Variant report

Variant	rs9379955
Chromosome Location	chr6:27033662-27033663
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:27026462..27028720-chr6:27031339..27033983,3	K562	blood:
2	chr6:27020688..27023464-chr6:27032968..27035001,2	K562	blood:
3	chr6:26922078..26923970-chr6:27032946..27034480,2	K562	blood:
4	chr6:26986842..26988770-chr6:27031968..27034490,2	K562	blood:

Variant related genes	Relation type
ENSG00000238621	Chromatin interaction
ENSG00000224843	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 9 )

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10456351	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10456352	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10946891	0.80[EUR][1000 genomes]
rs10946897	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10946898	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11756275	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12209886	0.81[EUR][1000 genomes]
rs12211984	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12523820	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12527111	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12527231	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13212021	0.84[ASN][1000 genomes]
rs2057348	0.80[EUR][1000 genomes]
rs2142685	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs35691005	0.80[EUR][1000 genomes]
rs4269366	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4403259	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4422620	0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4424065	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4434464	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4583981	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs62401067	0.82[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62402054	0.80[EUR][1000 genomes]
rs6930508	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6937880	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7451149	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7747454	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7768407	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9379956	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9379958	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9393789	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9461330	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9467978	0.80[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs994691	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948921	chr6:26556890-27443957	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	472 gene(s)	inside rSNPs	diseases
2	esv2758038	chr6:26695219-27095714	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	67 gene(s)	inside rSNPs	diseases
3	esv2759410	chr6:26695219-27095714	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	67 gene(s)	inside rSNPs	diseases
4	nsv1029124	chr6:26825468-27109774	Active TSS Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	244 gene(s)	inside rSNPs	diseases
5	nsv471636	chr6:26841084-27038175	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
6	nsv469625	chr6:26893739-27038175	Flanking Active TSS Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
7	nsv482537	chr6:26893739-27038175	Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
8	nsv965631	chr6:27007405-27037069	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
9	esv3369822	chr6:27007480-27037513	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

mRNA abundance (count:9)

SNP	Gene	Cis/trans	Tissue	Source
rs9379955	HCG11	Cis_1M	lymphoblastoid	RTeQTL
rs9379955	RP11-457M11.5	cis	Stomach	GTEx
rs9379955	RP11-457M11.5	cis	Esophagus Mucosa	GTEx
rs9379955	RP11-457M11.5	cis	Whole Blood	GTEx
rs9379955	RP11-457M11.5	cis	Heart Left Ventricle	GTEx
rs9379955	RP11-457M11.5	cis	Thyroid	GTEx
rs9379955	RP11-457M11.5	cis	Skin Sun Exposed Lower leg	GTEx
rs9379955	RP11-457M11.5	cis	Artery Tibial	GTEx
rs9379955	RP11-457M11.5	cis	lung	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:27028000-27034200	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr6:27029600-27034000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr6:27029600-27034200	Weak transcription	HepG2	liver
4	chr6:27029600-27034400	Weak transcription	GM12878-XiMat	blood
5	chr6:27030600-27034200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr6:27030800-27034200	Weak transcription	HMEC	breast
7	chr6:27033400-27033800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr6:27033400-27033800	Weak transcription	Gastric	stomach
9	chr6:27033400-27034400	Weak transcription	K562	blood

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