Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:30830841..30833196-chr22:30936778..30939588,2	K562	blood:

Variant related genes	Relation type
ENSG00000203606	Chromatin interaction

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1131603	1.00[ASN][1000 genomes]
rs13053196	1.00[ASN][1000 genomes]
rs13057281	0.86[EUR][1000 genomes]
rs13058535	1.00[ASN][1000 genomes]
rs17730748	1.00[ASN][1000 genomes]
rs17738020	1.00[ASN][1000 genomes]
rs1807507	1.00[ASN][1000 genomes]
rs34102711	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34318316	1.00[ASN][1000 genomes]
rs34471369	1.00[ASN][1000 genomes]
rs34886169	1.00[ASN][1000 genomes]
rs34911581	1.00[ASN][1000 genomes]
rs34964064	1.00[ASN][1000 genomes]
rs35057984	1.00[ASN][1000 genomes]
rs35074129	1.00[ASN][1000 genomes]
rs35246430	1.00[ASN][1000 genomes]
rs35617977	1.00[ASN][1000 genomes]
rs35765517	1.00[ASN][1000 genomes]
rs4449240	1.00[ASN][1000 genomes]
rs4820834	1.00[ASN][1000 genomes]
rs4820840	1.00[ASN][1000 genomes]
rs5753263	1.00[ASN][1000 genomes]
rs67384221	1.00[ASN][1000 genomes]
rs67401267	1.00[ASN][1000 genomes]
rs7292248	1.00[ASN][1000 genomes]
rs73168654	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829171	chr22:30598030-31043578	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv915818	chr22:30708245-31346302	Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	82 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30928200-30938000	Weak transcription	Lung	lung
2	chr22:30933400-30937800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr22:30933600-30937600	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr22:30933600-30937600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr22:30933800-30937600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr22:30934000-30937800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr22:30934600-30937800	Weak transcription	Ovary	ovary
8	chr22:30935000-30937600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr22:30937400-30937600	Enhancers	K562	blood
10	chr22:30937400-30937800	Active TSS	HepG2	liver

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