Variant report

Variant	rs1304902
Chromosome Location	chr5:107023656-107023657
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	chr5:107023431..107026443-chr5:107031056..107034359,3	K562	blood:

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10045032	0.88[ASN][1000 genomes]
rs11960012	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12656808	0.81[ASN][1000 genomes]
rs12657205	0.81[ASN][1000 genomes]
rs12658128	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12658772	0.86[ASN][1000 genomes]
rs12659199	0.88[ASN][1000 genomes]
rs13160949	0.87[ASN][1000 genomes]
rs13171567	0.90[ASN][1000 genomes]
rs13171805	0.86[ASN][1000 genomes]
rs13188836	0.89[ASN][1000 genomes]
rs13189126	0.87[ASN][1000 genomes]
rs1388133	0.87[ASN][1000 genomes]
rs1455527	0.87[ASN][1000 genomes]
rs1490827	0.94[JPT][hapmap];0.82[ASN][1000 genomes]
rs1490839	0.87[ASN][1000 genomes]
rs1559244	0.81[ASN][1000 genomes]
rs1559245	0.87[ASN][1000 genomes]
rs1586728	0.89[ASN][1000 genomes]
rs1602386	0.90[ASN][1000 genomes]
rs17430751	0.86[ASN][1000 genomes]
rs1823993	0.90[ASN][1000 genomes]
rs1826239	0.89[ASN][1000 genomes]
rs1895414	0.90[ASN][1000 genomes]
rs4957706	0.88[ASN][1000 genomes]
rs4957708	0.93[ASN][1000 genomes]
rs4957709	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4957710	0.86[ASN][1000 genomes]
rs4957711	0.87[ASN][1000 genomes]
rs56201232	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62357894	0.87[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6596745	0.90[ASN][1000 genomes]
rs6596746	0.87[ASN][1000 genomes]
rs6863281	0.82[ASN][1000 genomes]
rs6891467	0.87[ASN][1000 genomes]
rs723799	0.86[ASN][1000 genomes]
rs73200667	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7349802	0.91[ASN][1000 genomes]
rs7349825	0.90[ASN][1000 genomes]
rs7446408	0.87[ASN][1000 genomes]
rs7708158	0.82[ASN][1000 genomes]
rs7715219	0.88[ASN][1000 genomes]
rs7727931	0.90[ASN][1000 genomes]
rs7732343	0.89[ASN][1000 genomes]
rs873136	0.89[ASN][1000 genomes]
rs923622	0.84[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv34018	chr5:106720912-107110506	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:107018800-107029000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr5:107023400-107023800	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr5:107023400-107024000	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr5:107023600-107023800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr5:107023600-107024200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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