Variant report

Variant	rs28491830
Chromosome Location	chr3:158248689-158248690
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:158248140..158250406-chr3:158251926..158254670,2	K562	blood:

Extended variants
information (count: 48 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs12486595	0.91[ASN][1000 genomes]
rs12487004	0.93[ASN][1000 genomes]
rs12487933	0.86[AMR][1000 genomes]
rs1435638	0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs1435639	0.84[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs16829072	0.91[ASN][1000 genomes]
rs16829079	0.91[ASN][1000 genomes]
rs2363654	0.86[AMR][1000 genomes]
rs2363657	0.91[ASN][1000 genomes]
rs28669117	0.86[AMR][1000 genomes]
rs4522814	0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs5025785	0.86[AMR][1000 genomes]
rs59112782	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs59502510	0.91[ASN][1000 genomes]
rs67074371	0.82[AMR][1000 genomes]
rs6762774	0.82[AMR][1000 genomes]
rs6769314	0.82[AMR][1000 genomes]
rs6770005	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6795710	0.91[ASN][1000 genomes]
rs6797871	0.91[ASN][1000 genomes]
rs6804401	0.86[AMR][1000 genomes]
rs73020715	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs73020720	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs73022714	0.91[ASN][1000 genomes]
rs73022726	0.91[ASN][1000 genomes]
rs73022742	0.91[ASN][1000 genomes]
rs73172118	0.81[AMR][1000 genomes]
rs73172127	0.83[AMR][1000 genomes]
rs7619886	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs939115	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs939116	0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs9681065	0.82[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9811282	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9812307	0.80[AMR][1000 genomes]
rs9815348	0.86[AMR][1000 genomes]
rs9819130	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9830994	0.86[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs9849688	0.86[AMR][1000 genomes]
rs9854620	0.86[AMR][1000 genomes]
rs9858498	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002378	chr3:157715428-158673414	Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv1014381	chr3:158070451-158350118	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1004124	chr3:158146715-158808638	Genic enhancers Strong transcription Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
4	nsv1014557	chr3:158176582-158251602	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv877690	chr3:158184263-158296916	Flanking Active TSS Enhancers Strong transcription Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	esv2763312	chr3:158193512-158420588	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
7	nsv916167	chr3:158240540-158320581	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
8	nsv877691	chr3:158245883-158359667	Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs28491830	GFM1	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:158246600-158261000	Weak transcription	Primary T helper cells fromperipheralblood	blood

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