Variant report

Variant	rs8026404
Chromosome Location	chr15:59997696-59997697
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:59997520..59998026-chr19:1268910..1269742,2	Hela-S3	cervix:
2	chr15:59992550..59995081-chr15:59995698..59998010,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000099622	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs11629681	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11634157	0.96[CEU][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12161993	0.87[YRI][hapmap]
rs12438078	0.96[CEU][hapmap];0.86[TSI][hapmap];0.87[EUR][1000 genomes]
rs12439645	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12439658	0.83[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12439707	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12442896	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12443297	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12904505	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs16941544	0.81[YRI][hapmap]
rs17191002	0.86[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17236867	0.85[EUR][1000 genomes]
rs17302608	0.88[YRI][hapmap]
rs1871504	0.85[CEU][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2306357	0.88[CEU][hapmap]
rs3087328	0.84[CEU][hapmap];0.86[TSI][hapmap]
rs3843695	0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3848119	0.86[EUR][1000 genomes]
rs3936513	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4775200	0.96[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6151441	0.96[CEU][hapmap];0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6151443	0.80[LWK][hapmap];1.00[YRI][hapmap]
rs6151446	0.96[CEU][hapmap]
rs6151447	0.92[CEU][hapmap]
rs6151448	0.95[CEU][hapmap]
rs6151449	0.92[CEU][hapmap]
rs6151450	0.91[CEU][hapmap]
rs6151457	0.81[YRI][hapmap]
rs6494139	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs6494140	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7162645	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7173534	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7173827	0.88[CEU][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs7178211	0.88[CEU][hapmap];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs754642	0.87[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv527307	chr15:59103328-60018487	Enhancers Genic enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	145 gene(s)	inside rSNPs	diseases
2	nsv533240	chr15:59858093-59998176	Flanking Active TSS Strong transcription Enhancers Weak transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs8026404	GTF2A2	cis	parietal	SCAN
rs8026404	GTF2A2	Cis_1M	lymphoblastoid	RTeQTL
rs8026404	GTF2A2	cis	cerebellum	SCAN

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:59989800-59998400	Enhancers	Hela-S3	cervix
2	chr15:59993000-59998000	Weak transcription	HMEC	breast
3	chr15:59994400-59997800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr15:59996600-59997800	Weak transcription	A549	lung
5	chr15:59997400-59998200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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