| Tag | Content |
|---|
EnhancerAtlas ID | HS129-14980 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr16:88893250-88894580 |
Target genes | | Number: 16 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf12 | MA0742.1 | chr16:88893455-88893470 | GGCCACGCCCTCACT | + | 6.64 | | SP1 | MA0079.4 | chr16:88893453-88893468 | CAGGCCACGCCCTCA | + | 6.04 | | SP4 | MA0685.1 | chr16:88893453-88893470 | CAGGCCACGCCCTCACT | + | 6.1 | | ZNF263 | MA0528.1 | chr16:88893623-88893644 | AGAGGAGCAGGTGGAGAAAAA | + | 6.03 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AACACATGGC AGCAACACGG TCAGGGCACT CTGCACCGAC CCGATGGGGC TGGGGGCCAA 60
TCCCTGGGGG GGCGTGAGCC CCGCTGCCCA GCTGGGTCTA CAGATATGCA TACATGCTCA 120
CACGCCCACA GCAGGGACTG AGCGGGGTCA CAAGGCCTGT GAGAGACAGA GGAGCCTCAA 180
ACCAGGCCCA AAGACCCCAG AGCCAGGCCA CGCCCTCACT CCCTGGCACC CTTCTCTGCC 240
TCTGTGGATC AGATGAAAGG AGAATCACAG CCCTCCCAGG GAGATGCCCC TCCAGGCCCA 300
CCTGTCCGGA GAGGATCAGC CTCGCTCTAA CACTGAATGC CCTAAGGCCA CTGTGAGCCC 360
TGCCCCTTAA GTCAGAGGAG CAGGTGGAGA AAAACCAGAT GTGGAGGGGC AGCTGAGGCT 420
GGACAGGAGC AGCTCCGAGT GGCTGGGGTG GGGACGGCTC CTGACACACC CAGAGAGCTC 480
CAGGACAGGC AGGAGGCTGT CTTTCCCGCC GTGCCTTGAC CTCCGGAGGG CGTGGGCACT 540
GCTGACCAGC CATGAGCAGA GCGTGCCATC TGGCTTCCCT CAGTGGCCCT GTCTGCTTCT 600
TGTTTTTTGT TTTTGTTTTT TGAGATGGAG TTTTGTTCTT GTCACCCAGG CTGGAGTGCA 660
GTGGTGCGAT CTCAGCTCAC CACAACCTCT GCCTTCCAGG TTCAAGTGAT TCTCCTGACT 720
CAGTCTCCCG AGAAGCTGGG ATTACAGGTA TGTGTCACTA CGCCCGGCTA ATTTTGTACT 780
TTTAGTAGAG ACGGGGTTTC TCCATGTTGG TCAGGCTGGT CTCGAACTCC CAACCTCAGG 840
TGATCTGCCC GCCTCAGCCT CCCAAAGTGC TGGGATTACA GGCATGAGCC CGGCGGCCCT 900
GTCTCTTTCT TAACTCGGGG GCTCCAGGCT TGGGTCACTC GACGGGGAGA CTGGGGTGGG 960
GCTGGAGAGA CACCCCTGCC TGGCAAGCTC AGCCCCTGGG GCAGCTGGGC AGGGACCGCC 1020
ATCCGCTGCC AGGCCCTGGA GCTCCCACCC AGTGTCGACA GCCCTCCCCA CGGTCCAGGG 1080
GCACCCTCGC CGCCTGCAGC CAGCTCCTCG CTAGGGCAGA CGGCGATCGC CAGCTTCTCC 1140
AACAGAGGAG CCCTGGCCTC ACAGGGACAC TCACTCCGCG CTGCAGCCGC TCACGGGATG 1200
TGGGGTCTGC AGCGCCCAGT GTGGGGCAGG GAATGCAAAG CTCAGCGTTT GCCAGGAAAG 1260
TTCAGGAAGC TTTGCAGAAG GTGAGAAGCT TCCCCAGGTC TGGTCAGCAG TGTCTGTGCG 1320
ACTGCTTCCC 1330
|
