| Tag | Content |
|---|
EnhancerAtlas ID | HS038-13622 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr22:26565730-26567260 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr22:26565742-26565752 | GGGGCGGGGC | - | 6.02 | | Klf1 | MA0493.1 | chr22:26566288-26566299 | TGGGTGTGGCT | - | 6.14 | | Myog | MA0500.1 | chr22:26566778-26566789 | GACAGCTGCAG | + | 6.62 | | Tcf12 | MA0521.1 | chr22:26566778-26566789 | GACAGCTGCAG | + | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TAAGCGCCCC GAGGGGCGGG GCGGGCAGGG GGCAAAGTTG CCGGGAGAGC GGGGCAGCCA 60
GGGGTCGGGG CTGACCAGGG CGACTCAGGC ACCACCCGCC GGGATGGGAA GCGGTGGTGG 120
CTGTCCAAAA TCGGGGCTAG GAACCGCACG TCCCCTTGGC CCGGGCTGAT GGGAGTGTGG 180
AGGCGGGGAT GTGTTGAAGG ACTCGGGCGC TTCCCTGCTT CGGCTGCGGG CTCCCTTTCG 240
GTCTTCCCCG GCTGCGGGGC TGATTCTCCT TTGCAGCCAA AGAGGTTCTC CTTGGAGTGG 300
GGTCGCCTCC AAACCCCAAA TTCCCGGCGC TTCTCTGCAA CCGCACCCGG GGCTAGGTGC 360
CAGATAATTA TCTTCCTCTC CGGGAGAGGA CAGGAAGGGG GGTGAGAAGC TGACCCACCC 420
TGCAACTGAG GACTAGACTC AAACAGTGCA TTTGCCGCTC CCCCCGACAC CACAGAAACC 480
CTTGACTCCT TTGGTTCAGG CTACCCCGAG GGTCTGTGTT CCTGGATCGA TCTCAGCCAA 540
GCGTCAGGAT ACCGGACTTG GGTGTGGCTT TCGCTAGAGG CCGGTGGAGG GGGCTGAGGG 600
CTCTGAGAAC TTGGTAGGGG AGGGAGAAGA GATGTTAGTT AGCAGTTGGG AACCTGAACG 660
GGCTCCCCTC TACTCTCTCC CCTACTGCCT AGCATCTCTG ATCACTGTTA GGAATGGGGG 720
GTGAGGGGTG TTAGTTTCAT CTACCACGTG TTTGTTGAAG GGGAAGAGGG GCCCAAATTT 780
AGCAGAGAAT GACAGCTCCT CTTTCTCAGA CCTGGAACCA TACCCTCTCT CCACCCCGGT 840
AAGGTACCCC AGGAAAAGTT ATGGGTGGGG GAGAGGGCCA GATAGAGAGA GGGGTGCAAC 900
GCCTAACTCA CCCAAAGCTA ACCCTCAGAG CTTCGGGGGT TTTCTCAGGC ACCTAGGAGA 960
CCCGAAAATC AATGGGAGGG TTAGTTGGCC ACAGGACCCG GCCTTCTTGC AAGGTCCCAG 1020
AAATGCGCTC CTCACGTGTA AAAAAGCAGA CAGCTGCAGG GTCTGCCCAG GCTGAAGACA 1080
GAGGGAGCGC AGGCACTATG CTTATCTGGG GCTCCGCCTC TGTCATTTGC ACCGTCTTGA 1140
CTCGGAGTTG GGGGACAGGC GGTGTTCTTC TCCGGGGAGT TCTGGACCCC CAGCGCGCGC 1200
ACCTGCTTTC AGCACCAAAG GCCCTGGACA GCTCTCAGCT CCATGGGCCC TGGCTCTGGG 1260
TCCCTTTCCC TTCAACCCTT CCCGGTGGCC TGGAGTGCCC CCCTCAGCAT AAATCAGGCA 1320
TTTTATCCCC CATCTCCCCG TCTTTTTAAA TGTAGAGCCC AGAGTGCAGA GCAAAGGAAA 1380
TTGTTCATCA CCTTTTGTTT AACAAAGCAT ATCATTGAAG AACCCCCACC CCTTTTTTAT 1440
GGGGCAATAA TGTCCACAAT TTACACCAGG TCTGGACAGT TTCTCTGGGA AAGATAGGGA 1500
AAGAGATTTG GTTTAAACAA ATCGTTTCCA 1530
|
