| Tag | Content |
|---|
EnhancerAtlas ID | HS050-13592 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr11:102245230-102246120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXA1 | MA0148.4 | chr11:102245446-102245462 | CTTTGTTTACCTAATC | - | 6.09 |
|
| | 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 |
| GH11I102374 | chr11 | 102245532 | 102246131 |
|
Enhancer Sequence | CCACTTGAGG AGGCAGTCTG CCGGTTCTCA GATCTCCAGC TGCGTGCTGG GAGAACCACT 60
GCTCTCTTCA AAGCTGTCAG ACAGGGACAC TTAAGTCTGC AGAGGTTACT GCTGTCTTTT 120
TGTTTGTCTG TGCCCTGCCC CCAGAGGTGG AGCCTACAGA GGCAGGCAGG CCTCCTTGAG 180
CTGTGGTGGG CTCCACCCAG TTCGAGTTCC TGGCTGCTTT GTTTACCTAA TCAAGCCTGG 240
GCAATGGCGG GCGCCCCTCC CCCAGCCTCG CTGCTGCCTT GCAGTTTGAT CTCAGACTGC 300
TGTGCTAGCA ATCAGCGAGA CTCCGTGGGC GTAGGACCCT CCGAGCCAGG TGTGGGATAT 360
AATCTCTTGG TTCGCCGTTT TTTAAGCCAG TCTGAAAAGC GCAATATTCG GGTGGGAGTG 420
ACCCGATTTT CCAGGTGCGT CCGTTACCCC TTTCTTTGAC TCGGAAAGGG AACTCCTTGA 480
CCCCTTGGGC TTCCCAAGTG TGGCAATGCC TTGCCCTGCT TCGGTTTGCA CACGGTGCGC 540
GCACCCACTG GCCTGCGCCC ACTGTCTGGC ACTCCCTAGT GAGATGAACC CGGTACCTCA 600
GATGGAAATG CAGAAATCAC CCGTCTTGTG CGTCGCTCAC GCTGGGAGCT GTACACCGGA 660
GCTGTTCCTA TTCGGCCATC TTGGCTCCTC CCCTCCTTCA ATAAATATTT GTTGAGCATG 720
AGCACCAGTG CCAAATACTG TGCCTAATCA CAGTGGTTGC TGTCAAGGAG TATATACACT 780
AGCTGGCGAG ACTAGTGTGC AAAAGACAGG GTTAAAGGGC CAGCAGAGAG GCGAAGGTTG 840
CATATGTATT GGAGTATTGC GTTGGAAGAT GCTTTCTTTT TAAGCTTGTA 890
|
