Tag | Content |
---|
EnhancerAtlas ID | HS073-09823 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr22:37336500-37338000 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU2F2 | MA0507.1 | chr22:37337029-37337042 | TGCATTTGCATAT | + | 7.22 | POU2F2 | MA0507.1 | chr22:37336893-37336906 | ATATGCAAATGCA | - | 7.22 |
|
| 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 |
GH22I036940 | chr22 | 37336858 | 37337922 |
|
Enhancer Sequence | TGTGTGTGCA TGTTGGTGTA GTTGGAGGAA GGGGTTGCTC TTTGAAACCT CAATTGCTAT 60 TGTAAGTGAT ACAGCTCCAG TGACTGGAGG AACACCAGGG TCCTTAGTCT TGCGCCGATT 120 TAAATAAAAC GACACGGAAA CACATGGAGT GGTTTTAAGG AGTGGAGAGT TTAATAGGCA 180 AGAAAGAAGG AAGAAGCTCC CCTGTACAGA GACAGAGGGA GGGGGGATCC AAAGCTGAGA 240 GAGGAAACCC TGAGTGCCAC AGAAATAAGC CAGTTATATG AGGAGGCTAG AGAAGGCAGT 300 ATCTGATTTG CATAGGGCTC AGGGGATTGG TTTGACCAGG CATGTCATTC ATGTAACCCC 360 TGAAAAACCT GGCCCTTTCA CCCTAGCATT TTAATATGCA AATGCAGGGC GCCATGATGT 420 TCTACACAGG TGGGACTATG TGGGGGTGGC CATATTGCCA GGCAAACATG GGGACAAGGA 480 AAAGATGGCG GGAATCCCCA TGTTTGGGTG GACCCAGTTT CTAACGGTCT GCATTTGCAT 540 ATCAAAGGTT GCCAGCCTGA TTCTAAGAGC CGGGGCTTTC CTGCTAGACA AGAAACGTTT 600 TTTGGAGCTG CTTTTAAAAC AGAAACGAAA ACTTCCCAAG GACCACTTTT CCTCTTTATC 660 TGCCTCAAAT AATTTTTTAA TAATTCCTAT AACACAAGGA AATGAATTCT GCCAAACAGA 720 AGGGCCTTTG GTCTTTGGGG CACTACAGTG GGTACATGAT GGCGTGTGGA ACACCACGCA 780 ATGGAGGGAG ACGCAGGGCA CTCCTGGGAA AATCCAGGAG GGATGAGGGA AGAGGAAAGA 840 CAGTGAGGGA AAGGAGGATA AAGAACACAC TTTTAAAAAA TCGTTCATTA TTATCTGAAA 900 TTCCAACACA ACTGAACGTC CTGTATTTTT CCCTAGTCAT GAGAGTGAAA AACTAAATAG 960 AGACTGAGTT CCCCATACAA ATAACTGAGA GTGATCGAGA GCTTATTCCT GGCAGGCCCC 1020 ATTCGAGTGA CCTCTAAGAT CAATTCATTT AGATACTATG GAAGTGGAAG ATACTATCTT 1080 TATCATTTTT GTCATTGAGG AAACTAAGGC ACAGAGATGT CATACAACTT GCCCCAGGTC 1140 TGCCAGCAGG TAAGGGGCAG AGCCAAGATT TGAACTGTAG CCCTGTGTCT CAGAGCCTGC 1200 CCTCAAAAGG TAAGTCTCTC ACCTAAAGAT CCATACGGAG ATGTAAGATG ATCCATGTTG 1260 GTTGGCAAGA CAGAAAAATC CATAAACCAA ATAAATTGAT TTGGTGGCAG GGGGAGATTG 1320 AATCAGAGGT GACCCTGAAA AGTGTCTGTT TATCTGGGAG CTGAACACTG AAGGTGCAAT 1380 TCTCACCCAT TGGAGTCCAG AGAGACCTTC CCTGGAGGAC TGCAGCTCCC TCATCTGTCT 1440 TCCCCTGAGA ACCCAGCCCA GAGCCATGCA TGTAGTAGGT GATCATTGAG GTGAGCAAGG 1500
|