Tag | Content |
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EnhancerAtlas ID | HS101-22312 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr19:49160120-49160850 |
Target genes | Number: 41 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GLI2 | MA0734.2 | chr19:49160303-49160318 | CAATGTGGGTGGCCT | - | 6.23 |
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| 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 |
GH19I048656 | chr19 | 49159932 | 49161150 |
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Enhancer Sequence | TGGTATGGCG GTAGACCGGG TGCCCCTCGT CTAATTACAG GAGTCCTTAA AAGCAGAGAA 60 CCTTTCCCAG CCATGGTCAG AAAGAGATGT GAGGATAGAA GAGGCAGGAA AAATCTGAAA 120 TGTGAAAGGG ACTCGACCTG TCGTGGTTGG CCGTGAAGAT GGAAAAAGGG GTCATGAATC 180 AGGCAATGTG GGTGGCCTCT AGAAACTGGG AATAGAAAGG AAACAGATTC TCTCTTAGAG 240 GCTCCAGATG GAATGCAGCC TCGTTAGCAC CTTGATTTTA GCCCAGTGAA ACCCATGTGA 300 GGCTTTTGAT CTGTAGCGTG TAAGATGATA AATTTGTGTT GTTTCAGCTG CTGAGTTTAT 360 GGTAATTTGT TATGGCAGTA ACAGGAAAGG AATTCGACAG TTCTCTGTTA CTGAGCACGT 420 GAGGGAATTC TACGTCCCCA CCTTCATACA ACTGAGTGGA ACCACATGAG TAATCCCGAT 480 GAATGAGCTG TGATTGGAAG GGCCGGGAGT CGTTCCTGGA CCAAAGCTGT TTTGCTTGCA 540 TAAGACCATT CAGTGCTTTT CCTCTTTCCT TGTCTCAGTG ATCAAGGATG CCCTGGGTTA 600 CGGGTGGTGC TACAAGGTGG TGAACATCTC TCAGCCTGGG TCCTTGACTG TGTGGAAAAC 660 CAACCTTTGC CAACTTGCAT GGAACATGTA TATGAACAAG AAAGAAACTT TGTGTTTTCT 720 TTTTCTTTTT 730
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