| Tag | Content |
|---|
EnhancerAtlas ID | HS042-01779 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr1:58540250-58541700 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MITF | MA0620.2 | chr1:58541008-58541026 | TGTGGTCATGTGACTTTT | + | 6.35 | | MITF | MA0620.2 | chr1:58541008-58541026 | TGTGGTCATGTGACTTTT | - | 6.35 | | Nr5a2 | MA0505.1 | chr1:58541347-58541362 | GAATTCAAGGTCACA | + | 6.08 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TATATATATA TATATATTTG AGAAACAGAT GGTATCTCAG AGCCTCAAGT CTGTTGGCTT 60
GTAACAGCAA GGCAACGAAC TTTATGCCAA CAAGTAAACT CGTCTTCCCA GGAAAATGGC 120
AAACCCCTCA ATCACGTGGC CTCCAGTGAT ACTGCCAGTA TGAAGTGTTT AGATTCCCCA 180
GGCGAAAATA AGAAACTTTG CCACAGCAGT AACTAGAAAG AAAAGACTGT GGTTTAGGGA 240
GATAAGGAAA GGCAGGGAAC ATTTCCTGAA CTTCTAGTCA GCATCATGTA ATATGCTACG 300
TGCCTGTCAT CTATCAGCTC ACTCTGTCCC CCGGGAGCAG GGATGCAGAC TCCAGCCTTC 360
ATGGCTTCAA AGTGCACCAT GTTATGGACA AACAAAGTTT CCAAAGCTGA ATTGTGAAGG 420
TGCCAGGCAA ACACTTCCAC CAACAGAACC CAGCTCAAAT ACTACCTCTT CCATCCAGCT 480
TGCATAACTT TATCTGCTCT TTAGTTTGTT CCTTCTCTGG ATTCTAAAAG CTTGTCCCAG 540
CCAATTAAAT TCCAACCACC TAGGAAACAG AGAATTTCTT TTCTGTTCAT CTCTGTTCTT 600
TAGGAATTAT TGTTTAATCA CTTTTTTAAT AGAAAGCATT TTAAGGTGGA TTGAGAAGAA 660
AAGAGGGCAT GGTAGTTAGT AAAGTCTGTT CAAAAATACT CTGGGATTCC TTATTTACAC 720
ATGGTGAGAT TGTACTTCTC CTCCCCGTGA AAGATAAGTG TGGTCATGTG ACTTTTTTGG 780
CTAATGAAAT TGTGAGCAGA AGCAATCTGT GTCACTTCCA AGTGGAAGGT TTAGAGCCAG 840
TGCACAGTTT GCCACATTCC CTTCCTTACT AAAGTTACTG TGGAGGCCTG TGTCAAGAAA 900
AAGCCTCTAT CTTTGAGTGA GGATGATAAG GCAGAGAGCT CCCTGGTGAT TGTGTATGTT 960
GGCCTATAGA AGGAGCAAAA CCTGTGTAGT ATTAAACCAT CTTGATTTGT GTATGGAATG 1020
TTTGTTACTG CAGCATAAAT TAAGCTGTCC TGATTGATTC AAAAGGATTT GTCAAAAATG 1080
ACATAGAAGT GTCCTCAGAA TTCAAGGTCA CAAATGCAGC TGGGCTTCAA GAATGTACTA 1140
GAACCAAGGT CTAGAGAGCT GTCCGACTCT CTCTCCCTCT CCTGTATTCC CCTCTGTGTG 1200
TCCTCCAACT CTGCTGCCTT TCTCTGGCTC TATCTCTGTC CCTCTTTGTG AATCTCTCTG 1260
TTTTTCTTCC TGCTCCTCCA GTCTACCCAG GTGGGAAGTA GAGGGAAGAT GTTTTCACCA 1320
ACGCTATTGA GAATATCTGT TACAAGTCTT TCTCTCTCTC TCTCTCACAG GCACACACAC 1380
ACACACAAAC ACAATACTCG GCTTCATTTC CAAATTTCTA GAGAAGGGAC TCTGATCAGC 1440
TCAACTTAAA 1450
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