Variant report

Variant	rs9638846
Chromosome Location	chr7:27753692-27753693
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:27746088..27747969-chr7:27753217..27755020,2	MCF-7	breast:
2	chr7:27751979..27753711-chr7:27767653..27770152,2	MCF-7	breast:
3	chr7:27747436..27749954-chr7:27752214..27754351,3	K562	blood:
4	chr7:27747506..27749954-chr7:27752851..27754917,2	K562	blood:

Extended variants
information (count: 30 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs11763499	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11766320	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11973028	0.81[CHB][hapmap]
rs17155666	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17611937	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17685046	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2108309	0.83[CHB][hapmap];0.80[ASN][1000 genomes]
rs2237337	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs2285930	0.84[CEU][hapmap]
rs2391486	0.89[EUR][1000 genomes]
rs55714615	0.86[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs55738305	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56137979	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs61538692	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62449631	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs62454807	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62454947	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6462043	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6950949	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6957836	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6958125	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6974060	0.94[EUR][1000 genomes]
rs6974991	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7808062	0.91[EUR][1000 genomes]
rs960293	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs960294	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9638847	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9639563	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9639564	1.00[CEU][hapmap];0.93[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949025	chr7:27578167-28075172	Active TSS Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs9638846	TAX1BP1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:27749400-27755000	Weak transcription	Small Intestine	intestine
2	chr7:27749600-27754400	Weak transcription	HMEC	breast
3	chr7:27749800-27754400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr7:27750000-27753800	Weak transcription	HUVEC	blood vessel
5	chr7:27750000-27754200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr7:27750000-27754200	Weak transcription	NH-A	brain
7	chr7:27750000-27754400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr7:27750200-27753800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr7:27750200-27753800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr7:27750200-27754000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr7:27751200-27756800	Enhancers	HepG2	liver
12	chr7:27751400-27755600	Enhancers	Fetal Intestine Large	intestine
13	chr7:27751400-27756400	Enhancers	Fetal Intestine Small	intestine
14	chr7:27753600-27755200	Enhancers	Duodenum Mucosa	Duodenum

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