Variant report

Variant	rs112902133
Chromosome Location	chr15:50708433-50708434
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:11)
CpG islands
(count:0)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:11 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	NFYB	chr15:50708252-50708575	K562	blood:	n/a	n/a
2	FOXA1	chr15:50708058-50708520	HepG2	liver:	n/a	n/a
3	FOXA2	chr15:50708071-50708462	HepG2	liver:	n/a	n/a
4	HCFC1	chr15:50708124-50708461	K562	blood:	n/a	n/a
5	NFYA	chr15:50708368-50708565	Hela-S3	cervix:	n/a	n/a
6	NFYB	chr15:50708328-50708571	GM12878	blood:	n/a	n/a
7	MXI1	chr15:50708222-50708534	HepG2	liver:	n/a	n/a
8	ZNF384	chr15:50707955-50708497	K562	blood:	n/a	n/a
9	RFX5	chr15:50708363-50708572	HepG2	liver:	n/a	n/a
10	E2F6	chr15:50708312-50708738	H1-hESC	embryonic stem cell:	n/a	n/a
11	NFYA	chr15:50708313-50708532	K562	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:50647163..50649970-chr15:50707470..50713022,5	MCF-7	breast:
2	chr15:50664439..50666411-chr15:50707371..50708947,2	MCF-7	breast:
3	chr15:50646196..50649637-chr15:50705519..50710625,4	K562	blood:
4	chr15:50647220..50649637-chr15:50708002..50709799,2	K562	blood:

No data

No data

No data

Extended variants
information (count: 5 )
Associated
traits (count: 0)

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	nsv1045456	chr15:50592472-51019873	Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
2	nsv948579	chr15:50645530-51045564	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	119 gene(s)	inside rSNPs	diseases
3	nsv524613	chr15:50656449-50868779	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv904210	chr15:50702058-50786024	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
5	esv3394728	chr15:50707960-50712658	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:50698200-50715800	Weak transcription	Primary T cells from cord blood	blood
2	chr15:50704400-50710400	Weak transcription	K562	blood
3	chr15:50708000-50708800	Enhancers	HepG2	liver

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dbSNP/dbVar ID: rs12345 /nsv7879
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