| Tag | Content |
|---|
EnhancerAtlas ID | HS095-07843 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:112818620-112819750 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RUNX3 | MA0684.1 | chr12:112818702-112818712 | AAACCGCAAA | + | 6.02 | | ZEB1 | MA0103.3 | chr12:112819608-112819619 | CCCACCTGCCC | + | 6.14 | | ZNF263 | MA0528.1 | chr12:112819553-112819574 | CGAGGAGGGAGGGAGGGAGAG | + | 6.68 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTGCCGTTTC CAGAAACACA CAGTAATGGC TTTTAATTCA TTTCTATAAA TGTTCGTTGT 60
GCGTAAAGCC AAACTGCACG CAAAACCGCA AAACACAAAA GATCCCTCGC ATGCCGTTTA 120
TAGCCAGAAG ATAGGCCATC CTCTCTGCGC CCTACCCCAG AAAGCTCTCC TTACGGCAGT 180
AAAAATTTGA TGACACCCCA TGCTACCTAC ACATCAAAAT GTCATCCCAC AAAGTGGAAG 240
GGGAGCAGTG TCAGCATCCG TTGGCCTCCA TGAAACGACA CTGCCAGTAT TCCCACCTCT 300
AGGCAAACAC GAACCCAAGT GAAGTCGATG GAAAGTTCCC ACCAACCAGG CATATTTGGT 360
TCCCTTCTGC CCCCAAGGCC AAGCAGCTCA ACTGATGAGA TCTGCTGTTG CACCTGCCAC 420
GGCTCTGAAC CCGGGATGCT TGGCGACCCC CGGGGCACAC AAAAAGGCCC TGCGGCCTAA 480
CGCGCCAGTG ACCCTTCCCC GAGAGTGCAT GGAGGGCCGC TGGAGCATCC CTCTCGCTGT 540
CCACAGCGCC CGCTTCCCTG ACAAAGGCCC CGTGTCAATC CATCCGAGAC ACAACACAGA 600
GAAGTTGCTG GATTGCCCAT CGCGGACCCG CAGCTGCCAC TACCCTCTCC CGGAAAAAAA 660
CCAAACCAAA CCAAACAAAA AAAACAGAAC TAGGGAAGAA AAGGATGGGA GGGTACACAG 720
CGTGAAAATC AAAATGTTCC CAAAGCTAAG CAACCTGGGT GTGCCCTGGA AGTGGGTCCT 780
GGGGGCCCGT GGGGGAGGGG AGGGAGGGCC CGGGTGGTGG CGGTGGCTCC TCTGGGGCAT 840
GAAGGCCGAG CCAGGCGCTA GCCTAATAAA ATGCCGGGTG TCGGAACGCT CAAAAGAAAA 900
CCACAAATGA AATCCCCTGC GGGCGCCAGG CCCCGAGGAG GGAGGGAGGG AGAGCGGGGC 960
GGGCGGTCCG CAGACCTGCG GCCGCGGCCC CACCTGCCCG CCCCGCGCCC ACACACACCT 1020
GCCCCGGCAG CCGCCGGGAG GCGAGGCCGC GGCTGAGGCG AGGAGGGGGC CCGACCCGGG 1080
GGTGCCGGGC GAGTGGGTCA GTCCGATGGC GGGGGCCGGG GGCCGCCTCG 1130
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