Variant report

Variant	rs3135314
Chromosome Location	chr6:28861320-28861321
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ZNF263	chr6:28861186-28861585	HEK293-T-REx	kidney:	n/a	chr6:28861373-28861394

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:28861105..28864204-chr6:28976259..28979273,3	K562	blood:
2	chr6:28830882..28836292-chr6:28860588..28866545,10	MCF-7	breast:
3	chr6:28861105..28863398-chr6:28977409..28979121,2	K562	blood:
4	chr6:28828478..28839935-chr6:28855092..28866386,31	K562	blood:
5	chr6:28858916..28861710-chr6:28875406..28878163,2	MCF-7	breast:
6	chr6:28859779..28861420-chr6:28890604..28892940,2	MCF-7	breast:
7	chr6:28859278..28869415-chr6:28906395..28912460,18	K562	blood:
8	chr6:28693274..28695982-chr6:28860211..28863205,2	K562	blood:
9	chr6:28858686..28861504-chr6:28861818..28863578,3	MCF-7	breast:
10	chr6:28823126..28835109-chr6:28859268..28867076,23	K562	blood:
11	chr6:28802724..28808694-chr6:28856997..28865691,21	K562	blood:
12	chr6:28853385..28858171-chr6:28860346..28864278,7	MCF-7	breast:

No data

Variant related genes	Relation type
ZNF90P2	TF binding region
HCG14	TF binding region
ENSG00000225173	Chromatin interaction
ENSG00000204709	Chromatin interaction
ENSG00000233366	Chromatin interaction
ENSG00000213916	Chromatin interaction
ENSG00000204713	Chromatin interaction
ENSG00000225595	Chromatin interaction

Extended variants
information (count: 38 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs1061625	0.81[ASN][1000 genomes]
rs172326	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1794588	0.80[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs184094	0.87[ASN][1000 genomes]
rs2013652	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs209127	0.83[ASN][1000 genomes]
rs209140	0.90[ASN][1000 genomes]
rs209147	0.83[AFR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs209151	0.90[ASN][1000 genomes]
rs209165	0.92[ASN][1000 genomes]
rs209172	0.90[ASN][1000 genomes]
rs209177	0.88[ASN][1000 genomes]
rs209180	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2097424	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2148007	0.86[ASN][1000 genomes]
rs2269553	0.81[ASN][1000 genomes]
rs2894066	0.81[ASN][1000 genomes]
rs3132377	0.81[ASN][1000 genomes]
rs3132380	0.80[ASN][1000 genomes]
rs413972	0.92[ASN][1000 genomes]
rs422331	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs429369	0.92[ASN][1000 genomes]
rs4484511	0.86[ASN][1000 genomes]
rs743847	0.85[ASN][1000 genomes]
rs7750338	0.92[ASN][1000 genomes]
rs7769221	0.92[ASN][1000 genomes]
rs9257269	0.82[ASN][1000 genomes]
rs9257270	0.81[ASN][1000 genomes]
rs9257274	0.83[ASN][1000 genomes]
rs9257280	0.83[ASN][1000 genomes]
rs9257281	0.85[ASN][1000 genomes]
rs9257328	0.92[ASN][1000 genomes]
rs929042	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv883518	chr6:28792477-28911802	Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	56 gene(s)	inside rSNPs	diseases
2	nsv883519	chr6:28792477-28936556	Transcr. at gene 5' and 3' Genic enhancers Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	57 gene(s)	inside rSNPs	diseases
3	nsv427748	chr6:28831888-28999434	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	62 gene(s)	inside rSNPs	diseases
4	nsv601212	chr6:28833225-28893927	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases
5	nsv462667	chr6:28834646-28893927	Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Bivalent/Poised TSS Genic enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	47 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:28849400-28863000	Weak transcription	Right Atrium	heart
2	chr6:28853400-28863000	Weak transcription	Fetal Kidney	kidney
3	chr6:28859600-28861600	Weak transcription	HepG2	liver
4	chr6:28860600-28862800	Enhancers	K562	blood

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