Tag | Content |
---|
EnhancerAtlas ID | HS048-16231 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr17:47194950-47195820 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr17:47195373-47195386 | TGCAGCTGTTTCT | + | 6.29 | Myog | MA0500.1 | chr17:47195372-47195383 | CTGCAGCTGTT | - | 6.02 | Tcf12 | MA0521.1 | chr17:47195372-47195383 | CTGCAGCTGTT | - | 6.62 |
|
| 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 |
GH17I049117 | chr17 | 47194955 | 47195668 |
|
Enhancer Sequence | TTTGTTGGAA AGCCACCCAA CAGAGTGACC CAAACAGGAG CATCCAGGAA CCACGAACAA 60 TGGTCTTTAC ATGAGCAAGA AATAAACTTT TATTGTATGT TAGGCCACTA AGATTTCTTA 120 GTAGCTATTA TCCTGTGCCG ACTGTTTCAG CTGTGAGAGG GGACTGTGTG CTATTTAGTC 180 TCTGTTCCTC CAGCTCTGTC CTCCTCCCTA CTCCACCCTG TTCTGTGATC CAGGAGGACA 240 TCCATTGTCT GTGTGACCCA TGCTCCCTTC TCCTCTTGTT TCCAGCTGGG TTCAGTCAAT 300 GGGAAGAACC AGCAAGAGAT GAGAAAGTAG GAAAGGAAAG AGGGCAGAGT ATTTATTCCT 360 TCAGCTCCCA CCTGGCCAGG CTGAAGTTGA GCAAGCAACA GCTGTGGTTC CTTCACCTAA 420 GGCTGCAGCT GTTTCTGGGT TCAGCTATCA CTGTTGCCAC ACCTTGTTCA CTCAAGCCTA 480 AGGCAATAAC AGCTTCCTGC TCTTGCTAGT CCCTGAGTGC TTCCCCAACC CTTGTTGGTT 540 TCCTTAACCC TATGCACATC TCTGTAAAAA GGCCCTTGTT CAAACTCCCT GCAGTTACCC 600 CCTTTTGAGT GTGCCAGGTT TTCTCTCATG AAACTGACAT TGACTGATGT CAGTTTAAAC 660 TTATTTAAGG AAGTTTAAAT ATTCATCAAA GGTCCCTTGA AACTTCTTCT TCTTATTATT 720 TTGAGACAGG GTCTTGCACT GTTCTCTAGG CTGAAGTGCA GTGGTATGAT CACGGCTCAC 780 TGCAGGCTTG ACCTCCCGGG TTCAAGTGAT CCTCCCACTT CAGCCTCTCA AGTAGCTGGG 840 ACCAGAGGTG TGTGCCACCA TGCCCAGCTA 870
|