Variant report

Variant	rs73378304
Chromosome Location	chr7:65640747-65640748
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	chr7:65640707..65643373-chr7:65647388..65648894,2	K562	blood:

Extended variants
information (count: 41 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10950024	0.87[EUR][1000 genomes]
rs10950025	0.84[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs10950027	0.83[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs10950028	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10950029	0.83[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs11760805	0.84[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs11767833	0.90[EUR][1000 genomes]
rs12666485	0.84[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs12671834	0.87[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs12673308	0.84[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs160640	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs160641	0.82[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs2244226	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2451953	0.82[EUR][1000 genomes]
rs2460427	0.84[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs2465121	0.88[EUR][1000 genomes]
rs313818	0.82[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs313823	0.81[EUR][1000 genomes]
rs316305	0.84[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs316306	0.84[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs316316	0.84[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs316320	0.82[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs316324	0.84[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs316328	0.85[EUR][1000 genomes]
rs4441996	0.82[EUR][1000 genomes]
rs6460276	0.87[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs67302640	0.84[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs67397473	0.83[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs67688847	0.80[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs6960870	0.84[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs73136346	0.82[AFR][1000 genomes]
rs73376394	0.92[EUR][1000 genomes]
rs73376401	0.87[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs7782212	0.80[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7786728	0.83[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs7787063	0.84[AFR][1000 genomes];0.91[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2761079	chr7:65092426-65689733	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Genic enhancers Strong transcription Enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
2	nsv532124	chr7:65371521-66234730	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	125 gene(s)	inside rSNPs	diseases
3	nsv1021186	chr7:65492601-65663438	Active TSS Strong transcription Genic enhancers Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv971172	chr7:65616238-65653268	Weak transcription Strong transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1026559	chr7:65617368-66370805	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	116 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs73378304	RP4-756H11.3	cis	Muscle Skeletal	GTEx
rs73378304	RP4-756H11.3	cis	Thyroid	GTEx
rs73378304	GS1-124K5.11	cis	Thyroid	GTEx
rs73378304	RNU6-96P	cis	Thyroid	GTEx
rs73378304	GTF2IRD1P1	cis	Thyroid	GTEx
rs73378304	GS1-124K5.4	cis	Esophagus Mucosa	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:65636000-65643200	Weak transcription	Skeletal Muscle Male	skeletal muscle
2	chr7:65636200-65641600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr7:65636200-65648200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr7:65636800-65648000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr7:65639200-65641800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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