Tag | Content |
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EnhancerAtlas ID | HS051-07081 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr12:133234560-133235880 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MSC | MA0665.1 | chr12:133234653-133234663 | AACAGCTGTT | + | 6.02 | MSC | MA0665.1 | chr12:133234653-133234663 | AACAGCTGTT | - | 6.02 | MYF6 | MA0667.1 | chr12:133234653-133234663 | AACAGCTGTT | + | 6.02 | MYF6 | MA0667.1 | chr12:133234653-133234663 | AACAGCTGTT | - | 6.02 |
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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 |
GH12I132657 | chr12 | 133233950 | 133240725 |
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Enhancer Sequence | GTAAGGAAGA CAGGCACACA GCTCAGTAAC AGTGAAAATC ACCCAAAATC TGATCCTAAC 60 TCTTATCAAA TGAACATGGA AATAAGGACG TGTAACAGCT GTTCACAAAC ATCAATGTAT 120 ACATCTGCGT GCATATGTAT GCACAAACAT GCCTACAGGT TCCTCGGGGA GTAACACGTG 180 CGTATGTGTA AACACGTGCG TGTGTGCACG TAAACATGTC TACATGTTCC TCACAGCGTA 240 ACCATGGGCA TGCATATACA TAAACACATG CGTGTGCGTA GACATGTCTG CGTTTCTCAT 300 TGAGTAACCA CGTGCATGCG TACAGGCAAA CACGTGCATG TTCGTAACTA TGTCTACATG 360 TTTCTCACGG CATAACCATG TGCATGCACA TACATAAACG CATGCGTGCG TAAACATGTC 420 TACGTTTCTG AGTAACCACG CGCATGCGTA TAGGCAAAGA CATGCGTGTG TGCGTAAACA 480 TGTCTGCGTT TCTGAGTAAC CACGTGCATG CATACAGGCA AACGTGCACG TTCATAACCA 540 TGTCTACATG TTCCTTGCTG AGTAACACAC AGAAGACTCA GGCTGCTTTC TAGAAAAAAC 600 GAGCCTGTTT TCATGTCACT AGCAAAGCAA CTGGCAACCG TCAGTGCTTC CCTTTCACTG 660 GAGGAAACAT CTGTGGTGAA TACTGCAAAC ATAAGGAGAC CTAAAGAAGA CACGCACACT 720 ATGATCCACT CGGCTCCATC AAGCTTCAAC ACTTGGCCAC TCTGACTTCC TTTGTGAGAC 780 GATTAGAGTG AAGCCCTGTG TGACCCCAAC CTATTCCCTC CTCACACAGA AGTAAAGACA 840 ACCCTTATTC TGGTGTTCAT CAACCCCATG CAGGCATTTG TACTGGTCCT ATTTGTATAT 900 AACCACCAAA AAAAAAAAAA AAAAAAAAAA AAAAGAGCAG TTTCCATGTT TTTAAGTTTT 960 ACATACACGG AGGCATAAGG GTCTTCCTTC AACCTGATTT TTGCTTTTTT CTCCAAAGTG 1020 GTTTCAAACT GTCAGTGTTG TAACCTGTAG CTGCAATTCA ACCCTTTGAA CTCTGGTATA 1080 GTGTATCTCA TTCCCTACAA AATGGCAATT ATCCATTTCT GGTTGATGGA CACTTATGCC 1140 ATCCCCAAAC TTGGTGTTAA ACACAGCCCA AATCTGTAAG GAACCCCTTA CCTCTCCGTG 1200 ACAGGGCAGC CCTCACCTCT CTGTGATGAG GGGAGCCCTC ACCTCTCCGT GACGGAGGGA 1260 GCCCTCACCT GTCCGTGATG GGAGGAGCCC TCACCTCTCC GTGATGGGGG GAGCCCTCAC 1320
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