| Tag | Content |
|---|
EnhancerAtlas ID | HS098-18007 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr14:75100940-75102180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXP1 | MA0481.2 | chr14:75102154-75102166 | TACTGTTTACAT | - | 6.11 | | RELA | MA0107.1 | chr14:75101575-75101585 | GGGAATTTCC | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_33641 | chr14:75098154-75110709 | H2171 | | SE_64046 | chr14:75100941-75102385 | HSMM |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr14 | 75101713 | 75102000 | | chr14 | 75101225 | 75101552 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I074634 | chr14 | 75100972 | 75102202 |
|
Enhancer Sequence | TGGGGATAGA CTCTTTCCTA AGCGTTCTTG ACAGGGGAAA AAGGTTAGGG GGCATAAAGG 60
TTTTCAGGGT GTGGAAAGTA AAAATGGATT TTCAGGTAGA ACATGAGAAA GAGAAAGGGC 120
TGGAAAAGAA GGCTGGGATA CAAGCGTATG GGATACACAT CAGCTTTGGC TGCAAGTTAC 180
AGAAGCTGGC TCTGGCAAAC ATAAGTGGCG AAAGAGAATT TGTTGGAAAG ATACATGGTA 240
CTGAAGGAGG CCTTCAACAC TCAGGCCTGA GAAGGGACCA GGGCAGCTTT GGGGGTCTGG 300
GTAGCGGGAA CTCATGAGCT GTCTGGCTTT GGATGATTCT AAAGCAACTG CCTTCCATTA 360
TGGGTAATGA CTCCAACTCA GATTCAAATT CCCCAGGAAA AAGTCTGACA GATCTTGGGT 420
CTATGCTCAC CCTTTGAGAA TGGAGGGTTG GGAGAGTCCT GTGGCTGGCA GCCCCACCAG 480
GAATGCATGG AATTGGGGAG TTTGAGTTTC CCAAAGGAAA GCTGAGTTTC TGTTACTCAA 540
GGAAGGGAAG AAGTGCTGGG CATATGTGCA CAGCAGATGT TCTCTACACA TGGGATGTCA 600
ATTGAGAGAG GTGGGGGATG GATGGGGTGG GGGATGGGAA TTTCCAGGAC GCTGCAGAAC 660
CTGCCATAGG GGCCAAGGCT CCTGCCACAG CCCTGGATTG CATCTCCCTC TCCTCCTATA 720
AAAGCAAGCT CAGGAAAAGA ACATTGTTTC TGTTCTTGAC AGCTCCATAG AATTGTCTCC 780
TTAGCTTCCA GTCACGCTCA GCTCCTGCTA GAATAATTAC CACCCACCTG TTCTCCATAC 840
AAGAATTCAC AGCCAGTGGA CACACATCTG GCCTGTAAAA GACATGCTTG GAAGTCTCCC 900
AGGCTGCTTG GAACAGGCAG GAGACAACAC AGGGTCAGCC ACTAATTCAA AGGCAAGGAA 960
ACAGCTGGCC TGAGAGCTAT GGTCACTGGA GCCTAAGTGG CAGCGAACTC CTCCCCTGCC 1020
AGGCAGCTCA ATGGATGTGG GACAGGTGTG TCCTGAGACA AACAAACCCC CTGAGACTCA 1080
GAGGAGGTTT GAGTGCTGGG CCCTGTCCTC TTCTTCCAGC ACATGGCTGT CTTCCCCACC 1140
CCCATCTGCT TCTCTAGTGG GTGGAGGGGG CTAATACCCT GCCTTTCTTG GAGTTCCTTT 1200
ATTTTTCTTC CCATTACTGT TTACATCACT CCCTTCTAAA 1240
|
