Variant report

Variant	rs28503184
Chromosome Location	chr15:77936217-77936218
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RAD21	chr15:77935884-77936227	H1-hESC	embryonic stem cell:	n/a	chr15:77936049-77936062 chr15:77936051-77936063 chr15:77936046-77936065 chr15:77936051-77936061 chr15:77936117-77936136
2	CTCF	chr15:77935785-77936343	MCF-7	breast:	n/a	chr15:77936048-77936061 chr15:77936045-77936063 chr15:77936119-77936137 chr15:77936008-77936016 chr15:77936121-77936134
3	CTCF	chr15:77935938-77936318	MCF-7	breast:	n/a	chr15:77936048-77936061 chr15:77936045-77936063 chr15:77936119-77936137 chr15:77936008-77936016 chr15:77936121-77936134

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:77917075..77919713-chr15:77934421..77936689,2	MCF-7	breast:
2	chr15:77922761..77925687-chr15:77933695..77936379,3	K562	blood:

Variant related genes	Relation type
ENSG00000259666	TF binding region
ENSG00000169783	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs11630768	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11633639	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11634778	0.87[ASN][1000 genomes]
rs11635239	0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11638318	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11854903	0.83[AFR][1000 genomes]
rs11855155	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13329256	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13329323	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16969027	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1877298	0.83[AFR][1000 genomes]
rs1995972	0.83[AFR][1000 genomes]
rs2292415	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2292416	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2292417	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28374408	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28515899	0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs28649029	0.81[AFR][1000 genomes]
rs56717248	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56941158	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60886924	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs74025333	0.95[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs74025334	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74025342	0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs74025352	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8026671	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8028788	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9652488	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9806280	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9972481	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 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	nsv904415	chr15:77845959-77943935	Weak transcription Flanking Active TSS Strong transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv904416	chr15:77845959-77967416	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv904418	chr15:77851535-77963887	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv904419	chr15:77897197-77943935	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	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

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77927200-77940600	Weak transcription	Right Atrium	heart
2	chr15:77933200-77937000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:77933800-77936600	Enhancers	Fetal Muscle Leg	muscle
4	chr15:77934000-77936800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
5	chr15:77934200-77939200	Weak transcription	Fetal Intestine Small	intestine
6	chr15:77934800-77942600	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr15:77935000-77937800	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr15:77935800-77936800	Weak transcription	Fetal Brain Female	brain
9	chr15:77935800-77940800	Weak transcription	Rectal Mucosa Donor 29	rectum
10	chr15:77935800-77942600	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr15:77936000-77936400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr15:77936000-77936800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr15:77936000-77937000	Bivalent Enhancer	HepG2	liver
14	chr15:77936200-77936400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr15:77936200-77936400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr15:77936200-77938600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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