Tag | Content |
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EnhancerAtlas ID | HS187-05426 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr12:13331900-13333150 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Ar | MA0007.3 | chr12:13332193-13332210 | AAGTACATCCTGTTCCA | - | 6.14 | NR3C1 | MA0113.3 | chr12:13332193-13332210 | AAGTACATCCTGTTCCA | + | 6.03 | NR3C1 | MA0113.3 | chr12:13332193-13332210 | AAGTACATCCTGTTCCA | - | 6.07 | NR3C2 | MA0727.1 | chr12:13332193-13332210 | AAGTACATCCTGTTCCA | - | 6.07 | RREB1 | MA0073.1 | chr12:13332385-13332405 | CCCCACAACACACAAACACA | + | 6.22 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_00070 | chr12:13330671-13333635 | Adipose_Nuclei | SE_02366 | chr12:13331663-13333083 | Astrocytes | SE_26715 | chr12:13331506-13333248 | Esophagus | SE_36302 | chr12:13331995-13332979 | HMEC | SE_45692 | chr12:13331216-13333293 | Osteoblasts | SE_55863 | chr12:13331367-13333242 | u87 | SE_64909 | chr12:13331775-13332957 | NHEK |
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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 |
GH12I013177 | chr12 | 13330681 | 13333248 |
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Enhancer Sequence | GGTCTGGGTC ATCTGGCTTC TACCCAGACT CGCGTCAGCC TCCACACTGT GATTATCCAT 60 GACACTTCAG CCAGCAGCAT CTCCACAGCA CAGTTTATCA AAAAAAAAAA AAAAAAAAAA 120 GATCCTTTCC CAGGAACTGG GAACGCGTTT CATTTAGCTT CATTTAAAAT ACATTGTTAA 180 AGCGATGTGC TCCACGGAGC TGCCAAATGC TATAAATATG TATGAAGTCG CAGTAGCCTC 240 CTACACCCAT GGAGAGGCCA GTTTTGGGAT GGATAACAGA CAGGGGGAAT TTTAAGTACA 300 TCCTGTTCCA CTAACACTTG CTTCTTTTCC ATTCTGTTCT TCCTCCTTTT GCTCTCTCCT 360 GCTCACTAAC CCCCCTCACC CCAGCAGAAA AAATAATTGC TACGAGGGCT GAGCCTGAAG 420 ATTTCTTTTT TTTTTTTTCC TTAAAGTGTT GCAAAACCTT AAAACTGTAA GGGAATAACA 480 GCTTTCCCCA CAACACACAA ACACAGCTCT CCTCTGGCAA ACAGGAAACA CTCCCAGGGC 540 TGTGGGCTCC TGAGCCAGGA AATGGGTCTT TGCTGCTCTG GTTACCTTCT CCTCAGGTTC 600 TTCCTGGGCA TTCAATGCAG TTAAAAATAG TAACCACCAA AACCAGAAGA AAAGATGATT 660 TCATTGTCTA ACCGCTGCAA CTTGTGGCCT GATTTGGGTG GTGGCAGAGA GGGAGCTAAT 720 CCTCTGAGTT GGCGCCTTGG GAATTCTCTT AGGGTCGAGC TGGTCCCTGC CCCAGGATTT 780 CAAAACGGGG TATCCCTGAG GAGCCAGCCC AGCTCAGGAG GGCGGCGTGT TAGGCAGAGC 840 CAGCTTACCA CACTCGTGCA CACTGTGGGT GAGGCAGCTG GTGGAAATGC AAGATCTCTC 900 CGTGGCCCAG CCTGTGAGCA GTGCAGGTGG CACACACCCG CCCTGGCTTG GGAAGGCAAG 960 GCTGGGGGCG GAGCCTGTCT GCTATCTGAG CTAGTCATTC CTGCAGTGGT CTGGGTAGTG 1020 TGCATCCTCA GCTGGCCCTG GCAGGCATAA GAATTTGTAG AGTATGCTCA GTTCCACTCA 1080 GCATAGGGAG CTGTCACAGT GACAGGTACA GAAGGGACCC AGTGGGCTTC TAAGGCTATG 1140 TGAAGACAAA GATAGTTTGA GAAGGTACTT TATCGGGGAA CCTGCCCTGA TATTCATGTA 1200 GGTTCTTTTC TATTTTCCCT AAGCATTGGC CAGCTTGAGA AATAAAGGGA 1250
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