| Tag | Content |
|---|
EnhancerAtlas ID | HS108-39225 | Organism | Homo sapiens | Tissue/cell | K562 | Coordinate | chr8:53931100-53932280 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXF2 | MA0030.1 | chr8:53931153-53931167 | ATTGTTTATGTTAA | - | 6.03 |
| | | 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 |
| GH08I053018 | chr8 | 53931209 | 53932262 |
| Enhancer Sequence | TTTAATATGT ACAAAATGCT GTTGACTTTC CTTTTATTTG GTATGTCATG TTTATTGTTT 60
ATGTTAAAAA TGCAAAAGGG GGGGCAGGGC CAAGATGGCC CACTAGGAAC AACAACAATC 120
AGAGGCTCCC ATTGAAAAGA AGCATATTTA GTATGTGAAT CCTTCACTGG CAACCAATAT 180
ATTCAGGTTC TCTCGTCAGA ATTGACTAGG CAGCTGATGT GATCCGCGGA AAGGAAGGAA 240
GAGCAGTGTG GTGCAGCGGC CCACCTGAGA GCCACATGGG GCAAGGGAGC ACCCGCTTCC 300
CGGCCAAGGG AGGCAGTGAG TAAACATGCT ACCTAGCTGG GGAAACTGTG TTTTATCCAC 360
AGAACTGTGC AACCCATGGA TCAAAGATTC CACTTGCAAA CCCACACCAC TGGGGCCCAG 420
AGTCCCAACC CCCAACCCTG GAGCCCTGCA GATTCTCAGT AGCCTCTCAG CTGGAATCTG 480
CCTAAGCCTA CTGTGCCCCT TGAGGCGGGG GGAGGGGCGA CCAACACCAC AGCTGAAGCT 540
GCCTGCTGCC TAAGCTGTTT GAGCTCCTTG GGGGAGGGGC AGCAGCCAAT ACTGGGACTG 600
ATAGCAACCT AACACATTAA GCTCCCAGGG TGGGGAAGGG CAGCAGCTAT CTCTATTGCT 660
CCAGGCCACA CTTTTCCCCT GCTGAAGCCA GGGAGGCTGG ACGGCTTGGT CTCCAAGAGG 720
TGTCCCCCAC AGCCCAACAC ACCAGCTGTG GCAGACTGCG GCCAGAGCAC CTCTTCAGGC 780
CTGACCCTGA CACACCCTTC CTCACTGGGT GGGGCTTCCC TGCAGGAACT CCAACAACTC 840
CAGCCAGAAG CTCAGGGACA GAACCCGGAT CTCCCTAGGC CTGAGCACTT AGAGGGAGGG 900
GTGGTCACAG TCTCTGCAGA CCAGCAGACT TAGCCTTTCC TCCTGGTAGT TCTGAGGAAT 960
CCCAGCAGTC CAGATGAGTG GGTTTTCCCC CCAGCGAAGC ACACCCCCTC CACCAAGGGA 1020
AAGTCAAAGT GCTTCGTTAA ATGGGTCATG TTCCCTGTGC CACCCAACTG GGTGAGACCC 1080
TGTCTGTTGT CAGACATCCT ATACAGGAGC ATTCCTACTG GCATCAGGTC AGTGCCCCTC 1140
AAGGTAGAAG ATCCCAGAAG AAGGAGCAGG CATTCATCTT 1180
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