Variant report

Variant	rs6731242
Chromosome Location	chr2:234578693-234578694
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:234577799..234579592-chr2:234583305..234585773,2	K562	blood:

Extended variants
information (count: 30 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10929251	0.94[CEU][hapmap];0.82[JPT][hapmap];0.81[ASN][1000 genomes]
rs10929252	0.94[CEU][hapmap];0.82[JPT][hapmap];0.81[ASN][1000 genomes]
rs1113193	0.81[CHD][hapmap];0.82[JPT][hapmap]
rs12053462	0.84[TSI][hapmap]
rs12472689	0.84[TSI][hapmap]
rs12474980	0.84[TSI][hapmap]
rs12476197	0.84[TSI][hapmap]
rs12479240	0.82[JPT][hapmap];0.82[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs17854828	0.94[CEU][hapmap];1.00[CHD][hapmap];0.82[JPT][hapmap];0.81[ASN][1000 genomes]
rs17862847	0.94[CEU][hapmap];1.00[CHD][hapmap];0.82[JPT][hapmap];0.81[ASN][1000 genomes]
rs17862857	0.81[TSI][hapmap]
rs17863766	0.88[CEU][hapmap]
rs17863773	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17864684	1.00[CEU][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17868325	0.84[TSI][hapmap]
rs1823803	0.82[JPT][hapmap]
rs1901813	0.81[CHD][hapmap];0.82[JPT][hapmap]
rs2248733	0.94[CEU][hapmap];0.82[JPT][hapmap];0.81[ASN][1000 genomes]
rs4114768	0.81[ASN][1000 genomes]
rs4485562	0.84[TSI][hapmap]
rs6706988	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.89[TSI][hapmap];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6713902	0.82[JPT][hapmap]
rs6728792	0.82[JPT][hapmap]
rs7608713	0.81[CHD][hapmap];0.82[JPT][hapmap]

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	nsv529419	chr2:234229606-234670426	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
2	nsv876013	chr2:234338227-234579915	Weak transcription Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
3	nsv428072	chr2:234393609-234624769	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
4	nsv876015	chr2:234518011-234579915	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	9 gene(s)	inside rSNPs	diseases
5	nsv1010936	chr2:234549011-234640221	Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
6	nsv1013712	chr2:234558457-235495825	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs6731242	SPP2	cis	parietal	SCAN
rs6731242	FBXO36	cis	parietal	SCAN
rs6731242	USP40	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:234554600-234587800	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr2:234559800-234592800	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr2:234577400-234579800	Enhancers	Liver	Liver

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