Tag | Content |
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EnhancerAtlas ID | HS047-08769 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr12:121332170-121333060 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr12:121332749-121332761 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr12:121332753-121332765 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr12:121332757-121332769 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr12:121332761-121332773 | AAACAAACAAAC | - | 6.32 | Foxd3 | MA0041.1 | chr12:121332765-121332777 | AAACAAACAAAC | - | 6.32 | Zfx | MA0146.2 | chr12:121332508-121332522 | GAGGCCGAGGCGGG | - | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 121332201 | 121332483 | chr12 | 121332578 | 121332677 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I120894 | chr12 | 121331847 | 121332832 |
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Enhancer Sequence | TTTATAAAGT CAGAGTATAC AGTCAAAGGC TATCAGGCAA AGCTTGAAGA TTTAGTCAAG 60 TTTGGAAGGT CAAGCTAAAC AAGGTCTAGA CAAAACTTAA ACAACAAAAC AAAGTCAGGC 120 ACTGTACGTA GGTCACAATG ACTGTATAAC TAGCTTGAAG AAGAAATGAA CAAAACTTTC 180 TTTGCTACAC CTGCCCTATC TAGGTCAAGA GTGAAGCCCA AGCCTGAGGC CTCAGATGAA 240 GGGAAGTGGG TGTGCCTGTC AGGCATGGTG TGGGATAAGG AAACAGATAA ACTACTGGCC 300 AGGCGCAGTG GCTCATGCCT GTAATCCCAG CACTTTGGGA GGCCGAGGCG GGTGGATCAC 360 CTGAGGTCGG GAGTTCAAGA CCAGCCTGAG CAATATGGAG AAACCCCGTC TCTACTAAAA 420 ATACAAAAAA TTAGCTGGGT GCGGTGGCGC ATGCCTGTAA TACCAGCTAC TAGTGGGGCT 480 GAGGCAGGAG GATCCCTTGA ACCCGGGAGG TGGAGGCTGC AGTGAGCTGA GATCGTGCCA 540 CCGCACTCCA GCCCGGGCAA CAGAGTGAGA GTCCGTCTCA AACAAACAAA CAAACAAACA 600 AACAAACCTG CTAACAGCTC CTCCTCAGGC ATTTTTAGAA GGGTAGAAAA CCGTACCATG 660 CATTCCAAGG AAAAGCAGGG AAAGATGAGG ATCATCCACT CTACTGTTCT TTCTTCATTT 720 AAGTAGATCA TGAAGGAAAC TGTCTTCAAA ATCAAGATAA AACTAACATG AAAAAACAGG 780 TCGGGCATGG TGGCTCACGC CTGTAATCCC AGCACTTTGG GAGGCAGAGG TGGGTGGATC 840 ACCTGAGATC AGGAGTTGGA GATCAGCCTG GCCAACTCGG TGAAACTCCG 890
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