Variant report

Variant	rs12439483
Chromosome Location	chr15:35472043-35472044
allele	A/G
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	MAFF	chr15:35471982-35472272	HepG2	liver:	n/a	chr15:35472132-35472150
2	MAFK	chr15:35472031-35472268	IMR90	lung:	n/a	chr15:35472137-35472148 chr15:35472133-35472148 chr15:35472138-35472149 chr15:35472136-35472150 chr15:35472129-35472146 chr15:35472133-35472149 chr15:35472138-35472149
3	MAFF	chr15:35472016-35472271	K562	blood:	n/a	chr15:35472132-35472150
4	MAFK	chr15:35471981-35472258	HepG2	liver:	n/a	chr15:35472137-35472148 chr15:35472133-35472148 chr15:35472138-35472149 chr15:35472136-35472150 chr15:35472129-35472146 chr15:35472133-35472149 chr15:35472138-35472149
5	MAFK	chr15:35471967-35472244	K562	blood:	n/a	chr15:35472137-35472148 chr15:35472133-35472148 chr15:35472138-35472149 chr15:35472136-35472150 chr15:35472129-35472146 chr15:35472133-35472149 chr15:35472138-35472149

No.	Distal block	Cell Line	Cell type
1	chr15:35470643..35473276-chr15:35479917..35482066,2	K562	blood:
2	chr15:35466950..35469719-chr15:35470407..35472296,2	K562	blood:
3	chr15:35470907..35473908-chr15:35474557..35477034,3	K562	blood:

Variant related genes	Relation type
ANP32AP1	TF binding region

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10444865	0.98[ASN][1000 genomes]
rs11073085	0.81[EUR][1000 genomes]
rs11632681	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11635872	0.99[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12232307	0.97[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12591832	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12900262	0.89[ASN][1000 genomes]
rs12906317	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12911934	1.00[JPT][hapmap]
rs12917029	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13313465	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1380089	0.89[EUR][1000 genomes]
rs1458883	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs16960582	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs16960585	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1903077	0.86[EUR][1000 genomes]
rs2166157	0.97[AMR][1000 genomes];0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28448413	0.87[ASN][1000 genomes]
rs4597271	0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4923912	0.81[EUR][1000 genomes]
rs4924584	0.86[ASN][1000 genomes]
rs4924607	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59469657	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59766603	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62006772	0.85[ASN][1000 genomes]
rs67156387	0.92[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs8024405	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8026065	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8027994	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8031065	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs9972525	0.97[AMR][1000 genomes];1.00[ASN][1000 genomes]

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	esv3350109	chr15:34668106-35534229	Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv904073	chr15:35467096-35686267	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:35458800-35473200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr15:35466000-35473400	Weak transcription	NHLF	lung
3	chr15:35470800-35473400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr15:35471600-35472200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr15:35471800-35472200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr15:35471800-35472200	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr15:35472000-35472200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr15:35472000-35472200	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr15:35472000-35472600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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