Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:15005280..15007907-chr6:15011280..15013327,2	K562	blood:

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

rs_ID	r²[population]
rs1259064	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1259065	0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1259066	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1259072	0.85[AFR][1000 genomes];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1259075	0.82[AMR][1000 genomes]
rs2147203	0.82[EUR][1000 genomes]
rs2327870	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4715951	0.89[CEU][hapmap]
rs4715952	0.81[EUR][1000 genomes]
rs67121944	0.85[AMR][1000 genomes];0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6902553	0.82[EUR][1000 genomes]
rs6918145	0.82[EUR][1000 genomes]
rs7741200	0.82[EUR][1000 genomes]
rs7750114	0.82[EUR][1000 genomes]
rs927628	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9367854	0.82[EUR][1000 genomes]
rs9370790	0.82[AMR][1000 genomes]
rs9383006	0.81[EUR][1000 genomes]
rs9383008	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9383009	0.82[AMR][1000 genomes]
rs9396547	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1031668	chr6:14774036-15044308	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv538138	chr6:14774036-15044308	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv970723	chr6:14997807-15023765	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:14976000-15006400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:14984600-15006600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr6:14986600-15018000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:14993600-15007200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr6:15001800-15009200	Strong transcription	HUES48 Cell Line	embryonic stem cell
6	chr6:15002400-15006600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr6:15002800-15009600	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:15003600-15009200	Strong transcription	HUES6 Cell Line	embryonic stem cell
9	chr6:15003800-15009200	Strong transcription	iPS-18 Cell Line	embryonic stem cell
10	chr6:15004200-15006400	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr6:15005200-15009200	Strong transcription	H1 Cell Line	embryonic stem cell
12	chr6:15005800-15009200	Strong transcription	HUES64 Cell Line	embryonic stem cell
13	chr6:15006000-15009200	Strong transcription	iPS-15b Cell Line	embryonic stem cell

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