| Tag | Content |
|---|
EnhancerAtlas ID | HS142-01118 |
Organism | Homo sapiens |
Tissue/cell | NCCIT |
Coordinate | chr1:156662490-156663260 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:156663169-156663190 | CTTTCTTCCTCCTCCTCCCCT | - | 7.33 | | ZNF263 | MA0528.1 | chr1:156663166-156663187 | GCCCTTTCTTCCTCCTCCTCC | - | 7.36 | | ZNF263 | MA0528.1 | chr1:156663174-156663195 | TTCCTCCTCCTCCCCTCCTCC | - | 7.41 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_27277 | chr1:156660021-156664880 | Esophagus | | SE_29621 | chr1:156658694-156663018 | Fetal_Muscle | | SE_32899 | chr1:156660783-156664785 | H1 | | SE_33952 | chr1:156659478-156664985 | HCC1954 | | SE_68702 | chr1:156660181-156664908 | H9 |
|
| | 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 |
| GH01I156689 | chr1 | 156658793 | 156664790 |
|
Enhancer Sequence | GATCTGGCCC TGGCTGGGGG CGGGGGTGCT GTCTTCCTGC CAGGTTTCTG CCGCTGCCTG 60
GGAAGAGCCC AGCCCAGAGA TTCTTATCCA GGGCAGGAAC AGAACTGGTT TCTCGACTGG 120
CAGTGCCAAG GGGGACAGGG CAGGAGGAAG CCAAAAGGTC GGGAGGGCAG TGCCAGGCCC 180
AAAGGAGAGA GGTGGGAAGC CCTGGCCAGG GGACCTCCGA CGGTCACTAG AACAAGAGCC 240
TCAACCCCCT CTGCTGGGGC CCCGTCAGCC TGGCCCATCC ACCTTATTTG CCTGTGACTG 300
ATTCACTTTC CACAAAGACT CAGGGAGCCC CTCCCAGGCC CCCCACAGCC CACAGCCCTG 360
TCCCCCTTTT TCCTCAGGTG CGACTGGCCC AGCCAGGAGA AACACCTGGT TGGACTCAGC 420
TCCTCCCCTC CCCACCTCCC ACCACACTTG AAGCCTCCAG AGATCATTGG GGGAGGGGCA 480
GGGGAGCCTC AAGCGGTGGG GAACCCTGAA GACTGTCCTC AGAGCCTGCT GCCTTTTATC 540
CCCCGCCACA AAGGGGCCGG CAGCCACATG CCCATCCATC TTGCGCCTGT GGCGGTCCTT 600
AAGCAGTTCT TTGTTGGGAC CTAGGGTCAG AGGTGCTGGC CAGTACGCCC CCTCTCCTGG 660
GACCACCGCC CCTGGGGCCC TTTCTTCCTC CTCCTCCCCT CCTCCCAAGT GTCTCAGGAT 720
CTCTCCACTT TCTCCTGTGT CACCTCCCCT GTCCCCTCCC TTTCCTCTCC 770
|
