Tag | Content |
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EnhancerAtlas ID | HS095-06718 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:13332120-13333210 |
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 | TATGAAGTCG CAGTAGCCTC CTACACCCAT GGAGAGGCCA GTTTTGGGAT GGATAACAGA 60 CAGGGGGAAT TTTAAGTACA TCCTGTTCCA CTAACACTTG CTTCTTTTCC ATTCTGTTCT 120 TCCTCCTTTT GCTCTCTCCT GCTCACTAAC CCCCCTCACC CCAGCAGAAA AAATAATTGC 180 TACGAGGGCT GAGCCTGAAG ATTTCTTTTT TTTTTTTTCC TTAAAGTGTT GCAAAACCTT 240 AAAACTGTAA GGGAATAACA GCTTTCCCCA CAACACACAA ACACAGCTCT CCTCTGGCAA 300 ACAGGAAACA CTCCCAGGGC TGTGGGCTCC TGAGCCAGGA AATGGGTCTT TGCTGCTCTG 360 GTTACCTTCT CCTCAGGTTC TTCCTGGGCA TTCAATGCAG TTAAAAATAG TAACCACCAA 420 AACCAGAAGA AAAGATGATT TCATTGTCTA ACCGCTGCAA CTTGTGGCCT GATTTGGGTG 480 GTGGCAGAGA GGGAGCTAAT CCTCTGAGTT GGCGCCTTGG GAATTCTCTT AGGGTCGAGC 540 TGGTCCCTGC CCCAGGATTT CAAAACGGGG TATCCCTGAG GAGCCAGCCC AGCTCAGGAG 600 GGCGGCGTGT TAGGCAGAGC CAGCTTACCA CACTCGTGCA CACTGTGGGT GAGGCAGCTG 660 GTGGAAATGC AAGATCTCTC CGTGGCCCAG CCTGTGAGCA GTGCAGGTGG CACACACCCG 720 CCCTGGCTTG GGAAGGCAAG GCTGGGGGCG GAGCCTGTCT GCTATCTGAG CTAGTCATTC 780 CTGCAGTGGT CTGGGTAGTG TGCATCCTCA GCTGGCCCTG GCAGGCATAA GAATTTGTAG 840 AGTATGCTCA GTTCCACTCA GCATAGGGAG CTGTCACAGT GACAGGTACA GAAGGGACCC 900 AGTGGGCTTC TAAGGCTATG TGAAGACAAA GATAGTTTGA GAAGGTACTT TATCGGGGAA 960 CCTGCCCTGA TATTCATGTA GGTTCTTTTC TATTTTCCCT AAGCATTGGC CAGCTTGAGA 1020 AATAAAGGGA CAGAGTACAA AAGAGAGAAA TTTTAAAGCC AGGCGTCTGG GGGAGACATC 1080 ACATGTCTGT 1090
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