| Tag | Content |
|---|
EnhancerAtlas ID | HS184-17492 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr2:231904690-231906010 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr2:231904810-231904831 | TCTCCTCCCTCCTCCTCACCT | - | 6.05 | | ZNF263 | MA0528.1 | chr2:231904804-231904825 | GCCTTTTCTCCTCCCTCCTCC | - | 7.16 | | ZNF263 | MA0528.1 | chr2:231904807-231904828 | TTTTCTCCTCCCTCCTCCTCA | - | 7.24 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_35329 | chr2:231900709-231905823 | HepG2 |
|
| | 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 |
| GH02I231040 | chr2 | 231904744 | 231905530 |
|
Enhancer Sequence | CAAGTGATCC ACCCACTTTG GCCTCCCAAA GTGCTGGGAT TACAGGCATG AACTACCACG 60
CCCTGTCCCT CCTAAGCTTT TTGTAGACAC ATTGCTGTTG CCTGAGCCTG AAGAGCCTTT 120
TCTCCTCCCT CCTCCTCACC TGGCCAATCC CATTTGTGCA TTCAGAACTG GACTTCCTCC 180
TCCGGGAAGC CTCCCTTGAC CTTCCCTGCT CCCACTTGCA AGTTCACTGG CGAAATCCCA 240
GAACCCTTTA TCCCTTTGCT CTCTGAGCTC TTACCACATG ATTTCGTTCC CTTGTGAACA 300
TGATTTTGTT CCCTTGTGGG TTTAAACACC ATCTGCAGTC CCATTTCCTG ATACCCTGCC 360
TGGCATGCAG ACAGAGTGAA TGAATCCTCC CTTCCTTTTA AATAAACACT AATACTTTTG 420
AGATTTTAAC ACTTTGCAAG GGAATTGTTC TCTATGTTAA GCGCTTTCCT ACTTTTATAA 480
AAACATACTG AACAAAATTA AACCTCTCGC AAATGACTAA AGGTCGTGAG TGGAATTATA 540
ACTTATAGCC CACTGATTTC TTTGCAGCTT TTGCAGTGGG CAGAACTATT ATCTTCACAC 600
CAAATGGATT CATGTCACTA AGATTTCGCT AGTGGTTGGA TCTGTTTTTT TAAAGTTTTC 660
CAATTTCTTT CCTCACCGTC TGATGATAAT TCTTATTCTA GGTTGCTTGC CTTTTGGCAG 720
TGCCCTTTTA CCCAGTTCGT GGTACCTAAT CCAGCTGCCT TTGGGTTGAA AAACTAAGGA 780
TACAGTCTCT TTACCTTTGG GTGCGGGTTA AGAGTAAATT GGTCCTGAAT AAAGATTATG 840
AACAAGGATT TTCCTTGTTT TGGTTGCCTG AAGTCTTTTA AAAATAAATA AATAAATAAA 900
ATAAACAACC TAGTTCCTGT TGACTTTATA GATTACTAAA AAATGTATCT ATTCCTGCCA 960
AGAAATAGTT TGAACTAAAA TCAGAGGGAA CGTGCAGCTC TTTGAGTATT TTGTTTGGTG 1020
CTATGTAATT GTAATTAATT TCATGTCATT TTCATTGCTT TATTTCCTCA ACATGGTACC 1080
TACATCACAG GGCTTTTGTA AGAATTAAAT GAGATAACAT AGATAAAAGT AAAGCAATCA 1140
TTTTTAAAGT TCGGTTTTAA AAACCCACCC ACTTTTGCAA ATCAGACTCT GTGTTTTTAA 1200
TCAGACAGTT GAAACTAGGG CAGTTGACCG TTGGGGCACT TGATTTGCTA AACGAAATCT 1260
CTCAGTCTTG TGAAGTGGGA ACCATGTGAC CCTCTGACTC AGGTTTTGTG TTCTTCCTAG 1320
|
