Variant report

Variant	rs524908
Chromosome Location	chr15:44187991-44187992
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:44185248..44189822-chr15:44193811..44195914,4	K562	blood:

Extended variants
information (count: 91 )
Associated
traits (count: 14 )

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs10163054	0.95[CHB][hapmap];0.92[CHD][hapmap]
rs10438303	1.00[CHB][hapmap];0.94[CHD][hapmap]
rs1053492	1.00[CEU][hapmap]
rs11070408	1.00[CHB][hapmap];0.94[CHD][hapmap];0.84[JPT][hapmap]
rs11070410	0.85[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.90[TSI][hapmap]
rs11638972	1.00[CEU][hapmap]
rs11852767	0.91[ASN][1000 genomes]
rs11856495	0.85[ASN][1000 genomes]
rs11856795	1.00[CHB][hapmap];0.97[CHD][hapmap];0.88[ASN][1000 genomes]
rs12440573	1.00[CHB][hapmap];0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs12441127	1.00[CHB][hapmap]
rs12441861	1.00[CHB][hapmap];0.94[CHD][hapmap]
rs12441984	1.00[CHB][hapmap];0.84[JPT][hapmap];0.86[ASN][1000 genomes]
rs12702	1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs16944774	0.80[JPT][hapmap]
rs16950562	1.00[CHB][hapmap]
rs16965120	1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap]
rs16977724	1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap];0.86[ASN][1000 genomes]
rs16977798	1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap];0.86[ASN][1000 genomes]
rs1965795	0.86[ASN][1000 genomes]
rs2228368	0.81[ASN][1000 genomes]
rs2277531	1.00[CHB][hapmap]
rs2412823	0.81[CEU][hapmap]
rs2467402	0.95[CHB][hapmap];0.94[CHD][hapmap]
rs2788	1.00[CHB][hapmap];0.94[CHD][hapmap]
rs28413704	0.86[ASN][1000 genomes]
rs28437196	0.86[ASN][1000 genomes]
rs28476182	0.84[ASN][1000 genomes]
rs28509275	1.00[CHB][hapmap];0.97[CHD][hapmap]
rs28513374	1.00[CHB][hapmap];0.86[ASN][1000 genomes]
rs28519630	0.86[ASN][1000 genomes]
rs28524541	0.86[ASN][1000 genomes]
rs28531819	0.86[ASN][1000 genomes]
rs28564774	0.86[ASN][1000 genomes]
rs28583806	0.81[ASN][1000 genomes]
rs28590651	0.83[ASN][1000 genomes]
rs28636829	1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap];0.82[ASN][1000 genomes]
rs28679673	0.86[ASN][1000 genomes]
rs28684672	1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs28687459	0.86[ASN][1000 genomes]
rs28696802	0.86[ASN][1000 genomes]
rs28707214	0.86[ASN][1000 genomes]
rs28780699	0.86[ASN][1000 genomes]
rs28823973	0.91[ASN][1000 genomes]
rs28858500	0.90[ASN][1000 genomes]
rs28866846	0.88[ASN][1000 genomes]
rs2927085	0.86[CEU][hapmap]
rs2955969	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap];0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs3087657	0.92[ASW][hapmap];1.00[CEU][hapmap];0.81[MKK][hapmap];0.90[TSI][hapmap]
rs3736180	1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs3742982	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs3759790	1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap];0.86[ASN][1000 genomes]
rs3759791	0.95[CHB][hapmap];0.97[CHD][hapmap];0.84[JPT][hapmap];0.80[ASN][1000 genomes]
rs3816792	0.95[CHB][hapmap];0.97[CHD][hapmap];0.83[ASN][1000 genomes]
rs3825783	1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs3862142	1.00[CHB][hapmap];0.91[CHD][hapmap]
rs472385	0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs4997480	1.00[CHB][hapmap]
rs533143	0.85[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.82[GIH][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.87[MKK][hapmap];0.85[TSI][hapmap];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56909447	0.86[ASN][1000 genomes]
rs575082	0.80[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap];0.81[MKK][hapmap];0.93[TSI][hapmap];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs602370	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs61390361	0.88[ASN][1000 genomes]
rs663214	0.92[ASW][hapmap];1.00[CEU][hapmap];0.82[MKK][hapmap];0.93[TSI][hapmap]
rs667476	0.91[CEU][hapmap];0.95[CHB][hapmap];0.84[JPT][hapmap];0.83[YRI][hapmap];0.84[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs68079546	0.86[ASN][1000 genomes]
rs686666	0.95[CEU][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs688009	0.95[CEU][hapmap];1.00[CHB][hapmap];0.83[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs693919	0.80[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap];0.88[TSI][hapmap];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs694461	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap];0.93[TSI][hapmap];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7169322	1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap];0.85[ASN][1000 genomes]
rs7169382	0.81[ASN][1000 genomes]
rs7169988	0.90[CHB][hapmap]
rs7171750	1.00[CHB][hapmap]
rs7174208	1.00[CHB][hapmap]
rs7175032	1.00[CHB][hapmap];0.94[CHD][hapmap]
rs7175129	1.00[CEU][hapmap];1.00[CHB][hapmap]
rs7179388	0.86[ASN][1000 genomes]
rs7183809	0.86[ASN][1000 genomes]
rs8023458	1.00[CHB][hapmap];0.94[CHD][hapmap]
rs8023508	1.00[CHB][hapmap];1.00[CHD][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs8032649	1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap];0.86[ASN][1000 genomes]
rs8040839	0.84[ASN][1000 genomes]
rs9944216	1.00[CHB][hapmap];0.91[CHD][hapmap];0.88[ASN][1000 genomes]
rs9989313	1.00[CHB][hapmap];1.00[CHD][hapmap];0.84[JPT][hapmap];0.86[ASN][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	nsv1037786	chr15:43888926-44318587	Weak transcription Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
2	nsv542370	chr15:43888926-44318587	Weak transcription Genic enhancers Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
3	nsv431387	chr15:43929378-44862930	Weak transcription Strong transcription Active TSS ZNF genes & repeats Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer 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	158 gene(s)	inside rSNPs	diseases
4	nsv931051	chr15:43988761-44833518	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	154 gene(s)	inside rSNPs	diseases
5	nsv1050263	chr15:44093927-44204047	Strong transcription Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	n/a
6	nsv1044435	chr15:44176103-44507403	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

