| Tag | Content |
|---|
EnhancerAtlas ID | HS081-20774 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr9:101068650-101069820 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB3 | MA0638.1 | chr9:101069326-101069340 | CTATGACGTGGAAC | - | 6.07 | | YY1 | MA0095.2 | chr9:101069676-101069688 | CAAGATGGCTGA | + | 6.04 |
|
| | 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 |
| GH09I098305 | chr9 | 101067750 | 101070247 |
|
Enhancer Sequence | AGAGATGATC GTTACCAAGG GGTGGCACAC ACAGGCTGCT CTGAGAAGCT GTGGAGTGGA 60
GGGTTACTCA GGAGGTGGGC TGCAGGGAGG GAGGGTCGGG GGCCTTGCTG TCAGCCGGGT 120
CTTCTGGATG TCACCATCTG TCCCCACTTG TGGCCCTGCT GAGTCCTGCT GAGCAAATGC 180
AGACTGGGGA TGTGACAGCT GTCCAGTTCT CCTGCACCCC TATGACTGGT TCATGCACAG 240
ACCTGCCCAA GGCTACAGTG GAAGGGAACT TCAGATAAGA TCTCAGCTTT CTCCCTCACT 300
CTCTAGGGAA TACTAATATC CAGAAGGGTG AAGAGGTCTG CCCAAGGCCG CACAGCAATA 360
TGGTAGCAAA AATGGGCTGT GTTTTTAGAA ATTCACTCCA GTCTTTTTTC TATTAAACTA 420
AGCAGATCCC TTGTGTCTGA GACTTCTATT GTCCCCAAGC ACACACAGAC ACCCAGAATA 480
GCGACTACAT TTTTCAGCTG CCCTAGAGGC TAGGCGTGGC ATATTGCTAG CTTCTGGACA 540
ATGCCTGTAA ATAGAAGTGG TGTGCACATG TTCTGGGAAG TGTCTTTAAA GGGAAGAGGT 600
GTTGCTTTTC CTCCTTCCTA ACAGCTGGAG TGGAATGTGA TGGGTGGAGC TTCAGCATCC 660
GTCTTAGATC ACAAGGCTAT GACGTGGAAC CTGTGTAATG ATGATGTGGG GGCTGCAAGA 720
TGCAAGGAAC TGAGATTCTG GGAGCCTTAC CCCAGCCCTA GACTGCTTAC CTCTGGACTA 780
GGTTTACCTG AGAGGAACAT TTCCTGTCTC TTCAACCATT ATTATTTTGG GTTTTTCTGT 840
GACTTGCAGC TCTACTCCTA ACCAATAGAT GTCTTGACAG AAATGGACAG GGTAGAGGCC 900
AACTATGATC TGAAGCAGGG TGTCGAGGGT TTAACCCTTA TGGGTGGTCT AAGGGGAGGG 960
CGGGCTGCAG GGACAGCTCA GGTGGGTGTA GGGCAGAATG GTGGTGTGGT GGGCAGGAGG 1020
AAGAGCCAAG ATGGCTGACT GGTACAGGGA CCTCTGCTTT AGTGCAGCCC CTCCAAGAGG 1080
CCTTCTCTCT CACAAAGGCC CCTCTTCCCT TCGGCTTCAG CAGGGCAGCT TCAGGCGTCT 1140
GACAGCTGCA TGAACCATTT AACATCACAC 1170
|
