| Tag | Content |
|---|
EnhancerAtlas ID | HS048-26906 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr3:184362810-184363400 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr3:184363275-184363287 | AATTGTTTGTTT | + | 6.22 |
| | | 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 |
| GH03I184645 | chr3 | 184362947 | 184364010 |
| Enhancer Sequence | CCTGTAATCC CACCTACTTG GGAGGCAGGA GAATCACTTG AACCTGGGAG TCGGAGGTTG 60
CAGTGAGTCA AGATCGTGCC ACTGCACTCC AGCCTGGGGG ATAGAGCGAG ACTATGTCTC 120
AAAAATAAAA ATAAATTTCT GGGTTTTCTT TTAACTGACC AACACTATAT CCATTTTAAA 180
GATAGACTGA GCACCCTGGA GAAACTTGAC CCTGTGTTGC TCCCATCTCA GCCCCCAACT 240
ACCCATCTCT CCCTCCTGTC CATTAGCAAA GGAGAGCCCA GGGCTTCCAC CAGGCCTTCC 300
ACCTGCCCCA ACCTGCCTGC TCTGAACATT TTTAAGCATT CTTCAGGCAC CCGCTGCAAG 360
GGCACCTCTT CTGGGGAAAT ACCCCTGATC CCCAACACAG CTGGAGTCTC CTGCTCCAGG 420
CTTCTGGGCT CACACTTCCT GGCAGCTCTT ATCAGGCTGC TTGGTAATTG TTTGTTTTTC 480
CAACACTGTT TCACAATTAC TGTGCAATTT ACAAACTTGA CAACTCAGTG TGATCCAGCT 540
ACTGCAGAGG TGCCACCCAG GTGCTGATTC CTGCAGGGCC AGCCCTTCCA 590
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