Tag | Content |
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EnhancerAtlas ID | HS141-01214 | Organism | Homo sapiens | Tissue/cell | NB4 | Coordinate | chr1:154643740-154645010 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYB | MA0502.1 | chr1:154643959-154643974 | AAATGCACCAATCAG | + | 7.1 | NR2C2 | MA0504.1 | chr1:154644927-154644942 | TGACCCTTGCCCCCT | - | 6.39 | STAT1 | MA0137.3 | chr1:154644696-154644707 | TTTCTGGGAAA | + | 6.02 | STAT3 | MA0144.2 | chr1:154644696-154644707 | TTTCTGGGAAA | + | 6.32 | Stat4 | MA0518.1 | chr1:154644696-154644710 | TTTCTGGGAAAGGG | + | 6.56 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGGATTGTA AATACAGCAA TCGGCACTCT GTATCTAGCT CAAGGTTTGT AAACACACCA 60 ATCAGCACCC TGTGTCTAGC TCAGGGTTTG TGAATGCACC AATCCACACT CTGTATCTAG 120 CTACTCTGGT GGGGACTTGG AGAACCTTTG TGTGGACACT CTGTATCTAG CCCATCTAGT 180 GGGGAGGTGG AGAAACTTTG TGTCTAGCTC TGGGATTGTA AATGCACCAA TCAGTGCCCT 240 GTCAAAACAG ACCACTTGGC TCTACCAATC AGCAGGATGT GGGTGGGGCC AGATGAGAGA 300 ATAAAAGCAG GCTGCCGGAG CCAGCAGTGG TAACCCGCTG GGGTCCCCTT CTACACTGTG 360 GAAGCTTTGT TCTTTGCAAT AAATCTTGCT ACTGCTTACT CTTTGGGTCC ACATTGCTTT 420 TATGAGCTAT AACACTCACC GCGAAGGTCT GCAGCTACAC TCCTGAAGCT AGCGAGACCA 480 TGAGCCCACT GGGAGGAAAA AACAACTCCA GACGCGCTGC CTTAAGAGCT GTAACACTCA 540 CCGCGAAGGT CTGCAGCTTC ACTCCTGAGC CAGCGAGACC ACGAACCCAA CAGAAGGAAA 600 AATCTCCGAA CACATCCAAA CATCAGAAGG AACAAACTCC AGTGCGCCAC CTTAAGAGCT 660 GTAACACTCA CCACGAGGGT CCGCGGCTTC ATTCCTGAAG TCAGTGAGAC CAAGAACCCG 720 CCAATTCCAG ACACGTTTTG GCAACCCAGA TGGGACTTTC GCCTATCGCC AAGTGGTGAG 780 ACAATCGCCG AGCAGTGAGA CCATCGCCTA TTGCTGAGCA GTGAGTACCA TCGGACCCCT 840 TTCACTTGCT ATTCTGTCCT GTCTTTCCTT AGAATTTGGG GGCTAAATAC CGGGCACCTG 900 TTGGCCAGTT AAAAGCGACT AGCATGGCCG CCGGACTAAA GACATGGGTG TCAGGCTTTC 960 TGGGAAAGGG CTCTCTAACA ACCCCTGACT CTTCTTCGGA GTTGGGACCG TTTGCCTAGA 1020 ACCAGCTTCC ACTTTTCCTG TACTTCTGGG CTGAGCCGAG GGTCGACAGA GAGGAAAGAC 1080 ATGCAGCTCC GGGGTCCCAA CAACAAGTTG GTTGACCCTG CGGTCATGAG CGGAACTCTC 1140 AAAGGCATGT TGCCCAAGCG AGACTCACCC ATCTATCCTA TCTATCCTGA CCCTTGCCCC 1200 CTGGGTCCTA ATGCCTTCCA GACAAACTTC CTTTTGCCTC TCTTCTCTGA GGTTAGGCCC 1260 ACTTCTAAAA 1270
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