Tag | Content |
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EnhancerAtlas ID | HS095-08982 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr14:51823240-51824600 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ALX3 | MA0634.1 | chr14:51824450-51824460 | TTTAATTAGA | - | 6.02 | HSF1 | MA0486.2 | chr14:51824116-51824129 | TTCTAGAACTTTC | + | 7.04 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34141 | chr14:51822245-51825005 | HCC1954 |
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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 |
GH14I051355 | chr14 | 51822246 | 51825005 |
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Enhancer Sequence | TCATTTGCTA TTCCTCTCAC AGTAGAGGAA AGCCAAGTGA GTTGCGTAAA TGGAATAATT 60 ACATTTCCTA TTCCTGGGCG ACACATTTGC CAATTCTTTC TTAATAGCAT TAGAGCCAGG 120 CACGGTGGCT CAAGCCTGTA ATCCAAGCAG TTAGGGAGGC TGAGGTGGGA GGGCTTGAGC 180 TCAGGAATTC GAAACCAGCC TGGGCAACAT GGTGAGACCT TGTCTCTACT AAAAATATAG 240 CTGTGCTCAG TGGCACACGC TTGTGGCCCC AGCTACTTGG GAGGCTGAGA TGGAAGGACT 300 GCTTGGGCCT GGAAGGTTGA GGCTGCAGGA GCTGTGATTG TGTCACTGCA CTCCAGACTG 360 CACGGCAGAG CGAGACCCTG CCTCAAAAAA AAAAAAAAAA AAAAAAAGCA TTAGAATAGA 420 TAGATGCAGG AAAACCCCCT GTGTACATGC AAAAGGTAGT AGTTGTTAGC ATAACTTAAA 480 GCATAGATCT CTGGACATAA TGAAAAAGAG GCCGCACTGG TCCACAGATT AGAAAGATAC 540 ATATGTAGAG AAAATGATTT TTGAGCCTCC TTTAAAGATA CTATTCCAAC TTAATTCATA 600 AACATAATGA TAGCATTCCT CACTTACTTT ACAGCTACTT CATCATTTTG TCCCATCTAG 660 AGAAGACTCA TCTCTGATAG GATAACTCTC ATTTATCTCC TGTGTGGCTG GGACTCCCAC 720 CCATAAGCCT ACATAATTAG AGGCCTGCAG GAGATTCACA TTCCTTCTCT TGGTTTGTCT 780 TTTAAAAACT CCCATTTGTT CAGTTTCCCT GGCACATCAT ACATGTTCTT GCCTTCCTTT 840 CCTTCTTCTC AGGCCCCCAG GCCACTACAG CACGTTTTCT AGAACTTTCC TGAGATATAA 900 TGCCTTTATC TAAACACTCT GTGGCTGAGT TCTGGTAAAT AATGACAGGC ATGTGTGGAC 960 TTGTGGGCAG AAGTAGGTTT TGCCTCTGTG CTTTTTCTCA GTGGGAAGCC CAGGAGGCTG 1020 GCCCTGTTTC AACCTCCAGA TCTTTCTTTT TATGAAGATA ATGATGATCA CAGAGTCATA 1080 TTATTGGCCT CCCTGCGGGC ACTCAGAGGC AGCCAGCCCA ACGCTCTCAT GTTTCTTTGC 1140 CTTTCATTTG AAAACAACAT GTAGGGGCAC ATAGACAGGG TCAAGATAAT TTAAAAGAAG 1200 AATTTTTGAA TTTAATTAGA TAATACTTCT TCATAACATA CTTGGTTCAT TTGCACAGGG 1260 TATGGCAGCA TGCAAGGGAC TTCCACATGT ATGATGCTAT ATAGTACTTG AAACATTGGA 1320 GCTGTTTCTT TTCTGATTAT ACAAGTGTTA AAGCAAATGT 1360
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