Variant report

Variant	rs73236158
Chromosome Location	chr4:56469596-56469597
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:56468709..56470290-chr4:56471936..56473680,2	K562	blood:
2	chr4:56469594..56472542-chr4:56706462..56708819,2	K562	blood:
3	chr4:56466882..56469712-chr4:56475375..56477433,2	K562	blood:
4	chr4:56465744..56469712-chr4:56475129..56477433,3	K562	blood:

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs12510765	1.00[ASN][1000 genomes]
rs4333263	1.00[ASN][1000 genomes]
rs4412048	1.00[ASN][1000 genomes]
rs4631105	1.00[ASN][1000 genomes]
rs4864552	1.00[ASN][1000 genomes]
rs4864562	1.00[ASN][1000 genomes]
rs4865031	1.00[ASN][1000 genomes]
rs6554281	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6554299	1.00[ASN][1000 genomes]
rs6554309	1.00[ASN][1000 genomes]
rs6554311	1.00[ASN][1000 genomes]
rs6554312	1.00[ASN][1000 genomes]
rs6554314	1.00[ASN][1000 genomes]
rs6554317	1.00[ASN][1000 genomes]
rs6828640	1.00[ASN][1000 genomes]
rs6838362	1.00[ASN][1000 genomes]
rs6842779	1.00[ASN][1000 genomes]
rs6856478	1.00[ASN][1000 genomes]
rs73236146	1.00[ASN][1000 genomes]
rs7668437	1.00[ASN][1000 genomes]
rs7691573	1.00[ASN][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	esv3328582	chr4:56164136-56486156	Enhancers Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
2	esv2755990	chr4:56317136-57143037	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	40 gene(s)	inside rSNPs	diseases
3	nsv10496	chr4:56336946-56841137	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
4	nsv998179	chr4:56425126-56694339	Flanking Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	nsv932636	chr4:56438618-56667329	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr4:56464200-56475800	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr4:56465400-56479400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:56465600-56476000	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr4:56468800-56470400	Weak transcription	K562	blood
5	chr4:56469400-56470200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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