| Tag | Content |
|---|
EnhancerAtlas ID | HS048-28977 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr5:1385250-1386200 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr5:1385881-1385902 | ATCACGTTTCACTTTCCCATT | + | 6 | | IRF2 | MA0051.1 | chr5:1385880-1385898 | GATCACGTTTCACTTTCC | - | 7.05 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GCGTGGCCGG CTGGAGCCCA TGGCCAGCAG CCATGGCTGA GGGCATACTT CAAAACGGTC 60
ATTTCTGTCC CACTAATACT GTGTAAATAT GTATGCCATC CAATTTTTAA CCAAATAAAA 120
TGTTCTGTCT GACGGGTCCC TTCATCTATA TGACAAACAG TTTTAAGTAA AGAGGATCTC 180
AGCTTGCAGA ATAAGTAAAA TTGTTTAAAT TCTAGATAAA TGTGTTCAGT GCTTGATGGG 240
CTAATGCTGG CTGGATTTGT GAAGGTCAGT CATATACATG AAAATTCTTC TGCATTCACC 300
TTAGAAGAGC GATATTTTTA GGCGAACAGA GCTTGCGATA TTTTCTTTCC GTGCCACCTG 360
CCCGCTTGGT GTCTGGCCCT GCGTCCTCAG AGGACCATGG TGGGCTGGTG TTCTTGGAGA 420
GGAGGCCTCT CCAGGGCCAC CAAGAGGGGG CTGTGGCCCA GGCTGAGCTC TTCTAGTGGC 480
ATGAGGGACA CGCTTTATTC ATGTGAGCGT TGTGAGGTGG GAAGGGAGGC CAGCCAGGGG 540
AAGGGTAGAA GAATGCCTGT TGCTTGGGTC GGAGGCTCGA TGGACTTTCA CTGCTGGACA 600
TAGTGTGAAC ATGGGAGACG CAGGTTCAGC GATCACGTTT CACTTTCCCA TTCCCCGGAC 660
CTCAAACTCA GGCCTGTGTA ACTAAAGGTT CTGTGCTGCC AGGCTGGGCG TTTCCCCCAG 720
GGAAGGCACG AGAGAGCGAA TGCAGGGCCG GCCGCGGGGC CTGGGGACTG TGCCGCTCAG 780
CACCACCCAC AGGGCGTTCC TTGGGGCGTG GCCTGGGCCG GGGCGGTAGG ATCCCTTGGA 840
CAGGGCCGTG TCTGGCTCAC AGGAAGCTGC CCTCATGGAA CGGGGTGCAG TGGGGTGTTC 900
GTGGTCCTGC TGCCGTTGGC TGGGCGCAGC CATCCCTGCC GGCTCCCCCG 950
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