Variant report

Variant	rs17734856
Chromosome Location	chr15:42045160-42045161
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:42028222..42030756-chr15:42044005..42046072,2	K562	blood:
2	chr15:42039177..42040902-chr15:42043568..42045872,2	MCF-7	breast:

Extended variants
information (count: 53 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs1105881	0.96[CEU][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs1107858	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11632424	0.85[EUR][1000 genomes]
rs11634956	0.86[CHB][hapmap];0.86[JPT][hapmap];0.85[ASN][1000 genomes]
rs11637341	0.88[EUR][1000 genomes]
rs12440747	0.96[CEU][hapmap];0.86[CHB][hapmap];0.93[JPT][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12441300	0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1531140	0.92[CEU][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap]
rs16952372	0.92[JPT][hapmap]
rs16971976	0.86[JPT][hapmap]
rs17676742	0.96[CEU][hapmap];0.86[CHB][hapmap];0.92[JPT][hapmap]
rs17677199	0.96[CEU][hapmap];0.86[CHB][hapmap];0.93[JPT][hapmap];0.88[EUR][1000 genomes]
rs17677991	0.96[CEU][hapmap];0.86[CHB][hapmap];0.93[JPT][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17678138	0.96[CEU][hapmap];0.86[CHB][hapmap];0.93[JPT][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17678552	0.96[CEU][hapmap];0.86[CHB][hapmap];0.93[JPT][hapmap];1.00[YRI][hapmap];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs17678767	0.96[CEU][hapmap];1.00[YRI][hapmap];0.85[EUR][1000 genomes]
rs1918310	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.80[AFR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2004162	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2241522	0.92[CEU][hapmap];0.84[JPT][hapmap]
rs2277535	0.92[CEU][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap]
rs2303516	0.92[CEU][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap]
rs2303518	0.92[CEU][hapmap];0.92[JPT][hapmap];0.82[ASN][1000 genomes]
rs2305654	0.92[CEU][hapmap];0.92[JPT][hapmap]
rs2412622	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2577960	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28444909	0.88[EUR][1000 genomes]
rs28701757	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28754734	0.86[EUR][1000 genomes]
rs3743024	0.92[CEU][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap]
rs3959569	0.80[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs4923905	0.96[CEU][hapmap];0.86[CHB][hapmap];0.93[JPT][hapmap]
rs4923914	0.92[CEU][hapmap];1.00[YRI][hapmap]
rs4924564	0.86[CHB][hapmap]
rs4924570	0.92[JPT][hapmap];0.82[EUR][1000 genomes]
rs4924575	0.96[CEU][hapmap];1.00[YRI][hapmap];0.84[EUR][1000 genomes]
rs4924576	0.92[CEU][hapmap];0.84[JPT][hapmap];1.00[YRI][hapmap]
rs4924580	0.82[ASN][1000 genomes]
rs62002066	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs62002090	0.88[EUR][1000 genomes]
rs62002091	0.82[EUR][1000 genomes]
rs7171123	0.84[ASN][1000 genomes]
rs8035855	0.84[CHB][hapmap];0.86[JPT][hapmap]
rs9672298	1.00[CEU][hapmap];0.93[JPT][hapmap]
rs9672360	0.96[CEU][hapmap];0.93[JPT][hapmap]
rs9920903	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1049514	chr15:41958482-42081210	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv1048655	chr15:41978391-42049360	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region miRNA	6 gene(s)	inside rSNPs	diseases
3	nsv931223	chr15:41989960-42781757	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	81 gene(s)	inside rSNPs	diseases
4	nsv1036086	chr15:42004962-42091451	Strong transcription Weak transcription Flanking Active TSS Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	nsv1041861	chr15:42016097-42062287	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
6	nsv1054671	chr15:42016097-42098896	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
7	nsv1044347	chr15:42023805-42049360	Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv1038894	chr15:42038152-42077452	Flanking Active TSS Weak transcription Strong transcription Active TSS Transcr. at gene 5' and 3' Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs17734856	MGA	cis	lesional skin	skin_eQTL
rs17734856	MGA	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:41972400-42065200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr15:42003800-42056000	Weak transcription	Colonic Mucosa	Colon
3	chr15:42009800-42056800	Weak transcription	Fetal Heart	heart
4	chr15:42017400-42062600	Strong transcription	Primary T cells fromperipheralblood	blood
5	chr15:42019400-42060600	Strong transcription	Primary T helper cells fromperipheralblood	blood
6	chr15:42025000-42045800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr15:42025200-42065400	Weak transcription	Pancreatic Islets	Pancreatic Islet
8	chr15:42029000-42052200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr15:42029000-42054200	Weak transcription	Small Intestine	intestine
10	chr15:42029200-42048400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr15:42030400-42046400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr15:42035400-42054400	Weak transcription	Pancreas	Pancrea
13	chr15:42035600-42046600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr15:42035800-42047600	Weak transcription	NHEK	skin
15	chr15:42035800-42058200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr15:42036000-42052800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr15:42036000-42058400	Weak transcription	Psoas Muscle	Psoas
18	chr15:42038800-42051000	Strong transcription	Primary B cells from peripheral blood	blood
19	chr15:42039000-42064400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr15:42039600-42049000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr15:42039600-42062600	Strong transcription	Monocytes-CD14+_RO01746	blood
22	chr15:42039800-42049200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr15:42040000-42049600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr15:42040000-42061400	Strong transcription	Primary monocytes fromperipheralblood	blood
25	chr15:42040200-42048400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr15:42040200-42049400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr15:42040200-42059800	Strong transcription	Primary T helper cells PMA-I stimulated	--
28	chr15:42040200-42064400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr15:42040600-42063000	Strong transcription	HUES64 Cell Line	embryonic stem cell
30	chr15:42041600-42054600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr15:42041800-42047200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
32	chr15:42041800-42053400	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr15:42041800-42055800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr15:42041800-42056800	Weak transcription	Esophagus	oesophagus
35	chr15:42041800-42058200	Weak transcription	Gastric	stomach
36	chr15:42042000-42046400	Weak transcription	Stomach Smooth Muscle	stomach
37	chr15:42042000-42047200	Weak transcription	Brain Angular Gyrus	brain
38	chr15:42042000-42053000	Weak transcription	HMEC	breast
39	chr15:42042000-42053600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr15:42042000-42057000	Weak transcription	Right Ventricle	heart
41	chr15:42042000-42057200	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr15:42042200-42046200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr15:42042200-42046600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr15:42042200-42046600	Weak transcription	NHDF-Ad	bronchial
45	chr15:42042200-42047800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr15:42042200-42055800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr15:42042400-42046600	Weak transcription	Osteobl	bone
48	chr15:42042400-42048600	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr15:42042400-42054600	Weak transcription	Rectal Smooth Muscle	rectum
50	chr15:42042400-42054800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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