| Tag | Content |
|---|
EnhancerAtlas ID | HS048-07320 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr11:77801480-77802420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP2 | MA0593.1 | chr11:77801854-77801865 | AAGTAAACAAA | + | 6.62 | | GLIS1 | MA0735.1 | chr11:77801792-77801808 | TGACCCCCCAGGTAGA | + | 6.1 | | GLIS3 | MA0737.1 | chr11:77801793-77801807 | GACCCCCCAGGTAG | + | 6.37 | | KLF5 | MA0599.1 | chr11:77802124-77802134 | GCCCCGCCCC | + | 6.02 | | POU4F2 | MA0683.1 | chr11:77801734-77801750 | GTACATATTTAATGAC | + | 6.44 |
|
| | 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 |
| GH11I078090 | chr11 | 77801135 | 77802719 |
|
Enhancer Sequence | ACACCCGGCT AATTTTTTTG TATTTTTAAT AGAGGTGGGG TTTCACCGTG TTAGTGAGGA 60
TGGTCTCGAT CTCCTGACCT GGTGATCTGC TGAGTCTGTC CCGCAGACTC TGGCTGAGCA 120
ATGGATGAAA GAAGTACACT GACACAGGTG TTTTGCCTGA CAGCGCAGCT AGGGCTCAGC 180
ACCACTGACG AGAGAGTGCA GCAGCCACCG AGAGAGTGCA GTCCCAATAA GCTGGCCCTG 240
CTCGCATTTA TGTAGTACAT ATTTAATGAC AAAGGGTTGA AGCAAACACA GTTTGTGGGT 300
AATAAACATT GTTGACCCCC CAGGTAGAGA GCAGTCCTGT GCTCGAATGA TCAAAGGTTG 360
GTTTCTGGAG ACAGAAGTAA ACAAATTTAT CTAGATAAGT TTCTTTACAT TCCCTTGTTA 420
TCTGCCCTTT GCTCTCAGGC TCCGGATAAG AAAATTTGAC TGCCTTCAGC CATAATTCCC 480
TTCCGAAGCT TTTGGAAAAC CTCCCGGCCT TCCAAGAAGG TTTGCGTCTT TCCCTATAAC 540
TTTTTCTTAC AACTTTTCCC ACCACCCTGA CAGAACTCCT ACAGTGATCC ACCCGCCTCA 600
GCCTCCCAAA TTGCTAGGAT TACAGGTGTG AGCCACCACA CCCAGCCCCG CCCCGCCCTT 660
TTTTTTTTTT GAGTCAGTCT TACTCTTTGG TGCAGGCTGG AGTCCAGTGG CATGATCATG 720
GCTCACTGCA GCCTCAACCT CCTGGGCTCA AGAGATCCTC CCACCTCAGC CTCCTAAGTA 780
GCTGGGGCTA CAGGCCTACA CCACCCCAGC TGCCTAATTT TTTTTTTTTT TTTTTTGAGA 840
CAGAGTCTTG CTTTATCGCC CAGGAAGGAG TGCAGTGGCG CGATCTCGGC TCACTGCAAG 900
CTCTGCCTCC CAAGCTCACA CCATTCTCCT GCCTCAGCCT 940
|
