| Tag | Content |
|---|
EnhancerAtlas ID | HS049-01363 |
Organism | Homo sapiens |
Tissue/cell | Fetal_spinal_cord |
Coordinate | chr11:62162120-62163220 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr11:62162459-62162478 | GTGCCACAAGAGGGCAGCA | + | 6.35 | | E2F6 | MA0471.1 | chr11:62163138-62163149 | TCTTCCCGCCC | - | 6.14 | | KLF16 | MA0741.1 | chr11:62162758-62162769 | GCCCCGCCCCC | + | 6.02 | | KLF5 | MA0599.1 | chr11:62162758-62162768 | GCCCCGCCCC | + | 6.02 | | SP4 | MA0685.1 | chr11:62162755-62162772 | CCGGCCCCGCCCCCACT | + | 6.01 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_26858 | chr11:62161922-62163261 | Esophagus | | SE_30860 | chr11:62162186-62163321 | Fetal_Muscle |
|
| | 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 |
| GH11I062394 | chr11 | 62161921 | 62170750 |
|
Enhancer Sequence | GAGCTTGTCT TACCAATTCT CCAGTTCACA AGGAAATTTA CTCTAGTTAT TAAAGATTAC 60
CGTAGGCTCA GCTTGTGGCC ACTTGACCTC TTTAGCTGGG CAGCCCAGGT GCTAGGGTAC 120
GTATGGGGTC GTCAGCCCCT TTGTGCAAAG CCAAAGTGTG TATTTTTGCC CTCAGACCTG 180
AGTTGTACCA AAAGCCACCT CCACCAGCCT GGGAGTTCTG TAAATGGAGA CCACGTACAG 240
TTCTTGCTTT TGCCCCACAG CTTGTCCATG GCTCACTGTC AAACAGAGAA ATGAGCCTGA 300
CAGCATCTGA AAGGGGAAGA CAATCTTTTT ATCACTTCTG TGCCACAAGA GGGCAGCAAA 360
CTATAAACTA TCCATGGCTT CAGCCGCCCA AAGGGAAGGT ACTCTATCTG GATCAGAGCA 420
GTCTATTTAG AAAATTTGGA ACCAAAAGAA CATTCCTCTT CCTGACCTTC ATTTTCGTCC 480
AAATACTACA ATTTATTTTA GAGCAGAATT GTCCAAAACA CAAACGCTAG CAAATGGCCC 540
GAAGAACCCA CCCAGATCAA CAGTGGAAGC TCGCTCTGCC CTGGGCGCTG CCAGATGCCG 600
GATGCCAGAT CCCACGGTGA ACAAGCTCTG GCAGCCCGGC CCCGCCCCCA CTTGCTCCTT 660
CCAGCCAGGA AGACAGATAC ATCGTCATGT GGCTCACCCA CCAAAATGGT GGGATAATAA 720
GGAGCACAAG ACGGGCCCTG AGCCAAGGCC AAGTGTCCCC AAGCAGGAGT TGCTGCAGTC 780
AGGACTCAGC CCCACTGCTG GGCTGCAGAG AAGAGTCCTG GGTAAGGAAG GGCCTTGATC 840
TCGTAGCTGT TGCATAATAC ACATTTTTCT CAAATAATAT TCCTAGACTT CTTCCTCTCT 900
AGCTTGAGGG ATTGTAAACT CTGAGACCAA AGGAAGGAGT GGGGCACACG TTAGTCCCCT 960
TCAGTGTCCT GTTGTCAGAG GTGATGGTGT GTGGGGAAGG CTGGGAAGGG ACACTCGTTC 1020
TTCCCGCCCC CCACCTGCTC CTCTGAAGTC CTCCCATCAG CCTTCATCTT TGCACAAAAC 1080
CATCACTGCA TTTGGATTTT 1100
|
