Variant report

Variant	rs8025968
Chromosome Location	chr15:77839616-77839617
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr15:77838960..77839788-chr15:77925715..77926415,4	MCF-7	breast:
2	chr15:77839042..77839906-chr15:77876314..77877043,2	MCF-7	breast:
3	chr15:77837272..77839702-chr15:77860514..77863715,3	MCF-7	breast:
4	chr15:77837146..77840341-chr15:77840841..77844639,4	K562	blood:
5	chr15:77838034..77840169-chr15:77924048..77926294,2	K562	blood:
6	chr15:77839369..77839946-chr15:77923059..77923563,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000169783	Chromatin interaction
ENSG00000259420	Chromatin interaction

Extended variants
information (count: 98 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:91)

rs_ID	r²[population]
rs11630540	0.97[ASN][1000 genomes]
rs11630557	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11630916	0.81[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11630926	0.89[ASN][1000 genomes]
rs11631274	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11634174	0.88[CEU][hapmap];0.84[JPT][hapmap]
rs11635226	0.83[EUR][1000 genomes]
rs11635567	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11635606	0.89[ASN][1000 genomes]
rs11636231	0.83[EUR][1000 genomes]
rs11636529	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11637932	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11639293	0.88[CEU][hapmap];0.84[JPT][hapmap]
rs12898370	0.88[CEU][hapmap]
rs12898656	0.88[CEU][hapmap]
rs12899390	0.91[ASN][1000 genomes]
rs12901100	0.90[ASN][1000 genomes]
rs12901471	0.88[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12901732	0.83[CEU][hapmap];1.00[CHB][hapmap];0.81[JPT][hapmap];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12901765	0.91[ASN][1000 genomes]
rs12901998	0.80[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs12902072	1.00[CEU][hapmap];0.92[CHB][hapmap];0.92[JPT][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12902379	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12902698	0.82[CEU][hapmap];0.81[JPT][hapmap]
rs12902896	0.88[CEU][hapmap]
rs12902898	1.00[CEU][hapmap];0.92[CHB][hapmap];0.92[JPT][hapmap];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12902925	0.81[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12902948	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12904200	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12904208	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12904212	0.87[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.91[ASN][1000 genomes]
rs12904254	0.88[JPT][hapmap]
rs12904348	0.86[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.91[ASN][1000 genomes]
rs12904533	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12904584	0.91[ASN][1000 genomes]
rs12904709	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12904823	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12905044	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12905318	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12909292	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12909645	0.88[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12909808	0.88[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12910512	0.91[ASN][1000 genomes]
rs12910513	0.91[ASN][1000 genomes]
rs12910594	0.88[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.91[ASN][1000 genomes]
rs12910951	0.88[CEU][hapmap];0.82[CHB][hapmap]
rs12910975	0.88[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.91[ASN][1000 genomes]
rs12911649	0.88[CEU][hapmap]
rs12911854	0.87[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.91[ASN][1000 genomes]
rs12911963	0.88[CEU][hapmap]
rs12912386	0.81[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.91[ASN][1000 genomes]
rs12913005	0.83[EUR][1000 genomes]
rs12914098	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12914932	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12915057	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12915548	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12916515	0.88[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12916642	0.88[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12916682	0.88[CEU][hapmap]
rs12916822	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12916833	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12916973	0.88[CEU][hapmap]
rs12917044	1.00[CEU][hapmap];0.92[JPT][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12917175	0.88[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12917314	0.88[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12917431	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17394732	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs34020536	0.89[ASN][1000 genomes]
rs34075648	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34607443	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs34829483	0.81[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs35577135	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35657172	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs55883527	0.83[EUR][1000 genomes]
rs59418918	0.97[ASN][1000 genomes]
rs62009067	0.89[ASN][1000 genomes]
rs62009069	0.91[ASN][1000 genomes]
rs62009071	0.87[ASN][1000 genomes]
rs62009087	0.97[ASN][1000 genomes]
rs7176307	0.88[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7176875	0.96[ASN][1000 genomes]
rs7180732	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7181283	0.88[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];0.91[ASN][1000 genomes]
rs8032405	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8033067	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8033654	0.81[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs8040318	0.88[CEU][hapmap]
rs8040702	0.88[CEU][hapmap]
rs8041398	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8041520	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8042307	0.88[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:7 , 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	nsv1043284	chr15:77740632-77884026	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	nsv570139	chr15:77762493-77865459	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
5	nsv570140	chr15:77787469-77851535	Flanking Active TSS Weak transcription Active TSS Enhancers Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
6	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
7	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

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs8025968	RP11-307C19.1	cis	Heart Left Ventricle	GTEx

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77827000-77845400	Weak transcription	Fetal Kidney	kidney
2	chr15:77829400-77844800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr15:77833800-77843200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr15:77834000-77841200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr15:77834200-77840800	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr15:77836200-77840400	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr15:77836200-77841000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
8	chr15:77836200-77841000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr15:77836200-77841000	Weak transcription	Fetal Thymus	thymus
10	chr15:77836200-77841200	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr15:77836200-77841200	Weak transcription	K562	blood
12	chr15:77836200-77841400	Weak transcription	Brain Anterior Caudate	brain
13	chr15:77836200-77846600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr15:77837000-77840400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr15:77837800-77839800	Enhancers	Fetal Heart	heart
16	chr15:77838000-77839800	Enhancers	Right Ventricle	heart
17	chr15:77838600-77840800	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr15:77838600-77849800	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr15:77838800-77843400	Weak transcription	Placenta Amnion	Placenta Amnion
20	chr15:77838800-77849000	Weak transcription	Gastric	stomach
21	chr15:77839000-77840400	Weak transcription	Primary hematopoietic stem cells	blood
22	chr15:77839000-77840800	Weak transcription	Placenta	Placenta
23	chr15:77839000-77841200	Weak transcription	Spleen	Spleen
24	chr15:77839000-77842800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr15:77839000-77842800	Weak transcription	HSMMtube	muscle
26	chr15:77839000-77843000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr15:77839000-77844400	Weak transcription	Stomach Mucosa	stomach
28	chr15:77839600-77840000	Genic enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr15:77839600-77840000	ZNF genes & repeats	Brain Hippocampus Middle	brain

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