Variant report

Variant	rs73431712
Chromosome Location	chr7:119666070-119666071
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	chr7:119664746..119667649-chr7:119667923..119670710,3	K562	blood:

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10224732	1.00[EUR][1000 genomes]
rs10279248	1.00[EUR][1000 genomes]
rs10280627	0.83[ASN][1000 genomes]
rs10280758	0.83[ASN][1000 genomes]
rs17142497	0.83[ASN][1000 genomes]
rs17142550	1.00[EUR][1000 genomes]
rs1989217	0.83[ASN][1000 genomes]
rs2214705	1.00[ASN][1000 genomes]
rs55997859	1.00[ASN][1000 genomes]
rs57059935	1.00[ASN][1000 genomes]
rs58183333	0.83[ASN][1000 genomes]
rs58192464	0.83[ASN][1000 genomes]
rs58717470	0.83[ASN][1000 genomes]
rs59032327	0.83[ASN][1000 genomes]
rs59303341	0.83[ASN][1000 genomes]
rs59447974	1.00[ASN][1000 genomes]
rs59585910	1.00[ASN][1000 genomes]
rs60883005	1.00[ASN][1000 genomes]
rs61485753	1.00[ASN][1000 genomes]
rs6951188	0.83[ASN][1000 genomes]
rs6962109	1.00[ASN][1000 genomes]
rs6963042	0.83[ASN][1000 genomes]
rs6967778	1.00[ASN][1000 genomes]
rs6973663	0.83[ASN][1000 genomes]
rs6975320	0.83[ASN][1000 genomes]
rs6979383	1.00[ASN][1000 genomes]
rs6979384	1.00[ASN][1000 genomes]
rs6980091	1.00[ASN][1000 genomes]
rs6980267	1.00[ASN][1000 genomes]
rs6980402	1.00[ASN][1000 genomes]
rs73423841	1.00[ASN][1000 genomes]
rs73423843	1.00[ASN][1000 genomes]
rs73423854	1.00[ASN][1000 genomes]
rs73431755	0.83[ASN][1000 genomes]
rs73431761	0.83[ASN][1000 genomes]
rs73431762	0.83[ASN][1000 genomes]
rs73431766	0.83[ASN][1000 genomes]
rs73431767	0.83[ASN][1000 genomes]
rs73431773	0.83[ASN][1000 genomes]
rs73431782	0.83[ASN][1000 genomes]
rs73431793	0.83[ASN][1000 genomes]
rs73433665	1.00[ASN][1000 genomes]
rs73433666	1.00[ASN][1000 genomes]
rs73441608	1.00[ASN][1000 genomes]
rs73441610	1.00[ASN][1000 genomes]
rs73441658	1.00[ASN][1000 genomes]
rs73441659	1.00[ASN][1000 genomes]
rs73441660	1.00[ASN][1000 genomes]
rs73721058	0.83[ASN][1000 genomes]
rs7777407	1.00[EUR][1000 genomes]
rs7785001	1.00[ASN][1000 genomes]
rs7799093	0.83[ASN][1000 genomes]
rs7805422	1.00[ASN][1000 genomes]
rs7805993	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470388	chr7:119464310-119790102	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	esv2753623	chr7:119532049-119770049	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv831112	chr7:119585169-119776619	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv1024054	chr7:119638121-119700508	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	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	chr7:119656400-119668400	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr7:119661800-119668600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr7:119664200-119667800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr7:119664600-119667800	Weak transcription	NHLF	lung

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