Tag | Content |
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EnhancerAtlas ID | HS059-00955 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:28305490-28306940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr1:28306314-28306333 | GACTGCCATCTGCTGGAAA | - | 6.59 | NFIC | MA0161.2 | chr1:28306415-28306426 | TACTTGGCACA | + | 6.32 | Nfe2l2 | MA0150.2 | chr1:28306249-28306264 | CAGAGTGACTTAGCA | + | 6.35 | STAT1 | MA0137.3 | chr1:28305791-28305802 | TTTCCCAGAAA | - | 6.02 | STAT3 | MA0144.2 | chr1:28305791-28305802 | TTTCCCAGAAA | - | 6.32 | Stat4 | MA0518.1 | chr1:28305788-28305802 | TCATTTCCCAGAAA | - | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 28305641 | 28306639 | chr1 | 28305616 | 28305920 | chr1 | 28305951 | 28306585 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I027979 | chr1 | 28305616 | 28306712 |
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Enhancer Sequence | ACCCAAAAAC TTATTTTAAC CTTCACGTTG AGGGTGAAGT CCCTAAGATC TTAGTGTGAG 60 GGAATTTCTA TAAATGGGAA AGATTAATAG GTTTAGTGAC TTGCCCCTAG ATCACAAACA 120 AGCAAGTAGC TAGAACTTGG GGCCCCTGAC TCCAAATCTA GGCTCTGGTC ATTGTGTCAT 180 AATGAATGAA TGATTTTTGG GGTGAAATGT TTTAGGGTAG AAAAGAGAAG TGAAAACACA 240 AGGCCCTGAT TTCTTGTTAG AAACAATAAC AAACAAAAAG CCATTTCCCT CCAATTCTTC 300 ATTTCCCAGA AACAGTCCTG GGTATAGGCC TTACGTCTTT CAGTGAGAGA ACAGCCCCAG 360 AATAGAACTG AGAACAGTGA CCAATAAATA TGGCATCAAC ATTTGTCATA TCTGGAACCT 420 CCTTACTTAC TATACCTTGT AGTTGTAACC AAGATACTGC ATCACTGAAA TTGACCTTGG 480 GAAATGGGTG ATTTAAATCC ATTTCTCAGA ACTGCAGACA GTTTTGAGAA ACATGGCAGT 540 GTATCAAAAC TCAAATCCCA TCTGCAACCA ACACCTAAAA CATACACAGA TCATACTGCT 600 GTGGGAAAGA TACTTTATTT GTATAAATAA AAAGAAGTTA TATCCCTTGC TCTTTTTATC 660 TCCCTGCTTC TGCCACCTTC TTCAGTTAAA CAAGGTCCTA ACTTTGGCTT TCTTCTTCAT 720 CCTGCTCTAT TAACCTTCTT GTTCTTTCCC CTTGCCCAAC AGAGTGACTT AGCACCAGGG 780 TTCCTGTGTA AATAAGATAA AGCTGCCTCT TCCTCAAGAC ATTTGACTGC CATCTGCTGG 840 AAAATCACTG TAATATATAA ATATACAAAT CTAAGATAAC TGTAACATAA TTGGCCAGAA 900 CTTATACTTC CATACGCAGA AGTCCTACTT GGCACAGAAG TTGTGCAGAT ATGTAACTGC 960 AAATCTTTGA CATCCTTAAC CCAGTGGCAC TTCAAAACAG ACGGACTAGT CAACTGGACC 1020 AGACACTAGA TCACTCTGGG CTCAGCTGGC CACTTACAAT ACAAGGCTTG GCTTAGGTGC 1080 ACTTGGGTCT CTTTTAGTGC TAATATTTTA CAATAGAATT GTCATGCCTT ACATTCATAT 1140 GAGGGATTCA ATCAATGTTT GCTGAGTAAA TTCATATTAA TCTCACAAAT GATTCAGTGG 1200 AGGACTGTAG TCCAGGTCTT ATGCCTCAAT TCAGTTCAAA CATTAAACCA TTCAACTAAT 1260 AATAAATTCT TATTATGTTC ATGGTGTTGA AGAGTTCTTT AATTCCATTT CACCCATTAC 1320 AGCTTTACAA ACTAAGCCAA CCTCCACCAG ATGCACAGTC TACTATGATC TGTCTGTAGC 1380 AAAAAACTTT TTTAAGTGAG TCAGTTTGAC TTTCTTGTAA GACTCAACAA AGGCAGTAAC 1440 TCATATTTTG 1450
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