Variant report

Variant	rs11630780
Chromosome Location	chr15:56128445-56128446
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs1042477	0.94[ASW][hapmap];0.92[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.90[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];0.97[TSI][hapmap];0.92[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11071228	0.92[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs11632977	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11633263	0.85[ASN][1000 genomes]
rs11633313	0.89[AFR][1000 genomes];0.95[ASN][1000 genomes]
rs12102014	0.91[AFR][1000 genomes];0.80[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12102020	0.92[AFR][1000 genomes];0.80[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12232351	0.84[ASN][1000 genomes]
rs12898589	0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12910830	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13380185	0.92[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs16976585	0.89[ASN][1000 genomes]
rs2288344	1.00[AFR][1000 genomes];0.80[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2288345	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2414444	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35040841	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56093337	0.82[AFR][1000 genomes]
rs56333939	0.99[AFR][1000 genomes];0.80[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs60890210	0.87[ASN][1000 genomes]
rs7162435	1.00[CHB][hapmap];1.00[CHD][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.81[MEX][hapmap];0.85[YRI][hapmap];0.84[AFR][1000 genomes];0.80[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs7175686	0.99[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs7176225	0.92[AFR][1000 genomes];0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs8024944	0.91[AFR][1000 genomes];0.80[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs8026172	0.92[AFR][1000 genomes];0.80[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs8028559	0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv457157	chr15:55722213-56255774	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
2	nsv569539	chr15:55722213-56255774	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv833017	chr15:55965957-56157912	Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active 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	8 gene(s)	inside rSNPs	diseases
4	esv3366380	chr15:56003224-56141650	Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs11630780	CYP19A1	cis	parietal	SCAN
rs11630780	PRTG	cis	Artery Tibial	GTEx

Chromatin state (count:87 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56095800-56128600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr15:56106000-56131200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr15:56112600-56133600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr15:56115400-56148000	Weak transcription	Ovary	ovary
5	chr15:56115800-56129800	Weak transcription	Hela-S3	cervix
6	chr15:56116400-56129000	Weak transcription	NHLF	lung
7	chr15:56116400-56129600	Weak transcription	NHDF-Ad	bronchial
8	chr15:56116400-56133400	Weak transcription	Fetal Lung	lung
9	chr15:56116600-56150600	Weak transcription	Right Ventricle	heart
10	chr15:56116800-56162200	Weak transcription	Fetal Heart	heart
11	chr15:56117600-56131200	Weak transcription	Small Intestine	intestine
12	chr15:56118600-56151000	Weak transcription	Fetal Kidney	kidney
13	chr15:56118800-56147000	Weak transcription	Gastric	stomach
14	chr15:56118800-56149200	Weak transcription	Brain Cingulate Gyrus	brain
15	chr15:56118800-56151400	Weak transcription	Brain Anterior Caudate	brain
16	chr15:56119200-56133000	Weak transcription	Primary T cells from cord blood	blood
17	chr15:56119400-56134800	Weak transcription	Rectal Mucosa Donor 29	rectum
18	chr15:56120000-56136800	Strong transcription	Liver	Liver
19	chr15:56120000-56144800	Strong transcription	Skeletal Muscle Female	skeletal muscle
20	chr15:56120000-56147800	Weak transcription	HepG2	liver
21	chr15:56120600-56146600	Weak transcription	Pancreas	Pancrea
22	chr15:56120800-56147200	Weak transcription	Thymus	Thymus
23	chr15:56121200-56147200	Weak transcription	Spleen	Spleen
24	chr15:56121800-56135600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
25	chr15:56122000-56136600	Strong transcription	Fetal Intestine Large	intestine
26	chr15:56122200-56129000	Weak transcription	Placenta Amnion	Placenta Amnion
27	chr15:56122200-56135400	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr15:56122200-56136000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr15:56122400-56136800	Strong transcription	Primary neutrophils fromperipheralblood	blood
30	chr15:56122400-56145200	Weak transcription	Rectal Mucosa Donor 31	rectum
31	chr15:56122600-56134200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr15:56122600-56152000	Weak transcription	Fetal Thymus	thymus
33	chr15:56122600-56153800	Weak transcription	Primary T cells fromperipheralblood	blood
34	chr15:56122600-56154800	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr15:56122600-56156600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
36	chr15:56122800-56129600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
37	chr15:56122800-56132600	Weak transcription	Monocytes-CD14+_RO01746	blood
38	chr15:56122800-56134800	Weak transcription	Rectal Smooth Muscle	rectum
39	chr15:56122800-56141600	Weak transcription	Primary T helper cells fromperipheralblood	blood
40	chr15:56122800-56147200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr15:56122800-56147600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr15:56122800-56156000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr15:56123000-56136800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr15:56123000-56140200	Weak transcription	Dnd41	blood
45	chr15:56123200-56137600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr15:56123800-56128800	Strong transcription	Adipose Nuclei	Adipose
47	chr15:56123800-56137000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr15:56124200-56130000	Weak transcription	HUVEC	blood vessel
49	chr15:56124600-56129600	Weak transcription	Cortex derived primary cultured neurospheres	brain
50	chr15:56124600-56129600	Strong transcription	Fetal Intestine Small	intestine

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