| Tag | Content |
|---|
EnhancerAtlas ID | HS044-06799 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr2:9970390-9971310 |
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 | CACACACCAA CATGCCCAGC TAATTTTTGT ATTTTTATTA GAGACGGGGT TTCACCATGT 60
TGACCAGGCT GGTCTCAAAC TCCTGACCTT GTGATCCACC CACCTCGGTC TCCCAAAGTG 120
CTGGGATTAC AGGCGTGAGT CACTGTGCCC AGCCCTAGAC TTTTATTTAA AATGAGACTT 180
CTGTGGCTCT GTTACTCTCC TTCCTGGAAG GGAGGGAGGA GCAAGACCGG TTTGCCCCAA 240
GCCTATAAAT GGAATAAACC AGTCCCCAAC AGGTTCTGCA ACTTGCCTGA GATCTTATCG 300
CTCCTGAGTT TGGGAAACTC TTGAGTTATT TAAGCCACAC TCTTAGAAGG TTGTTTTGCT 360
TCTGTTTAAT TGGGGCTGTG CCTTCTGGCT GTTGAGCTCC TTTGACAAAG TGATTTTGCA 420
TCCAGAGTAC TTTATTCATT CATCCATTCA TTCACTAAAA AAACCTTTAT TAAGCACTTG 480
GTCTGTTAGC AGAAAAAGTA GGCTCTTTGG AACAGGCAGA ACTGAGTTAA GTTCCCTCTT 540
GGCCTCTTGC TGGTTGGGTG ACCTGATTAG TCCTCCTGAG CCTCAGTTTC CTTTACTGTT 600
TAATGACAAC AGTTAAGAGA TCATTTGGGT AATGGGCCTG GTACAGTGCC TGACAGAGTC 660
TGTGCCTAGC AAATACGCAC TCCTTATCCT TCCCCAGGGC TATGCAAACT GCAAGTGGTT 720
TCAGTTTCAG TTATGGGCAG ACCAGGCTAC CAGCAGGCCT TGGAGCGCCT GGAGGATCCA 780
TTCAGAGGGC AAGTGCTGGA TACTCTCTTC TCTCTAGCAG GAACATGGAG GGTGGATGAG 840
AAGCAGCAAG GATGATGTTT GCTTTCTGGA TCATCCCTGT GCCTTGTGAT TAGCATTTAA 900
TAGGCTCCCA GAAAGCTTTG 920
|
