Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:34028224..34029930-chr11:34073891..34075941,2	K562	blood:

Variant related genes	Relation type
ENSG00000135387	Chromatin interaction

rs_ID	r²[population]
rs10082562	0.81[ASN][1000 genomes]
rs10768043	0.80[ASN][1000 genomes]
rs10836144	0.89[ASN][1000 genomes]
rs10836145	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10836146	0.89[ASN][1000 genomes]
rs10836147	0.90[ASN][1000 genomes]
rs11032481	0.89[ASN][1000 genomes]
rs11032482	0.89[ASN][1000 genomes]
rs11032485	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11032487	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11032489	0.80[ASN][1000 genomes]
rs12277616	0.81[ASN][1000 genomes]
rs12576882	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12577490	0.90[ASN][1000 genomes]
rs12789531	0.81[ASN][1000 genomes]
rs12799109	0.89[ASN][1000 genomes]
rs2139177	0.90[ASN][1000 genomes]
rs7121633	0.87[ASN][1000 genomes]
rs7122747	0.90[ASN][1000 genomes]
rs7952389	0.87[ASN][1000 genomes]

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:34026600-34035000	Weak transcription	Fetal Intestine Large	intestine
2	chr11:34028000-34029600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr11:34028200-34029200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr11:34028800-34029200	Enhancers	K562	blood
5	chr11:34029000-34036000	Weak transcription	Duodenum Mucosa	Duodenum

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