| Tag | Content |
|---|
EnhancerAtlas ID | HS047-23111 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr22:45664550-45665860 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr22:45665048-45665067 | GCGCCGCCAGGGGGCGCCC | + | 6 | | KLF5 | MA0599.1 | chr22:45665096-45665106 | GGGGCGGGGC | - | 6.02 | | MAX | MA0058.3 | chr22:45665531-45665541 | AGCACGTGGT | - | 6.02 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_29166 | chr22:45664444-45665041 | Fetal_Intestine_Large | | SE_29166 | chr22:45665146-45666889 | Fetal_Intestine_Large | | SE_35362 | chr22:45665143-45666883 | HepG2 |
|
| | 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 |
| GH22I045267 | chr22 | 45663771 | 45666551 |
|
Enhancer Sequence | CCTGCCCTCG TCTCTCCCAG CACAGGAGAG CGCCGTGGGT TTGCTGACCG CGTCCCTGCT 60
GAAAGGCGAC TCCGGGAGCA CAGGCTTCTG CCCTCTCCTG ATGTCCCTAG CAGCGCCGGG 120
CACGCAGCAG TGCTCGCTGG GTTTTTGTTG CACCTTTGAG AGGAAAAGGA GCTCGGTGTC 180
CCCTGCAGCC CCTGGAAGTG AGGCGAAGAA GGCCAGGATG GAGTTGGGTG GGCACCCGCC 240
TGTGGTCGTA CCCGGATCGT GGAGGCCGCG GGCCCTGAAC CCTAGACACT GGGCGGGACC 300
CTCCCTCCAT TATAAAAAAA AGTAATAAAG CAAAAGCATC TCGCGACTGC GCTGCCATAA 360
TGGCAAATGT GTCGAAATTA TACGCGAAAA CAATTGCTTC CCCCTGAGAG GGCATTCTTC 420
TGATGCTAAT AGAAATTGGG GGAGTCAGCC TTGCTGTGGG CGCGGCACCG CCCCCTCCCC 480
GGCCGAACCG CCCGCGTTGC GCCGCCAGGG GGCGCCCGAC ACCAACGCGA GGCTCCACGC 540
GCCAGCGGGG CGGGGCTGAG AGGAGGTGGG GGCGGAGCCT GGGTAGGCGG AGGCGGAGGC 600
GGGGGCGGGG GCGGGGGCGG GGGCGGGGGC GGGGGCAGGC CCCGGGCGGC GAAGCCGCGC 660
TCCACAGCCA GGACCCTGCT CTCCCGGCCC CGGCCCACCC TTGCGGTCCC GGCTGCACCC 720
AAACCCGACC CCCTGCACTT CTCACCTCCC GGCGTAGTGC ATACTGTTCC TTCCACCGGG 780
AACACGCGGA ATACCTTCCC CGTTCAAGAT CTAGTCGAGG CACCACCGCC TCCAGCAAGC 840
CTTCCCGAGC CTCAGGCTGA ACCAGGCACC TCCCTTGGGC TCCTACAGGT CCCCTGGCCA 900
CACTGTCACT CTGTATTCTT CTCCTGGGAC AGTGGACAGT GAGTCCCCCG GCCGGGATGG 960
GGCTGGGTCA CCCACGATCC TAGCACGTGG TGAGTGGGTT TCAGGTGAAT AAATCTGGGA 1020
GCCGGGAGCC CCAGGCAGCT TACTCAGATG ATCGATGGTG GAAGTCCTGT CCCTCCACCC 1080
ACCTTTGCTT AGAGCCTGGG ACCACAGACG CTCAGTAAGT AACTGGGCTC CCTGGCTCCT 1140
GCCCCAGCCT GTCAGCCCCC ATCTATAACT TCTGAGGGCT GAATCTTCCT CCTGCAGAAC 1200
CTCGGGCTCT GAAGGTGATC CTTAGTAGGC CAGCTTGCAG CCCAGCCTTT GCATCTAACA 1260
CCCTCCCCGC TTTTCACAGT CTCTCCCTGT TCCCTTGTTC AGTTGGGGTG 1310
|
