Variant report

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	STAT5A	chr14:81471839-81472267	K562	blood:	n/a	n/a
2	ARID3A	chr14:81471969-81472276	K562	blood:	n/a	n/a
3	ATF3	chr14:81471966-81472205	K562	blood:	n/a	chr14:81472094-81472109 chr14:81472098-81472105 chr14:81472097-81472105 chr14:81472095-81472106
4	ZNF143	chr14:81471982-81472133	K562	blood:	n/a	n/a
5	JUND	chr14:81471887-81472946	K562	blood:	n/a	chr14:81472097-81472106
6	JUN	chr14:81471844-81472340	K562	blood:	n/a	chr14:81472093-81472106 chr14:81472097-81472106
7	JUN	chr14:81471926-81472205	K562	blood:	n/a	chr14:81472093-81472106 chr14:81472097-81472106
8	JUND	chr14:81471936-81472268	HepG2	liver:	n/a	chr14:81472097-81472106
9	POLR2A	chr14:81471903-81472108	ProgFib	skin:	n/a	n/a
10	RCOR1	chr14:81471975-81472175	K562	blood:	n/a	n/a
11	CREB1	chr14:81471945-81472212	K562	blood:	n/a	chr14:81472095-81472108
12	CEBPB	chr14:81471918-81472255	K562	blood:	n/a	n/a
13	ATF1	chr14:81471911-81472280	K562	blood:	n/a	n/a
14	CREB1	chr14:81471908-81472356	K562	blood:	n/a	chr14:81472095-81472108
15	JUN	chr14:81471974-81472219	HepG2	liver:	n/a	chr14:81472093-81472106 chr14:81472097-81472106
16	CEBPB	chr14:81471982-81472273	K562	blood:	n/a	n/a
17	EP300	chr14:81471988-81472154	K562	blood:	n/a	n/a
18	CUX1	chr14:81471751-81472098	K562	blood:	n/a	n/a
19	TEAD4	chr14:81471868-81472224	K562	blood:	n/a	n/a
20	IRF1	chr14:81471917-81472148	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:81467255..81470490-chr14:81470537..81472087,4	K562	blood:

rSNPs within LD-proxies of this variant (count:19)

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	nsv869348	chr14:80921098-81535754	Weak transcription Strong transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv1052999	chr14:81468860-81599074	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
3	nsv542144	chr14:81468860-81599074	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:81455800-81492200	Weak transcription	Fetal Thymus	thymus
2	chr14:81468000-81486600	Weak transcription	Thymus	Thymus
3	chr14:81468400-81472600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr14:81470400-81477200	Weak transcription	Dnd41	blood
5	chr14:81470800-81474800	Enhancers	K562	blood
6	chr14:81471400-81472800	Enhancers	Fetal Heart	heart

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