Variant report

Variant	rs1505258
Chromosome Location	chr1:75802788-75802789
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	chr1:75802617..75804536-chr1:75804779..75807311,2	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs1004053	0.91[CHB][hapmap];0.91[JPT][hapmap];0.96[ASN][1000 genomes]
rs10493571	0.85[CEU][hapmap];0.83[CHB][hapmap];0.88[ASN][1000 genomes]
rs10493573	0.81[CEU][hapmap];0.83[CHB][hapmap];0.89[ASN][1000 genomes]
rs10874149	0.96[ASN][1000 genomes]
rs11163074	0.90[CHB][hapmap];0.90[JPT][hapmap];0.93[ASN][1000 genomes]
rs11163089	0.88[CEU][hapmap];0.83[CHB][hapmap];0.88[ASN][1000 genomes]
rs11163095	0.88[ASN][1000 genomes]
rs11163114	0.82[CEU][hapmap];0.84[CHB][hapmap]
rs11163154	0.82[CEU][hapmap];0.84[CHB][hapmap];0.89[ASN][1000 genomes]
rs11163155	0.89[ASN][1000 genomes]
rs11163185	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1144297	0.82[CEU][hapmap]
rs12030510	0.81[CEU][hapmap];0.83[CHB][hapmap]
rs12038999	0.89[ASN][1000 genomes]
rs12404058	0.81[CEU][hapmap];0.83[CHB][hapmap]
rs1249655	0.82[CEU][hapmap];0.82[CHB][hapmap];0.86[ASN][1000 genomes]
rs1249656	0.82[CEU][hapmap];0.84[CHB][hapmap];0.89[ASN][1000 genomes]
rs1249657	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1249659	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1249660	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1249670	0.90[CHB][hapmap];0.90[JPT][hapmap];0.96[ASN][1000 genomes]
rs1249675	0.90[CHB][hapmap];0.90[JPT][hapmap];0.96[ASN][1000 genomes]
rs1249838	0.88[CEU][hapmap]
rs1249839	0.89[CEU][hapmap]
rs1249845	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12562924	0.81[CEU][hapmap];0.83[CHB][hapmap];0.89[ASN][1000 genomes]
rs12726507	0.82[CEU][hapmap];0.84[CHB][hapmap];0.88[ASN][1000 genomes]
rs12744088	0.86[CEU][hapmap];0.84[CHB][hapmap];0.88[ASN][1000 genomes]
rs12756704	0.82[CEU][hapmap];0.84[CHB][hapmap];0.89[ASN][1000 genomes]
rs1343517	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1613680	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1700893	0.82[CEU][hapmap];0.84[CHB][hapmap];0.89[ASN][1000 genomes]
rs2135142	0.86[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2657206	0.81[CEU][hapmap];0.83[CHB][hapmap];0.89[ASN][1000 genomes]
rs6593571	0.96[ASN][1000 genomes]
rs6656537	0.81[CEU][hapmap];0.83[CHB][hapmap]
rs6658610	0.81[CEU][hapmap];0.83[CHB][hapmap];0.89[ASN][1000 genomes]
rs7548993	0.86[CEU][hapmap];0.84[CHB][hapmap];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3368999	chr1:75524762-75933220	Bivalent/Poised TSS Strong transcription Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1013952	chr1:75716654-75936048	Weak transcription Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv535004	chr1:75716654-75936048	ZNF genes & repeats Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:75797400-75804600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:75799800-75803800	Weak transcription	Fetal Brain Male	brain
3	chr1:75800000-75803400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr1:75800600-75805000	Weak transcription	HepG2	liver

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