Variant report

No.	Distal block	Cell Line	Cell type
1	chr14:31675035..31677201-chr14:31702573..31705087,3	K562	blood:
2	chr14:31674892..31678549-chr14:31702210..31703744,3	MCF-7	breast:
3	chr14:31701418..31703156-chr14:31707210..31709221,2	K562	blood:
4	chr14:31699229..31701573-chr14:31702357..31705028,3	K562	blood:

Variant related genes	Relation type
ENSG00000092148	Chromatin interaction

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10132373	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10135213	0.95[EUR][1000 genomes]
rs10138200	0.95[EUR][1000 genomes]
rs10148827	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10151563	0.95[EUR][1000 genomes]
rs1041088	0.95[EUR][1000 genomes]
rs10872849	0.84[EUR][1000 genomes]
rs11156660	0.85[EUR][1000 genomes]
rs11156661	0.85[EUR][1000 genomes]
rs11626839	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs12184973	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12434266	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs12588620	0.84[EUR][1000 genomes]
rs12889162	0.95[EUR][1000 genomes]
rs2378848	0.84[EUR][1000 genomes]
rs4981825	0.85[ASN][1000 genomes]
rs4981828	0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs5024655	0.95[EUR][1000 genomes]
rs61995523	0.81[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6571403	0.95[EUR][1000 genomes]
rs6571404	0.95[EUR][1000 genomes]
rs7146274	0.84[EUR][1000 genomes]
rs7147686	0.83[EUR][1000 genomes]
rs7156178	0.85[EUR][1000 genomes]
rs7494025	0.95[EUR][1000 genomes]
rs8022573	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9788563	0.95[EUR][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	nsv901587	chr14:31501505-31752664	Strong transcription Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
2	nsv1050054	chr14:31501703-31733642	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
3	esv2830427	chr14:31639110-32000034	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31699600-31703400	Weak transcription	Placenta	Placenta
2	chr14:31699600-31703800	Enhancers	HepG2	liver
3	chr14:31699600-31707600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr14:31701800-31708600	Weak transcription	K562	blood
5	chr14:31702400-31703400	Enhancers	A549	lung
6	chr14:31702600-31703000	Enhancers	Fetal Heart	heart
7	chr14:31702800-31703000	Enhancers	Hela-S3	cervix
8	chr14:31702800-31703400	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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