| Tag | Content |
|---|
EnhancerAtlas ID | HS082-09112 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr12:112818580-112819750 |
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 | TCAAGCACGT CCAAATGTCT CGGCCAATGT GATCCGATCA CTGCCGTTTC CAGAAACACA 60
CAGTAATGGC TTTTAATTCA TTTCTATAAA TGTTCGTTGT GCGTAAAGCC AAACTGCACG 120
CAAAACCGCA AAACACAAAA GATCCCTCGC ATGCCGTTTA TAGCCAGAAG ATAGGCCATC 180
CTCTCTGCGC CCTACCCCAG AAAGCTCTCC TTACGGCAGT AAAAATTTGA TGACACCCCA 240
TGCTACCTAC ACATCAAAAT GTCATCCCAC AAAGTGGAAG GGGAGCAGTG TCAGCATCCG 300
TTGGCCTCCA TGAAACGACA CTGCCAGTAT TCCCACCTCT AGGCAAACAC GAACCCAAGT 360
GAAGTCGATG GAAAGTTCCC ACCAACCAGG CATATTTGGT TCCCTTCTGC CCCCAAGGCC 420
AAGCAGCTCA ACTGATGAGA TCTGCTGTTG CACCTGCCAC GGCTCTGAAC CCGGGATGCT 480
TGGCGACCCC CGGGGCACAC AAAAAGGCCC TGCGGCCTAA CGCGCCAGTG ACCCTTCCCC 540
GAGAGTGCAT GGAGGGCCGC TGGAGCATCC CTCTCGCTGT CCACAGCGCC CGCTTCCCTG 600
ACAAAGGCCC CGTGTCAATC CATCCGAGAC ACAACACAGA GAAGTTGCTG GATTGCCCAT 660
CGCGGACCCG CAGCTGCCAC TACCCTCTCC CGGAAAAAAA CCAAACCAAA CCAAACAAAA 720
AAAACAGAAC TAGGGAAGAA AAGGATGGGA GGGTACACAG CGTGAAAATC AAAATGTTCC 780
CAAAGCTAAG CAACCTGGGT GTGCCCTGGA AGTGGGTCCT GGGGGCCCGT GGGGGAGGGG 840
AGGGAGGGCC CGGGTGGTGG CGGTGGCTCC TCTGGGGCAT GAAGGCCGAG CCAGGCGCTA 900
GCCTAATAAA ATGCCGGGTG TCGGAACGCT CAAAAGAAAA CCACAAATGA AATCCCCTGC 960
GGGCGCCAGG CCCCGAGGAG GGAGGGAGGG AGAGCGGGGC GGGCGGTCCG CAGACCTGCG 1020
GCCGCGGCCC CACCTGCCCG CCCCGCGCCC ACACACACCT GCCCCGGCAG CCGCCGGGAG 1080
GCGAGGCCGC GGCTGAGGCG AGGAGGGGGC CCGACCCGGG GGTGCCGGGC GAGTGGGTCA 1140
GTCCGATGGC GGGGGCCGGG GGCCGCCTCG 1170
|
