Variant report

Variant	rs72730744
Chromosome Location	chr15:78099752-78099753
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:78097066..78100710-chr15:78102142..78106147,5	K562	blood:
2	chr15:78099210..78100960-chr15:78102155..78104684,2	K562	blood:
3	chr15:78097737..78099826-chr15:78103179..78105100,2	MCF-7	breast:

Extended variants
information (count: 61 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs11072672	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11072677	0.94[ASN][1000 genomes]
rs11072678	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11852404	0.90[ASN][1000 genomes]
rs11852704	0.94[ASN][1000 genomes]
rs11855944	0.90[ASN][1000 genomes]
rs11857499	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11857839	0.94[ASN][1000 genomes]
rs11857968	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11858003	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12441624	0.90[ASN][1000 genomes]
rs12441953	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12906902	0.90[ASN][1000 genomes]
rs12911998	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12912051	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12914963	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs34000202	0.90[ASN][1000 genomes]
rs35265558	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs35487286	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35840713	0.81[EUR][1000 genomes]
rs35977825	0.81[EUR][1000 genomes]
rs36055448	0.81[ASN][1000 genomes]
rs4075024	0.94[ASN][1000 genomes]
rs4075981	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4304989	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4886913	0.86[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4886916	0.90[ASN][1000 genomes]
rs4886923	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4886925	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4886940	0.86[EUR][1000 genomes]
rs4886945	0.86[EUR][1000 genomes]
rs56061966	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs58455314	0.83[AFR][1000 genomes]
rs60777884	0.82[AFR][1000 genomes]
rs61085022	0.82[AFR][1000 genomes]
rs7164311	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7170767	0.90[ASN][1000 genomes]
rs7175762	0.90[ASN][1000 genomes]
rs7175927	0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7181312	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7182069	0.90[ASN][1000 genomes]
rs72730767	0.86[EUR][1000 genomes]
rs72730772	0.86[EUR][1000 genomes]
rs72730774	0.86[EUR][1000 genomes]
rs72730775	0.83[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1040852	chr15:77160237-78137541	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv916323	chr15:77485765-78121259	Enhancers Strong transcription Weak transcription Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	esv1806097	chr15:77817889-78301377	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
4	nsv529491	chr15:77932659-78751516	Genic enhancers Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
5	nsv833061	chr15:77998374-78121905	Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv833062	chr15:78035206-78220358	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv904421	chr15:78041789-78129964	Bivalent Enhancer Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv904422	chr15:78055479-78106177	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv904423	chr15:78059488-78119345	Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Enhancers Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv904424	chr15:78059488-78158893	Enhancers Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv471255	chr15:78063585-78131097	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv570171	chr15:78064664-78131097	Bivalent Enhancer Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv904425	chr15:78064664-78153850	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
14	esv1833316	chr15:78081307-78328108	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
15	nsv570172	chr15:78088127-78111702	Bivalent Enhancer ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
16	nsv904426	chr15:78090630-78264164	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78074400-78100800	Weak transcription	Fetal Intestine Small	intestine
2	chr15:78092800-78101200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr15:78094200-78102400	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr15:78096600-78104200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr15:78096800-78102600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr15:78097200-78100800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr15:78097200-78101400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr15:78097400-78102000	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr15:78098800-78101000	Enhancers	Brain Cingulate Gyrus	brain
10	chr15:78099000-78099800	Bivalent Enhancer	Fetal Muscle Leg	muscle
11	chr15:78099000-78102400	Enhancers	Fetal Brain Male	brain
12	chr15:78099200-78100800	Enhancers	Fetal Brain Female	brain
13	chr15:78099200-78100800	Enhancers	Ovary	ovary
14	chr15:78099200-78102800	Weak transcription	Gastric	stomach
15	chr15:78099400-78099800	Enhancers	A549	lung
16	chr15:78099400-78101200	Enhancers	Brain Hippocampus Middle	brain
17	chr15:78099600-78100800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr15:78099600-78100800	Enhancers	Fetal Stomach	stomach
19	chr15:78099600-78101400	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr15:78099600-78101600	Enhancers	Brain Angular Gyrus	brain
21	chr15:78099600-78102400	Weak transcription	Fetal Heart	heart
22	chr15:78099600-78104200	Enhancers	Fetal Muscle Trunk	muscle

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