Tag | Content |
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EnhancerAtlas ID | HS060-18849 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr2:25780530-25782010 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEOX2 | MA0706.1 | chr2:25780992-25781002 | AGTAATTAAC | + | 6.02 | Znf423 | MA0116.1 | chr2:25781716-25781731 | TAACCCTTGGGGGGC | - | 6.06 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 25780615 | 25780755 | chr2 | 25781272 | 25781487 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I025557 | chr2 | 25780071 | 25782268 |
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Enhancer Sequence | CTTTGTATAT TTAACAAACA GCCCAGGTGA TTCTTTCCAG GGAATTCTGG GAAGCACTGC 60 TTCCCCACAA ATTAGAAGTT CTTACTAACA CAAAGAGGTA AAAAATTGAG ACAGGGGTAA 120 AACTATCAGA AAGTGATTCA GTTGCTGCTT CCTACAGATG ATGTAATTAT CTACTTGGAA 180 GTCCAAGAAA AGGAACTGAA AAATTATTAG AACCACATAT TGACAGAAGA ACCAGTGAGA 240 CTTCAAGACA GAAATGTCCA TGAGATCTCT GAATGTAGGA GTCTTAACCT AAACAAGAAG 300 AACGAGCTGG AACTAAGAAC TGCAGAAATT TATTAGCGTC TGGGGTGGAG TGAGGGGCAT 360 GTAAAAGCCG GAACTGTGAG AAAACATTCA GAAAGAAGGT GTGCAAGAGA ATGCCGGGGA 420 GCACAGGATC TGGCTCATCA AAGGCGATCC AAAGGCTTAA TGAGTAATTA ACATGCACAT 480 TTCATAGCTA GACATTTCGT AGTCACTAAA TGAAGATATA CAACATATAA CACACATGGA 540 TTAAATTTAT TTAGAGAAAG AGTTCAACCC TAAATCTGTA CCTGTAGATC TCAGAAAGCA 600 TGAGGTATTC AGGCAATAAT CACTGATAAA TTTGAGTTAA TGCAGAAACA GATAAGCAAT 660 TCACACTACT GGGTCACAGA GAACACAGTG ATCTTCCCAC ACATGGAAGC AGAAGATGCA 720 CTCTCCAGTG CAGCTCTGGT GGCCATCTGC AAGAACAAAA AAAAGATCTA AAGTTGACAA 780 AAGGGCTGTG GCTAAGTGAT GACTGCCACA GGAAATTGCT CATTTGAAGA ACTGCTTGGT 840 TTAAGCTAAG TCATACACTT CTTTGTAATG GAAAAACCTC CTTGTCATCG CTCTAAGAAT 900 AATCAGGCTA CAGTTGAAAA AATGCCTTAT TGTTTCATAA ACTACACACC AATTCTTTAT 960 TTGATCGCAT CCATCTTTTT AAACAGCTGG GTCCATTTTG AATGTTCTCG TTTTAAACTT 1020 AGCATTTTTG CAGCTGTAAG TGGTTTTATG AATAAATCGT GCATGCAAAC AACACAGTAG 1080 AATTGGGCAA CGTTCAGATG ATTGAAAGGA GCAATATCTA AAACATCCCA AGCAACCTAC 1140 TGAAAATGCG GATAAAGGTT ATCAGGATAT CCCAGACTAT TCCCCCTAAC CCTTGGGGGG 1200 CTCTAGAAAG TCCAGAATTT CAAAGGGAGG CCTCTGGTCA ACGAAGCAGT CACTTTAGCT 1260 CTAAGTCAGC TGTCGAATGG GAGAGTTTCA GAGCACTTCT CCCCAGGCCT CCATAACACC 1320 ATCAACAAGA GTAAAAAGAT GAACCCAGAG CCCTGCATGT TCCTGGCAAC CAACACCCTC 1380 TCAACTAACA CATTGCCACA GTGCCATGAT CTGCCTATCT GGGGTTAATT CCAGCACGAC 1440 CTTTATATCA GGTTATACTT TTTAAAAATA AGAAATCCAA 1480
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