Variant report

No.	Distal block	Cell Line	Cell type
1	chr6:117989002..117991438-chr6:117994299..117996624,2	K562	blood:
2	chr6:117988434..117990727-chr6:117995010..117997280,2	K562	blood:
3	chr6:117986656..117990988-chr6:117991172..117993909,4	K562	blood:

Variant related genes	Relation type
ENSG00000153989	Chromatin interaction

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10457318	0.82[EUR][1000 genomes]
rs10872153	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11961040	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12205963	0.80[EUR][1000 genomes]
rs13211542	0.88[ASN][1000 genomes]
rs1501474	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1532680	0.81[EUR][1000 genomes]
rs1827327	0.89[ASN][1000 genomes]
rs1967194	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2062663	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2088870	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs210639	0.81[AFR][1000 genomes]
rs4946273	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9285426	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9320614	0.81[EUR][1000 genomes]
rs9320616	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9320617	0.86[AFR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9374674	0.86[AFR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9387491	0.81[EUR][1000 genomes]
rs9401019	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9401023	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9489238	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9765895	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9767060	0.86[EUR][1000 genomes];0.89[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	nsv532050	chr6:117528154-118203005	ZNF genes & repeats Enhancers Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv5449	chr6:117954646-117999751	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:117969400-117995800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr6:117971800-117989800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr6:117973000-117990600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
4	chr6:117973800-117995600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr6:117978000-117995600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr6:117982600-117990000	Weak transcription	HUES6 Cell Line	embryonic stem cell
7	chr6:117984600-117991000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:117985600-117990400	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr6:117985800-117991200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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