| Tag | Content |
|---|
EnhancerAtlas ID | HS091-33118 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr22:38502600-38503850 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr22:38503260-38503273 | GGGGACAGCTGCT | - | 7.04 | | Nr5a2 | MA0505.1 | chr22:38503116-38503131 | GAGTCCAAGGTCACA | + | 6.07 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28205 | chr22:38503175-38509317 | Fetal_Intestine | | SE_29187 | chr22:38503057-38509293 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 38503347 | 38503493 | | chr22 | 38502839 | 38502975 |
|
Enhancer Sequence | AAAGAGCACC CTGACTTCCA GGGGCTCCCC TTCACACATT GGAGGGAGAA CAATTAGTTA 60
AAATTTCCTT CCGAACCTTC CCACTTGCCT CACCACCAGG CCCCACCCCA CCTCTCCCAC 120
TCAGCCCCTG CGCCCAAGCC CTGGCTCATG CCTGCCTGCT GCCCGCTCAT GGCTGTGCGC 180
AGCCCGCTGC CATGCTCCCT TGGAAAGCCC TCTCTTCTCT CCATCTAGCC AAGCTGACTC 240
CCTCAGCTCT TTTCTTTCCC CTGTGTCACT GAAGCCCTGC TTGGCGGAAG GCCCTGGAGC 300
TACGGAGAGG AAGGAAGGCT CTGCGGCGCT CCCAGTCTTG GGAGGGATAG GGGCAGGTGA 360
GTTAACTTCT GGTTATCATA GCTAAGGTAT CCAGGGGCAG TAAGTAGGGG CCAGGGCAAA 420
CGGTTTATGC TTATTAATTC ACGTCATCCT CTCAAGAACC CTGGGAGGCA GTTATTATGA 480
TTCTCTCCAT TCCTCAGATA GGTAAGTGGA GGCATAGAGT CCAAGGTCAC AAAACTAGTC 540
ACTGGTGAAG CTGGGCTTTG AACCCACCAC GAGCTAAGAA CGGACAGAAT CATCTGTTGG 600
AGTCCAGGGG GAGGGGTGAC TGGACTTGCC CCAGGGAGTC AGAGGAGGCT TTGGGAAGGA 660
GGGGACAGCT GCTTCCCAAC TGGACGGCAG GGGGAGGGAC CGGTGGCTCT AGGCTGAGAG 720
GACAGCAGGA CAGCAGCCCC GCAGCGGGGA CACCAGCAGA GGGCCCACTC TTCCGGGGGG 780
CTGGGCTGTG TTGGGGGTGT CAGGAGAAGC TGCTGGATCG ACAGAGCCAG GGACCCCTCA 840
CTGAGAAGCC TGTGTTCAGT TCTACGGGCA GTGGGGCCGT GGAACGGTTC TGCTCCTGGG 900
AGTGACATGG TCAGGTCCAT GTGGCTGCTC CCTGGGAGGC TGCAGTGAGG AGGGCTGCAG 960
TGAAAGGACC TTTCTCTTCC TTGGGCCTCC ATTCACTCTG GCATCTCAGG CAATGACTAG 1020
CTCTTTGAGA CTCAGTTTCT TCCTCTATAA AATGGAGGCA GAAATGCCAC CAGCCTCCTA 1080
GGGCTGCTAG AGGCTTGAAC GACTATTGCA GGGAACCGTG CCCCACAGAG CCGGGTGCTG 1140
GGAAGGGCAG CCACGGTCAT CCTCCCTGGG AAGGGCATCT GGTAGGCTGG GCCCTCTCCT 1200
TGGAACATAG CCCACTTTCC TCGAGTGACC CCTCCAGGCC CTGGGGCCTG 1250
|
