| Tag | Content |
|---|
EnhancerAtlas ID | HS048-22489 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr2:242641740-242643150 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr2:242641756-242641766 | GGGGCGGGGC | - | 6.02 | | Zfx | MA0146.2 | chr2:242641755-242641769 | CGGGGCGGGGCCTG | + | 6.18 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 242641903 | 242642065 | | chr2 | 242642157 | 242642400 |
| Enhancer Sequence | CCAGGTGCGT CACGGCGGGG CGGGGCCTGG CGATGCTGGG CGGGGCTTGC GGCCTCGACC 60
CCGCCCACAT ATTAGGTCCC GCCCCTACCC AGGCCCCGCC TCATCTCCGC CCCCAGCTCC 120
GGCCCCGGCC CCGCCAGGTC CCGCCCGTCC CTGTCCCGTC TGCAGGAGGA GCTGGCGCCC 180
GCTGCGGGGC TCCGGGCCTT GGGGGCTCCG GGGTCTGGGC CTCCGCCTGG CTGTGCGCCC 240
GTGTGCGCCG GCCTCTTGTG TGACCGCGGC TGGGGAGGGC GTGCGGGCCG CGGGGCGTCT 300
CTCCCCGGCA CTGGGGACTG CGGCGCGGAG GCGGGGAGGG CGGTGCCGAG TCGGCCCTGG 360
TGGGCGGGCT GTGCTGTTTC CAGGTGGCAG CAGGTCGGCG CCCCCAGCGG CTGAGCGGAC 420
GGTGCTTTCC CTCACTTTAC ACACCAGGGA AGGTCCAGCG CTGCCGAGCA GCCTGCTCAG 480
GGTCTCCCGC TCGTAGAGGG GCAGACCCCA CGCGGGACCC CTGACGTCGG CCCGGGATGG 540
GCACAGCTTT GGGGTCGCGG TGTTTGGGGT TGTGCCGGGT GGCTCTGGAG GGCCCTTGTG 600
GGGGCGCTGC ACTGGGGATC CTCATGGTCT TCGGCCTGGC ACCCGCCCAG GGGCTGAGAC 660
AGTGGCGAGT GAGCCGTGGC CTGGAGCTGG AGACCGCTGC CCTAGAGGGA CGCCCGATTC 720
TGCCCATGTG CTCCGCTGTC TCTTGGGGGT CTGAGTAGTG GGGGGTTCCC TGGGTAGAAG 780
AGTCAAGCTG GGGAGCACGC TGGAGGGGAG GCCTTCTCTA TCCTGGTGCC CAGCCAGTGG 840
GCTGGCCTCC CAAGGAGGGT TGACTTTGTG TGTGTCTGGG AGGCTGTGCC AGCCGGGAGG 900
CTGTGCCTCT GTCCTCTAGG GGAGCTGGGA AAACACTGGG GCTGGAAGCA TCAGATGCAT 960
AAGATAGAGT TAGGTTTAAA ATGATTGCCT GGTAACTGTG AACAGCAGAT GGGAGGGTGG 1020
CCAAGACTGG AGGAGGCAGC CCCCCTTAGG AGCCTGTGTC AGCTGTGCAG GGGGCGGAGG 1080
TTGGCCTGGT CTAGGGGGTA ACAAAGCAGA CGCGAAAGCA GCACGGGGGT CCTCCTGGCA 1140
GACTGTGGGG AATGGTTGCG CTAGCCACAG GGACTATTTA AGTAAAATTA AAAATTGAAT 1200
GGCGTTAGTC CCATTTCCAG TGCTCAGTAG CTCCCTATGG CCACCACTGT CTTGGGCAGC 1260
TCAGAGAGAA CATTTCTTTT CTTTTTCTTT TTTTGATTTT TTTTGAAATG GAGTCTCACC 1320
CTGTTGCCCA GGTTGGAGGG TATGATCTCA GCACACTGCA ACCTCCACCT CCCAGGTTCA 1380
AGCAATTCTC ATGCCCTAGC CTCTCGAGTA 1410
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