| Tag | Content |
|---|
EnhancerAtlas ID | HS022-05191 |
Organism | Homo sapiens |
Tissue/cell | CD4+ |
Coordinate | chr16:2751020-2752350 |
Target genes | | Number: 12 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr16:2751883-2751894 | AGGGTGTGGCC | - | 6.32 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_41895 | chr16:2751543-2755377 | LNCaP |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 2751650 | 2751713 | | chr16 | 2752094 | 2752169 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I002701 | chr16 | 2751544 | 2755377 |
|
Enhancer Sequence | TGGTGGGGCT GGGGCCCTGG GAAGCCGTGT CAGCAGCTCG GGGTCCGCGA ACAGGGCTGT 60
CCCCATGTGG CACCTGTGCT CTTCTGCCAC CGTCTTGTGA CTTCTGGCTG GGAGGGAACA 120
ATGTCTCCTG CCCGTGGTGG GCACCTGCCT CCCGGGGCAG CTTCAGGTCT TCGACCTTAG 180
CACTTCTGGG TGGATTCCAA ACCCATTGCA AAGAACGGGT GTCCTCCCCC TTCCTTGATT 240
ACGACCTGCT TGGCACGCTT CATCCCTTGG GGACCCCTTC TCCCAGTTCA TGTAGGGAAG 300
CCGCTGGGCT GACCAGCTGT CCCGGCTGTG GGGTGGGACC CTGCGGGGTG CTGGGAGGTG 360
GCCAGACCGG ACCCAGGGTC CCCAGTGGTC AGCAGGGGAT TGCAAGCAGG GCTTGGAAGT 420
GGCTGTGAGG ACACAGGGGC TCCGGGGGGC ATGGCCGTGA GTGCTCCCAG GGGTACCCTT 480
AGCTGCTTGG GCCCATGCCG GCACCCCTGT GGCCGCCTCA CTGGGCTGGG TCCACTGCTG 540
CCCACTGGGT CAGCCGCCAG CTATACAGGA GCAGCAGGTA GCTGCGGGCT GCTCTCCCGG 600
CCGTTGGTCC AACTGCGCAG GTCTTAGAGA GGCCAAAGTG TGAGCCTCGT CCAGCTGCTT 660
TTTGGCTTGG TCATCTGCTG CTGTCATGCT TATTGTGATT TGCGTATTGC CTTTTAATTT 720
TCCCTTTAAA AGCACAGAAG TGCCTGGTGG CCCAGGGTAG CCAGCCATGG GCCAGATGCC 780
TGGCCAGAGA GACAGGTTGG CCCTGGACCT GCATTGGCCT GGCCTGCCTG GTGACCCGGA 840
GGGAGGCAGG TTGGAGTGGC CTAAGGGTGT GGCCAGCAGG CTGCAGCAGA CCCGCCCTGG 900
CCGAACTCCT GGACAGCACA GCTCCTCCAG CGGCTTTCGG TCCAGTCAGC TGGTCCCAGG 960
CTCTTCCCTC CAGGTTTTCA GAGCCGCCCT CCACTCTCCT CCCGCTGCCC CCCTCCCTCC 1020
GCCCCAGCTC AGGGACCCGT CTGTGCTCCG TCCCCCTGGG GCAGCAGCCC CTTTTGGCCC 1080
AGCTGGAAGC GCCAAGGAAA GCTCAGGGTC CTCACAGAGG AAGAGCTCGC CCCATGCCAT 1140
GCCACGGCGT GGGGTGCCGC CCCGTGTGCT CGTGCAGGTG TTCCGGGGAT TTGTTTTCCA 1200
TCCATTTCCT GAAGCGTCGG CAGTCTTTGC TGTGGCTTTC GCGGTGGCAG GCGCGTCCTG 1260
AGGCTGGTCA TGTCAGCCTG GCTGGGTCTC TCAGGCTTCA CTGGGCTGCG TCTCAGGCTA 1320
TGTCTCCTTG 1330
|
