| Tag | Content |
|---|
EnhancerAtlas ID | HS118-08963 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr19:927720-929090 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr19:927797-927812 | AGGTCTTTGTGACCT | - | 6.63 | | HOXA13 | MA0650.2 | chr19:928276-928287 | GTTTTATTGGC | - | 6.14 | | ZEB1 | MA0103.3 | chr19:927887-927898 | CCCACCTGCCC | + | 6.14 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27633 | chr19:924004-930287 | Fetal_Intestine | | SE_28572 | chr19:924338-929404 | Fetal_Intestine_Large | | SE_57993 | chr19:924590-928562 | VACO_9m | | SE_69171 | chr19:924614-929396 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GATGGGGGGC TGGGTGCCGC CCTGGTGGCC TCCGGACCGC CAGGCTCTCC TGGTCACAAC 60
CCAGCGCTAT GGCCCTGAGG TCTTTGTGAC CTGGGACCTC TGTCCCCACA ACAGATGGAA 120
CAGAGGCTAT TTTGGAACAT GCCCTCCTCG CTTTCTCCCA GGGGCCACCC ACCTGCCCCC 180
CACTGCCTTT TCACCCATGG GGCCGAAAGA CTCAGGGGTC TGGGTAAAGG GTGTCTAGGG 240
CAGAGGGGCC ACAGGACTCT CTTGTCCGGT GACTGGGGAG GCTTGGGGGT GTCTGCTGTG 300
CAACACTGAC CTGGGTGGGG TCGGGTCACA GGAGGGATCT GAGTCCCAGG GGTCCCTGCC 360
TCCTCGTCTC TCCAGGCCTT GTCTGCCCAG GAGCTGTGTA TGAGTCTTGG GGGCTCCTTT 420
GCCAGGGTAA GGGTTGGGGG TGGCCTCCTG GGCCCAGCTG CCTCTCGGGA GGGTGGAGCT 480
TTGCCCCCTC CGCTGTCCCC ATGATGTGCC TTCCCTCTGG GGTGTCACTC CAGGCCTGTT 540
GGGTTCTGCC CGGCCTGTTT TATTGGCGGC CTGGGCGGGT GGAGGTGTGG CCTGGGCTAG 600
GGGGTGGCTC GGGTGGGACC CAGGCCCCAG GAGTCTCTGT TCTTCACCCA GGCCATTAGG 660
ACTGGCCCTG GGTGGAAGGC ACTCTAGGCT GGGTGAGTGT GTTGCCGTCC GAGACATCTG 720
GCCCACTCGG GATCCCAGAG GACCGGGAAA CTCCAGACCC CTGTTGCCCT GCAGAGATTG 780
TGGGGTCTGC GTGGGAGGCT CTGTGGTCAC CCAGACCTGG GTTCAAATCC CACCGCCATG 840
TCTCCAAGCA GAGGATCCCT GAGCCTCAGT TGTCCTCAAC CATGAAATGG GACCGCCCTG 900
GTGCCCCCTT CTCTGACACC TGTTGGTGCC CACCTTAACC TCCTGAACTC GATTCATCCC 960
TCCTTGAGTG CCATGGGTTG GGGGGGTACT GTTACCCACA CTGTTTTGCA GGTAGGGAAC 1020
CTGAGGTCCA GAGAAGTTGT GGCTTGGGCG TTGCTGTTGA GTTGTGTGAT GGGGGGAGGG 1080
TTAGCCCAGG GCCCGTATAC AACAGGCGCT CAATCTCCAG TCTGGCCTGA GATGGGAGGA 1140
TACCTAGATA CCTGGAGGCC AGGCTGGGCC GCTCCAACAG GGACTCAGGC AGCGACTGGA 1200
ACTTAGAACC CACCTGACTG GGGCCCGGAG CCCGCTGGCC AATCACAGGC CAGGAACGCC 1260
CATTCCCCCA CCCTGCTTGT GAAGCAATAA TCCAAGATCT CCTGGGGCAG ACAGTCTGGC 1320
CACAGCGTGT TTCTCTGTGG CCCCGTGCGG GGCGACCTTG CTACCCAGGC 1370
|
