Variant report

Variant	rs1249665
Chromosome Location	chr1:75782119-75782120
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:75770101..75774631-chr1:75777492..75782800,4	K562	blood:

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

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

rs_ID	r²[population]
rs10493569	0.82[ASN][1000 genomes]
rs10493572	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10493574	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10493575	0.82[ASN][1000 genomes]
rs12122907	0.82[ASN][1000 genomes]
rs12408190	0.82[ASN][1000 genomes]
rs12408226	0.82[ASN][1000 genomes]
rs12408827	0.90[ASN][1000 genomes]
rs12410333	0.82[ASN][1000 genomes]
rs12411159	0.90[ASN][1000 genomes]
rs1249666	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1249667	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1249668	0.82[ASN][1000 genomes]
rs1262045	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1505259	0.82[ASN][1000 genomes]
rs17096776	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17096782	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17096851	0.82[ASN][1000 genomes]
rs17096888	0.82[ASN][1000 genomes]
rs17097953	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17097955	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17581457	0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17584397	0.82[ASN][1000 genomes]
rs17643802	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17644957	0.82[ASN][1000 genomes]
rs1858630	0.82[ASN][1000 genomes]
rs1858631	0.82[ASN][1000 genomes]
rs1876033	0.82[ASN][1000 genomes]
rs1913118	0.82[ASN][1000 genomes]
rs1936359	0.82[ASN][1000 genomes]
rs3899859	0.82[ASN][1000 genomes]
rs4949666	0.90[ASN][1000 genomes]
rs58890548	0.82[ASN][1000 genomes]
rs60194830	0.82[ASN][1000 genomes]
rs74089232	0.82[ASN][1000 genomes]
rs74089237	0.82[ASN][1000 genomes]
rs74089238	0.82[ASN][1000 genomes]
rs74089245	0.82[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:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:75780400-75782400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr1:75780400-75782600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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