Tag | Content |
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EnhancerAtlas ID | HS127-08229 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr12:122937830-122939100 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr12:122938068-122938089 | CTTTGCTTTTGCTTTTGCTTT | + | 6.38 | IRF1 | MA0050.2 | chr12:122938074-122938095 | TTTTGCTTTTGCTTTTGCTTT | + | 6.55 | IRF1 | MA0050.2 | chr12:122938080-122938101 | TTTTGCTTTTGCTTTTTTTTT | + | 6.59 | SP2 | MA0516.2 | chr12:122938614-122938631 | AGAAGTCCCGCCCCCCT | + | 7.2 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27577 | chr12:122937897-122938918 | Esophagus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 122938394 | 122939019 | chr12 | 122937953 | 122938289 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I122452 | chr12 | 122937012 | 122939112 |
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Enhancer Sequence | AGAATTACAA AGAACCTTCT TAAGGGTGGG GGAGATTATA AAGTACATTG ATCAGTTAGG 60 GTGGGGCAGA AACAAATCAC AGTGGTGGAA TGTCATCAGT TAAGGCTATT TTCACTTCTT 120 TTGTGGATCT TCAGTTGCTT CAGGCCATCT GGATGTATTC GTGCAGCACA GGAGATATGA 180 TGGCTTAGTT TGGGCTCAGA GGCCTGACAA TTTCCTATTC ATGCTTTCTT GTGGTTTGCT 240 TTGCTTTTGC TTTTGCTTTT GCTTTTTTTT TTTTTTTTTT TTTTTGAGAC AGAGTCTCAC 300 TCTGTCTCCC CAGGCTGGAG TGCAGTGGTG CAATCTTGGC TCACTGCCAC CTCTGCCTCC 360 CAGGTTCAGG CGATTCTCCT ACTTCAGCCT CCCTAGTAGC TGGGACTACA GGCCTGCGCC 420 ACCACACCTG GCTAATTTTG TATGTTTAGT AGAGACGGGG TTTCGCCCTT TAGGCCGGGC 480 TGGTCTCGAA CTCCTGAACT CAGGTGATCC GCCTGCCTCG GCCTCCCAAA GTGCTGGGAT 540 TACAGGTGTG AGCCACTGCT CCTGGCCTTT CCTATGGTTT TCTAAGTGTG CGTGTGCATG 600 CACACACACA CGTGCACGCA CACACGCACC CTCTGGCATG CATCTCCTTG GCCCAGGTGG 660 GCCCAGATGG GCCCAGGTCT GTCCACCCTG AATATACCAT GATCAGGGTA AAGTGAGTAT 720 TGCACAGTCA ACTATAACAT TCACTACTGT GCTTCCATTT TCAAAGACTG AAGCAGAGAC 780 TACCAGAAGT CCCGCCCCCC TCAAAGCCAT TCTACCCTCT TCCTGTATCT GATTCTTCCT 840 GCCATGTGAC ATCCAGAATG AAGACATTTC CTAACTTCCT GTGTTATTAG GGATGGCCAT 900 GAAAATAAGT TCTGGCCAAG CTGAAGTAGC CCATGCAACC TCTTGGAAGT GTGTGTGTGT 960 GTGTGTGTGT GTGTGTGTGT GTGTGTAAGA GATGGAGGCT TGCTCTGTTG CCCAGGCTAG 1020 AGTATAGTGG CATGATTACA GTTCACTGCA AACTTGAACT CCTGGGCTCA AGCGATCCTC 1080 CGGCCTCAGC CTTCGAGTAG TTACGATTAC AGGGGTGAGC TACAGTGTCC AGTCCAGGCA 1140 GTTTTCTTAA AGGGAGAGGG CAAACATTTA TCTTTCTTTT CTCCCTCCTG CTGATAGGAT 1200 GTGATATTGT GACATAATAA GAAATAGGCC GGGCATGGTG GCTCACGCCT GTAATCCCAG 1260 CACTTTAGAA 1270
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