Tag | Content |
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EnhancerAtlas ID | HS047-30324 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr7:4834030-4835420 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr7:4835262-4835274 | TCTATTTTTAGT | - | 6.27 | MEF2B | MA0660.1 | chr7:4835262-4835274 | TCTATTTTTAGT | - | 6.32 | MEF2C | MA0497.1 | chr7:4835261-4835276 | TTCTATTTTTAGTAG | - | 6.57 | SPIC | MA0687.1 | chr7:4834758-4834772 | AAAAAGGGGAAGGA | + | 6 | STAT1 | MA0137.3 | chr7:4834799-4834810 | TTTCCTAGAAA | - | 6.14 | Stat4 | MA0518.1 | chr7:4834796-4834810 | CCCTTTCCTAGAAA | - | 6.81 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 4834766 | 4835034 | chr7 | 4834243 | 4834734 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I004794 | chr7 | 4833941 | 4834831 |
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Enhancer Sequence | TTTGGGTCCA CACTGCCTTT ATGAGCTATA ACACTCATCG CAAAGATCTG CAGCTTCACT 60 CCTAAAGCCA GCAAGACCAC GAACCCACTG GGAGGAACGA ACAACTCCAG ACGCGCCGCC 120 TTAAGAGCTG TAACACTCAC CGCGAAGGTC TGCAGCTTCA CTCCTGAGCC AGCGAGACCA 180 CGAACCCACC AAAAGGAAGA AACTCCGAAC ACATCCGAAC ATCATAAAGA ACAAACTGCG 240 GACACGCAGC CTTTAAGAAC TGTAACACTC ACCGCGAGGG TCCGCGACTT CATTCTTGAG 300 GTCAGTGAGA CCAAGAACCC ACCAATTCCG GACACAAAAG AATCCAGACC CAAGGCCACA 360 TACTGCATGA CTCAGGTCAG AGGCGTGGGA GCCACAGCAA CCGCGTCTTA AATAGGGGCT 420 GGGTAAAAAC GAGGCTGAGA CCTGCGGGGC TGCATTCCCA GGAGGACAGG CATTCTTAGT 480 CACGGGATGA GACAGGAGGT CAGCACAAGG TACAGGTTCA AGATGCGGGT CCCAAAGACA 540 CTCCTGATAA AATAGGATGC TGTAGAGAAG CTGGCCAAAA CCAAGACAGC AACGACAGTG 600 ATCTCTAGTC ATCCTTGCTG CTCGTTAGTT GCTAATTATA ATTCATTAGC ATTCTAAAAG 660 ACACTCCCAC CAGCGCAGTG ACAGTTTCCA AATGCCACGG TAACGTCAGG AAGTTACCTA 720 TGTAGTCTAA AAAGGGGAAG GACCCTCAGT TCCAGGAAAT CTTCATCCCT TTCCTAGAAA 780 ACTCATGAAT AATCCGCCCC TTGTTTAGCA TGTAATCAAG AAATAACTCT AAATATACTC 840 ACTAGCGCTC ATGCTGCTGC TCTGCCTTTG GAGTGGCCAT TTTTTTTTTT TTTTTTGAGA 900 CAGAGTCTTG CCCTGTTGCC CAGGCTGGAG TGCAATGATG CAATCTCGGC TCACTGCAAC 960 CTCCACCTCC TGGTTTCAAG CAATTCTCCG GCCTCAGCCT CCTGAGTAGC TGGGATTACA 1020 GGTGTGTGCC ACCACCCCCA GCTAATTTTA TTATTTATTT ATTTTTTTTT TTTTTGAGAC 1080 AGAGTCTTGC TCTGTTACCC AGGCTGGATG GAATACAATG GCACAATCTC AGCTCACTGC 1140 AACCTCCGCC TCCCAGGTTC AAGTGATTCT CCTGACTCAG CCTCCTGAGT AGCTGGGATT 1200 ACAGGCGCTT GCTACCATTC CCAGCTAATT TTTCTATTTT TAGTAGAGAC GGGGTTTCAC 1260 CATGTTGGCC AGGATGGTCT CAAACTCCTG ACCTCAGGTG GTCAGGCCTT GGCCTCCCAC 1320 AGTGCTGGGA TTACAGGCGT GAGCCAACGC GTCTGTCCCA CCCAGTTAAT TTTTGTATTT 1380 TTAGTAGAGA 1390
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