Variant report

Variant	rs11636649
Chromosome Location	chr15:78031458-78031459
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:78021356..78025369-chr15:78027266..78032240,6	K562	blood:
2	chr15:78029860..78033858-chr15:78038839..78041859,3	K562	blood:
3	chr15:78025745..78027955-chr15:78030465..78032674,2	K562	blood:
4	chr15:78029999..78032267-chr15:78076792..78079270,2	MCF-7	breast:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10851896	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10851897	0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11072664	0.90[EUR][1000 genomes]
rs11072670	0.90[ASN][1000 genomes]
rs11630598	0.90[EUR][1000 genomes]
rs11631237	0.89[ASN][1000 genomes]
rs11636173	0.87[ASN][1000 genomes]
rs11637968	0.90[ASN][1000 genomes]
rs12438542	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12442435	0.81[ASN][1000 genomes]
rs3935682	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3935683	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3935684	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3935685	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs3935831	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4072803	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4076998	0.80[ASN][1000 genomes]
rs4468571	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4886901	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4886904	0.87[AFR][1000 genomes];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58619842	0.90[ASN][1000 genomes]
rs58813188	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs58831466	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs60917280	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61331678	0.90[EUR][1000 genomes]
rs62007780	0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62007781	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs62007784	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62009151	0.90[EUR][1000 genomes]
rs67133828	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs72730707	0.81[ASN][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	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	nsv833060	chr15:77816654-78035204	Weak transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
4	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
5	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
6	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
7	nsv570150	chr15:78004743-78038124	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	nsv904420	chr15:78025267-78078903	Weak transcription Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78029800-78031600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
2	chr15:78029800-78032800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:78030000-78031600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
4	chr15:78030200-78033800	Enhancers	H1 Cell Line	embryonic stem cell
5	chr15:78030400-78032000	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr15:78030400-78032800	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr15:78030600-78033400	Enhancers	K562	blood
8	chr15:78031000-78031600	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr15:78031000-78031600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr15:78031000-78032000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr15:78031000-78032400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
12	chr15:78031000-78032600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr15:78031000-78032600	Enhancers	Brain Germinal Matrix	brain
14	chr15:78031200-78031600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
15	chr15:78031200-78031600	Enhancers	Gastric	stomach
16	chr15:78031200-78031600	Enhancers	Lung	lung
17	chr15:78031200-78032200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
18	chr15:78031200-78032200	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr15:78031200-78032400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr15:78031200-78032400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
21	chr15:78031200-78032600	Enhancers	Fetal Brain Female	brain
22	chr15:78031400-78031600	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr15:78031400-78031800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
24	chr15:78031400-78031800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
25	chr15:78031400-78031800	Bivalent Enhancer	Fetal Stomach	stomach
26	chr15:78031400-78032000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
27	chr15:78031400-78032200	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr15:78031400-78032400	Bivalent Enhancer	Fetal Muscle Leg	muscle
29	chr15:78031400-78032400	Weak transcription	Spleen	Spleen
30	chr15:78031400-78033000	Enhancers	Fetal Brain Male	brain

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