Tag | Content |
---|
EnhancerAtlas ID | HS145-15647 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr22:24255560-24256700 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr22:24255933-24255951 | ATTTCCTTCCCTCCCTCC | - | 6.45 | KLF16 | MA0741.1 | chr22:24256256-24256267 | GGGGGCGGGGC | - | 6.02 | KLF16 | MA0741.1 | chr22:24256352-24256363 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr22:24256257-24256267 | GGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr22:24256353-24256363 | GGGGCGGGGC | - | 6.02 | SP1 | MA0079.4 | chr22:24256351-24256366 | CGGGGGCGGGGCTTG | - | 6.23 | ZNF263 | MA0528.1 | chr22:24255838-24255859 | CTCTTCCCTTCTTCTTCCTTC | - | 6.61 |
|
| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_37758 | chr22:24249966-24257197 | HSMMtube | SE_56738 | chr22:24255405-24256233 | VACO_400 |
|
| 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 |
GH22I023907 | chr22 | 24250157 | 24258315 |
|
Enhancer Sequence | CCAGGGGTTA AGAGGGAGCT TGAGGCACCA GAAAGAGCTA TAGTCACAGC CACCTGTGAA 60 AGCCATCTCT GAGGTCCCTT CCTGTCACAA CAGCTGGGCT CCTGACTCAG ACCAAGACAG 120 CTTTTGTTTC TTTTCCTTTC TAGCCCCCCA CTTCCCACCC ACCTTTCTGC TTTCTCATAT 180 GGGCTCATTA TGGTTTATAG GGCTGGGGAA CGTTGCCTCT TCTGCCCTCC ATTTCTCCCA 240 TCTCCCTTCT TTCCCCTCCA CTTTTTCTGA GTCCACTTCT CTTCCCTTCT TCTTCCTTCC 300 CTCTGGGACG CTGCACAGTT CCTTCCACCC GGCACGGCCT GGGACTCTAG ACTCCCTCTG 360 AAGGCACGGA AGTATTTCCT TCCCTCCCTC CGACCCGATC TTTCTGCCCT TGATTCAAAA 420 CAATCTGAGG TCCCTAGGCC CTTCCCTTTC CGCCTCTGCG CTCCCCATGG GGTCCGGTGT 480 AGTTTTCCCG CCCCTTCCCT GCAGCTCCCG AGACCACCCG GACACAACGG AGCCATCCAG 540 CGCCCTCAGA GGCCCTGGGC ACACGGGCAG ATGGTCACCG CCTCCTAAGG GAGCAGCGCG 600 CGCCCGTTGC TCGCTGCCCG TTGGTTGTTG CTGGTAGCTC CGGAGGGCGG GGTTGGCGAG 660 GAAAGTGAGT CCGTATGTCC CCAGCATGCT CCGCGCGGGG GCGGGGCTCT AAGGGGGCAG 720 GCGAAGGCGG AACTGGCGTG GTCAAACCAA CCTATCAGCC TCCAGCATGC TCCGTGTGGG 780 AGCGGGGTTC CCGGGGGCGG GGCTTGGTTT GTGTGCCCTT CCGGCGTTTC GCCCCTGCGT 840 TCTCTGAGAT GCTCCCACGC AGATGTATGG GCCTAATTCG CTAATATCCA CTCTATATCC 900 TGTTCCATCC TCTTGTAATG GGCGTTTGGA GTGTTGCCAA TTTTTTGCTG TTATAATGAT 960 TGTAATAGCA TATTAAAAAA CTTGAACATA GTTTGATTGT AATAACATTA AATATAGCAT 1020 CTTAAACATA CAGTTTGAGC GTGCCAACCT GATGGGTGTG GAATGTAATA TTCATTATAA 1080 CTTTGATTTT CATTTCCCTA CTTTGAGTAA GTTTGAACTT CTCTTTATGT AATTATTGAC 1140
|