| Tag | Content |
|---|
EnhancerAtlas ID | HS183-14764 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr9:140710510-140711890 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB3 | MA0638.1 | chr9:140711800-140711814 | CAGTGACGTGGCAC | - | 6.51 | | RARA(var.2) | MA0730.1 | chr9:140711180-140711197 | TGACTTTTTTGTGACCT | - | 6.12 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_59052 | chr9:140703092-140735559 | Ly3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TCAGGTGAGA GGCAGCTTCC TGCCGGAGCC CCACATTCTG CTCGTATTAG CACGTATTAG 60
CACGGAGGTC ACCCCGACAG ACAAGAACTT AACGTGTTTG GATGCACGCA CATGTGTGTT 120
TGCAGATAGA GCCGACAAGT TACCTGAGCC CTTTATCCTC TAGAAATGTC ACTTGTGCCA 180
TAAATCACGA GTCATGCTTC CCCCAGCACA GACTTCGGCA TGAGAGAAGG AGCAGGTTGT 240
TGGGTCAGTC CAGCTAAAAG CAGAGGAACG GACTTGGCCT AAGAATTACC TTTGTTACCG 300
AGTTCATGCG AACATTCTTC AACAGGTTAG GGCTGTCGTA GTTCTATTTT AATACTCCAG 360
TCATTTTCTA AATATTCTCT GTTCTCTGGG CTTCCCTAAC AGTGAGGTGA TGTCCCAACG 420
CTTCTCAGGC TGCGTGGACT CCTTGTTCCT GGGTTGCTCA GGACGCTCAT GGAGTAAGGC 480
TTGCCCAGCG CCCTTCCCCA GCTGGGCTTG GTCCCCTGAC CGCCCAGCAG CTGCGTCTCC 540
TTTCCCTGGA TTCTGGTCTT GAGCATTTCC TCCGCAAATG TGCCCGAGAT TGGAGAAGTC 600
AAAGCTCCTC TGAGTCATAA GGGAAAGTTA TGCACACTTA AATTTAGCTG AACACTCATT 660
TTTATAGTAT TGACTTTTTT GTGACCTCGA TAAACTTGGT TCATGGTGAA AGGCAGTCTC 720
TGTCCTTGGT ATGGTAGAAA GGCCTGGTGG TGAGGACCCA CGCCAGACAG ACGCGAGGCA 780
GACACGGGAC ACATGCCAGA TGGGCAGACG CGAGGCACGT GGTTCTGAGG GCTCCTCAGA 840
GGCCCACATG CCAGGACCGC CCAGCCGCCC TCCTCCAGAT CTACCCGGCC ACCCTCCCCC 900
AGGCCTGCCC AACCACCTTC CCCCAGCCCT GAGAAACCCT CGACCGCCAC CTCCCCTGCC 960
ACCCTCCCCC AGCCCTGAGG GGCCTGTGGG CTCCTTGTCG GGAGCAGGCT GGGCTGCAGG 1020
TGTCACCACA GCCTGGTCCA GCTATAGGCT TCTCTAGTAT TAGCACCTCT GCCCCTCACA 1080
GTGCCTAGTG GCCCAGGCCC AGCTCTGTCC CCATGTTACA GATGGGGACA CCGAGCCACG 1140
GCCAGGACCA GTGACTTGCC GAGGTTGTGG GCTGGGGTGC TCCTGGCTGA TCCCCGGGTT 1200
CTTGGCTCCC TGAGAGTGCG AGATGCCGTG TCTGTGAGGT GCCTGCAGCA TCGAACGCTT 1260
CGGATACAGA ACCAGTTTTC TTCCTCATTT CAGTGACGTG GCACCAGCTG GCTTTTGCTG 1320
ACCATTGTGG CAACAGGCTG AGGCTGTGGC CTGGGTTCAC CACTACTCTC TATTTTTCAG 1380
|
