Tag | Content |
---|
EnhancerAtlas ID | HS051-23188 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr6:27124940-27126270 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr6:27125675-27125695 | CCCAAAAACAACCACCACGC | + | 6.68 | STAT1 | MA0137.3 | chr6:27125851-27125862 | TTTCTGGGAAA | + | 6.02 | STAT3 | MA0144.2 | chr6:27125851-27125862 | TTTCTGGGAAA | + | 6.32 | Stat4 | MA0518.1 | chr6:27125851-27125865 | TTTCTGGGAAATAA | + | 6.06 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH06I027157 | chr6 | 27124780 | 27126450 |
|
Enhancer Sequence | TGTGTTGCGT GGAGACGGGA GGTCAAGAAA AGCTTCCTTG ATTTGAAAAG CTTTCTTGAG 60 TTGAAGCTGA AGCATTAAAC AAATTTAACC AGGTAAAGAG AAGAGGCCGG GCGCGGTGGC 120 TCACTCCTGT AATCCTAGCG CTTTGGGAAG CCGAGAGGGG CGGATCAGTT GAGTTCAGGA 180 GTTTAAGACC AGAATGATTT TACAGAAAGA AAATCATTTG GTATCAAGGG GAAAACACGA 240 CCAGGACCTT GACTCTAGAG GCTACGTTCC TAAAACAGCA AGCGGGGCAG GAGGGAAGTC 300 CCACGGAGCT TTGGAGCCAC AGGAGAGGCA CTTTTATCTC CCTCTTCTGG CAAACTAGGT 360 ATGAAAGGGA GAAAGAAATT TCACTCTGAG GTGCGAGCGC CGCCGGACAT TTCCTGACGG 420 CTCAGGTGGG CAGGCTGAGT GCGCGAGCGC CTCACTGGCT TCTCATAGGT ACCTGGGTCA 480 GGACGAAGCC ACATAGTTCC TCGTGATGAG AAACTCACTT CTGGCACCTG TCGAGATGCC 540 AGATTCCATG CCAAGCCCCC GAAGATTCTG ACTAGTTTGG CAAAAAATGG GATCTGGCAG 600 GTCCACTTCA AAGCAGCGCC CTCTTCCTTT TGTTGCCAAA GATCTGAGGA CCACACTGCT 660 AAACTGAGCA AGAAACATGC GTGGGTTGGA GATAGAAGTG AGAATAATGA GTTTACAAGC 720 ACAGTATTAC CAACCCCCAA AAACAACCAC CACGCTGGGA AAATTCCATA TAATGAAACT 780 TAATGTGTTA CCTTTGGCTT CTTTGCCATA AGCAAAATAT TGGGGACGGG GAGTGGATAA 840 GGAAGTAAAC TGGGTAGGTG TGTAAATAAG GACGAAAGAC TGCACCATTC TTTAGATGAC 900 AAAAACAGAC GTTTCTGGGA AATAAGCAAA GGAAGAGCCC CACAAGCAGC GGCCTCTGGT 960 GGCGTGCCGT GATCGTATAG TGGTTAGTAC TCTGCGTTGT GGCCGCAGCA ACCTCGGTTC 1020 GAATCCGAGT CACGGCAGTA CCTTGATGTC GCCTCAATTT CTCAACGTAC TGAGCAGTAC 1080 CTTGACGTCG CCTCAATTTT TCAACATACT GGAGTGGAGA CAGTCTCGGA AAAACCCTTG 1140 CAAAATTGAA TTGACTTACG ATCTAATCTG TACACAAAAA ACACTAGTAT TCATCATGGT 1200 GCCCCAACCA GTCAGCCAAG CAGAGAGTGT CTACGCTTGT TGCCTTGTCT TTTTTTTCCC 1260 CTCTCCAAAG ATTCTCTTCC CAACCCTACC CAAGCCCTAC AGTCTTGTTG GCATTGGCTG 1320 TATGTGAAGA 1330
|