| Tag | Content |
|---|
EnhancerAtlas ID | HS184-08688 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:120835340-120836810 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr12:120836324-120836345 | CTCTCCCCACCTCCCTGCTCT | - | 6.23 | | ZNF263 | MA0528.1 | chr12:120835904-120835925 | CCTCCCCACCGTTCCTCCTCC | - | 6.5 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_65438 | chr12:120835400-120836605 | Pancreatic_islets |
|
| | 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 |
| GH12I120397 | chr12 | 120835401 | 120836605 |
|
Enhancer Sequence | AATGCAGATG TATTCAGCTT CCCCTTCAAA GGGTGCCAGA CAAAATACAG GACGCCTAGT 60
TAAGTTGAAA TTTCAGATAA TCAACCAATA CTTTTTGAGT GTAAGTATGT CCCATGCAAT 120
ATTTGGGACA TACTTATACT TTGTTTTTTG TCTGCTTTTG TTATTTATCA GAAATTCACA 180
TTTAACTGGA AGTCCTGTAT TTTTATTTGC TAAATCTGGC CACCCTGCCC TCCTGGGATC 240
CCACCCCGTC TCGCAGCCCG GTGCCCACCG CAGGCGGGTA CACCCTGCGC GGTGCAGTCA 300
CTCCGGGCGC AGCCTGGCAA CGCGGCCACA AAGGGAGCCC GGGAGGCGGA ATCTTTCCAC 360
ATGCCTGATC AATGGGGGCG CGGAGACGGC GGCGCAAACA GGCCTGAGAC AGCCGCACAA 420
AGAGGAGGCC CCTCGGTCGC TCCCGCCTTC CATTGATCCT GGTCCTTTGT GGCTCGGACA 480
ACGGGGGCGC GGGAGGCGCC TTGCGGGGAC TTGGCCGTTT CTCATTAGAG GGAGAAGGCC 540
TGTGAGCACC CCCGTCCCGC CAGCCCTCCC CACCGTTCCT CCTCCCGTGG GCTCCAGGCC 600
TCAGGTCTGG GGCTGTCCAA ACCTATCAGG GGAACTGGGC AGGGCACAGG GTGGGGTCGG 660
ACCAGGCTAG GAAGGTCTGG AGCCTGCCTG TGGGGGCCAG CCACCCAGCC CCCGCCTCCT 720
GAGGACCCCC CAGTCTCCTC TGGCGGGCCC TCTCTGTCCC CTTGGTTACA GGCAGGTTTT 780
GCACAGTCTC TGTTTTTTTA TTTATTGAGC AAATATTTAT TGAGCGTTTG TTCCAAGCTG 840
TTCCCACTCC CTCCTGCCCC CATGGCCACT TAAACTAGCC AATTCCTCCT CCAAGCATCA 900
CCTCTCTGGG AAAGCACCTC TCAGTCCTCT CTCACCTCAG GTTGGGTAGT GAAACCCCAC 960
TACACATACA CACACCCCGT GTGCCTCTCC CCACCTCCCT GCTCTTCATT CATGATAAAA 1020
ATGACTAACA ATTATGAAGT ACTTACTATG CCTGCCATGC TAAACATTTT ATTGCTGTCT 1080
CCTTTAATTC TCATAACACC CCTCTAGATT GGAGCTACTA TGATCTCCAT TTTCCAGAGG 1140
TGGAAACTGA GGTTTGGCAT GCTAAAATGG TCACCCAAAG TCATACAGCA AGCGGTAGAG 1200
TGGAGATTTG AATGCAGGTG ATGAATTGCA GTTTGAGATC TTCACATCCC AAGTTCCAGA 1260
CTCTATGCAG GATTCATTGC TGTGGCCCAG TAATGAACTG TTTACTCCAT CAGCACATTT 1320
ACCCACTGTA CTGTGTCTAT TTGGCCTTTT CCGTCTGTGT TCCCCACTAG ACTGATTGGT 1380
CTGTGACCGC AGCACCCAGC ACAGAGAAGG TGCCCAGGGT ATATTTGCTA ATCTGAACTA 1440
TTGGGTTTAA GAATTTTGGT TGGGCGCGAT 1470
|
