| Tag | Content |
|---|
EnhancerAtlas ID | HS048-30211 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr5:138897260-138898270 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr5:138898206-138898218 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr5:138898210-138898222 | GTTTGTTTGTTT | + | 6.32 | | NHLH1 | MA0048.2 | chr5:138897574-138897584 | CGCAGCTGCG | + | 6.02 | | NHLH1 | MA0048.2 | chr5:138897574-138897584 | CGCAGCTGCG | - | 6.02 |
|
| | 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 |
| GH05I139517 | chr5 | 138896810 | 138898710 |
|
Enhancer Sequence | TGAATGAAGA CACAGGCAGT TGGGACAGAG AGAAGCGAGT GGGATGTGGA GGTGACCCGA 60
TGAAATACTG GCCCGGAGAT ATGAGGCATG AGGCGGGGAG CACGAGGGTG TCGAAGGGCC 120
AAAATGTGGT AAGAGAAGCC GGAGGAGTGT GAGGACAGGT GGAAGGGATC CAATGTGGGA 180
TCTAAGGGGT CTGAGACCAC CGTGGCCGCG GGAGGCAGGA GAAGGTACCG CAGAGCTCCC 240
GGTGATGTGT CAGGAGGCCC TACACTCGCG CGTGCACTGG CTCGCAGTTT GGACAGAGAC 300
CCTACAGGCC AGGCCGCAGC TGCGCCCAGA CCACCCCCAG CGGGTGAAGA CTGCCGCGGC 360
GGCGCAGTTC CCGGCATGCC TCCGGCCGGT GACTTCATCC GGCCCGGGGC CAAGGCCCGG 420
CCTCCGCTAG AGGGCGCTGC TCTCAGCAGC CGCGCCGCCC GGATGGACTC GCGCCAGAGT 480
AGGACAAGAG AGGCAGGCGG CGGCTGCTCC GTGCGGCTCC CACGCCTCTC GGGCGGCAGG 540
TCCTGCCTCG GACCTGGGAC CACTGGCTGG CGCCTGTGGC TCACATCTCC ACGCCTTTGC 600
CCGCTCCTCC CAGGAGCCCG AGTCAGAAAC CTGTGCTTCA CCCTCGAGAG CGCTGCCATC 660
CTCCCCCTCA ACCAGACGGG CATGGCGTCT GGTTGTCCGT CCTGTCTTCT CATCGTCTCA 720
GAGCCCTTCC CTGACCCCTA CCCTCTCTCA GACCAACAGG ATGATGACAG GAAGAGGATC 780
CAGGACCAAC TCCTAGCGGT GACCTTGAGA AAACAATCTC ATACCCCAGT TTCCCTTACA 840
ATGCAATGGA AATAATACTA ACAACCCTGG AAGAGTGTTG GAAGGACTAA ACGAAATCAT 900
CTTTTTCAGT ACTAAGCAGA GGCTCAGTGA GCATCAGCGT TTTTTTGTTT GTTTGTTTGT 960
TTTCTTGAAA CTGGTTGGAG CCCAGGCTGG AGTGCAGTGG CATGATCTTG 1010
|
