| Tag | Content |
|---|
EnhancerAtlas ID | HS147-00832 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:27193310-27194710 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TP53 | MA0106.3 | chr1:27193597-27193615 | GGCATGCACCAGCATGTC | - | 6.13 | | TP53 | MA0106.3 | chr1:27193597-27193615 | GGCATGCACCAGCATGTC | + | 6.17 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_26621 | chr1:27193611-27195235 | Esophagus | | SE_34025 | chr1:27193917-27194938 | HCC1954 | | SE_34526 | chr1:27193835-27194826 | HCT-116 | | SE_64263 | chr1:27194021-27194814 | NHEK |
|
| | 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 |
| GH01I026867 | chr1 | 27193925 | 27194757 |
|
Enhancer Sequence | CCACCATGCC CGGCTAATTT TTGTATTTTT AGTAGAGACG GGGTTTCACC GTGTTAGCCA 60
GGATGGTCTC GATCTCCTGA CCTCGTGATC CGCCCGTCTC GGCCTCCCAA AGTGCTGGGA 120
TTACAGGCGT GAGCCACCGC GCCCGGCCTA TTTTGTTTAT TTTTATATGG AGTCTCGCTC 180
TGTTGCCCAG GCTGGAGTGC AGTGGTGCAA TCTCGGCTCA CTGCAACCTC TGCCTCCTGG 240
GTTCAAGCGA TTCTCCTGCC TCAGCCTCCT TAGTAGCTGG GATTACAGGC ATGCACCAGC 300
ATGTCCAGCT AATTTTTTGT ATTTTTAGTA GAGACGGGGG TTTCACCATG TTGGTCAGGC 360
TGGTCTCGAA CTCCTGACCT CGTGATCCAC CCACCTTGGC CTCCCAAAGT GCTGGGATTA 420
CAGGCGTGAG CCACCACACC CGGCCTATTT TTTATTTATT TTTTATTTTT TATTTTTGAG 480
ACAGGGTCTG GCTCTGTCAC CCCAGGCGTG ACAGTGGCTT TTGGTCTCAA GCAATCCTCC 540
CACCTCAGCC TCCTGGTAGC TGGGACTATA GGTGCCTGCC ACCGCACCCA GCTAATTTTT 600
TATTTTATTT TTAGTAGAGA CAAGGTTTCA CCATGTTGGC CAGACTGGTC TCAAACTCCT 660
GGGCTCAAGC GATCCTCCTG CCTCAGCTTC CCAAAGTGCT AGGGTTACAG GCTTGTGCCA 720
CCTCACCCAG CCTCAAATGT CAGCTATTAA CGAATCCTTC CAGCTTCAAT AAGTCTAGGA 780
TTTGGCCAGC ATTTTTATGC CTAAAGCAGA ATCATGAGGC AGGCCCAGTC CTGAGGGGCA 840
GCCTTATTGC CAAAGCTGAC CTGCACGCCT GCTGAGCCCC CTGAGAATGC TGCCCTCACA 900
TCAGGTGGTC ACTCTTCCAC CTGGCAAGAT GGAGAGAGCT AAGCCCAGGG TCCAAGCTTG 960
GCCACACCAA TAGGACTCAA AACTGAAGGG TTTTTGTCAG AACTCCTGCT TCTACAGGGG 1020
AAGCCGGCAG GACCACTCTG ATGCCTTCTG GGTCCCCTGT TTTCTCCCTT CCTTTCCTAG 1080
AGGTGTGTCA GATTTCAAGG CTCCAAACCA GGGACTCTAG GCAGGGCAAG TAACTCCACT 1140
CAGATCTAGA GGTGACCTGA TTTCTCTCAC CAGACAGGTC TGGTGACTCT CTCTTAATGG 1200
GCTACATCCT GGGAAAGGAA CTTCTTTCTT TTCTCTCAGC CTCTGACTTT TGTCTGTTAG 1260
CTCTGGACCA CTCGTGGTTG TCCCATATGG GGAGAAGTGA GCTGCCCTAA GGTAGTGTGT 1320
CGGTGTAAGG ATTTTAAACC AGATGCTGTG CATTGGAATA TCTCTAAATC AGATGCTTAC 1380
CAGGGCTAAA TGTGAGCTGG 1400
|
