| Tag | Content |
|---|
EnhancerAtlas ID | HS073-09762 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr22:31101570-31102960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxq1 | MA0040.1 | chr22:31101741-31101752 | TATTGTTTATT | + | 6.62 | | ZNF263 | MA0528.1 | chr22:31101827-31101848 | GGAGGAGGGGGAGGGAAGTGT | + | 6.08 | | ZNF263 | MA0528.1 | chr22:31101824-31101845 | AGTGGAGGAGGGGGAGGGAAG | + | 7.25 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 31102484 | 31102589 | | chr22 | 31101581 | 31101740 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I030705 | chr22 | 31101481 | 31103130 |
|
Enhancer Sequence | CGTCTGGCCT CCCCAGTATT TTTGCGCCTT TGGTGGAGTG TCTGCTGTGA GTTCTTCAGC 60
TGCTGCTACT GAACCTTGTA CGTTTCTCAG GGAGGGTCTG TTAATCCAAG ATTGGGGCCT 120
GACAAGAAGT CTGAAACGTT TGTGACAGTG AGCCTGCACT AGCTTTGGTC ATATTGTTTA 180
TTGATCTCCT GCAGTGACCA CAATGTGCAA GGCAGTGTGA GTGACAGACC TGCATACCAC 240
TGTCACACAA CTGGAGTGGA GGAGGGGGAG GGAAGTGTGC ACACACCCTG GTTATTTAGT 300
AAGAGGCCAA CAGGTTGAGG CAAAGTGCTT TGTGGGAGCC CCTGGATATT CAAACATGTG 360
GCTTTCACTT CCCCTGTAGT CTTTTGGGAT ACAGCTGGCA AACTATGTCA GTAAAGAAAG 420
ACAGGTCTAT GAAAAGGCTG TGAGGTTCCC TAGAACAAGA TCAGTATATG CTTATCCCAA 480
GGGGAAAGAG AGGGGAAATG GGCCTGTTCC CTGGATGACT GCTGGATGCT GACACGTGGA 540
GAGAGGAGAT GGTAAGAAAC ACCTCTGAAC AAAATTGAAA TTGGCAGCTT GGTGTGTGGT 600
GAATCACACA GCAGGTGTCA CCACACGGAG ATGTGGCTTT AAGAGGCCCC TTTCATAATC 660
ATACACACGG AGCAAACTGT CAATAAGTTT TGGGGTCATG CTGGGTGCTG TACACTTTTT 720
TTCTTTTATG TGCGATGCTT TGCCACGTTG CCTTACTTTT TTTTTTAAGA GTCCTTGGAG 780
TTCTGATTGC TTAGTGATGC TTCATTCCAT TTGGCATCTT GTCACACGCA CAGCCACAGC 840
TCTACATTTA ATACCGATTT AACAATCTTG ACTCACACCA TTTGATCTGC ATTGCTGGGC 900
CATTGCCTGA AACCAAGAGG AGGGCAGATG GTGTGGCTGA GCTTGCATAG GAAACTGCCA 960
GATTGCATTG TCCTTTGAAG CAGCAGGAGG TGCCGCCTTC CTAATACAGT GTGTGGTTTC 1020
CCTGGGCTCA CCAGATGAAG CCCTGACCCT CGGCGTGATA GTCACTGTCC TTCACAGCCA 1080
GGTCCTGCCT CTCTTTTCCC TATCACTCAT CTTCTTCCAG CCTTGACCCT TCTTCTAACA 1140
AACTTGCCTT ACTCCCCCTT TGCAAGCCAC ATGTGTTTCA TTCCTCACTC CAGATCTTCC 1200
TGCCATCCCC TCAGCCAGAA GGACCCCTCC TCATTGCTGC TGAAATCCTA TCTGGGTAGG 1260
CTTAATCCCA GGGTCATCTC AGCATGGACC TGTATGGATT TCCTGCAACG ATCTGGAGGA 1320
ACTGTCCTTC TTCTGGATGC CTTTTTGTGT ATTTCATTTG GCCATGCACC CCATCAGCTG 1380
GGTATTCGTC 1390
|
