| Tag | Content |
|---|
EnhancerAtlas ID | HS047-02940 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:207174550-207175580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELF5 | MA0136.2 | chr1:207175391-207175402 | AACTTCCGGGT | - | 6.14 | | TFAP2A | MA0003.3 | chr1:207175303-207175314 | TGCCTGAGGCA | - | 6.02 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_26663 | chr1:207174076-207177334 | Esophagus | | SE_27711 | chr1:207174549-207176229 | Fetal_Intestine | | SE_31518 | chr1:207174225-207175679 | Gastric | | SE_33873 | chr1:207174470-207177225 | HCC1954 | | SE_34694 | chr1:207175413-207177474 | HeLa | | SE_57640 | chr1:207174392-207175686 | VACO_503 | | SE_57951 | chr1:207174806-207175106 | VACO_9m | | SE_57951 | chr1:207175382-207175652 | VACO_9m |
|
| | 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 |
| GH01I207001 | chr1 | 207174816 | 207177209 |
|
Enhancer Sequence | TGCTAAACTG CCCTAGCTTC ATGACAGCAT CCAATCCCTA GTAATTTCCA TATATACTAA 60
TCCTGTGCCA GAAATGGCAA TGAATTCAGA ATGGATCCCC ACTGCCCTGA GACTCACCTC 120
AAAATCCTAC AGCAGGACAC CAAACCTTAC ATGAGATGTG TCCCTGCCTT ACTCCTGCTG 180
AGCATCATTC TACCGTTCCT TTGGAATGCC ATCCCTCGCT GCATTGAGGC AATATATCTG 240
ATTTTGTTGG ATTTCAGGTG TGTGCCTGGT GGTCTTATCT CAGGAGCACT GGGCTGGTGG 300
AAGAGATGGT GATTGTTATC AGATGGCATG ATGGTGACAG TGAGGGGAGG CAGACCCAGG 360
GCTTGAGAAG GACAGAGGAC AGGTGAGCAT TTCCTCACCC AGGACAGGCC AGACGTGCTC 420
CCTGAACTGT TGCCTGTGCT GGGTGTTTGC CATCAGCCAT TTTTCCCTCT GATTTTATCA 480
CTTCCAATAT AGGTATGTGC ATTAATGTAG GTATGTGCAT TCTTAGAGAT TCATTCCTTT 540
GGCTTACACT AACGACTTTT CTTACACAAA AGACCTCAGT GAACCTTGGG AGAGAAGGCA 600
GTTCTTGGGG AGGAGAAAGA TTGAGACTGG GAAGGCACAT GTAGCTGCTT TGTATTCTAC 660
CCTCTGGTTG GCCTTAGTGC CCTCTTTTTG CTTGGTCTCT GGGCACTGAA TCCTTCTAGG 720
AATCTTCTTA GTTTTAGGCA CTGGTTTTAA TCCTGCCTGA GGCAGTTGCA ACCACCTTTT 780
CTGAGCTAAC AACAATCTCC ACCCCCTTAC CTAGGAAGCA CCTGCAACTT TAGTCAGATG 840
GAACTTCCGG GTGTCTCACC TGGGAGAGAG AGCTATGTAG CCCTTAGGAG GAGTTCAGTG 900
TTGTTAACCT AGTGCAGCAG AATTGTGAGC GGGGCTGAGC CTCTGCCTCA GCCTCAACTC 960
CATTGGGGCT GCGGACAGGA GGGAAAATTG GGGGTGGGGA ACTCAGCCTT GCTTGTTGGA 1020
GCACTATTTT 1030
|
