Tag | Content |
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EnhancerAtlas ID | HS060-28087 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr5:134148380-134149850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-3 | MA0672.1 | chr5:134148727-134148737 | TTCAAGTGGT | - | 6.02 | RUNX1 | MA0002.2 | chr5:134149739-134149750 | TTCTGTGGTTT | + | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 134149600 | 134149729 | chr5 | 134149024 | 134149356 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I134813 | chr5 | 134149050 | 134149720 |
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Enhancer Sequence | CAGTGTCGTA ATCTCAGCTC AACTGCAACC TCTGCCTCCT GGGTTCAAGC GATTTTCCTG 60 TTTCAGCCTC CCTAGTAGCT GGGATTACAG GCACCCACCA CCACGCCCGG CTGATTTTTG 120 TATTTTTAGT AGAGATGGGG TTTCACCATA TTGGCCAGGT TGGTCTCAAA CTCCTGACCT 180 CAGGTGATCC ACCTGCCTTG GCCTCCCATA GTGTTGGGAT TATAGGTGTG AGCCACTGTG 240 CCTGGCCAAT AAAGTCATTT TTTTTTTTTT GAGACGGAGT CTCGCTCTGT CACCAGGCTG 300 GAGTGCAGTG GCTTGATCTT GGCTCACTGC AACCTCTGCC TCTCAGGTTC AAGTGGTTCT 360 CCTGCCTCAG ACTCCCAAGT AACTGGAACG ACAGGCACGC GCCACCATGC TTGGCTAATT 420 TTTTTTGTAT TTTTACTAGA GACAGGGTTT CACCATGTTG GCCAGGATGA TCTTGATCTC 480 TTGACTTCGT GATCCGCCTG CCTCGGCCTC CCAAAGTGCT CAGATTACAG GCGTGAGCCA 540 CCACGCCCGA CCACATTTCA TTTTTTAAAT TTATCTGTTA CCATGTAACA AATCAAAACT 600 TAGCAGGTTA AAGCAATAAA CACTTATTAT CACATAGTTC CTTATGGTCA GGAAATCAGG 660 AGCAGTTTAG TCAGGTAGTT CTGGCTTAGG CGCTCGTGAG ATTGCAGTCA TCTGCAGGCT 720 TGACTGTTGC TGGATGATCT GCTTCCAACA TCAGTCACTT TGATGTAGAT AGGATGCCTC 780 AGTTCTTCAC CTCTTTGCCT GTCCTTACCC ACATGGCAGC TGGCTTTCCC CACAGTGAGT 840 GATCAAAGAG AGCAAAGAGA AAGCTTTAGT GCTTTTTATG ACTGTCTCTG AAATTACACA 900 CTGTCACTTC CACTTTATTC TTTATGGGGT TTTTTTTGTC TTGTTTTGTT TTGTTTTGGA 960 AACAGAGTCT GACTCTGTTG CCCAAACTGG AGTGTAGTGG TGCGAACTCA ACTCACTGCT 1020 GCCTCAGCGA TCTTCCCACC TCAGCCTCTT GAGTAGCTGG TACTATGGGT GCACCACCAT 1080 GCCCTGTTAA TATATATTTT AAAATGTTTT TTTTTTTAGA GTCGAGGTCT CACTGTGTTG 1140 CCTAGGTTGG TCTGAAATTC CTGGGCTCAA GTGATCCTCC TGCCTCAGCC TCCCAAAGTG 1200 ATGGTATTAC AAACATGAGC CACCATGCCC AGCCCACTTT CTTCTATTAG AAGGAAGTCA 1260 TTAAGTCCAG CCCACACTCA AGAAAAAAGA CTATTAAATA ATTTGTAGCC ATGTTTTAAA 1320 AACATCTGTC ACTTTTTGAC ATTATGGTAG TTTCCTCTTT TCTGTGGTTT TAGTTGCCAT 1380 AGGTTAACCA CAGTCTGAAA CTATTACAGT ATTTTGAGAC CACATTCATA TAACTTTTAT 1440 TACAGTATAT TGCTATAATT GTCCTATTTT 1470
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