| Tag | Content |
|---|
EnhancerAtlas ID | HS064-09886 |
Organism | Homo sapiens |
Tissue/cell | GM18507 |
Coordinate | chr22:31101440-31103030 |
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 | CGGCTAATTT TGTATTTTTA GTAGAGTCGG GGTTTCTCCA TGTTGGTCAG GCTGGTCTCG 60
AACTCCCGAC TTCACATGAT CCACCTGCCT TGGCCTCCCA AAGTGCTGGG ATTACAGGGG 120
TGAGCTACCG CGTCTGGCCT CCCCAGTATT TTTGCGCCTT TGGTGGAGTG TCTGCTGTGA 180
GTTCTTCAGC TGCTGCTACT GAACCTTGTA CGTTTCTCAG GGAGGGTCTG TTAATCCAAG 240
ATTGGGGCCT GACAAGAAGT CTGAAACGTT TGTGACAGTG AGCCTGCACT AGCTTTGGTC 300
ATATTGTTTA TTGATCTCCT GCAGTGACCA CAATGTGCAA GGCAGTGTGA GTGACAGACC 360
TGCATACCAC TGTCACACAA CTGGAGTGGA GGAGGGGGAG GGAAGTGTGC ACACACCCTG 420
GTTATTTAGT AAGAGGCCAA CAGGTTGAGG CAAAGTGCTT TGTGGGAGCC CCTGGATATT 480
CAAACATGTG GCTTTCACTT CCCCTGTAGT CTTTTGGGAT ACAGCTGGCA AACTATGTCA 540
GTAAAGAAAG ACAGGTCTAT GAAAAGGCTG TGAGGTTCCC TAGAACAAGA TCAGTATATG 600
CTTATCCCAA GGGGAAAGAG AGGGGAAATG GGCCTGTTCC CTGGATGACT GCTGGATGCT 660
GACACGTGGA GAGAGGAGAT GGTAAGAAAC ACCTCTGAAC AAAATTGAAA TTGGCAGCTT 720
GGTGTGTGGT GAATCACACA GCAGGTGTCA CCACACGGAG ATGTGGCTTT AAGAGGCCCC 780
TTTCATAATC ATACACACGG AGCAAACTGT CAATAAGTTT TGGGGTCATG CTGGGTGCTG 840
TACACTTTTT TTCTTTTATG TGCGATGCTT TGCCACGTTG CCTTACTTTT TTTTTTAAGA 900
GTCCTTGGAG TTCTGATTGC TTAGTGATGC TTCATTCCAT TTGGCATCTT GTCACACGCA 960
CAGCCACAGC TCTACATTTA ATACCGATTT AACAATCTTG ACTCACACCA TTTGATCTGC 1020
ATTGCTGGGC CATTGCCTGA AACCAAGAGG AGGGCAGATG GTGTGGCTGA GCTTGCATAG 1080
GAAACTGCCA GATTGCATTG TCCTTTGAAG CAGCAGGAGG TGCCGCCTTC CTAATACAGT 1140
GTGTGGTTTC CCTGGGCTCA CCAGATGAAG CCCTGACCCT CGGCGTGATA GTCACTGTCC 1200
TTCACAGCCA GGTCCTGCCT CTCTTTTCCC TATCACTCAT CTTCTTCCAG CCTTGACCCT 1260
TCTTCTAACA AACTTGCCTT ACTCCCCCTT TGCAAGCCAC ATGTGTTTCA TTCCTCACTC 1320
CAGATCTTCC TGCCATCCCC TCAGCCAGAA GGACCCCTCC TCATTGCTGC TGAAATCCTA 1380
TCTGGGTAGG CTTAATCCCA GGGTCATCTC AGCATGGACC TGTATGGATT TCCTGCAACG 1440
ATCTGGAGGA ACTGTCCTTC TTCTGGATGC CTTTTTGTGT ATTTCATTTG GCCATGCACC 1500
CCATCAGCTG GGTATTCGTC CTTCTCTCTC CGTTAGATCA ATACCTCCCT CCTCCCCACC 1560
GGAACATAGG GCCATGTCTT CTCAATGTAG 1590
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