| Tag | Content |
|---|
EnhancerAtlas ID | HS145-21748 | Organism | Homo sapiens | Tissue/cell | NHBE | Coordinate | chr5:176119830-176120960 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxo1 | MA0480.1 | chr5:176120021-176120032 | TGTAAACAGCA | - | 6.14 |
| | | 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 |
| GH05I176692 | chr5 | 176119654 | 176120597 |
| Enhancer Sequence | AGCTCCTGAG CAGGGGACCC CTCGGGCTGC CTTTTCCATC TTCTTGGCCC TGCCTCATCC 60
TCCCCTAGGG CTGTTTGCTC CCTCCAGAGC AGGCGACCAT AATTGCTGCT TTCCACAATG 120
ACATAAAAAT CTAAGAGGCA CAATCAATAC AGCGCACACA CATCATCGTC TTTCATTGCA 180
AACGATAAAA GTGTAAACAG CAGGGGTGGC GGCAGCTCTG GAGGCTGCAG TGGGGGCAGG 240
GCGGGCTGCC ACCACTTCCC TGACTGTCAC CCTTCTTCTG GGACACAGGG CTCTTCCAGG 300
TGCGAGCGGG AGTGCCTTCC CCACTCTGGG GAGTGGCACC CCTCATTAAA GCCCATTCAG 360
GGAAGTGGTT TTTCCTGTTT TTGCTTCCAG ATGCAGCAAC CCCAGTTTCT TTAACCCGAC 420
TTCAGAAATC CAATTTGTCC TCTGTACTTT AAAAGCTTTT CCCTTGCTTC CCCTGCATCC 480
AAAATACAGA GCTAGGGGTG GCTTCTGGTG GCAGAAGAAC TTGTTGGGGT TTTGCCTGTC 540
ACAAGCCCAT GAACTGACCT CGACCCCATT TTAACCCCAG CTCTTGACAG CCAACTTCTT 600
TCGCCACCTG TCCAGCCTGC CACCCACAGC TTTTCTTGGA ACGTGCACAG AAACCATTAT 660
ATCCCCAGCT CCCACACACT CCCGGCGACG ACTTCCTCAA ACTAGTTACT TAATGAACGT 720
CATCCAATTC CGATTCCGTC TTGCTGTAGT CTCATTTGCG AAAGCCAATC TGCTTTATGA 780
TTCTAACCTC TGGCTAGCAA CTGCTCCCAA TTTCATGTCA TCCATAAACT TGATGAACGA 840
TTAGCTTGCT TCTCTGCAGT CATTCATTTA TTTATTCAAC CGGTATTTAG TGAGCGCCTA 900
CTGGATGCTG GGTGCTGGAT ACAGAGTTAC AGGAGACGCA GGTCCTGGGC TGAAGAGACT 960
CCTGTGGGGA GGCGGAGCCC ACGTGAAAAT GGTTCCCATT TATGTGATCT GTGCTCAACT 1020
GGGGCAGGGG AGAGAGCCAG CTCCTTCTTG GTGCGGGGGG CGGGGGGCAG TTTACATTTG 1080
CCTGAAGATG CTGGAGGGGA TTTTGGCAGC TGGAGAAGGA ATGACGTTCC 1130
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