Variant report

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	RCOR1	chr6:15106593-15107814	K562	blood:	n/a	n/a
2	EP300	chr6:15106637-15108016	K562	blood:	n/a	n/a
3	BHLHE40	chr6:15106719-15107788	K562	blood:	n/a	n/a
4	MAX	chr6:15106758-15107139	K562	blood:	n/a	n/a
5	TEAD4	chr6:15106558-15107947	K562	blood:	n/a	n/a
6	UBTF	chr6:15106875-15107037	K562	blood:	n/a	n/a
7	MYC	chr6:15106703-15107057	K562	blood:	n/a	n/a
8	TAL1	chr6:15106616-15107893	K562	blood:	n/a	chr6:15106807-15106825
9	CBX3	chr6:15106008-15107878	K562	blood:	n/a	n/a
10	TBL1XR1	chr6:15106863-15107648	K562	blood:	n/a	n/a
11	TBL1XR1	chr6:15106764-15107582	K562	blood:	n/a	n/a
12	GATA1	chr6:15106470-15108923	K562	blood:	n/a	chr6:15108734-15108745 chr6:15106808-15106825 chr6:15107298-15107307
13	CEBPD	chr6:15106593-15107904	K562	blood:	n/a	n/a
14	GATA2	chr6:15106745-15107756	K562	blood:	n/a	chr6:15106808-15106825 chr6:15107298-15107307
15	GATA2	chr6:15106563-15107062	K562	blood:	n/a	chr6:15106808-15106825
16	MYC	chr6:15106701-15107806	K562	blood:	n/a	n/a
17	TEAD4	chr6:15106597-15107576	K562	blood:	n/a	n/a
18	GATA1	chr6:15106602-15108186	PBDE	blood:	n/a	chr6:15106808-15106825 chr6:15107298-15107307
19	MAX	chr6:15106742-15107830	K562	blood:	n/a	n/a
20	ARID3A	chr6:15106725-15107548	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:15103632..15105300-chr6:15106507..15108224,2	K562	blood:
2	chr6:14882855..14884940-chr6:15106180..15108933,2	K562	blood:
3	chr6:15106427..15109667-chr6:15111584..15114479,3	K562	blood:
4	chr6:15106242..15108900-chr6:15209959..15212920,4	K562	blood:
5	chr6:15069920..15071454-chr6:15106788..15108446,2	K562	blood:
6	chr6:15069954..15071516-chr6:15106946..15109346,2	K562	blood:
7	chr6:15092731..15095339-chr6:15106274..15108820,2	K562	blood:
8	chr6:15099407..15102397-chr6:15106486..15108344,2	K562	blood:
9	chr6:15102630..15105132-chr6:15106724..15108823,2	K562	blood:
10	chr6:15105604..15108959-chr6:15245974..15248979,5	K562	blood:

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	nsv830593	chr6:15049636-15244190	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1016007	chr6:15099585-15159098	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	esv2762580	chr6:15105917-15159110	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 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	chr6:15087400-15117600	Weak transcription	Right Atrium	heart
2	chr6:15090400-15109000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:15106800-15108000	Flanking Active TSS	K562	blood

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