508	0.84[MEX][hapmap]
rs1049518	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.95[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10519018	1.00[CHB][hapmap];0.96[MEX][hapmap]
rs1060896	1.00[CHB][hapmap];0.96[MEX][hapmap]
rs1145077	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.81[MKK][hapmap];1.00[TSI][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]
rs1145080	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1145084	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1145086	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1145089	1.00[CHB][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1145091	0.84[MEX][hapmap]
rs1145093	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1145097	0.98[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1153845	0.82[GIH][hapmap];0.96[MEX][hapmap];0.86[TSI][hapmap];0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1153855	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1153857	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1153858	0.84[MEX][hapmap]
rs1153860	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1153862	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11632752	1.00[CHB][hapmap];0.96[MEX][hapmap]
rs11632778	1.00[CHB][hapmap];0.96[MEX][hapmap]
rs11632920	1.00[CHB][hapmap];0.95[MEX][hapmap]
rs11636114	0.88[AMR][1000 genomes]
rs11637838	1.00[CHB][hapmap];0.95[MEX][hapmap]
rs11637920	1.00[CHB][hapmap];0.96[MEX][hapmap]
rs11639420	1.00[CHB][hapmap];1.00[MEX][hapmap]
rs11855414	0.90[AMR][1000 genomes]
rs12437840	0.80[MEX][hapmap]
rs12437887	0.80[MEX][hapmap]
rs12440038	0.80[MEX][hapmap]
rs12904150	1.00[CHB][hapmap];0.96[MEX][hapmap]
rs12908818	1.00[CHB][hapmap];1.00[MEX][hapmap]
rs12909409	0.90[AMR][1000 genomes]
rs12910764	0.90[AMR][1000 genomes]
rs12911186	1.00[CHB][hapmap]
rs12915314	1.00[CHB][hapmap]
rs1346266	0.83[MEX][hapmap]
rs1346267	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][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]
rs1346268	0.80[MEX][hapmap]
rs1365610	0.83[MEX][hapmap]
rs1426932	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1547487	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs1554521	0.80[MEX][hapmap]
rs1617634	0.98[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1617984	1.00[CHB][hapmap];0.98[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1706770	1.00[CHB][hapmap]
rs1719231	1.00[CHB][hapmap]
rs1719245	0.98[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1719246	1.00[CEU][hapmap];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1719247	0.84[MEX][hapmap]
rs1719250	0.91[CEU][hapmap];1.00[CHB][hapmap];0.95[MEX][hapmap]
rs17536527	1.00[CHB][hapmap]
rs2002035	0.86[AMR][1000 genomes]
rs2015295	0.85[AMR][1000 genomes]
rs2413768	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap]
rs2413772	1.00[CHB][hapmap];0.96[MEX][hapmap]
rs2413774	1.00[CHB][hapmap];0.96[MEX][hapmap]
rs2433601	0.85[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2433616	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2453533	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2461700	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2461705	1.00[CHB][hapmap];0.96[MEX][hapmap]
rs2467853	1.00[CEU][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2467858	0.88[YRI][hapmap]
rs2467862	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2467865	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2486274	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2486288	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2899375	0.88[AMR][1000 genomes]
rs35861938	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3759899	0.80[MEX][hapmap]
rs3809472	0.80[MEX][hapmap]
rs4395020	0.80[MEX][hapmap]
rs4774580	0.80[MEX][hapmap]
rs4775911	0.80[MEX][hapmap]
rs6493143	1.00[CHB][hapmap]
rs6493144	1.00[CHB][hapmap];1.00[MEX][hapmap]
rs6493145	1.00[CHB][hapmap]
rs7165039	1.00[CHB][hapmap]
rs7166580	1.00[CHB][hapmap]
rs7167146	1.00[CHB][hapmap];1.00[MEX][hapmap]
rs7171312	1.00[CHB][hapmap]
rs8024620	1.00[CHB][hapmap];1.00[MEX][hapmap]
rs8039138	1.00[CHB][hapmap]
rs8039352	1.00[CHB][hapmap];0.91[MEX][hapmap]
rs8039354	1.00[CHB][hapmap];0.96[MEX][hapmap]
rs8039540	1.00[CHB][hapmap]
rs872192	1.00[CEU][hapmap];1.00[CHB][hapmap];0.86[CHD][hapmap];0.82[GIH][hapmap];1.00[MEX][hapmap];0.89[TSI][hapmap];0.98[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs9921008	0.86[AMR][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	nsv916374	chr15:45058112-45769052	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	104 gene(s)	inside rSNPs	diseases
2	nsv932147	chr15:45319178-45872076	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
3	nsv869616	chr15:45401411-45736209	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	76 gene(s)	inside rSNPs	diseases
4	nsv569315	chr15:45446156-45772448	Flanking Active TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
5	nsv469721	chr15:45608881-45788002	Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases
6	nsv482380	chr15:45608881-45788002	Weak transcription Enhancers Active TSS Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	54 gene(s)	inside rSNPs	diseases

mRNA abundance (count:20)

