| Tag | Content |
|---|
EnhancerAtlas ID | HS184-15894 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr2:9970370-9971300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr2:9971102-9971123 | AAGTGGTTTCAGTTTCAGTTA | + | 6.62 | | IRF8 | MA0652.1 | chr2:9971106-9971120 | GGTTTCAGTTTCAG | - | 6.49 | | IRF9 | MA0653.1 | chr2:9971106-9971121 | GGTTTCAGTTTCAGT | - | 6.51 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_26755 | chr2:9970491-9973090 | Esophagus | | SE_64906 | chr2:9970407-9971570 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I009829 | chr2 | 9970041 | 9972970 |
|
Enhancer Sequence | TGAGTAGCTG GGACTACAGG CACACACCAA CATGCCCAGC TAATTTTTGT ATTTTTATTA 60
GAGACGGGGT TTCACCATGT TGACCAGGCT GGTCTCAAAC TCCTGACCTT GTGATCCACC 120
CACCTCGGTC TCCCAAAGTG CTGGGATTAC AGGCGTGAGT CACTGTGCCC AGCCCTAGAC 180
TTTTATTTAA AATGAGACTT CTGTGGCTCT GTTACTCTCC TTCCTGGAAG GGAGGGAGGA 240
GCAAGACCGG TTTGCCCCAA GCCTATAAAT GGAATAAACC AGTCCCCAAC AGGTTCTGCA 300
ACTTGCCTGA GATCTTATCG CTCCTGAGTT TGGGAAACTC TTGAGTTATT TAAGCCACAC 360
TCTTAGAAGG TTGTTTTGCT TCTGTTTAAT TGGGGCTGTG CCTTCTGGCT GTTGAGCTCC 420
TTTGACAAAG TGATTTTGCA TCCAGAGTAC TTTATTCATT CATCCATTCA TTCACTAAAA 480
AAACCTTTAT TAAGCACTTG GTCTGTTAGC AGAAAAAGTA GGCTCTTTGG AACAGGCAGA 540
ACTGAGTTAA GTTCCCTCTT GGCCTCTTGC TGGTTGGGTG ACCTGATTAG TCCTCCTGAG 600
CCTCAGTTTC CTTTACTGTT TAATGACAAC AGTTAAGAGA TCATTTGGGT AATGGGCCTG 660
GTACAGTGCC TGACAGAGTC TGTGCCTAGC AAATACGCAC TCCTTATCCT TCCCCAGGGC 720
TATGCAAACT GCAAGTGGTT TCAGTTTCAG TTATGGGCAG ACCAGGCTAC CAGCAGGCCT 780
TGGAGCGCCT GGAGGATCCA TTCAGAGGGC AAGTGCTGGA TACTCTCTTC TCTCTAGCAG 840
GAACATGGAG GGTGGATGAG AAGCAGCAAG GATGATGTTT GCTTTCTGGA TCATCCCTGT 900
GCCTTGTGAT TAGCATTTAA TAGGCTCCCA 930
|
