Tag | Content |
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EnhancerAtlas ID | HS042-07852 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr11:61772630-61773550 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr11:61772671-61772683 | AAACAAACAAAC | - | 6.32 | MYB | MA0100.3 | chr11:61773365-61773375 | GACAGTTGGT | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr11:61773531-61773546 | GAGGTCAGGAGTTCA | + | 6.22 | RARA | MA0729.1 | chr11:61773531-61773549 | GAGGTCAGGAGTTCAAGG | + | 6.73 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I062004 | chr11 | 61771581 | 61773472 |
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Enhancer Sequence | CACTGCACTC CAGCCTGGCA ACAGAGCGAG ACTCCGTCTC AAAACAAACA AACAAAAAAA 60 TGTCTCTCTC CTCTCTTTCA AATGAGCAGC TGCCCGAGAA CCCACAGGAA TGGATGGAAG 120 GATAGAAAAA GGCAGAAAAG ACACCCGCGG GACACTTTGG AAGCCAGTGC CATCTCTCTG 180 TTCTCTAACA GTGCTAAGAA AGGATGGGCC TGTGGGTAAT CATTCTGATC AAAAGCCAAG 240 GCAGCAGCTG GACTGTGCCT CCAAACTGTT CTGGAGGAAG AAAATATGCA AAGAAAGATG 300 TTATTCAGGG CTGCAAGCAG CCTCCCTCTT CTGCTCAATC TCCCTCTTTC TCTCTGAAAT 360 TCTTCCCACC CACGGGTGCC AGCTTTTTCT GTCCCATGAT GTCGGGGGTT GGGACGGGGG 420 ATGGGAGAAC TGACTGCCTG ACTCCACCTG ACCAGCTGCC TGCAATCTGT AGGTCGTGGA 480 GTATAGGAGA TCCAGACTGT TCCCCAGACA CCAACTGCCA GCCTTTAAGT GTCCTCCATT 540 TGCTACCACC CAGGGGACCA AGGGTTTTTC TCTCCCACAA ACCATATAAT TGGACTCACA 600 GCCTTTTTCT TTTAGGAGAG CTTACTGAGG GGTTGATAGG AAGGGCACTG ACAAGATGGG 660 GGGCTACCAG CTTCCCCAGG GGAAGTGACT CCTAGGCCAA GACTTTACAG CGTGAATTTG 720 TGTTTCTCTG ACTTGGACAG TTGGTTAAGA TTAAAAAGGA GAAGCCATTT TTCAGCGTGT 780 GGATGGCCAC CTCCCCAGAA GAGTTTCTCT TCTGGGAATA AAATAGGAAC CAAGGGGCTT 840 GATGCAGTGG CTCACGCCTG TAATCCCAGC ACTTTGGGAG GCTGAGGCAG GTGGATCACC 900 TGAGGTCAGG AGTTCAAGGC 920
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