SNP	Gene	Cis/trans	Tissue	Source
rs1145076	C15orf63	cis	parietal	SCAN
rs1145076	SLC28A2	cis	cerebellum	SCAN
rs1145076	CTD-2651B20.4	cis	Artery Tibial	GTEx
rs1145076	CTD-2651B20.3	cis	Muscle Skeletal	GTEx
rs1145076	CTD-2651B20.4	cis	Nerve Tibial	GTEx
rs1145076	CTD-2651B20.3	cis	Esophagus Muscularis	GTEx
rs1145076	BMF	cis	parietal	SCAN
rs1145076	CTD-2651B20.3	cis	Thyroid	GTEx
rs1145076	CTD-2651B20.3	cis	lung	GTEx
rs1145076	CTD-2651B20.3	cis	Skin Sun Exposed Lower leg	GTEx
rs1145076	GATM	cis	parietal	SCAN
rs1145076	CTD-2651B20.3	cis	Heart Left Ventricle	GTEx
rs1145076	SPATA5L1	cis	multi-tissue	Pritchard
rs1145076	CTD-2651B20.3	cis	Nerve Tibial	GTEx
rs1145076	CTD-2651B20.4	cis	Skin Sun Exposed Lower leg	GTEx
rs1145076	GATM	cis	cerebellum	SCAN
rs1145076	GATM	cis	multi-tissue	Pritchard
rs1145076	CTD-2651B20.3	cis	Adipose Subcutaneous	GTEx
rs1145076	CTD-2651B20.3	cis	Artery Aorta	GTEx
rs1145076	CTD-2651B20.3	cis	Artery Tibial	GTEx

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:45676400-45684800	Enhancers	Fetal Intestine Large	intestine
2	chr15:45679000-45686200	Weak transcription	Left Ventricle	heart
3	chr15:45679000-45693800	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr15:45679400-45688800	Enhancers	Liver	Liver
5	chr15:45681800-45685000	Enhancers	Duodenum Mucosa	Duodenum
6	chr15:45682600-45686200	Weak transcription	Ovary	ovary
7	chr15:45682800-45686000	Weak transcription	Brain Substantia Nigra	brain
8	chr15:45682800-45693800	Weak transcription	Brain Angular Gyrus	brain
9	chr15:45683000-45685600	Enhancers	Primary B cells from peripheral blood	blood
10	chr15:45683000-45686000	Weak transcription	Brain Cingulate Gyrus	brain
11	chr15:45683200-45685800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr15:45683200-45686000	Weak transcription	Brain Anterior Caudate	brain
13	chr15:45683200-45686200	Weak transcription	Brain Inferior Temporal Lobe	brain
14	chr15:45683200-45686600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr15:45683200-45691600	Weak transcription	Cortex derived primary cultured neurospheres	brain
16	chr15:45683600-45685000	Enhancers	Primary B cells from cord blood	blood
17	chr15:45683600-45685200	Enhancers	Primary monocytes fromperipheralblood	blood
18	chr15:45683600-45685200	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr15:45683600-45685400	Weak transcription	Pancreas	Pancrea
20	chr15:45683800-45685400	Weak transcription	Brain Hippocampus Middle	brain
21	chr15:45684000-45684800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr15:45684000-45685000	Enhancers	Primary hematopoietic stem cells short term culture	blood
23	chr15:45684000-45685000	Flanking Active TSS	GM12878-XiMat	blood
24	chr15:45684200-45685000	Flanking Active TSS	Fetal Intestine Small	intestine
25	chr15:45684400-45684600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr15:45684400-45684600	Flanking Active TSS	HepG2	liver
27	chr15:45684400-45684800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr15:45684400-45684800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
29	chr15:45684400-45684800	Enhancers	NHEK	skin
30	chr15:45684400-45685000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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