| Tag | Content |
|---|
EnhancerAtlas ID | HS052-29652 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr5:424090-425430 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TFAP2C | MA0524.2 | chr5:425382-425394 | CGCCCCAGGGCA | + | 6.22 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_37211 | chr5:424409-425770 | HSMMtube | | SE_45637 | chr5:423502-425669 | Osteoblasts | | SE_58626 | chr5:366707-441100 | Ly1 | | SE_59696 | chr5:390329-441740 | Ly4 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 424613 | 424702 | | chr5 | 424842 | 424963 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I000424 | chr5 | 424316 | 425316 |
|
Enhancer Sequence | TGGTGAGTGC GTGGGTCCCT GGCAGGGGGC TCCCGACATC TGGGATGCAT TCTACCCTGG 60
TGTGGAAGGA AACAGAGGGC AAGAGGGGGT GGGGGCGTTA AACCACATGT CCCTGGTGGA 120
GGGACGGGGG CCGGTGCTGA GCTCTGTGTA CCCTGTGATG GTGTGGGGGT GTTAACCCAT 180
GTGTCTCTGG TGGGTGGGAG AGGGCTGGGC ACTGAGCTCT GTGCACCCTG TGATGGTGTG 240
GGGGTGTTAA CCCATGTGTC TCTGGTGGGG GGGCGAGGGC CGGTGCTGAG CTCTGTGCAC 300
CCTGTGATGG TGTGGGGGCT TTAACCCACG TGTCTCTGGT GGGTGGGAGA GGGCTGGGCA 360
CTGAGCTCTG TGCACCCTGT GATGGTGTGG GGGTGTTAAC CCATGTGTCC CTGGTGGGGG 420
GGCGAGGGCC GGTGCTGAGC TCTGTGCACC CTGTGATGGT ATGGGGGTGT TAACCCATGT 480
GTCTCTGGTG GGTGGGAGAG GGCTGGGCAC TGAGCTCTGT GCACCCGGCG ATGGTGTGGG 540
GCTGTGACGC CTCTGGGCAT GCGTGATGAG TCAACCGTGA GGCCTGCTGT GGTGGACAAG 600
CCAGGTCGAT GAGAATGTAA AACTCTGCAG TAGGTTTATA CTCTAGTTGT ACCTTTATTT 660
AAAACTTATT AAAATATTTT TTAAAATGTG CCCCACATCT GCCAAGGGCT GGCAAACTGG 720
GAGAGCCTCT GGCTGTGGCT GGCGTGAGTG GCTGAGCCCA TGGCATCTGC TGAGCTTTTT 780
GGTTTCACCC TCTTCTCTTG CAAACAGATA CTTGGGGTTT TCACTTCTGC TATTTGACCA 840
TTTCTTCTTC CAGCTCCTCA TTGAATCAGA GAACTCCTCC CCATCGGACA TGTCAGGGCA 900
AAGGCCTCCC ACCCTGTCCC AGAGCCCTGC CCACCTTGCA GACCCTCCAG GCACTGTGGT 960
CCCCCTGGCC ACAGCACAGT CAGCCCTGGG TCATGGCCCC TCAGAGCCCC AGTGGTGGCC 1020
CTTGCTGTCT CCTGGCTGCA ATTCAATGCC ACAAGGCCCT CAGACCCCAG CACCCCACAA 1080
GGCCCTCTGA CTCCAGCACT GTAGCTGGGC AGGCCCCCTG GGCTCAGCTT TCCACCCATT 1140
TGTGGACCCA TGACCTCCTG GGGACCTTGG GTGCAGACGG TCCCCATGGC AGAGGTACCT 1200
GTGGGTCTGC CTGTTTCTGT GTCTTTCCCA CCCACTGGGT GCCTGGTGGA AGGACCAGCT 1260
CTCCACAGGC CCCAGATCTG TTGCCACGCA CACGCCCCAG GGCACATCTT TCATTTAGGT 1320
AGCTAGGGAC AATAAAGTTT 1340
|
