| Tag | Content |
|---|
EnhancerAtlas ID | HS038-06563 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr14:69764800-69766080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MSC | MA0665.1 | chr14:69765378-69765388 | AACAGCTGTT | + | 6.02 | | MSC | MA0665.1 | chr14:69765378-69765388 | AACAGCTGTT | - | 6.02 | | MYF6 | MA0667.1 | chr14:69765378-69765388 | AACAGCTGTT | + | 6.02 | | MYF6 | MA0667.1 | chr14:69765378-69765388 | AACAGCTGTT | - | 6.02 | | RFX5 | MA0510.2 | chr14:69765366-69765382 | GGTTGCCACAGCAACA | + | 6.22 | | RFX5 | MA0510.2 | chr14:69765366-69765382 | GGTTGCCACAGCAACA | - | 6.35 |
|
| | 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 |
| GH14I069298 | chr14 | 69765601 | 69765750 |
|
Enhancer Sequence | AGTCACTCAG CTACAAGTTC AGACTAGAGA CATTCAGGAC TGGTTAAAGA AAGCAGCCCC 60
TCTCTCAGGA AGAGTCAGGA GGGCAGAGGA GTTACAGCCT CTCAACAGCA ACGTTGGGGC 120
CTGCCAATGC CAGTTCCTGA TGCCCCCCTC TTTCTCAGGG CTGGTGAGTG CCCAGCGCCC 180
TTCACCTGCA TTGGCAGGAT TCTGTTCTAG CTGTGTGTGG CCCTCTCTCT GCCCCTGGAG 240
GGCCCTCCCT CCTTCAGCTT GTAGATAGGG AGTGGAGTGG GTAAGGAGGT GTTGCTGGAG 300
AAGTGGCCTA TATCACAAGA AGGTGTGGGA ACCCCTCTGG CGGGAGTCAT CTCATAGCTC 360
TTCCAACCTG TTGGTAGGGA ATGATAGAAC AATTCCAAAT CTCTGCACTT CACAATCAGC 420
CTCCCGTTCC CTGTCGCCAC TTCCCACGTC CTCCACCATG TTCCATCCTC ACAGACACTT 480
TGGGGGCAAC TTCCCCTGCA GTTGCCCAAG CCAAGTAGTC AGCAGGAGCT TCATGGCTGT 540
TAGCTGGAGC GGAAGGCTGG CTGCCTGGTT GCCACAGCAA CAGCTGTTGT AAGTAAGTGG 600
TCCTTGTGAC AGAAGACAAT TTAATAAGCC AGATCTGGGG GCCTAGTGGG AAGGTTGCTA 660
GTGGCTTTAC TGGGTATCTT CTGTGGTGCT GGAGCTGTAG GCAGGCAGGT GTGACTGAGG 720
AGAGTTGGAG TCGGGGGAGG CCAGGCATCT GCCTTTACCC AAGGGCTGGA GGCTTTTGTC 780
CTGCAGAGGT AGGCCCAGCC AAGAGGGAGC TGCCTCCTGT GTCTTCAGAG ATCCCGACAC 840
TCAACTCTGG ACATCACCCA AGGCCGAGGC CTTGCACTTC TGCTCCCAGC TAGAATGAAC 900
TAGCTTGTAT CAGAGCAGTT CTTCTGCTGA GAACAACTGG ACAATTTGGA TGAAGCATAA 960
GAAACATCTG TGTGCAGTTG AGACTGAGGC AGACAGGACA GGTGTCCATA TCTAGGGCCC 1020
GATTTCAGCA CGTGCAGTAG CCCTGGGAAA ATGGCATGCT GTTTCTGCAT CTCTGTGCTC 1080
CTAGTAAAAC AGCAAAACTC CTGGAAAGAG TTGCCTATCC TTGCTGTGCT GTTTCTCTCC 1140
TTTCATTCTT TCTTGAATCC ACTCCAGTGA GGTTTTTGTC CCTACTGTTC CTCCAGAATT 1200
GTTTGTCAAG GCTGTTCTCA CTTCATTTGC TCCCTAAGGG ATCTCGCCTC AAGTCTCAGG 1260
TTCCTAGGAA GCTGACTCGG 1280
|
