| Tag | Content |
|---|
EnhancerAtlas ID | HS184-17997 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr20:31489950-31491100 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXH1 | MA0479.1 | chr20:31490935-31490946 | TGTGGATTGGG | - | 6.14 |
| | | 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 |
| GH20I032902 | chr20 | 31490401 | 31490550 |
| Enhancer Sequence | TGGAACTAGA TATAAGCACG GTTCTGGGAT GGTTTTGAGC AGAGAACTGG TGTGGTCTGG 60
CTTATATGTT GCAGGTGGAG TGTCCATGGG CAGGGGTGGT GGTGAACACA CCAGTGAGGA 120
GGCCATTGCA ATAGTTGAGG CTGCATAGGA TGGTGGCCTG GAGCTGGGCT GTGTTGTGGG 180
ATGGAGGGAC TGGAGATGTA TTTTTGGGGT AGGGTAGAGA ATATATTTAC ACACACAAAC 240
ACAGAGACAC ATGTTCCCTT CCTTCAGCCT GGGTGACAGA GCAAGACCCT GTCTTCAAAA 300
AAAACAAAAG ACTCCATTCA GGTCAGACAC GGTGGCTCAC TTCTGTAATC CTAGCACTTA 360
GGGAGGCCAA GGCAGGAGGA TCCCTTGAGG CCAGGAGTTC AAGACCGGCC TGGGCAATAC 420
AGCAAGATCC CATCTACACA AAATATTTAA AAATTAGCTG GGAGTGTTGG CACACCCCAT 480
GCATTCTTGT CTGCATGCAG TGCAATGTAC AGGCCGGCAG GTGGCACAAT TGACCACTTG 540
CTGGTCTCCC GTTTTGGCGA TGCCATCTTA GGGCATATCC TCTGCGGGTG GGGCCTGGCA 600
TTGGCACCCC AACCTCTGCC TCTGGAGTCA GCCTCAGCCT CCAAGGCAGT GTGGGCCTGA 660
GGGTCTGGCT TCCTTGCAGC CAGCCTCACC TGAGTTCTCA GATGGTTCGA GCCAGGAGCA 720
AATCTGACGG AGCGGGTGTG GTAGCAGGAG CCGGTGCTGA GTGTGTGGAC TGACCCCCGG 780
CGTCTCCCCG ACTGTCCCCT CTTCCTTCAC TTCTGCCACC ACCACCTAGT TGAAGCCACC 840
GTCATCTCCC ACCTGAACTG CTTGCCCTGG CCCTCTTAGC AGCCTCACCG TGTCCCCTCA 900
GGCCACATTT CCTGACCCAC GGCCATCAAC AAATCTGATC CAGCCAGGGC CCTGTATGGA 960
GCCTTCAACG GCTCCTGGCC AGGGCTGTGG ATTGGGCCCT GCCCATCTCG CCCATGTCCT 1020
CTCATGCCCT CTCCTCCTGG CCCACCTGGT GCCCACCACA CCGGCCTTGC ATAGGCTGCT 1080
CCCTCCGGCT GAAGCCTCAC CCCTCCCCTG GGCTCCCCGG GGCTGACTCC TTCTCACCCT 1140
TCAGGTCTCC 1150
|
| |
|
|
|
