| Tag | Content |
|---|
EnhancerAtlas ID | HS098-34377 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr20:23160600-23161850 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr20:23161604-23161625 | AAAAAGAAAGAAAAAGAAACC | - | 6.04 | | IRF1 | MA0050.2 | chr20:23161598-23161619 | AAAGAAAAAAAGAAAGAAAAA | - | 6.67 | | NR2C2 | MA0504.1 | chr20:23161154-23161169 | GAGGGTCAAAGGTGA | + | 6.06 | | Nr2f6 | MA0677.1 | chr20:23161155-23161169 | AGGGTCAAAGGTGA | + | 6.35 | | Rxra | MA0512.2 | chr20:23161155-23161169 | AGGGTCAAAGGTGA | + | 6.47 |
|
| | 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 |
| GH20I023179 | chr20 | 23160438 | 23161830 |
|
Enhancer Sequence | CAAGTCTTCC AGGAAGGCTC TCCCAGCACC ATCCTCACCT GCAGGTGGGT TTTGCACCAC 60
ATCTATGCTT TGACCTGGGC TGCTGTTGGA CAGTTGCCAT GAGCCCAGAC CTCTCTGAGA 120
GCATGTGGAG CACCCTTTAT GACACAAACA AGAGCTCAAG GATGGTGGCT GGGGTTCAGT 180
CTGCCGCTGC AAATACCAAA AGCTGTCCTC ATTGAGTCAT CCCTCCCAGA GCAGGAAGAG 240
CAGAGGTTCT GGGAAACAAC CCCAAGGAGA GAGACAGGGC ATTTGTGAGC TGTGCAGCCT 300
CCCTGCTGGG ACATAGGGAA CTCTAGCTGG AGATGAGCAG GGCCTGAGTC TGAGGGTGGC 360
CCTGCTGAAA GCACAGTAAT AGGAGTTATA ATCAGCTAAG AGCAGGAAAT CTACTTTATT 420
TTTCTAATGT TATTCTTTGC TTTCTAGATA AAACAGCATG TAAGCATCTC TGCAGTTGCT 480
GTCCCCAGAG CCCACTTCCT GGATATTGCC AGCTGCCTGG ACCAACCTTT CCGAAAGATC 540
AGCCAGGTCA CAGTGAGGGT CAAAGGTGAG CCACGGGCCT CAGCAGCTGC TGAGTGGATG 600
GTGCGTGGGA CTCAGGAAGT GACGTTCTCT CCCCGCCCAG CCCCCTTCCT CAGTCTATTG 660
CTCCGAATCC TGGACCACAC ACTGCGTGCT GAGGCTCCAT CGCTGTGCTG GGTGAGGGGT 720
GGAGGACTGT CCAGCTGACA GCCACCCAGG AGGCCTGCCC AGGAGACCCA GCCCAGCCTC 780
TCCTTGGAAC CTGAAGAACT CCAGGCAGCT GATGGGACAC TGGGGCCCAG GTCAGCCCCT 840
CCCCTTCCCT GAGGTTGCCT GAGGACGCCT TCACTGTTCT AGAGAAGGAG GCCCTCCCCA 900
TGGCTGGGGA CAGTCACAGC AGCTGCAGAC AGATGATGGG AGGGAGCATT CTTTCCCTAA 960
CCCTAGAGGC GGGCGAGCAT TCACCAAGTG TTGTTGTTAA AGAAAAAAAG AAAGAAAAAG 1020
AAACCAGGAT TGTACCTGAG GTCAGGCAGA CAGTGCTCAA CTCAGCACTG GGAAGATTGC 1080
TAGAAGCCTT GGGCCTATCT AGGAAGACTG GGCCAACATG CGATCCCCTC TGCAAGGTGG 1140
AGGCCATGCA CCTGCCTCCT GCTCCTGAGC TCCGGTATCC TCACTGTGAC CCAGGCCCCA 1200
CTGCAGCAAA GAGACACTGG GAATTAGCCC TTCTGTCCCC TCCTTGCCAG 1250
|
