| Tag | Content |
|---|
EnhancerAtlas ID | HS150-07331 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr3:33618900-33619570 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata4 | MA0482.1 | chr3:33619087-33619098 | TCTTATCTCCT | + | 6.14 | | Lhx3 | MA0135.1 | chr3:33619535-33619548 | GATTAATTAATTT | - | 7.82 | | POU6F1 | MA0628.1 | chr3:33619536-33619546 | ATTAATTAAT | + | 6.02 | | POU6F1 | MA0628.1 | chr3:33619536-33619546 | ATTAATTAAT | - | 6.02 | | PROP1 | MA0715.1 | chr3:33619542-33619553 | TAATTTGATTA | - | 6.02 | | TCF3 | MA0522.2 | chr3:33619179-33619189 | AACACCTGCT | + | 6.02 |
|
| | 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 |
| GH03I033577 | chr3 | 33618660 | 33621460 |
|
Enhancer Sequence | GAACATTAGC ATTGCACCAT CATTCCTGAC ACAAAAACAC ATCTTACACC TAAGTGGACA 60
GACAGGCCTA CAGGAGACAA AAGAAGTATT CAAATGGAAG GAAATGTTGA AGGTACAAGC 120
ATGAAACAAA AAAACGAACA TTATAGTGTA AAAAAAAAAC CACTATGGTA ACTAGTAACT 180
AATAAAATCT TATCTCCTTT AATCCTGACA TCCAATGAGG CAGTAAATTA CTATTCAATT 240
TTACAGATGG TGCTATGGTC TAACTGACTG ACCTTCTACA ACACCTGCTT CATTCATATG 300
TAGAAATCTT AATCCTCAAG GTGATGGTAT TAGGAGATAG GTGGGGCCTG TAGGAGCCAA 360
TTTGCCCTAA TGACTGGGAT TAGTGCCTTT ACAAAAGAGA CCCCAGAAAG CTAGCTAGCT 420
CCTTCTAACA TTTGAAAACA CAATGAGAAG GCATCATCTG TGAACAAAGG AATGGGTCCT 480
CATCAGACAC CAAATTTGCT GGTTCTTTAA TCTTAGACTT CCTAGTCTCC CAAACCATGC 540
CGAATAAACT TCTGTCATTT AAAAGTACAT AATCTATGTT ATTTTGTTAC AGTAGCCTGA 600
ACAAACTAAG ATGAGGAAGC TAAAGCCTAG AGAGAGATTA ATTAATTTGA TTATAGCCAC 660
ACTACTAGTA 670
|
