Variant report

Variant	rs1724627
Chromosome Location	chr15:52702026-52702027
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:52700906..52703355-chr15:52710486..52712910,2	MCF-7	breast:
2	chr15:52696768..52698806-chr15:52701704..52704430,2	K562	blood:
3	chr15:52694162..52695707-chr15:52701924..52704599,2	MCF-7	breast:
4	chr15:52701268..52703457-chr15:52706501..52708965,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs1526169	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1534200	0.86[AFR][1000 genomes]
rs1615235	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs1669864	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1669866	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1669877	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1724585	0.83[EUR][1000 genomes]
rs1724592	0.95[AFR][1000 genomes];0.91[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1724624	0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1724625	0.90[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs1724626	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1724630	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1724635	0.97[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs17707852	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1972160	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2444015	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2444019	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2462847	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2462848	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2462849	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2600902	0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs8033579	0.86[AMR][1000 genomes];0.84[EUR][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	esv1846455	chr15:52501831-52714452	Strong transcription Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	17 gene(s)	inside rSNPs	diseases
2	nsv471245	chr15:52607262-53187165	Weak transcription Strong transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	52 gene(s)	inside rSNPs	diseases
3	nsv1041421	chr15:52661342-53148286	Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Bivalent/Poised TSS 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	51 gene(s)	inside rSNPs	diseases
4	nsv1054899	chr15:52662365-52803756	Enhancers Genic enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1724627	MYO5A	cis	Artery Tibial	GTEx

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:52644600-52730200	Weak transcription	Esophagus	oesophagus
2	chr15:52663200-52711400	Strong transcription	Monocytes-CD14+_RO01746	blood
3	chr15:52663400-52708600	Strong transcription	Primary monocytes fromperipheralblood	blood
4	chr15:52665200-52720600	Weak transcription	Pancreas	Pancrea
5	chr15:52668800-52730400	Weak transcription	Aorta	Aorta
6	chr15:52673800-52730200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr15:52674000-52703800	Weak transcription	Fetal Brain Male	brain
8	chr15:52676000-52705600	Weak transcription	Fetal Stomach	stomach
9	chr15:52676400-52709800	Weak transcription	NHLF	lung
10	chr15:52676400-52721400	Weak transcription	Gastric	stomach
11	chr15:52676600-52706400	Weak transcription	Lung	lung
12	chr15:52676600-52718600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr15:52677000-52730000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr15:52679800-52729600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr15:52679800-52740000	Weak transcription	Spleen	Spleen
16	chr15:52680600-52719800	Weak transcription	NH-A	brain
17	chr15:52680800-52716400	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr15:52680800-52730000	Weak transcription	Brain Angular Gyrus	brain
19	chr15:52680800-52740200	Weak transcription	Thymus	Thymus
20	chr15:52681000-52706800	Weak transcription	Brain Substantia Nigra	brain
21	chr15:52684000-52719800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr15:52684800-52719800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr15:52684800-52730000	Weak transcription	Brain Hippocampus Middle	brain
24	chr15:52685000-52717000	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr15:52685400-52706200	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr15:52685400-52711000	Weak transcription	NHDF-Ad	bronchial
27	chr15:52685400-52730000	Weak transcription	Brain Cingulate Gyrus	brain
28	chr15:52685600-52708000	Weak transcription	NHEK	skin
29	chr15:52687000-52714800	Weak transcription	Psoas Muscle	Psoas
30	chr15:52687000-52715000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr15:52687200-52706200	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr15:52689600-52707400	Weak transcription	Fetal Heart	heart
33	chr15:52689600-52730200	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chr15:52689600-52730200	Weak transcription	Left Ventricle	heart
35	chr15:52689600-52730400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
36	chr15:52689800-52703000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr15:52689800-52706800	Weak transcription	HSMMtube	muscle
38	chr15:52694000-52702800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr15:52694400-52702600	Strong transcription	Primary neutrophils fromperipheralblood	blood
40	chr15:52695200-52703400	Strong transcription	Primary B cells from peripheral blood	blood
41	chr15:52696000-52730200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr15:52696200-52719800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr15:52697000-52709800	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr15:52697200-52703800	Weak transcription	Rectal Smooth Muscle	rectum
45	chr15:52697200-52715000	Weak transcription	Skeletal Muscle Male	skeletal muscle
46	chr15:52697200-52718400	Weak transcription	Dnd41	blood
47	chr15:52697200-52720000	Weak transcription	Ovary	ovary
48	chr15:52697200-52730000	Weak transcription	Brain Inferior Temporal Lobe	brain
49	chr15:52697200-52730400	Weak transcription	Stomach Smooth Muscle	stomach
50	chr15:52697200-52738600	Weak transcription	Fetal Brain Female	brain

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