| Tag | Content |
|---|
EnhancerAtlas ID | HS076-02447 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:53753940-53755190 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr1:53754214-53754235 | TCTCCCTTTCTCTTTCTCTTA | + | 6.45 | | KLF13 | MA0657.1 | chr1:53753994-53754012 | CACAAGTGGGCGTGGCAG | - | 7.24 | | KLF14 | MA0740.1 | chr1:53753997-53754011 | AAGTGGGCGTGGCA | - | 7.73 | | MYCN | MA0104.4 | chr1:53754091-53754103 | GGCCACGTGGTG | + | 6.07 | | MYCN | MA0104.4 | chr1:53754091-53754103 | GGCCACGTGGTG | - | 6.07 | | SP3 | MA0746.2 | chr1:53753998-53754011 | AGTGGGCGTGGCA | - | 6.71 | | SP8 | MA0747.1 | chr1:53753998-53754010 | AGTGGGCGTGGC | - | 7.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 53754594 | 53754800 | | chr1 | 53755120 | 53755170 |
|
Enhancer Sequence | TTCTCTCTAC ATGGGGATCC TCCTCCTTCC TTAGGTTGCC AAGAGGATGA AAGTCACAAG 60
TGGGCGTGGC AGGGCTTTGT TCCTTCTGAA GCTCAGGACA AAGCACTGGG CTTCCCTCCT 120
GCCTGGGAGC CTTCAGGACG GCATGGAGTT TGGCCACGTG GTGGGTAAGG AAAGGATGGG 180
GCCTGCGGCA TGGCTGGGGA GGCCAGGAGC AGCTGTACGA GGAAATGAGG GCTCCTTGTC 240
TCGGGTGGGG GCCGCTCTTG CTCTGTTCTC TCTCTCTCCC TTTCTCTTTC TCTTATGTGG 300
AGACTGGTAG CTCTGTTGCT AGGAGACAAG GAAACCCAGT TATCACCAGC CACGGCGTTA 360
GATGGGACTC CGGTCTCCAT TGTCCCCACC TCTGCCTCTG GGACGACTGT TACCCCTAAA 420
CAGGGGCTCC TGGGTCCCCG CCAGCCCCAC TATCCTCCAC ATGCTTTTGC CTGAGCCTTT 480
TGTCTCGGGC TCACGCTGCT GAAGCTCTGC CTCTGGACTG CTGGGTCCTT CCCCGCCCCC 540
TTCTCATCTC CTTTTTAATT TAACAAATGT CACAGAATGA CCTGCCGGGT GTAAGTTTGC 600
TTTGAGGATT AGGGCCTGGA AAATAAATCA TGGAGAGACA AAGCCCTGAG TGTAGGGGGC 660
AGGCCTGGGG CTCAGCTCTG GCCTCTACCT CCCCCTGCCT GCCTCTGCTA CCACCCAGCT 720
GGCCATGGAG GCAGGAGCTC CTAGGCTCAG CCCACCCAGG GTAGAGGAAC GGGCCAGAGC 780
CTCAAAGTCT TGGCTGGGTA GCCTTGGGCA AGTCACTCAA CCTCTTTGAG CTTCAGTGTT 840
CTCCGTTACA AAACTCAGAA AATGACAGTA TCTGCTTCAT GAGGCTGCTG TGGTTATCAA 900
AGGCATTAAT GCACACAGAG AGCTTAGCAC ACGATAAAGG CTTAAGAAGC ACCAGCTGCC 960
ACTGGCACTC CTGGAATTAT GGTCGGGGTC CTCAAGAACA GCAGCAGGGA GGCCTGGAGG 1020
ACACGCTAGG GCTCCTTCTG GGCAGAAGGG CTTGACAGGG CTGTTTCTAG CTCCTGCTGC 1080
CACAGAAACA GGGTCCAACC TACAAGAGGG CTGTGAAGAA AGTCCAGAAA CAGGTCAGTA 1140
GAAACCAGCA ACTAAATATA TCTGTTTACC AGGAGCGCCC TGAGTGCGTG GCACAGAATG 1200
TTCAACTGGT TACCTCTCCT GAGCCTCACA GCCTCTCAAG GAAGATCTGA 1250
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