| Tag | Content |
|---|
EnhancerAtlas ID | HS024-06232 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr16:85815180-85816570 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr16:85816190-85816208 | GCTTCCCTCCTCCCTTCC | - | 7.14 |
|
| | 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 |
| GH16I085781 | chr16 | 85815381 | 85816472 |
|
Enhancer Sequence | AGGCCACCAC ACCCAGTTAC TTTTTAGTGT TTTTTTTTGC TTTTTTTTTT TTTTTTTGGT 60
AGAGAGGAGG TATTGCTATG TTGCCCACAC TGGTCTTCAA CTCCTGGCCT CAAGCAATCT 120
TACTGCCCTG GCCTCCCAAA GTGCTTACAG GCATGGGCCA CTGTGCCCAG CCTACTTATT 180
TATTTGTATT GCTGGGGAGA GTGTGAGTGC AGTTCCCCAC ATATGAAGAA ATCGCAGGGG 240
TCAGCACATC TGGAGTGCAA TGGACGAACC TTGCCCTGGG AAAACCACCT TTGTGATCTT 300
GGTATTTTCC CTGACAGGTA AATACGTTTT GCCTGTTTAA AGTGGCTGAT GACAGCCCCA 360
CTGTGATGGC TGTGGCCAGC AAGGACAGGA AACGCTGTTG GGTAATGGGG CGCACCGTGT 420
AAAGCAGGTC CTTGCCTCAT TCCAACCAGA AAGCCCTGGT GACGGGGATC TTGAGAGAGC 480
ATCTCCTAAC GGAAGGCTCC CAGGAAGCCA GTGGAGAGTC GCCTGAAGCG GGCAGTGAAA 540
CTGCTGCTGG GCACCTGCCA GCTCCTGGGC CAAACTCCAA GCCTCCCGGG CCCGCCTTCT 600
CCATCTGCAC GCTAGCAAAG CAGCTTGTCC ACTGTAACAA GTAAGAGCAA CCTCAGGGCA 660
GCTGGCAGTC CGTCACCCTC TGAGAAATTC CTCAGCCTTT CCACATCTTC TCCACGCTCA 720
TGAGCCTCCA CTGCTGGCTC TGGCCCTGCC GCCACCCAAC CCTGATAAAT GACACCTTTC 780
TACCTTAAGT TAATAGAGCT AATAATAGAG CAGCTCCTCC ACCATTCCTG CACCATGTCT 840
CCAAACACAA AGTTATTCTT CTATCCTATG CCAGGAAGGG GCCTTCTCCT CGGGGGCCTT 900
ATTTATATTC TTTCTGTGCC CAAGCCCCAG TTCTGCCTTC AAATCTGTGT AAGTCTTTAT 960
TTTCAGGGAA AAACAAAAGC ATTGAACCGG TTCCCTCTAG CTGCTGTCCA GCTTCCCTCC 1020
TCCCTTCCAT GACTGTTTCT TCAACTTCTT TAACAAGCCG CTAGTCTTGC TCCATGTCCT 1080
CACCACAGCT CTGTGCAATC TGCCATCTAA CCCATTCCCT TGCAGAGCAG CACTCCGGAA 1140
GTCTCCTGAC CACTGCCTGA TGGCCCCAAG ACTGCTACCC CCTCAAAAGC CTCCCAGCGG 1200
GAACCCACCA CTCTCAGGCA GGCCAGTCCA TTTCCAGCCT CTCCGACCTG AGGCCACCTT 1260
TCCCTCTGCT CTTCCCCACC CTGCAGGCCA CAGGTCCTTT CTCTGCCCTC CTTTCCTGCA 1320
TTCTCCCTGT CATTTATTTC CTTCAGTCTC TCACCTTAGG CAGGGGCTTC TAAAACTGCT 1380
TCCTAACCGG 1390
|
