| Tag | Content |
|---|
EnhancerAtlas ID | HS045-42214 | Organism | Homo sapiens | Tissue/cell | Fetal_lung | Coordinate | chr22:25030640-25031540 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYC | MA0147.3 | chr22:25031041-25031053 | GGGCACGTGGCT | - | 6.18 |
| | | 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 |
| GH22I024634 | chr22 | 25030768 | 25031567 |
| Enhancer Sequence | TAAACTAAAG CAAGGGAGGA GTGGCCGTTC TCTCTGTTCA TTCATTCACC TTTTCATTCA 60
TTCCTTCTTC CCTCCATTCC CCCATCTGTC CATCCTTCCC TGCCCTGATT GCTCATGCCA 120
CCGCCCCCCG CAGCCCCTCC TGACCTGGTC CTTTGGTTTC TCTTCAGGGA TTTCTGTCTC 180
CTCCCACAGG GCTGAGAATG GCAGCTCAGG GACAAGTAGG GGCTGGGGAC TGCTTAGTCT 240
CCCCAGTGGC TCTCAGGGGA TTTGAGGGTT TGACGCCAGC TGCCACCCCA GGCTGTGCCC 300
CTCCTCTGCT CAGGAGGACA TACAGGATGC AACACCCACT TAAACTCGAA GTTGCAAAGA 360
TGCAAATGAG ACTGGGGTCT CAGGCACCAG AGACCACCCG TGGGCACGTG GCTTTTGGGA 420
TTGGAGACCT GCTGCCACAG ATCTCTGAAG AGTCTGGACC TGCTGGGTCT CCCCAAGTGA 480
CTCTCTGGGG GTCTCCATAG CATGCCCTGC TGTGTGCATG ACGGTCACTG GTTGGGTAGG 540
GGTCTCTACT CTAAAGCTCC CTCTGCCGGC ATCCCCTCGA ACTCTCCCTT GGTGAAGAGA 600
GAGGATGTGG TTTGCCCCAG TGTTTTATCA AACAACTCTC TCCACTTCCT GTTTTAAGAA 660
GCTGGGAGTG GAAGAGAGCC TGGGGCTGGC CCCAGCTGCT GCTGCGAAAC AGGGGTCACT 720
GGACGCTGGG ACCCTGGCCG GGCTGGCTGG AGGCCTCAGG AAGAGGCCTG CTACAGTGTC 780
ATCCTGGCCA AGATTCCTCC CTGCAGAGGA CCCTGGCCAC GCTGCCACAG GGTCTGCTGG 840
GGCCACCAGA AGCCCATGCT CCTGCCTCCA TCTCTCCCCT CTGTGCTCAC CTCTCACCAG 900
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