Tag | Content |
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EnhancerAtlas ID | HS080-17996 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr2:1770190-1771630 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr2:1771393-1771403 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr2:1771393-1771403 | GGCACGTGCC | - | 6.02 | Nr5a2 | MA0505.1 | chr2:1770515-1770530 | GTGTTCAAGGTCAGG | + | 6.83 | ZNF263 | MA0528.1 | chr2:1770875-1770896 | TGAGGAGGGACGGCAGGGAGA | + | 6.26 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 1770800 | 1771620 | chr2 | 1771092 | 1771558 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I001766 | chr2 | 1770361 | 1770550 |
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Enhancer Sequence | TCGTACCAGA GAACCCCGGG ACCTGAACCC AGTGACTAGA GTCCTTTTGA AAAGACGGAA 60 GGCAGAGATG CAGAGGCCAA GGCCATGAGA GGCCGAGGCA GAGGCCTGGC CAGGGGTCTG 120 TGGGATCCCC AGCCACAAGG CCGCTGAAGA GGTCCTGGAG GAAGCATTCT CCCCAGCCTG 180 CAGAGGGAGC AGGGCACGCC CAAGCCCTAC CTTGGACTGC AGGCTTCTGA ACCCTGTAGT 240 TGAAGGCTGT AGTTTGCAGC TCTTTGTTAC AGCAGCCACA GGGAATGCGC CTCCAGCCTG 300 TCTGGAAGTC AGCTCTTCCC ACAGGGTGTT CAAGGTCAGG TGGGCTGCTC CCAGAGGAGC 360 AGGTGCAGGC AGAGACCACA GGCTGCTGGA GGGAAGGGGA TACCCAGCCT TTGCTGAGGC 420 TCTGTCCCAC TTCTGTTTGT CGTATTTTAG CCATTTGGGG TGCACCTAAC CACTGAGCTT 480 ATTCCTTCTC TAGCTCCCTA CCTCCACCAC CCAGACCGTC CCGCTGTGCA GCAGCCAGGC 540 AGCGCCTCTC TTCGGGGCCT CTCCCCCAGT CCCCCTGCTG AGCTCTGGAC ACTCTGGGAT 600 GGACCCCCCG CTCAGATCAG GCAGGGTCTG GGTCAGGCAG GGGCCAGGGG CTTAGCCCGC 660 AGTGGCCTGA GCCCAGGCAG CTCGCTGAGG AGGGACGGCA GGGAGAGACT TGGGTGTCCA 720 CCCTGCCTCA TGGGCTGCTG ACCCTCCCCA CACTCCATCC TGCCCTTCTG CCCTCCTGCC 780 CTGGCTGCCA CCTTGTCCCC TGGACTGGCT CTCAGAACAG CCGAGCACAT GGGGGATGGC 840 CCAGAGGGGT CCCGGCCCCC GACCAGGTAG GCATCTCTGG GTCAGCTGTG CCCCAGGGGG 900 ATGGGTTGAG TCTCAGACCG GCCAGTGCCC CAGGGACCCC TTTCCTTTCA CTTACAGGAG 960 AGTTCCTCTG TCTCACTGCC TGGGGGAAAA ACCAGCTGAG CCCGTCATGC AGATTTTCTA 1020 GGGAGCTGGG CCTGCAGGAG GCCTGGCTTT TGCCCTCTGC TCCTGGGAGG TGACCTCTCG 1080 GCCGGCCCTC AGAATGTCTT GACTAATAAG AGCGTCTTTC TTTACCTGGG GCCGTGGGCC 1140 ACCCTGGAGA GCCGATGCTT ACAGTGTGAC TTGTGGTGGG GCCCAGCCTC AGGCGGACCT 1200 GCAGGCACGT GCCGCACCGG ATCCCCAGAG TCCGAGCCCG CCCCACCCCC CACGCCCTCC 1260 GTGGGGCTGG TGCGGCCTCC CAGGTGCTGG TCCCCCAGCA CTTACCACTA AGCCGCCGCA 1320 CCTGCTTCCT TCTTATTCAC CCTGGCCCTC CCTCTGCCTC TCCACACCAC CAGGCTTGAG 1380 TTAACTCACA CCTCCTTCCT CTGTATCGTC TCTGCAGTAT TTCTCAAATG TACTAAAAAA 1440
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