| Tag | Content |
|---|
EnhancerAtlas ID | HS180-10133 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr11:120483400-120484550 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr11:120484154-120484165 | CTAATCCCCTT | - | 6.32 | | GSC | MA0648.1 | chr11:120484153-120484163 | GCTAATCCCC | + | 6.02 | | HNF4G | MA0484.1 | chr11:120483867-120483882 | AGAGACCAAAGTTCA | + | 7.09 | | IRF1 | MA0050.2 | chr11:120483929-120483950 | TCACACTTTCTGTTTCTTCTT | + | 6.2 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 120483447 | 120484361 | | chr11 | 120483837 | 120483981 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I120612 | chr11 | 120483220 | 120484689 |
|
Enhancer Sequence | GGGAATTATT AGACTTGACA CTAGAAGTTG TCAGTGTAGC CCTCATTATC GGGCTACTTT 60
GTGGTGGATG GGAACTGGCT TTGGGGCTTT GTCTGTGACA GGAGAGTGCT CCCTGCTGAC 120
TCTGGGTGGG TCAGACAGAG GCCATACCAG AGCTCTGAGC TTCCACCGTG TGTAGAGCCC 180
TGAGCGGGGC AGGGAACACA GGGACAAAGA GGAGTGAGGT AGGTAGGGGA GGAGGGTCAT 240
GGGCACATGG TGCAAACCCG AGTGTGTGTG TGAGAAAAAA GCATTTCTAA TCAGTGACCC 300
TCGTATTAAG CAGGGTTCTG TGTGTGAGTG GTGGGGTTGC TGGGATAAAG AGCCATTTGA 360
GGCTGGAGGG CTGGTCTCTG CCATTGGGGT CTTGGCTGGT GAGAATGAGG ATGATTACTC 420
ATATCCATGT GTCGTTGTGA CTCAGAGAGC TCGGGTTCTG GAGTTGGAGA GACCAAAGTT 480
CACAGCTGAG CCCAGCTGCT GCTTAGCTGA TTGGCCTTGG GTAAGTTCCT CACACTTTCT 540
GTTTCTTCTT CTCTTGTGTG GGGTATCATA ATAACTGCTT CCTGTTTCTC TGTGTCTTGT 600
ACAAGAAGAC ATGCCCCCAC AGTGGGACTA GCACTCAGGT CTTGTCAATT CTTGTCCTGT 660
GCTTTCTATA CCCTTCAGCC AAGGGAAGGG GGGCTGTCTG CTTAATTAGC TGATGTTGAT 720
AAGAGCTTTG GAGATACAAA GCTCTTGATA AGAGCTAATC CCCTTAATCT GTGTGGGGCT 780
GATGTGTGCA TGTGTTGTAC AAGGCAAATA GCACTGGGGG GATTGACCAG GAATGCAGGG 840
CAGCACACGG AGTGTGCATG TGTTTGCGTG TGTGCATGTG TACACATTGT TCTTGCTCCC 900
TTGAAAGGTG CTGCAGACAT GATGTGCAGG GATTCATGCC TCAGATGGAG CTTGGAGGAG 960
ATGCCCTCCG TGTTTTTCCA TCCCCAAAAT GCTGTGATTC TATCCTTGAT TGGAAGGTGG 1020
CTCCAGGTCC TGGGGCAGGG AAGCTCCTGA GCTCTGCAGG AGCGTCTGTG TGGTCCAAGG 1080
GAAGGATTTA AGAGCCCAGA GTCAGGTGTG GGGTGAGCTT TCTGCACACT GCCCTGCTCA 1140
CTGTCTCAGG 1150
|
