| Tag | Content |
|---|
EnhancerAtlas ID | HS120-03955 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr2:235916950-235917820 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Pou2f3 | MA0627.1 | chr2:235917678-235917694 | GCTGATTTGCATAAGA | - | 6.53 |
|
| | Number of super-enhancer constituents: 14 | ID | Coordinate | Tissue/cell |
| SE_05986 | chr2:235912983-235917339 | Brain_Hippocampus_Middle | | SE_05986 | chr2:235917353-235919355 | Brain_Hippocampus_Middle | | SE_29217 | chr2:235906866-235919843 | Fetal_Intestine_Large | | SE_31459 | chr2:235913090-235921057 | Gastric | | SE_35959 | chr2:235916580-235918312 | HMEC | | SE_41684 | chr2:235915069-235919429 | LNCaP | | SE_47485 | chr2:235913482-235917291 | Pancreas | | SE_47485 | chr2:235917415-235919493 | Pancreas | | SE_53059 | chr2:235915933-235919600 | Small_Intestine | | SE_56860 | chr2:235915685-235917299 | VACO_400 | | SE_56860 | chr2:235917478-235918554 | VACO_400 | | SE_64488 | chr2:235916492-235918506 | NHEK | | SE_65336 | chr2:235913309-235920314 | Pancreatic_islets | | SE_69100 | chr2:235913434-235917126 | H9 |
|
| | 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 |
| GH02I234998 | chr2 | 235906788 | 235921345 |
|
Enhancer Sequence | GCAGCTGGGG CTCTGTGGTC GCCTGGCATG AGCTCTGGGC TGCAGCCTCC CTGCAGGGCC 60
CAGGAGGGCC AGAGAGAAAA CGCCAGGAAG AACCAGCCGA GGCCTACTCA GGAACCATGG 120
CGAAATAAAG CAGGAGGCGG AGAACGCTTG AGGTGCTACC TCTTGTACCG CTTCTCCTTG 180
TAGGTGGTTA TTTTCTCCTC ATTCTCTTTT TGGTACCCTT TGTGTAGAAT AATGCTCCTT 240
AGGTACTTTC TAGTTGGAGA CAAGAAAGAA GCTTCTCCAA GCTCCCCTTG GTTCTGGCAG 300
TGTCCTCTGG CTCTGGATCA CTCTTGGTGC CCTTTCCAAG CACCTCTCCC TACTCGCTGT 360
AAAAACTCCA AGGCAAACAA GCTGTGAATT ATCAAAAGGC CACCGGCCTC TGGTGAACTC 420
ATTCTCCCGC TAGGAAACCT GTTGGGTAGG TTTTGTTCTA TTTTATCTCC ACCTGGTATG 480
GGCTTGTAGC AGAGGCCCTA CTGAAAAACG GGGTGATTCA CACACTTTGC TCATTTATGC 540
TTTGCTTTAA AAAAGAAAGC AATGGGAGCA GCTGGCTGCT GCCTGCCTGT TTTTGTCTGA 600
CTGTCCTGTA AGCTCTACCA CACCAGCACA ACACCGGGGT TCCAGCTGGC TTACAGGGGC 660
TGGGCTGACA TTTGCCCAAG GGACAGGTGG ACGGACAGCT TGTGTTCTCT GGGATTGTCT 720
AGAAATCAGC TGATTTGCAT AAGAATGTTT CCCCATAGCT GAGAGCTTAA TGTTCATCAC 780
TGACCCATTG GTGAGTTTGT TGAAATAGAG ATGGTTCCGG GTAGAATATA CTTGCCTCCT 840
AGCACCTGAA GGACTATTAC TTGGGATAAC 870
|
