| Tag | Content |
|---|
EnhancerAtlas ID | HS120-04813 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr4:1341980-1343270 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr4:1342683-1342701 | TAGGCCTTCCTTCCTTCC | - | 6.39 | | EWSR1-FLI1 | MA0149.1 | chr4:1342687-1342705 | CCTTCCTTCCTTCCTGCA | - | 7.69 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_24914 | chr4:1339567-1342392 | Colon_Crypt_3 | | SE_24914 | chr4:1342472-1342962 | Colon_Crypt_3 | | SE_24914 | chr4:1343064-1343662 | Colon_Crypt_3 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr4 | 1342603 | 1342723 | | chr4 | 1342200 | 1342317 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I001349 | chr4 | 1343065 | 1343662 |
|
Enhancer Sequence | TGTCTTAGGG TTCAGTAACA GTAACTGACT GGCCCACTGA GCCCAGGACA CACACAGGGC 60
CCTGCCCTCC TGCCCCCACC TGGGAGAGAA CCACCCGAGG GACACACCCA GGACATTTTC 120
TCGGGGCCCT GCAGTACCCG GCTCTGACGG GTGGTCATGT TCTGGGGTCG GGGCGTGTGG 180
CGTTGGGGAC CCCACTGCTC TGTGGTTGGT GCTTCTCTTC ATTCCCATTT GTGTGGTCTG 240
GAGCACATCC TGTAGGAGTT CTTGAGTGCA CAAATGTGAT TCAGAGAGAA ACGTGCATCT 300
TTTTCTTTGC TGCTGGACTT TTCGAAGGGA AAGAATAGAG CTTGCTGATG GGCGAGTTGG 360
TCCATCGCCT TTAGGGTATG TCCACCTCTG TTCACTTCCT CCAAGGAAAA CGCCGGAGGG 420
GATCTCTGCC GTCACCCTCA GGCAGCCAGA GATTCATGGG GGAAGCAAAA CTTCCCCTCG 480
GAGGGTGGAG CATAAGTCGA GGACACTGAT TATTCTGTAT CCTGTGTTTG TAAAATGGCA 540
GTTTATAGAT TGTTTATACA GTGATGGAGT GTTGACATTT TGATAGAAAA TTTCAGGTCA 600
GGTTTTGTGG CCTGCGCCAG GAAATCGAAT TCGCAATGGT TTATGTGGGG TCAGGAGCTG 660
GGAATAGGAG CATTCAGGAG GGGCTGGGAG ATGTCCCGAG CTCTAGGCCT TCCTTCCTTC 720
CTGCAGCAGG AGGCACCCAG CTGAAACAGT GTGCGTGCTG GGCGGTGTGC GTTGTGCCAG 780
GCGGTGTGTG TTTGTGCCGG GCGGTGTGCG TTGTGCCGGG CGGTGTGCGG TTTGTGCCAG 840
GCGGTGTGTG TTTGTGCCGG GCGGTTGGCG TTTGTGCCGG GCGGTGGGCG TTTGTGCCGG 900
GCGGTGTGTG TTGCGCTAGG TAACGTGTGT TTAAAGAGCC AGATGGTTTG TGTTTCAGGC 960
TTTGCTGTAA TGCCTCAGTT GTGAACACAG CTGTAGATGA TGTAGGTGGA TAGATGGGCG 1020
ACGTTCCAAT GACACTTTGT GAATGAACAC CGACATTTGA AGTGTATATG ATTTTCACAT 1080
TTCACCAAGT ATTTTTTGTT TGTATTGACA TTCTTGGCTT GTGGGCCACA CAGAAACAGG 1140
CAGGGGCTGG GGAGGTAGAT GTGGCCCTTG GGCAGTAGTT TGCAGACCCT GCTCTAGAAA 1200
AGGGGAGAAT GAAGATGGGA AGGCAGTGGT GGTCCCTGCC ACACGTGCGT GCGGCATCCA 1260
TGCACGGAGA GTCTCCCCCC GCCCATCCTC 1290
|
