| Tag | Content |
|---|
EnhancerAtlas ID | HS101-09569 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr12:4251860-4252640 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr12:4252182-4252203 | GAGTGAAAACTGAAAGTAAAA | - | 6.77 | | IRF1 | MA0050.2 | chr12:4252188-4252209 | AAACTGAAAGTAAAACTTGAA | - | 6.99 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_10702 | chr12:4251260-4252896 | CD19_Primary | | SE_11778 | chr12:4250259-4259106 | CD20 | | SE_58886 | chr12:4216067-4279606 | Ly3 | | SE_61003 | chr12:4215547-4279853 | HBL1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 4252128 | 4252433 | | chr12 | 4252200 | 4252569 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I004140 | chr12 | 4249781 | 4253415 |
|
Enhancer Sequence | CCATGAAAAT AACTTGAGGG GACACCTGGA AGAGCGCGGA CCACATTTCT GGAGTAGAGA 60
GGTGCAATGT CTTGCCCATA TTCACCCGAA TCTAGCAGTA GAGCTGATCC CAGCCCAGGT 120
GTGACAATTT GCAGATATGC GGATGACGGA CAGCTCCCAG GTCCAGGCCA GGCACTGCAG 180
AACGTTCTAT TCCTGCTGCT CACCTTCCCC CGCCCGCCCG CAAGCTCCAC CTGGAGGACC 240
TGGGTGGGGT GGAGCACAGG TTTGCTGAGA AATCTGGCTG AGAGATCTGA CCGTTAAATG 300
GGTTTCATCC TGAAATGACT TTGAGTGAAA ACTGAAAGTA AAACTTGAAA CCACCCACTT 360
CCCGCTGCTT CCTTCCCTCG AGCGCTGAGT GCAGCTAAGC CACTCCTGTC TTGTAGGGCT 420
TGCTCCTGCC TCGCCCTTCC CAGACCAAGC CCTGAACCCC ACTGACGGTC GTGCCTGAGC 480
CCCACCCTTG GCACCACCTC AAGGACTCTG TTCCTCCCCT CCCACTGCCC AGGCGGAAGT 540
CAAAACCGTG CGTACTGCAG AGGAGGCACA TCCTTCGAGA ACAGCGAACA CCCCAGCCTT 600
CTTATCAACC CTGACTCCTA TTCATATCCT CACCCTATTT ATTAAATAAG AACCAGTTCT 660
TTCATTTAAA AAATGGATCA AAGACGGCTG GGCGCAGCGT CTCACATCTG TAATCTCAGC 720
ACTTTGGGAG GCCAAGGCGG GAGGATCACC TGAGGTCAGG AGTTCGAGAC CAGCCTGGCC 780
|