mRNA abundance (count:14)

SNP	Gene	Cis/trans	Tissue	Source
rs524908	TGM5	cis	Lymphoblastoid	GTEx
rs524908	WDR76	cis	parietal	SCAN
rs524908	DUOX2	cis	parietal	SCAN
rs524908	AC011330.5	cis	Thyroid	GTEx
rs524908	NAP1L2	trans	lymphoblastoid	seeQTL
rs524908	CKMT1A	cis	Esophagus Mucosa	GTEx
rs524908	SERF2	cis	lymphoblastoid	seeQTL
rs524908	ZSCAN29	cis	Thyroid	GTEx
rs524908	ELL3	cis	multi-tissue	Pritchard
rs524908	STRCP1	cis	Whole Blood	GTEx
rs524908	STRC	cis	multi-tissue	Pritchard
rs524908	ZNF690	cis	multi-tissue	Pritchard
rs524908	ADAL	cis	parietal	SCAN
rs524908	TGM5	cis	lymphoblastoid	seeQTL

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:44156800-44206400	Weak transcription	Fetal Brain Male	brain
2	chr15:44166800-44193800	Weak transcription	Spleen	Spleen
3	chr15:44166800-44196200	Weak transcription	Osteobl	bone
4	chr15:44170600-44188800	Weak transcription	NHDF-Ad	bronchial
5	chr15:44173600-44208000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr15:44173800-44190000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr15:44173800-44193600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr15:44173800-44211600	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr15:44174200-44194200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr15:44174200-44195800	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr15:44174200-44195800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr15:44174200-44211600	Weak transcription	H1 Cell Line	embryonic stem cell
13	chr15:44176600-44192000	Weak transcription	Hela-S3	cervix
14	chr15:44176800-44193600	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr15:44177200-44192000	Weak transcription	A549	lung
16	chr15:44177200-44192800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr15:44178200-44197800	Weak transcription	NHLF	lung
18	chr15:44178400-44189400	Enhancers	Fetal Heart	heart
19	chr15:44179000-44192000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr15:44179400-44193600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr15:44180000-44195800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr15:44180800-44192400	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr15:44183200-44193000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr15:44183400-44191800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr15:44183400-44197800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr15:44184000-44188800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr15:44184000-44194200	Weak transcription	HUVEC	blood vessel
28	chr15:44184400-44190400	Weak transcription	Brain Germinal Matrix	brain
29	chr15:44184600-44188400	Weak transcription	Fetal Brain Female	brain
30	chr15:44184800-44190800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr15:44185000-44188400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr15:44185200-44188000	Enhancers	Left Ventricle	heart
33	chr15:44185400-44188000	Enhancers	HSMMtube	muscle
34	chr15:44185400-44188400	Enhancers	Pancreas	Pancrea
35	chr15:44185600-44188200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
36	chr15:44185600-44188200	Enhancers	Stomach Smooth Muscle	stomach
37	chr15:44186000-44188000	Weak transcription	Right Atrium	heart
38	chr15:44186200-44193200	Weak transcription	HMEC	breast
39	chr15:44186200-44197800	Weak transcription	NHEK	skin
40	chr15:44186400-44190600	Weak transcription	Ovary	ovary
41	chr15:44186400-44191000	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr15:44186600-44188600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr15:44186600-44192000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr15:44186800-44188400	Weak transcription	Brain Hippocampus Middle	brain
45	chr15:44186800-44188600	Weak transcription	Brain Inferior Temporal Lobe	brain
46	chr15:44186800-44189000	Weak transcription	HSMM	muscle
47	chr15:44186800-44190600	Weak transcription	Fetal Stomach	stomach
48	chr15:44187000-44188800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr15:44187000-44188800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr15:44187000-44190600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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