| Tag | Content |
|---|
EnhancerAtlas ID | HS048-10806 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr13:107569970-107570680 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr13:107570558-107570577 | CACTGCCCCCTACTGGCCG | - | 8.13 |
|
| | 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 |
| GH13I106915 | chr13 | 107567809 | 107573470 |
|
Enhancer Sequence | GGCCGGGGCC GGGGTCGGGG ACGCGGGGCA GGTTCGTGGC GCAGCCCGGG GAGACCTTGG 60
GCGAGGCCTC CAGGCGGGGA CGGGAAAGGG AACGGGAACG GGGACAGGGC GCAGGGCAGA 120
GGGCCGGGAC GGAAACGGGG ACAGGGCGCA GGGCAGAGCA CAGAGCGCAG GGGCGCAGAG 180
AAGGGGACGA AGACGGGGCC GGAGGCGCCT GAGGGGGGCT CCGTGCGGGA ATCGGCGGCG 240
CCACCCAGCC CCGCACATCG CCGAGAGAGG CCCGCGTGCT TCTGAGAGCG CCGCCCCTGA 300
CGTTTCTGCT GCGCGCTGGG ACCGAACCTA CAGGAAGCAA AACCCTAGAG GAAGAAGTCG 360
GCGGCTTTTT GGCTCGGAGA CAAAATGGAG CCCCGCGGAT GCAGCCTGGG CTCCCTCGGG 420
CGCATCCCCA GAAGCTGCGG GTGTCCCCGG AGGACTTGAA GTCCTCCCGT GCGTCTCGAT 480
GCCACCAGTT TTTGTTTCTT TGGTGAGGAA TCGGTTCACG GTGAAACTTC ATTCCTCAGC 540
CGGTGGGGAG CCGAGGCTGG GCCGGGCGGC GAGGGTTGCG CTGGGACGCA CTGCCCCCTA 600
CTGGCCGCTG CGCCGCGTTC CCAGCTGCTC GAGCGGGTGG TTCAGTGAAC TCGGATTAAT 660
TTAAATACAG CCGTAGATTT GGCTTTTTTC CCTCCCGGGC GAATCTAAAT 710
|
