Variant report

No.	Distal block	Cell Line	Cell type
1	chr6:37758926..37760720-chr6:37767100..37768812,2	K562	blood:
2	chr6:37761965..37764146-chr6:37767297..37769364,2	MCF-7	breast:
3	chr6:37764796..37769141-chr6:37786360..37788768,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000156639	Chromatin interaction
ENSG00000225945	Chromatin interaction

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1212636	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12198360	0.83[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs12211975	0.96[ASN][1000 genomes]
rs12523829	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs259714	0.82[ASN][1000 genomes]
rs259717	0.84[ASN][1000 genomes]
rs259721	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs259722	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs259723	0.93[ASN][1000 genomes]
rs4142102	0.96[ASN][1000 genomes]
rs4711515	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6458030	0.95[ASN][1000 genomes]
rs67133782	0.96[ASN][1000 genomes]
rs6915506	0.80[AMR][1000 genomes]
rs6926280	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6937655	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs72849338	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9349051	0.90[AFR][1000 genomes];0.84[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9369024	0.90[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs9369025	0.87[ASN][1000 genomes]
rs9380703	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9380704	0.92[AFR][1000 genomes];0.82[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs9470714	0.92[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	nsv1028825	chr6:37495154-38278320	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active 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 miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv1024016	chr6:37567651-37981590	Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 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	chr6:37759200-37768400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr6:37759800-37768600	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr6:37766400-37768800	Enhancers	Fetal Stomach	stomach
4	chr6:37766400-37775400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr6:37767400-37768800	Enhancers	HepG2	liver
6	chr6:37767400-37775400	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr6:37767400-37777000	Weak transcription	Right Atrium	heart
8	chr6:37767800-37768800	Weak transcription	Liver	Liver
9	chr6:37767800-37769600	Weak transcription	Aorta	Aorta

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