Variant report

Variant	rs8038115
Chromosome Location	chr15:77203340-77203341
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	chr15:77200931..77204903-chr15:77206482..77209699,4	K562	blood:
2	chr15:77202308..77207759-chr15:77221259..77225491,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000117906	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs11852605	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs11852935	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11854018	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs11854604	1.00[AMR][1000 genomes]
rs11855062	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11855359	1.00[AMR][1000 genomes]
rs11855501	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs11855827	1.00[LWK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11856288	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs11857316	1.00[AMR][1000 genomes]
rs11857437	1.00[AMR][1000 genomes]
rs11857794	1.00[AMR][1000 genomes]
rs11857800	1.00[AMR][1000 genomes]
rs11858343	0.86[AFR][1000 genomes]
rs11858497	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35402111	1.00[AMR][1000 genomes]
rs6495215	1.00[AMR][1000 genomes]
rs7164979	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs7166387	1.00[AMR][1000 genomes]
rs7169383	1.00[AMR][1000 genomes]
rs7169613	1.00[AMR][1000 genomes]
rs7170490	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7171670	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs7171966	1.00[AMR][1000 genomes]
rs7182749	1.00[AMR][1000 genomes]
rs73457178	1.00[AMR][1000 genomes]
rs8028181	1.00[AMR][1000 genomes]
rs8032135	1.00[AMR][1000 genomes]
rs8037292	1.00[AMR][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	esv3440794	chr15:76764595-77571114	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	esv3367577	chr15:77015618-77442634	Genic enhancers Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	esv1803942	chr15:77151005-77210457	Active TSS Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	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
5	esv2758388	chr15:77170550-77373448	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
6	esv2760041	chr15:77170550-77373448	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77198400-77203800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr15:77198800-77203600	Weak transcription	Placenta	Placenta

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