Variant report

Variant	rs707885
Chromosome Location	chr6:24224676-24224677
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs11754526	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11755011	1.00[ASN][1000 genomes]
rs11759157	0.83[ASN][1000 genomes]
rs12153942	0.83[CHB][hapmap];0.90[JPT][hapmap]
rs1340696	0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1417215	0.98[ASN][1000 genomes]
rs1615548	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1620407	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1621975	0.98[ASN][1000 genomes]
rs16888894	0.93[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs16888905	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1770461	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1770906	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1770908	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1770909	0.84[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1856837	0.98[ASN][1000 genomes]
rs2050820	0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55798554	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57859236	0.98[ASN][1000 genomes]
rs58339591	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6921861	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73394023	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73394032	0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs73394036	0.80[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73726623	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs73726632	0.86[ASN][1000 genomes]
rs73726634	0.84[ASN][1000 genomes]
rs7747779	0.83[AFR][1000 genomes]
rs793833	0.93[AFR][1000 genomes]
rs793834	0.84[ASN][1000 genomes]
rs793837	0.83[AFR][1000 genomes]
rs793857	0.91[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs793861	0.81[JPT][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	nsv1029930	chr6:23481989-24289948	Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv427746	chr6:24221299-24305709	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24206200-24231400	Weak transcription	Fetal Intestine Small	intestine
2	chr6:24206800-24227600	Weak transcription	Fetal Kidney	kidney
3	chr6:24214600-24235400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:24217800-24231600	Weak transcription	Rectal Smooth Muscle	rectum
5	chr6:24223800-24224800	Genic enhancers	HepG2	liver
6	chr6:24224600-24225000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:24224600-24225000	Enhancers	Pancreas	Pancrea

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