| Tag | Content |
|---|
EnhancerAtlas ID | HS108-09587 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr12:53264010-53264750 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EN2 | MA0642.1 | chr12:53264620-53264630 | CCCAATTAGC | + | 6.02 | | POU2F2 | MA0507.1 | chr12:53264212-53264225 | GTCATTTGCATGT | + | 6.08 | | POU2F2 | MA0507.1 | chr12:53264201-53264214 | CTCATTTGCATGT | + | 6.54 | | Sox3 | MA0514.1 | chr12:53264631-53264641 | AAAACAAAGG | - | 6.02 |
|
| | Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
| SE_23067 | chr12:53263490-53272120 | Colon_Crypt_1 | | SE_23945 | chr12:53263966-53269591 | Colon_Crypt_2 | | SE_26564 | chr12:53260695-53274096 | Esophagus | | SE_34862 | chr12:53263401-53270367 | HeLa | | SE_43420 | chr12:53263602-53268189 | MCF-7 | | SE_52377 | chr12:53263981-53269471 | Small_Intestine | | SE_56286 | chr12:53264201-53266907 | u87 | | SE_57699 | chr12:53264062-53266257 | VACO_503 | | SE_64566 | chr12:53263876-53266558 | NHEK | | SE_65517 | chr12:53264132-53266162 | Pancreatic_islets | | SE_67099 | chr12:53263476-53274484 | H2171 |
|
| | 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 |
| GH12I052869 | chr12 | 53263583 | 53270635 |
|
Enhancer Sequence | GGTCCCTGCC ATGGGTTATA GTGACAATTG AGGTTTCCAA GTACTTAGCA CATGCCTGGC 60
GCAGTTGGTT ACTTGTGGGG AGGGGCAGAG AAACGGACCC TAACGCACAC AGACAGGTAG 120
AGAAGAGGCA GACAATTGCA GGGCTGCTGG AGACAGTGCC TGGGCCCAGA CACCCTCTGG 180
CACTGGCCAG GCTCATTTGC ATGTCATTTG CATGTGCTCT GACACTTGTC ACTCCTGTCG 240
CTTCAGAGCC TCTGGGTCAC ACATTGTCTC TGTCCCTTCC TCATGTCACT TCCTGGATTC 300
CCAAGGGCTG AGGGGACCCC ACAGAGAGAA GAGAACCCCG AGTCTGGGGG TCAAGGAGCC 360
TGAGGGAGGA CCCGGAGTCT GAAAAGGGTG GGTGCTTTGG CCGCCTGGAA GCCTGGCTTA 420
GGGCGACCCC TGCAGGGCAA TCCTAGAATG GAGGGAGGAG GCGGAGAGGT GAGCTCGGGC 480
TCCCCCCAGC TCCCAGGGCG GCACCAGCCT GGCCCTTTTA CCTCCAACAC GCCCTATGCT 540
CCCTGGCACC CTGGAGTCTG AAGGCAGTCC ACCGACCTGG GCCAGATAGA ATCCAGAAAC 600
TCACAGCTGC CCCAATTAGC TAAAACAAAG GGGGTCAATG TGGGTTGTAC CAAGCATCAA 660
AGCAGGAATA TCTGGGGGCT CCAGGCCATC AGCAACACCA TCCAGATACC ACTGGACCTG 720
CACCAGTGCC TACCCTGGGT 740
|
