| Tag | Content |
|---|
EnhancerAtlas ID | HS024-16417 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr9:133342190-133343580 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nfe2l2 | MA0150.2 | chr9:133343549-133343564 | CAGAATGACTGAGCA | + | 6.66 | | RREB1 | MA0073.1 | chr9:133342198-133342218 | CTCCCCACCACCCCCAACCT | + | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_33497 | chr9:133340521-133351254 | H2171 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 133342243 | 133342627 | | chr9 | 133342849 | 133343053 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I130467 | chr9 | 133342925 | 133343088 |
|
Enhancer Sequence | GGCCGAGTCT CCCCACCACC CCCAACCTTT CCCTATAGCC CCCTTCCCGG GCACGTCCCT 60
GCTGGGGGCT GTCTGAGCCA GTGGCCTAGG CCGGGACTGA CCCCATGTGA TGGGGGATTG 120
AACTTCCACC CCAGCTGCCT ACACACGTGG CCTCTGTCCC CTGGGCTGAC CCCACAGAGG 180
TGTGGTCATC TGCCAGCCCG TTGCCAGGGC GGAGCCGCTC TGAGGCCATT TCCCAGTCCC 240
CCGAGCCAGA GGACACAGGG CTCACTCTCT CTCCTGCTCC CTGGGAGGCG GAGACCAGAG 300
CCCTGCTTGC CACCTCCGCA GTGTGTGTGT CTTGGTGTGT GTCACTTGGG GGGATGGCTG 360
GGGGATGTGA TGGCCGGCCG GGGGGATGTG ATCGGGAGCT GTTCTCCCAA TTCCCTGGAT 420
ACTAATTGCC CCTAGCGCTT TCCCCGGGAA CAGGTAGGCG CTCCAAGGGA CAGTCGCAGA 480
CAAAGCCTTT TATGGCACCA GCCCTTTTTG AAGTACAAGT TGCAATAAAA CATATTAGAA 540
GTTTTGCATC AAGATCCTTA GCCGCTCCCC AGGGCACCTT TCTTTTTAGC GACTCGATGG 600
CAGCCCTTGA CAAACAGCCT CAATCAATCA GGCCGGGGAA AAGCAACTCA GCGCACACAC 660
CAGAAAATTG CTCAGGTTTT TAAATAGCAG TCGCCAAGGC TGGCTGTGAG CTCTCGCTGC 720
AGCCAAGGTG CCGCGTGGTA GGGGAGGCGG CAGGGACGCA GCCCTGCCCC CGCCGCCAGC 780
AACCCATTAA GACCTGGAGT GCTGGGAGGG AAGACCTTCT CCACCATCTG TTGTTTTATT 840
ATTAAGAGGG GAGTTTACAA GAGCAAGCCC ATATGTTGCC AAACAAATTG TCAAATAGCA 900
GAGCTATTAA GGGAGCCGGG TTGGTGAGGT TTCTCCCCTG GTCTCCTTGA TGATATAGAA 960
TATGAAGCGT GTTTCATCTT TAAGAATAAT GAATTGGAGC CCCCACCCAG CTCTACCCTC 1020
ACGCCTCGAG TCCTGGATAG AGAGGGGCAG GGCCGACCCA TACGTTGCCC TTTCTTTCCG 1080
TTAAGTCCCC AGACAAAAGC AGCTTCTGGT TTTTCTAGCA TAGATGAGTC TCAGGAGCAC 1140
ACTGCTGTCC TTCCTTCTCA GGTTTTGAGG AGAAGGTGCT GAGCTCAGCT TCCATCCCAA 1200
ATAACCTTTT GAGCCGGAAA AGTTTGCCAG GGAAAGATGA GCATGGCCCC CTCGGCCACC 1260
TACCCTCTCC TGGAGATGGG TTTCATCAGA AATGACTGTG GGGAATCTGA GCACGTTCTA 1320
GAAGGAGGCA GAGGCAGTGT TTCTGCACCC AGGAAATGTC AGAATGACTG AGCAGTGATG 1380
AGGCCTCCTC 1390
|
