| Tag | Content |
|---|
EnhancerAtlas ID | HS043-08306 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr11:71211420-71212340 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr11:71212111-71212124 | AGAGACAGCTGCA | - | 6.36 | | Myog | MA0500.1 | chr11:71212114-71212125 | GACAGCTGCAG | + | 6.62 | | NR2C2 | MA0504.1 | chr11:71211746-71211761 | GGAGGGCAGGGGTCA | + | 6.26 | | Tcf12 | MA0521.1 | chr11:71212114-71212125 | GACAGCTGCAG | + | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr11 | 71211627 | 71211690 | | chr11 | 71211465 | 71211936 | | chr11 | 71211998 | 71212187 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I071500 | chr11 | 71211761 | 71211910 |
|
Enhancer Sequence | ACCGTTGACC CCCCGAGGAG ACATTAGGCG ATGACTGGAG ATGATTTTGG TTATCATGAC 60
TGGGCTGGGG TCTGTGCTCC CAGCATCCCG TGGGTGGAGC CCAGGGATGC TGCTGAATGT 120
CCTACTGTGT GCAGGATGGG CCCCTCCCAA CCCCACACCC AGCAGAGAAT TCTTTGTTCC 180
ACGTGTTGGT GGTGCCAAGG TTGAGGAATG CTGAACATTT GGGACTAGAA GACGTTTGGG 240
GCTGCATGGT TGTAAGGAAG AGATACTGTA TCTGGCTGAT TTCCGTGGAA AGGAACTTGC 300
TCAAAGAGTG ACTTAGAGGG TGGAAGGGAG GGCAGGGGTC ACAGGGTCTG GAAAGCTGGG 360
ACTCAGGCCA GGTGGCTGCT GCCCTATATC CCCTGCTGTG GCTGGACGGA GCCCACACGC 420
CACACCCAGC CTGGGCTGGA TGCCAATCTG CTCTGCCATC CCTGAGTCCC AGTGTCCCTG 480
GGTCACCAGG CAGTGGAGTG GCCAAGCCTC GGGTGATGGG CCCTGTCATC TGGCCACCCA 540
GGGCAGGAGA GGGAGCTGCC CCAGCTCTGG CCTCTGTAGT GGGAGGTGGG GGCTTGGCTC 600
CCACCAAGAT GTACTCAGGG GCGGGCTCCC CCAGATCAGG AAGGGGGTTC AGACACTATG 660
CAGCCAAAAG AGTGACGCAT GTGGGAGCAT CAGAGACAGC TGCAGGTAAA GGTGGAGACG 720
CTGCTGTCAT CTGCAGTGAC AGCTATGCGT GATCTGGACC CGCCCCTCCA GGCTTTTCCA 780
GCACACACGC CCAGCATCTG GTGGGGACTC TGGTAATTTA CTTTTTCACC TCTGGGACTT 840
GTGACCCGCT TTTGGTGCGT GCCAGTGTTT CAACAGCCCC ACAGTCCGTC TTTGCGGGGC 900
TGTGGTGTCA CAGGCCTCTC 920
|
