| Tag | Content |
|---|
EnhancerAtlas ID | HS003-37487 | Organism | Homo sapiens | Tissue/cell | A549 | Coordinate | chr5:127901410-127902830 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxq1 | MA0040.1 | chr5:127902067-127902078 | AATAAACAATT | - | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 127901851 | 127902318 | | chr5 | 127902382 | 127902681 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH05I128565 | chr5 | 127901500 | 127902734 |
| Enhancer Sequence | TGTATCTTTC AATGTTCCTT CTTAGTGTGA TTTTCTAATT CCTCGTCACT CCCTGTCATT 60
TATTGAAGTC TTGAGAACAC CTAAATCAAT CTCTTCCTCT CCAGTTCTAC TGCTGCCATA 120
ATTCTCCTGG AACAACATCC ATGTTAATAG TATATTTGAC ACTCTGGCCT CCAGCTTCCT 180
GGCCTTCCTT GTTTCCAATC ATAATTACAT CCATCCTACC TAAGCTGCTC ACCTCGTGGC 240
CACACATTGC TCTGGAATAG TGCAGCCCAA CAGGACTTCC TGCAATGATG AAAATGTTAT 300
ATAGCTGTGT AAGTTCACTG TCAACACAAA TATTTAATGT TTTCTCCGTT CTCTTCACAT 360
TTCTGCCTCT ATCAGCTGAT GATCTCACTT ATACTTCATT GAAATGATAA AAGAAATAAG 420
AGAAGAGCAC CTTCATTTTC AAAATCACTA CCCAATCTAG TAATCTGTCT CCACTTGAAC 480
TTCTTTGCTT CACCTCTTGC TAGTGGGAAG AAATGTCGAC TTTCAACCCA GAGGCCAAAT 540
CCTCCACTTT ATCCTTTGGA TCACATCACC TCCAGCTTAA CAAATGAAAT CACTCTTCAA 600
ACCCTTCCCT CTTTTCTTTA TCAGTACACC AGCATTCTTA AGTTATCTAT TATCTTAAAT 660
AAACAATTCT CTTTAGCCTT TGTGTCTCAT TCCAGTTTTT GTGATAATTC TTTGGGACCT 720
TTTGCTGCTG TTACTGTCTC ATCCTCTATT TATGTATTTA GCTACTGATA CCAATTTATT 780
AAGCTAGTTG ACTTAAGTAC CTGCAATGAC GACCTCAACC TCTACTCCTG GCTCAATACT 840
GATGAAGTAA TCTGCTTAGT TTCCAGGGAA CTGTTAAAGT TAATGAGTGC TTGGGGATTC 900
TCATCTGGAA ACCATTCCAA TGGTTAGAAC ATTCGCCGTA AGAAATTTTT CTTGTAGTGA 960
TTCTTTGATT CTTTGATCTG TCCCTTCACT TTAAGTTTTT CCTATGTACC TCTAATCAAG 1020
TCAACACAAA CCATCTCCAG GGATTTTACC TTGCCACTGG TTAGATAATT CTAGTTTGGT 1080
GAGTTGCCAC CCTTAGTTCC ACAAGTGTCT CTTCTGTCTT CAAAAGCCAT GGCTACAGTG 1140
TCACTTCCTG ACTGACTTGT TCCTCAGGGA GAAATACTGG CGGTGAACCC ACAGGAACCT 1200
GTGGGTCCAT AGCTCTGCTG AAGCTGCAAC CAAGTCAAAG TCCACCTATT TCTTCTTAAG 1260
CCTATGCCAA CTAAAGTTTC TCCTGACCAG TAGGCAAAAA GTACTCACTT TCTGGGTCAA 1320
AAAATGAATG CTAAGTTGCC AAATCCAGTG GATGTGATTT GGCATTCATT TTACTCATAG 1380
CCATTTAATC ATTTCATTCA ACTCAATCCC AACCTTTGAA 1420
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