| Tag | Content |
|---|
EnhancerAtlas ID | HS024-16152 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr9:104240490-104242120 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr9:104240993-104241012 | CAGCCACCAGATGGCAGAA | + | 6.95 |
|
| | 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 |
| GH09I101478 | chr9 | 104240578 | 104244329 |
|
Enhancer Sequence | GTGTTCAAAC TCACAAAAAT ATTTTAGAAG TAAGCAGGTC TAATATTCTG ATGGAAAACA 60
GACTAGTGCC AAAAAACAGA ATGAAAAGGG CAAAGCCAGT ATAAAATAAT AATTGCTAGT 120
AAGGTCAATG CAAAACTAAA TGGTGTCTGC AGTACAGAAA GTAAATCTGT TGCCTCAGAC 180
GCATCATAAG GTTTACACAC ATTTGGAGGA AAACTGTATA GTTTGTGAGT TATTGCAAAG 240
GGAGGATTGC CCAGGAACCA TACGAGGCTG CTGTGGAGCA GACTCAGCCA GTGCTCTCAT 300
ATCCATGGTC TCCCCTTGGG CACACAGAAA GACCTCATTT CCTAGTTTGC CTTCTCCAGG 360
TGGAGTCATG TGACTAGGGC TTGTCAGCAA AGTGACAGGT GTCACACCTG GGACAAGGTA 420
GTTGAGAACA GATGTGCCAT CTCGACTTTC TCTTTCCCCA TCTGCCAGCT GAATGGAGAG 480
CCCTGGTGGA TCTAGAGGAG GTACAGCCAC CAGATGGCAG AAGCCTGGGT CCTTGAATCC 540
TTTACATACA TATCCCAGTG TTGGGACGGC ATGGAACAGA TGTCCCTTCC GCTGCCCACC 600
TCCCAGTACC CTCCCAAACT AGAGTGGACT GTGTTGTGAG CAATACATAA ACCACTGTGT 660
CTAGACACCA ATAATTTTTG GACTTTATTA CAGCAGTTAG CCTACTCTGC CCTCTACAGT 720
TGTGTAGAAT ACCAAATGTA CAGTGACATG GTTAATTTCT CAAGTAGAGA AACAAGTTTC 780
ATTTCAGCCA CAGAAGCAGA TTGTACTATG GGACTCCAAA GGTGAGACAG ACTATCCTAG 840
TACTAAGAGA TCTGGATAGT ACCCAAAGAG GGAACAAAGC AAGGAGAGGT TTGAATTATG 900
CAACCCCAGT CTTGCTGGTT TGTGAACATC CAGCATATTG CAGACTGGTT GCTTCTTCCT 960
CTGCTCTGCT CAGCGCAATG GAGTTAACAA ACCATGTGGT TGAACGTGAT TGAACGTGGC 1020
CTCACCACTT CCACATCACT GCTGATGGAA GCCAATACTA GAATTGGGCT GAACTCCCAC 1080
TCCTGCAGTA TTGGCCTTGG AAAAGGAGGC ATTCGAGTGG ATTTCTGCTC ATACTATTAT 1140
CCCTGCCTTT GTTATTACCA CAAGGGAGCT GGATCAATCT AGAGGAGGGA ACTAGAGACA 1200
ATGAGATAGG GCAGGCAGTT TGGAAAATGC CAGGCACATA GTAAAGGCTA TCACTTACTA 1260
TGATATGTCA GGGGGGAAAG AAATGGAAAC ACCTAGAACT GACATCAGGA GAACCTTTGG 1320
TCCCAGGGAA TTTATCCTAC TGGGGACAAT AAAATCATTA ACATCTCACA TAGTCCTTTA 1380
CTTTAAAACT ACGTCTGTGA GACTGCTGTT CTACTGACAA TCAGGAAAAG AGAGGGATTT 1440
GGTTCAGAGG ACACATGGTC CCTACCTATA TTGATCAGCT TTGCTGGGGT GATTAACAGC 1500
CTCAAATCTT TATAACTTAA AGTGATAACA TGTATTTCTT GCATACGGGT TTGTGGATAG 1560
CTGTGGCTCA GTTGGGGTCA GCTCCAGAAT GTAGGTCAGA ATTAGCTCAT GCCACATGCC 1620
CCTCCTTCTA 1630
|
