| Tag | Content |
|---|
EnhancerAtlas ID | HS116-06270 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr11:43758210-43759050 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2A | MA0052.3 | chr11:43758450-43758462 | GCTATTTTTAGC | - | 6.44 | | MEF2B | MA0660.1 | chr11:43758760-43758772 | GCTAAAAATAGT | + | 6.11 | | MEF2B | MA0660.1 | chr11:43758450-43758462 | GCTATTTTTAGC | - | 6.92 | | MEF2C | MA0497.1 | chr11:43758449-43758464 | TGCTATTTTTAGCAA | - | 7.4 | | PRDM1 | MA0508.2 | chr11:43758242-43758252 | TCACTTTCAC | + | 6.02 | | RUNX1 | MA0002.2 | chr11:43758386-43758397 | TTCTGTGGTTT | + | 6.32 |
|
| | 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 |
| GH11I043735 | chr11 | 43757133 | 43759368 |
|
Enhancer Sequence | AGGAGAACAA GTTAGAGTGG TCTTATATTG CATCACTTTC ACTGTTTGTC TTTAATAAAA 60
ATGGAGGAAG TTGCTGCTGT TTTATTAACT TGCACCCTGC ATGCTTCTCT TCTTTGTTCT 120
TTGTTAAATA TGAGCTGGCG TGTGTTAAGA CTACGTTAGC ATTTGCTCTC AGGGACTTCT 180
GTGGTTTCTA AATTCAGCAC TGCTAAGCCC CTACACTGTT TGCCTGAATC AGTTGAGACT 240
GCTATTTTTA GCAACAAAAG GGAATTGAAA TAGCAATTTT CTTTCCATGT AATAGATTCC 300
CAAGAGGAAT ACTGATGCAA GCTCTCTATC ATTTTCTATT CCTACCACCC TCCTCCCAAA 360
GCCCTCAGAG GAAAGGCAGC TGTCATGGTT TGCGGCAGTA TTAATCTTTA ATCAATCGAG 420
TGTTTTCTGC ATTCAGGTGT TCGGGGGGAA AAAAGAGTCA CAAGAAGGAA CCTGTTTGGA 480
ATAACTAAGC TCTTAGGCAT GGACTTTACA GTCAGAATTT TGTGGGTAGT GGCAGGGAAT 540
AGACAGAAGA GCTAAAAATA GTGAGTTTGC TTCCAGTGTT GCTCTAGTCT ATTTTTGATG 600
TTTGATTTTG ATAAGGTTGA TTGGGTTCTT ACTAAAAATA TCTGTTCCTA GCAAGTTGAG 660
GACAAAAAGA GTAGAATATT TTTAACCTAC ACAAACTAAA GTATTTTTGT TGACTGTATA 720
AAATCTGGAA GTGGAGCCCT GGTCAGTTGC CAGTATTTTA TATAATCTGT AGCAAGCTAG 780
ACACTTCTGG ATGCCAAGTT GGGCTATTCT TTATAGTTGT CAGTTTCCAT CTTCTCAAAG 840
|
